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Sample records for a-570-892 carbazole violet

  1. 21 CFR 73.3107 - Carbazole violet.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false Carbazole violet. 73.3107 Section 73.3107 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3107 Carbazole violet. (a) Identity. The color additive is carbazole violet (Pigment Violet 23) (CAS Reg. No. 6358-30-1, Colour Index No. 51319). (b)...

  2. 21 CFR 73.3107 - Carbazole violet.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false Carbazole violet. 73.3107 Section 73.3107 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3107 Carbazole violet. (a) Identity. The color additive is carbazole violet (Pigment Violet 23) (CAS Reg. No. 6358-30-1, Colour Index No. 51319). (b)...

  3. 21 CFR 73.3107 - Carbazole violet.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false Carbazole violet. 73.3107 Section 73.3107 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3107 Carbazole violet. (a) Identity. The color additive is carbazole violet (Pigment Violet 23) (CAS Reg. No. 6358-30-1, Colour Index No. 51319). (b)...

  4. 21 CFR 73.3107 - Carbazole violet.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Carbazole violet. 73.3107 Section 73.3107 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3107 Carbazole violet. (a) Identity. The color additive is carbazole violet (Pigment Violet 23) (CAS Reg. No. 6358-30-1, Colour Index No. 51319). (b)...

  5. 21 CFR 73.3107 - Carbazole violet.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false Carbazole violet. 73.3107 Section 73.3107 Food and... ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3107 Carbazole violet. (a) Identity. The color additive is carbazole violet (Pigment Violet 23) (CAS Reg. No. 6358-30-1, Colour Index No. 51319). (b)...

  6. 76 FR 24855 - Carbazole Violet Pigment 23 From India: Rescission of Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-03

    ... Antidumping Duty Order: Carbazole Violet Pigment 23 From India, 69 FR 77988 (December 29, 2004). On January 28... order. See Initiation of Antidumping and Countervailing Duty Administrative Reviews, 76 FR 5137 (January... International Trade Administration Carbazole Violet Pigment 23 From India: Rescission of Administrative...

  7. 75 FR 27815 - Carbazole Violet Pigment 23 From China and India; Determinations

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-18

    ... (74 FR 56663) and determined on February 5, 2010 that it would conduct expedited reviews (75 FR 14468... COMMISSION [Investigation Nos. 701-TA-437 and 731-TA-1060 and 1061 (Review) Carbazole Violet Pigment 23 From... on carbazole violet pigment 23 from India would be likely to lead to continuation or recurrence...

  8. 75 FR 26716 - Carbazole Violet Pigment 23 from India: Extension of Time Limit for Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-12

    ... FR 977 (January 7, 2010). This administrative review covers the period January 1, 2007 through... International Trade Administration Carbazole Violet Pigment 23 from India: Extension of Time Limit for Final... administrative review of the countervailing duty order on carbazole violet pigment 23 (CVP-23) from India....

  9. 75 FR 29718 - Carbazole Violet Pigment 23 From India and the People's Republic of China: Continuation of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-27

    ... Five-Year (``Sunset'') Review, 74 FR 56593 (November 2, 2009); See also Carbazole Violet Pigment 23 From China and India, 74 FR 56663 (November 2, 2009). \\1\\ On December 29, 2004, the Department... 2010). See also Carbazole Violet Pigment 23 from China and India; Determinations, 75 FR 27815 (May...

  10. 75 FR 23239 - Carbazole Violet Pigment 23 From India: Extension of Time Limit for Final Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-03

    ... administrative review of the antidumping duty order on CVP 23 from India. See Carbazole Violet Pigment 23 from India: Preliminary Results of Antidumping Duty Administrative Review, 74 FR 68038 (December 22, 2009... International Trade Administration Carbazole Violet Pigment 23 From India: Extension of Time Limit for...

  11. 75 FR 34699 - Carbazole Violet Pigment 23 from India: Rescission of Countervailing Duty Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-18

    ... Investigation; Opportunity To Request Administrative Review, 74 FR 62743 (December 1, 2009). On December 31... Initiation of Administrative Review, 75 FR 4770 (January 29, 2010). Rescission of Countervailing Duty... International Trade Administration Carbazole Violet Pigment 23 from India: Rescission of Countervailing...

  12. 75 FR 977 - Carbazole Violet Pigment 23 From India: Preliminary Results of Countervailing Duty Administrative...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-01-07

    ... Affirmative Countervailing Duty Determination: Carbazole Violet Pigment 23 From India, 69 FR at 67321. These... Pigment 23 from India, 69 FR 77995 (December 29, 2004) (CVP-23 Order). On December 1, 2008, the Department... Request Administrative Review, 73 FR 72764 (December 1, 2008). On December 30, 2008, the...

  13. 75 FR 38076 - Carbazole Violet Pigment 23 from India: Final Results of Antidumping Duty Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-01

    ... Value and Antidumping Duty Order: Carbazole Violet Pigment 23 From India, 69 FR 77988 (December 29, 2004... Pigment 23 from India: Preliminary Results of Antidumping Duty Administrative Review, 74 FR 68038...: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). The Department intends to issue...

  14. 75 FR 33243 - Carbazole Violet Pigment 23 From India: Final Results of Countervailing Duty Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-11

    ... India: Preliminary Results of Countervailing Duty Administrative Review, 75 FR 977 (January 7, 2010... Administrative Review, 75 FR 26716 (May 12, 2010). Scope of the Order The merchandise covered by this order is... International Trade Administration Carbazole Violet Pigment 23 From India: Final Results of Countervailing...

  15. 75 FR 29719 - Carbazole Violet Pigment 23 From India: Continuation of Countervailing Duty Order

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-27

    .... See Notice of Countervailing Duty Order: Carbazole Violet Pigment 23 From India, 69 FR 77995 (December... (the Act). See Initiation of Five-Year (``Sunset'') Reviews, 74 FR 56593 (November 2, 2009). As a... India: Final Results of the Expedited Five-year (Sunset) Review of the Countervailing Duty Order, 75...

  16. 75 FR 25209 - Carbazole Violet Pigment 23 from India: Rescission of Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-07

    ... in Part, and Deferral of Initiation of Administrative Review, 75 FR 4770 (January 29, 2010... Review, 75 FR 10759 (March 9, 2010). In this notice we indicated that we would be conducting the changed... International Trade Administration A-533-838 Carbazole Violet Pigment 23 from India: Rescission...

  17. 75 FR 13257 - Carbazole Violet Pigment 23 from India: Final Results of the Expedited Five-year (Sunset) Review...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-19

    ...). See Initiation of Five-year (Sunset) Review, 74 FR 56593 (November 2, 2009) (Initiation Notice). On... International Trade Administration Carbazole Violet Pigment 23 from India: Final Results of the Expedited Five... (the Department) initiated a sunset review of the countervailing duty (CVD) order on Carbazole...

  18. 77 FR 1463 - Carbazole Violet Pigment 23 From the People's Republic of China: Final Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-10

    ... Duty Administrative Review, 76 FR 55003 (September 6, 2011) (Preliminary Results). DATES: Effective... People's Republic of China: Rescission of Antidumping Duty Administrative Review, 76 FR 53408 (August 26... International Trade Administration Carbazole Violet Pigment 23 From the People's Republic of China:...

  19. 75 FR 10759 - Carbazole Violet Pigment 23 from India: Initiation of Antidumping Duty Changed-Circumstances Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-09

    ... and Antidumping Duty Order: Carbazole Violet Pigment 23 From India, 69 FR 77988 (December 29, 2004... Order, Finding, or Suspended Investigation; Opportunity To Request Administrative Review, 74 FR 62743... Revocation in Part, and Deferral of Initiation of Administrative Review, 75 FR 4770 (January 29, 2010)....

  20. 75 FR 12497 - Carbazole Violet Pigment 23 from India and the People's Republic of China: Final Results of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-16

    ... China, 69 FR 77987 (December 29, 2004); Notice of Amended Final Determination of Sales at Less Than Fair Value and Antidumping Duty Order: Carbazole Violet Pigment 23 From India, 69 FR 77988 (December 29, 2004... 1930, as amended (the Act). See Initiation of Five-Year (``Sunset'') Review, 74 FR 56593 (November...

  1. 75 FR 62765 - Carbazole Violet Pigment 23 From India: Final Results of Antidumping Duty Changed-Circumstances...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-13

    ...-Circumstances Review, 75 FR 52930 (August 30, 2010). Although we gave interested parties an opportunity to... Antidumping Duty Administrative Review, 75 FR 38076 (July 1, 2010). Notification This notice serves as a... International Trade Administration Carbazole Violet Pigment 23 From India: Final Results of Antidumping...

  2. 75 FR 25840 - Carbazole Violet Pigment 23 from the People's Republic of China: Extension of Time Limit for the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-10

    ... Antidumping Duty Administrative Review, 74 FR 68780 (December 29, 2009) (Preliminary Results). The final... the Tariff Act of 1930, As Amended, 70 FR 24533 (May 10, 2005). This notice is published in accordance... International Trade Administration Carbazole Violet Pigment 23 from the People's Republic of China: Extension...

  3. 77 FR 38767 - Notice of Scope Rulings

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-06-29

    ... Rulings, 77 FR 32568 (June 1, 2012). This current notice covers all scope rulings and anticircumvention.... Multiple Countries A-533-838/C-533-839/A-570-892: Carbazole Violet Pigment 23 from India and the People's Republic of China Requestor: Nation Ford Chemical Co. and Sun Chemical Corp.; finished carbazole...

  4. 75 FR 74682 - Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation; Opportunity To...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-01

    ...: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003), the Department has clarified its practice with... Mushrooms A-337-804 12/1/09-11/30/10 India: Carbazole Violet Pigment 23 A-533-838 12/1/09-11/30/10 Certain.... 12/1/09-11/30/10 The People's Republic of China: Carbazole Violet Pigment 23 A-570-892...

  5. Synthesis and blue-violet two-photon excited fluorescence of a new organoboron compound

    NASA Astrophysics Data System (ADS)

    Cao, Duxia; Liu, Zhiqiang; Li, Guozhong; Liu, Guoqun; Zhang, Guohui

    2008-02-01

    A new A-π-D-π-A type organoboron compound, 3,6-bis(dimesitylboryl)- N-butyl-carbazole (abbreviated as BBC), with trivalent boron as electron acceptor and carbazole as electron donor and π-conjugated core, has been synthesized and its single and two-photon related photophysical properties experimentally investigated. Pumped by 720 nm laser pulses in femtosecond regime, it showed strong two-photon excited blue-violet fluorescence at 393 nm in toluene and 403 nm in THF. The measured two-photon absorption cross-section by two-photon fluorescence method in toluene and THF is 34 GM and 38 GM, respectively.

  6. Method for metabolizing carbazole in petroleum

    DOEpatents

    Kayser, Kevin J.; Kilbane, II, John J.

    2005-09-13

    A method for selective cleavage of C--N bonds genes that encode for at least one enzyme suitable for conversion of carbazole to 2-aminobiphenyl-2,3-diol are combined with a gene encoding an amidase suitable for selectively cleaving a C--N bond in 2-aminobiphenyl-2,3-diol, forming an operon that encodes for cleavage of both C--N bonds of said carbazole. The operon is inserted into a host culture which, in turn, is contacted with the carbazole, resulting in selective cleavage of both C--N bonds of the carbazole. Also disclosed is a new microorganism that expresses a carbazole degradation trait constitutively and a method for degrading carbazole employing this microorganism.

  7. Carbazole incorporated ratiometric chemosensor for Zn2+

    NASA Astrophysics Data System (ADS)

    Helal, Aasif; Kim, Hong-Seok

    2013-03-01

    An electron donating carbazole incorporated thiazole (3) based Zn2+ selective intrinsic chemosensor has been synthesized and investigated. It was found that electron donating substituents such as methyl and carbazole on chemosensor (1) produce remarkable red shift in emission upon complexation with Zn2+. The sensor shows a selective fluorescence response with Zn2+ over biologically relevant cations (Ca2+, Mg2+, Na+, and K+) and biologically non-relevant cations (Cd2+, In3+ and Ga3+) in an aqueous ethanol system. It also produce an enhancement in the quantum yield and a longer emission wavelength shift on Zn2+ binding with the potential of a ratiometric assay.

  8. Tetracyclo(2,7-carbazole)s: Diatropicity and Paratropicity of Inner Regions of Nanohoops.

    PubMed

    Kuroda, Yasuhiro; Sakamoto, Youichi; Suzuki, Toshiyasu; Kayahara, Eiichi; Yamago, Shigeru

    2016-04-15

    Three N-substituted tetracyclo(2,7-carbazole)s were synthesized to investigate the inner regions of nanohoops. One compound has a 5,5-dimethylnonane bridge between two neighboring anti-carbazoles, which can be used as covalently bonded "methane probes". These probes near the ring center are strongly shielded by local ring currents and exhibit a singlet at δ = -2.70 ppm in (1)H NMR. To visualize local and macrocyclic ring currents separately, we drew nucleus-independent chemical shift contour maps of tetracyclo(9-methyl-2,7-carbazole) and [n]cycloparaphenylenes (CPPs). Local ring currents make the interior diatropic, and paratropic regions exist only outside the ring. Macrocyclic ring currents in [5]CPP to [7]CPP generate deshielding cones, which are typical of antiaromatic [4n]annulenes. PMID:27015266

  9. Electrochemically Induced Synthesis of Poly(2,6-carbazole).

    PubMed

    Laba, Katarzyna; Data, Przemyslaw; Zassowski, Pawel; Karon, Krzysztof; Lapkowski, Mieczyslaw; Wagner, Pawel; Officer, David L; Wallace, Gordon G

    2015-10-01

    The formation of a poly(2,6-carbazole) derivative during an electrochemical polymerization process is shown. Comparison of 3,5-bis(9-octyl-9H-carbazol-2-yl)pyridine and 3,5-bis(9-octyl-9H-carbazol-3-yl)pyridine by electrochemical and UV-Vis-NIR spectroelectrochemical measurements and DFT (density functional theory) calculation prove the formation of a poly(2,6-carbazole) derivative. Both of the compounds form stable and electroactive conjugated polymers.

  10. 27 CFR 21.111 - Gentian violet.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2014-04-01 2014-04-01 false Gentian violet. 21.111 Section 21.111 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT....111 Gentian violet. (a) Gentian violet (methyl violet, methylrosaniline chloride) occurs as a...

  11. 27 CFR 21.111 - Gentian violet.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2011-04-01 2011-04-01 false Gentian violet. 21.111 Section 21.111 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT....111 Gentian violet. (a) Gentian violet (methyl violet, methylrosaniline chloride) occurs as a...

  12. 27 CFR 21.111 - Gentian violet.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2013-04-01 2013-04-01 false Gentian violet. 21.111 Section 21.111 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT....111 Gentian violet. (a) Gentian violet (methyl violet, methylrosaniline chloride) occurs as a...

  13. 27 CFR 21.111 - Gentian violet.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2012-04-01 2012-04-01 false Gentian violet. 21.111 Section 21.111 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT....111 Gentian violet. (a) Gentian violet (methyl violet, methylrosaniline chloride) occurs as a...

  14. 27 CFR 21.111 - Gentian violet.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Gentian violet. 21.111 Section 21.111 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT....111 Gentian violet. (a) Gentian violet (methyl violet, methylrosaniline chloride) occurs as a...

  15. Thermodynamics of the hydrodenitrogenation of carbazole

    SciTech Connect

    Steele, W.V.; Chirico, R.D.

    1991-10-01

    A thermodynamic analysis, based on accurate experimental Gibbs energies of formation, was completed for the key hydrogen-consuming steps in the HDN reaction network for carbazole. The results were compared with literature reaction studies. The concept of crossover temperature'' is shown to be a valuable tool in the interpretation of literature reaction-study results. Methods of nitrogen removal from aromatic materials are discussed in light of the findings of the thermodynamic analysis. It is concluded that the removal of nitrogen from heterocyclic aromatic nitrogen-containing compounds with conventional hydrodesulfurization catalysts, temperatures, and hydrogen pressures occurs under thermodynamic control'' with unavoidably high hydrogen consumption. The report also concludes that to reduce hydrogen consumption in the HDN of carbazole, pathways via 1,2,3,4a,9a-hexahydrocarbazole must be followed. Conditions under which these processes are possible are discussed. 36 refs., 9 figs.

  16. 75 FR 52930 - Carbazole Violet Pigment 23 From India: Preliminary Results of Antidumping Duty Changed...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-30

    ... Review, 75 FR 10759 (March 9, 2010) (Initiation). In this notice we indicated that we would conduct the...: Rescission of Administrative Review, 75 FR 25209 (May 7, 2010). In the notice we indicated that, in... within 270 days after the date on which we initiated the changed-circumstances review.'' See 75 FR...

  17. 75 FR 14468 - Carbazole Violet Pigment 23 From China and India

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-25

    ... to its notice of institution (74 FR 56663 November 2, 2009) of the subject five-year reviews was... section 201.8 of the Commission's rules, as amended, 67 FR 68036 (November 8, 2002). Even where electronic... (C) of the Commission's Handbook on Electronic Filing Procedures, 67 FR 68168, 68173 (November...

  18. 1-Nitro-9H-carbazole

    PubMed Central

    Kautny, Paul; Stöger, Berthold

    2014-01-01

    In the title mol­ecule, C12H8N2O2, the nitro group is tilted slightly with respect to the carbazole moiety [angle between the least-squares planes = 4.43 (9)°]. In the crystal, the mol­ecules are connected via pairs of N—H⋯O hydrogen bonds into dimers with -1 symmetry. The dimers in turn are arranged into layers parallel to (10-1). PMID:24526975

  19. Final report on the safety assessment of Basic Violet 1, Basic Violet 3, and Basic Violet 4.

    PubMed

    Diamante, Catherine; Bergfeld, Wilma F; Belsito, Donald V; Klaassen, Curtis D; Marks, James G; Shank, Ronald C; Slaga, Thomas J; Snyder, Paul W; Alan Andersen, F

    2009-01-01

    Basic Violet 3, Basic Violet 1, and Basic Violet 4 are triphenylmethane dyes that function as direct (nonoxidative) hair colorants. No current uses or use concentrations in cosmetics are reported. The term Gentian Violet is used synonymously with Basic Violet 1 and Basic Violet 3, although the chemical structures of these 2 dyes are not the same. The Cosmetic Ingredient Review Expert Panel noted that Basic Violet 1, 3, and 4 contain quaternary ammonium ions, and therefore the rate of penetration across the epidermis is expected to be slow. The panel concluded that because of the carcinogenic potential of these dyes, insufficient data exist to support the safety of Basic Violet 1, 3, and 4 in cosmetic formulation. Dermal absorption data and a risk assessment are needed to complete this safety assessment. PMID:20086192

  20. Carbazole hydroxylation by the filamentous fungi of the Cunninghamella species.

    PubMed

    Zawadzka, K; Bernat, P; Felczak, A; Lisowska, K

    2015-12-01

    Nitrogen heterocyclic compounds, especially carbazole, quinolone, and pyridine are common types of environmental pollutants. Carbazole has a toxic influence on living organisms, and the knowledge of its persistence and bioconversion in ecosystems is still not complete. There is an increasing interest in detoxification of hazardous xenobiotics by microorganisms. In this study, the ability of three filamentous fungi of the Cunninghamella species to eliminate carbazole was evaluated. The Cunninghamella elegans IM 1785/21Gp and Cunninghamella echinulata IM 2611 strains efficiently removed carbazole. The IM 1785/21Gp and IM 2611 strains converted 93 and 82 % of the initial concentration of the xenobiotic (200 mg L(-1)) after 120 h incubation. 2-Hydroxycarbazole was for the first time identified as a carbazole metabolite formed by the filamentous fungi of the Cunninghamella species. There was no increase in the toxicity of the postculture extracts toward Artemia franciscana. Moreover, we showed an influence of carbazole on the phospholipid composition of the cells of the tested filamentous fungi, which indicated its harmful effect on the fungal cell membrane. The most significant modification of phospholipid levels after the cultivation of filamentous fungi with the addition of carbazole was showed for IM 1785/21Gp strain.

  1. 21 CFR 589.1000 - Gentian violet.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Gentian violet. 589.1000 Section 589.1000 Food and... Substances Prohibited From Use in Animal Food or Feed § 589.1000 Gentian violet. The Food and Drug Administration has determined that gentian violet has not been shown by adequate scientific data to be safe...

  2. 21 CFR 589.1000 - Gentian violet.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Gentian violet. 589.1000 Section 589.1000 Food and... Substances Prohibited From Use in Animal Food or Feed § 589.1000 Gentian violet. The Food and Drug Administration has determined that gentian violet has not been shown by adequate scientific data to be safe...

  3. 21 CFR 589.1000 - Gentian violet.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Gentian violet. 589.1000 Section 589.1000 Food and... Substances Prohibited From Use in Animal Food or Feed § 589.1000 Gentian violet. The Food and Drug Administration has determined that gentian violet has not been shown by adequate scientific data to be safe...

  4. 21 CFR 589.1000 - Gentian violet.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Gentian violet. 589.1000 Section 589.1000 Food and... Substances Prohibited From Use in Animal Food or Feed § 589.1000 Gentian violet. The Food and Drug Administration has determined that gentian violet has not been shown by adequate scientific data to be safe...

  5. 21 CFR 589.1000 - Gentian violet.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Gentian violet. 589.1000 Section 589.1000 Food and... Substances Prohibited From Use in Animal Food or Feed § 589.1000 Gentian violet. The Food and Drug Administration has determined that gentian violet has not been shown by adequate scientific data to be safe...

  6. Antitumoral activity of trisubstituted dihydrobenzo(a)carbazoles. Part III.

    PubMed

    Segall, A; Pizzorno, M T

    2000-10-01

    Two recently synthesized, trisubstituted dihydrobenzo(a)carbazoles were investigated regarding their anti-HIV and antitumoral activity. The compounds showed some activity against melanoma, renal cancer and breast cancer cell lines.

  7. Carbazole degradation in the soil microcosm by tropical bacterial strains

    PubMed Central

    Salam, Lateef B.; Ilori, Matthew O.; Amund, Olukayode O.

    2015-01-01

    In a previous study, three bacterial strains isolated from tropical hydrocarbon-contaminated soils and phylogenetically identified as Achromobacter sp. strain SL1, Pseudomonas sp. strain SL4 and Microbacterium esteraromaticum strain SL6 displayed angular dioxygenation and mineralization of carbazole in batch cultures. In this study, the ability of these isolates to survive and enhance carbazole degradation in soil were tested in field-moist microcosms. Strain SL4 had the highest survival rate (1.8 x 107 cfu/g) after 30 days of incubation in sterilized soil, while there was a decrease in population density in native (unsterilized) soil when compared with the initial population. Gas chromatographic analysis after 30 days of incubation showed that in sterilized soil amended with carbazole (100 mg/kg), 66.96, 82.15 and 68.54% were degraded by strains SL1, SL4 and SL6, respectively, with rates of degradation of 0.093, 0.114 and 0.095 mg kg−1 h−1. The combination of the three isolates as inoculum in sterilized soil degraded 87.13% carbazole at a rate of 0.121 mg kg−1 h−1. In native soil amended with carbazole (100 mg/kg), 91.64, 87.29 and 89.13% were degraded by strains SL1, SL4 and SL6 after 30 days of incubation, with rates of degradation of 0.127, 0.121 and 0.124 mg kg−1 h−1, respectively. This study successfully established the survivability (> 106 cfu/g detected after 30 days) and carbazole-degrading ability of these bacterial strains in soil, and highlights the potential of these isolates as seed for the bioremediation of carbazole-impacted environments. PMID:26691461

  8. Carbazole degradation in the soil microcosm by tropical bacterial strains.

    PubMed

    Salam, Lateef B; Ilori, Matthew O; Amund, Olukayode O

    2015-01-01

    In a previous study, three bacterial strains isolated from tropical hydrocarbon-contaminated soils and phylogenetically identified as Achromobacter sp. strain SL1, Pseudomonas sp. strain SL4 and Microbacterium esteraromaticum strain SL6 displayed angular dioxygenation and mineralization of carbazole in batch cultures. In this study, the ability of these isolates to survive and enhance carbazole degradation in soil were tested in field-moist microcosms. Strain SL4 had the highest survival rate (1.8 x 107 cfu/g) after 30 days of incubation in sterilized soil, while there was a decrease in population density in native (unsterilized) soil when compared with the initial population. Gas chromatographic analysis after 30 days of incubation showed that in sterilized soil amended with carbazole (100 mg/kg), 66.96, 82.15 and 68.54% were degraded by strains SL1, SL4 and SL6, respectively, with rates of degradation of 0.093, 0.114 and 0.095 mg kg-1 h-1. The combination of the three isolates as inoculum in sterilized soil degraded 87.13% carbazole at a rate of 0.121 mg kg-1 h-1. In native soil amended with carbazole (100 mg/kg), 91.64, 87.29 and 89.13% were degraded by strains SL1, SL4 and SL6 after 30 days of incubation, with rates of degradation of 0.127, 0.121 and 0.124 mg kg-1 h-1, respectively. This study successfully established the survivability (> 106 cfu/g detected after 30 days) and carbazole-degrading ability of these bacterial strains in soil, and highlights the potential of these isolates as seed for the bioremediation of carbazole-impacted environments.

  9. Microgap ultra-violet detector

    DOEpatents

    Wuest, Craig R.; Bionta, Richard M.

    1994-01-01

    A microgap ultra-violet detector of photons with wavelengths less than 400 run (4000 Angstroms) which comprises an anode and a cathode separated by a gas-filled gap and having an electric field placed across the gap. Either the anode or the cathode is semi-transparent to UV light. Upon a UV photon striking the cathode an electron is expelled and accelerated across the gap by the electric field causing interactions with other electrons to create an electron avalanche which contacts the anode. The electron avalanche is detected and converted to an output pulse.

  10. Microgap ultra-violet detector

    DOEpatents

    Wuest, C.R.; Bionta, R.M.

    1994-09-20

    A microgap ultra-violet detector of photons with wavelengths less than 400 run (4,000 Angstroms) which comprises an anode and a cathode separated by a gas-filled gap and having an electric field placed across the gap is disclosed. Either the anode or the cathode is semi-transparent to UV light. Upon a UV photon striking the cathode an electron is expelled and accelerated across the gap by the electric field causing interactions with other electrons to create an electron avalanche which contacts the anode. The electron avalanche is detected and converted to an output pulse. 2 figs.

  11. Synthesis and characterizations of carbazole-isoindigo-carbazole oligomers for photovoltaic application

    NASA Astrophysics Data System (ADS)

    Lee, Ji-Young; Lee, Song-Mi; Lee, Soo-Hyoung; Kim, Dong-Hee; Lee, Sang Hee; Lee, Youn-Sik

    2016-08-01

    6,6‧-Dibromo-N,N‧-(2-octyldodecanyl)isoindigo was coupled to either 4-(N-carbazolyl)phenyl boronic acid or 9-phenyl-9H-carbazole-3-boronic acid to give two different conjugated molecules of P-II-P and C-II-C, respectively. The optical band gap/HOMO levels of P-II-P and C-II-C were 1.90/-5.60 eV and 1.85/-5.39 eV, respectively. Based on the experimental and calculation data, C-II-C is more highly conjugated than P-II-P. The performances of C-II-C-based photovoltaic devices were better than those of P-II-P-based devices, with the best power conversion efficiency of 0.44%.

  12. Synthesis and investigation of carbazoles and fluorenes containing tetrathiafulvalene core

    NASA Astrophysics Data System (ADS)

    Abashev, George G.; Shklyaeva, Elena V.; Syutkin, Roman V.; Lebedev, Konstantin Yu.; Osorgina, Irina V.; Romanova, Valentina A.; Bushueva, Anastasya Yu.

    2008-12-01

    For the first time carbazole- and fluorene-based monomers containing tetrathiafulvalene moieties were prepared. All the synthesized monomers were electrochemically polymerized in CH 3CN (CH 2Cl 2) media using (C 2H 5)N 4ClO 4 (1:1) as the supporting electrolyte. The properties of the resulting polymers were characterized by cyclic voltammetry (CV).

  13. Dame Sheila Patricia Violet Sherlock.

    PubMed

    Pepys, Mark

    2003-01-01

    Dame Sheila Patricia Violet Beckett Sherlock was the world's leading female physician-scientist of the twentieth century. Her brilliant, wide-ranging, original contributions to the investigation, diagnosis, classification, epidemiology, pathogenesis and management of liver disease played a leading role in the establishment of hematology as a medical specialty. Her rigorous, highly focused, studies combined experimental and laboratory investigations with meticulous clinical observation, encompassed most aspects of liver function, disease and treatment, and led directly to enormous benefit for millions of patients. Her remarkable individual personality also had a profound influence not only on her medical and scientific specialty but also on several generations of physicians throughout the world. She was the first female professor of medicine and head of a department of medicine in the UK, and the pioneer of women in modern medicine. The importance of her contributions to knowledge and her massive influence on training in and the practice of medicine related to liver disease were recognized by a glittering array of honours and awards from professional societies and academic institutions throughout the world, including 19 honorary degrees, and, very belatedly, election to Fellowship of The Royal Society in the last year of her life.

  14. Ultra violet disinfection: A 3-year history

    SciTech Connect

    Tubesing, R.R.; Lindeke, D.R.

    1998-07-01

    The Stillwater Wastewater Treatment Facility is one of nine wastewater treatment facilities operated by the Metropolitan Council Environmental Services in the Minneapolis-St. Paul Metropolitan Area. The facility services the cities of Stillwater, Oak Park Heights, and Bayport. In 1993, an ultra violet disinfection facility began operation to provide the disinfection for the Facility. This presentation discusses the reasons for using ultra violet disinfection in lieu of chlorination/dechlorination facilities, the operating performance, and operating cost factors.

  15. Biodegradation of crystal violet by Agrobacterium radiobacter.

    PubMed

    Parshetti, G K; Parshetti, S G; Telke, A A; Kalyani, D C; Doong, R A; Govindwar, S P

    2011-01-01

    Agrobacterium radiobacter MTCC 8161 completely decolorized the Crystal Violet with 8 hr (10 mg/L) at static anoxic conditions. The decreased decolorization capability by A. radiobacter was observed, when the Crystal Violet concentration was increased from 10 to 100 mg/L. Semi-synthetic medium containing 1% yeast extract and 0.1% NH4C1 has shown 100% decolorization of Crystal Violet within 5 hr. A complete degradation of Crystal Violet by A. radiobacter was observed up to 7 cycles of repeated addition (10 mg/L). When the effect of increasing inoculum concentration on decolorization of Crystal Violet (100 mg/L) was studied, maximum decolorization was observed with 15% inoculum concentration. A significant increase in the activities of laccase (184%) and aminopyrine N-demethylase (300%) in cells obtained after decolorization indicated the involvement of these enzymes in decolorization process. The intermediates formed during the degradation of Crystal Violet were analyzed by gas chromatography and mass spectroscopy (GC/MS). It was detected the presence of N,N,N',N"-tetramethylpararosaniline, [N, N-dimethylaminophenyl] [N-methylaminophenyl] benzophenone, N, N-dimethylaminobenzaldehyde, 4-methyl amino phenol and phenol. We proposed the hypothetical metabolic pathway of Crystal Violet biodegradation by A. radiobacter. Phytotoxicity and microbial toxicity study showed that Crystal Violet biodegradation metabolites were less toxic to bacteria (A. radiobacter, P. aurugenosa and A. vinelandii) contributing to soil fertility and for four kinds of plants (Sorghum bicolor Vigna radiata, Lens culinaris and Triticum aestivum) which are most sensitive, fast growing and commonly used in Indian agriculture.

  16. 76 FR 55003 - Carbazole Violet Pigment 23 From the People's Republic of China: Preliminary Intent To Rescind...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-06

    ... Republic of China, 69 FR 77987 (December 29, 2004) (the Order). On December 1, 2010, the Department... FR 74682 (December 1, 2010). On January 3, 2011, the Department received a timely request for... Administrative Reviews, 76 FR 5137 (January 28, 2011). Also on January 28, 2011, the Department requested...

  17. 75 FR 36630 - Carbazole Violet Pigment 23 from the People's Republic of China: Final Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-28

    ... Administrative Review, 74 FR ] 68780 (December 29, 2009) (Preliminary Results). This administrative review covers...: Extension of Time Limit for the Final Results of Antidumping Duty Administrative Review, 75 FR 25840 (May 10... Chloranil Comment 6. Surrogate Value for Benzene Sulfonyl Chloride BILLING CODE 3510-DS-S...

  18. Optical writing and reading with a photoactivatable carbazole.

    PubMed

    Garcia-Amorós, Jaume; Swaminathan, Subramani; Zhang, Yang; Nonell, Santi; Raymo, Françisco M

    2015-05-01

    The fluorescence of a carbazole chromophore can be activated irreversibly under optical control with the photoinduced opening of an oxazine ring. In proximity to silver nanoparticles, the quantum efficiency of this photochemical transformation and that of the emissive process increase significantly. The plasmonic effects responsible for such enhancements, together with the photochemical and photophysical properties engineered into this particular photoactivatable fluorophore, permit the optical writing and reading of microscaled patterns at low illumination intensities.

  19. Bioactive carbazole alkaloids from the stems of Clausena lansium.

    PubMed

    Du, Yi-Qian; Liu, Hang; Li, Chuang-Jun; Ma, Jie; Zhang, Dan; Li, Li; Sun, Hua; Bao, Xiu-Qi; Zhang, Dong-Ming

    2015-06-01

    Seven new carbazole alkaloids, claulansines L-R (1-7), and six known analogues (8-13) were isolated from the stems of Clausena lansium. Their structures were elucidated on the basis of spectroscopic analyses, including UV, IR, and NMR experiments (HSQC, HMBC, and NOE experiment). Compound 7 showed moderate anti-inflammatory activities. Compounds 3, 5, 6, 8, and 12 exhibited moderate hepatoprotective activities. PMID:25804252

  20. Carbazole and amide alkaloids from the stems of Clausena lansium.

    PubMed

    Du, Yi-Qian; Liu, Hang; Li, Chuang-Jun; Yang, Jing-Zhi; Ma, Jie; Zhang, Dan; Sun, Hua; Zhang, Dong-Ming

    2015-01-01

    Two new carbazole alkaloids, claulansine S (1) and claulansine T (2), and one new amide alkaloid, clauamide A (3), together with four known analogues (4-7) were isolated from the stems of Clausena lansium. Their structures were elucidated on the basis of spectroscopic analyses, including UV, IR, and NMR experiments (HSQC, HMBC, and NOE experiments). Compounds 4 and 6 showed moderate hepatoprotective activities. PMID:26095884

  1. Liquid organic hydrogen carriers: surface science studies of carbazole derivatives.

    PubMed

    Papp, Christian; Wasserscheid, Peter; Libuda, Jörg; Steinrück, Hans-Peter

    2014-10-01

    We review recent results towards a molecular understanding of the adsorption and dehydrogenation of carbazole-derived liquid organic hydrogen carriers on platinum and palladium single crystals and on Al2 O3 -supported Pt and Pd nanoparticles. By combining synchrotron-based high-resolution X-ray photoelectron spectroscopy, infrared reflection-absorption spectroscopy, advanced molecular beam methods and temperature-programmed desorption spectroscopy, detailed insights into the reaction mechanism are obtained. On Pt(111), dehydrogenation of perhydro-N-ethylcarbazole, H12 -NEC, starts with activation of the hydrogen atoms at the pyrrole unit, yielding H8 -NEC as the first stable reaction intermediate at ∼340 K, followed by further dehydrogenation to NEC at ∼380 K. Above 390 K, dealkylation starts, yielding carbazole as an undesired byproduct. On small supported Pt particles, the dealkylation sets in at lower temperatures, due to the higher reactivity of low-coordinated sites, while on larger particles with (111) facets a reactivity as on the flat surface is observed. Carbazole derivatives with ethyl, propyl and butyl chains show an overall very similar reactivity, both on Pt(111) and on Pt nanoparticles. When comparing the dealkylation behavior of H12 -NEC on Pt(111) and Pt nanoparticles to that on Pd(111) and Pd nanoparticles, we find a higher reactivity for the Pd systems.

  2. 21 CFR 73.2775 - Manganese violet.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... pyrophosphate complex having the approximate formula: Mn(III)NH4P2O7. (b) Specifications. Manganese violet shall.... Mercury (as Hg), not more than 1 part per million. Total color, based on Mn content in “as is” sample,...

  3. 21 CFR 73.2775 - Manganese violet.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... pyrophosphate complex having the approximate formula: Mn(III)NH4P2O7. (b) Specifications. Manganese violet shall.... Mercury (as Hg), not more than 1 part per million. Total color, based on Mn content in “as is” sample,...

  4. 21 CFR 73.2775 - Manganese violet.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... pyrophosphate complex having the approximate formula: Mn(III)NH4P2O7. (b) Specifications. Manganese violet shall.... Mercury (as Hg), not more than 1 part per million. Total color, based on Mn content in “as is” sample,...

  5. 21 CFR 73.2775 - Manganese violet.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... pyrophosphate complex having the approximate formula: Mn(III)NH4P2O7. (b) Specifications. Manganese violet shall.... Mercury (as Hg), not more than 1 part per million. Total color, based on Mn content in “as is” sample,...

  6. 21 CFR 73.2775 - Manganese violet.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... pyrophosphate complex having the approximate formula: Mn(III)NH4P2O7. (b) Specifications. Manganese violet shall.... Mercury (as Hg), not more than 1 part per million. Total color, based on Mn content in “as is” sample,...

  7. Discovery of novel N-substituted carbazoles as neuroprotective agents with potent anti-oxidative activity.

    PubMed

    Zhu, Daqian; Chen, Meihui; Li, Min; Luo, Bingling; Zhao, Yang; Huang, Peng; Xue, Fengtian; Rapposelli, Simona; Pi, Rongbiao; Wen, Shijun

    2013-10-01

    Carbazole moiety is an important scaffold with a variety of biological applications, for example, anti-oxidative stress. Our previous synthesized carbazoles were screened for their neuroprotective properties against two individual oxidative stresses. Some of the new carbazole derivatives were observed with modest to good neuroprotective effects on neuronal cells HT22 against cell injury induced by glutamate or homocysteic acid (HCA). Substituents introduced to the carbazole ring system play crucial roles in their biological activities. In particular, a bulky group favors the neuroprotective activity of the compounds. One of the new compounds, 6, showed the best neuroprotective effects, which might result from its anti-oxidative activity with a GSH-independent mechanism. These findings might provide an alternative strategy for the development of novel carbazole derivatives for the treatment of CNS diseases such as Alzheimer's disease.

  8. Holographic Optical Elements Using Polyvinyl Carbazole Holographic Material

    NASA Astrophysics Data System (ADS)

    Matsumoto, K.; Kuwayamo, T.; Taniguchi, N.

    1986-06-01

    We developed a new holographic material: polyvinyl carbazore material. The advantage or the material over conventional DCC material is that it has high durability against humidity and transparency. Some optical properties of the material and some applications are presented. We have already installed the holographic display element using polyvinyl carbazole in a commercialized 8mm movie camera. The letters "END" are displayed on an imaging plane of the finder system by using an image plane hologram. We also present the holographic lens of which aberration is well corrected at laser diode wavelength. We made this holographic lens using a new aberration correcting method.

  9. Adsorption kinetics of methyl violet onto perlite.

    PubMed

    Doğan, Mehmet; Alkan, Mahir

    2003-01-01

    This study examines adsorption kinetics and activation parameters of methyl violet on perlite. The effect of process parameters like contact time, concentration of dye, temperature and pH on the extent of methyl violet adsorption from solution has been investigated. Results of the kinetic studies show that the adsorption reaction is first order with respect to dye solution concentration with activation energy of 13.2 kJ mol(-1). This low activation energy value indicates that the adsorption reaction is diffusion controlled. The activation parameters using Arrhenius and Eyring equations have been calculated. Adsorption increases with increase of variables such as contact time, initial dye concentration, temperature and pH.

  10. Indigenous and enhanced mineralization of pyrene, benzo[a]pyrene, and carbazole in soils.

    PubMed Central

    Grosser, R J; Warshawsky, D; Vestal, J R

    1991-01-01

    We studied the mineralization of pyrene, carbazole, and benzo[a]pyrene in soils obtained from three abandoned coal gasification plants in southern Illinois. The soils had different histories of past exposure to hydrocarbon contamination and different amounts of total organic carbon, microbial biomass, and microbial activity. Mineralization was measured by using serum bottle radiorespirometry. The levels of indigenous mineralization of 14C-labeled compounds ranged from 10 to 48% for pyrene, from undetectable to 46% for carbazole, and from undetectable to 25% for benzo[a]pyrene following long-term (greater than 180-day) incubations. Pyrene and carbazole were degraded with short or no lag periods in all soils, but benzo[a]pyrene mineralization occurred after a 28-day lag period. Mineralization was not dependent on high levels of microbial biomass and activity in the soils. Bacterial cultures that were capable of degrading pyrene and carbazole were isolated by enrichment, grown in pure culture, and reintroduced into soils. Reintroduction of a pyrene-degrading bacterium enhanced mineralization to a level of 55% within 2 days, compared with a level of 1% for the indigenous population. The carbazole degrader enhanced mineralization to a level of 45% after 7 days in a soil that showed little indigenous carbazole mineralization. The pyrene and carbazole degraders which we isolated were identified as a Mycobacterium sp. and a Xanthamonas sp., respectively. Our results indicated that mineralization of aromatic hydrocarbons can be significantly enhanced by reintroducing isolated polycyclic aromatic hydrocarbon-degrading bacteria. PMID:1785924

  11. Indigenous and enhanced mineralization of pyrene, benzo(a)pyrene, and carbazole in soils

    SciTech Connect

    Grosser, R.J.; Warshawsky, D.; Vestal, J.R. )

    1991-12-01

    The authors studied the mineralization of pyrene, carbazole, and benzo(a)pyrene in soils obtained from three abandoned coal gasification plants in southern Illinois. The soils had different histories of past exposure to hydrocarbon contamination and different amounts of total organic carbon, microbial biomass, and microbial activity. Mineralization was measured by using serum bottle radiorespirometry. The levels of indigenous mineralization of {sup 14}C-labeled compounds ranged from 10 to 48% for pyrene, from undetectable to 46% for carbazole, and from undetectable to 25% for benzo(a)pyrene following long-term (<180-day) incubations. Pyrene and carbazole were degraded with short or no lag periods in all soils, but benzo(a)pyrene mineralization occurred after a 28-day lag period. Mineralization was not dependent on high levels of microbial biomass and activity in the soils. Bacterial cultures that were capable of degrading pyrene and carbazole were isolated by enrichment, grown in pure culture, and reintroduced into soils. Reintroduction of a pyrene-degrading bacterium enhanced mineralization to a level of 55% within 2 days, compared with a level of 1% for the indigenous population. The carbazole degrader enhanced mineralization to a level of 45% after 7 days in a soil that showed little indigenous carbazole mineralization. The pyrene and carbazole degraders which they isolated were identified as a Mycobacterium sp. and Xanthamonas sp., respectively.

  12. Micropropagation of African violet (Saintpaulia ionantha Wendl.).

    PubMed

    Shukla, Mukund; Sullivan, J Alan; Jain, Shri Mohan; Murch, Susan J; Saxena, Praveen K

    2013-01-01

    Micropropagation is an important tool for rapid multiplication and the creation of genetic variability in African violets (Saintpaulia ionantha Wendl.). Successful in vitro propagation depends on the specific requirements and precise manipulation of various factors such as the type of explants used, physiological state of the mother plant, plant growth regulators in the culture medium, and growth conditions. Development of cost-effective protocols with a high rate of multiplication is a crucial requirement for commercial application of micropropagation. The current chapter describes an optimized protocol for micropropagation of African violets using leaf explants obtained from in vitro grown plants. In this process, plant regeneration occurs via both somatic embryogenesis and shoot organogenesis simultaneously in the explants induced with the growth regulator thidiazuron (TDZ; N-phenyl-N'-1,2,3-thidiazol-5-ylurea). The protocol is simple, rapid, and efficient for large-scale propagation of African violet and the dual routes of regeneration allow for multiple applications of the technology from simple clonal propagation to induction or selection of variants to the production of synthetic seeds.

  13. Micropropagation of African violet (Saintpaulia ionantha Wendl.).

    PubMed

    Shukla, Mukund; Sullivan, J Alan; Jain, Shri Mohan; Murch, Susan J; Saxena, Praveen K

    2013-01-01

    Micropropagation is an important tool for rapid multiplication and the creation of genetic variability in African violets (Saintpaulia ionantha Wendl.). Successful in vitro propagation depends on the specific requirements and precise manipulation of various factors such as the type of explants used, physiological state of the mother plant, plant growth regulators in the culture medium, and growth conditions. Development of cost-effective protocols with a high rate of multiplication is a crucial requirement for commercial application of micropropagation. The current chapter describes an optimized protocol for micropropagation of African violets using leaf explants obtained from in vitro grown plants. In this process, plant regeneration occurs via both somatic embryogenesis and shoot organogenesis simultaneously in the explants induced with the growth regulator thidiazuron (TDZ; N-phenyl-N'-1,2,3-thidiazol-5-ylurea). The protocol is simple, rapid, and efficient for large-scale propagation of African violet and the dual routes of regeneration allow for multiple applications of the technology from simple clonal propagation to induction or selection of variants to the production of synthetic seeds. PMID:23179707

  14. Synthesis of Carbazole Alkaloids by Ring-Closing Metathesis and Ring Rearrangement-Aromatization.

    PubMed

    Dhara, Kalyan; Mandal, Tirtha; Das, Joydeb; Dash, Jyotirmayee

    2015-12-21

    Aprocess for the assembly of carbazole alkaloids has been developed on the basis of ring-closing metathesis (RCM) and ringrearrangement-aromatization (RRA) as the key steps. This method is based on allyl Grignard addition to isatin derivatives to provide smooth access to 2,2-diallyl 3-oxindole derivatives through a 1,2-allyl shift. The diallyl derivatives were used as RCM precursors to afford a novel class of spirocyclopentene-3-oxindole derivatives, which underwent a novel RRA reaction to afford carbazole derivatives. The synthetic sequence to carbazoles was shortened by combining the RCM and RRA steps in an orthogonal tandem catalytic process. The utility of this methodology was further demonstrated by the straightforward synthesis of carbazole alkaloids, including amukonal derivative, girinimbilol, heptaphylline, and bis(2-hydroxy-3-methylcarbazole).

  15. Novel Carbazole (Cbz)-Based Carboxylated Functional Monomers: Design, Synthesis, and Characterization

    PubMed Central

    Mondal, Ejabul; Lellouche, Jean-Paul; Naddaka, Maria

    2015-01-01

    A series of novel functional carbazole (Cbz)-based carboxylated monomers were synthesized and characterized. A Clauson-Kaas procedure, a deprotection step, amide coupling, and hydrolysis were utilized as key chemical reactions towards the multistep synthesis of monomers in good to excellent isolated yields. The design strategy was further extended to complex carbazole-COOH monomers incorporated arylazo groups as photoreactive moieties. In addition, photoreactive hybrid carbazole (Cbz)-pyrrole (Pyr)-based carboxylated monomers, comprising a pyrrole core linking a carbazole and a photoreactive phenylazide or benzophenone moiety through an amide spacer in the molecular structure, were also synthesized. The latter can be utilized for surface modification of polymeric films in their monomeric form or as polymeric microparticles (MPs). PMID:26478845

  16. Nitrogen Oxide Inhibitory Trimeric and Dimeric Carbazole Alkaloids from Murraya tetramera.

    PubMed

    Lv, Hai-Ning; Wen, Ran; Zhou, Ying; Zeng, Ke-Wu; Li, Jun; Guo, Xiao-Yu; Tu, Peng-Fei; Jiang, Yong

    2015-10-23

    Two new structurally unique trimeric carbazole alkaloids, murratrines A and B (1, 2), and 11 new carbazole dimers, murradines A-K (3-13), and four known analogues (14-17) were isolated from the leaves and stems of Murraya tetramera. The structures and relative configurations of 1-13 were elucidated on the basis of comprehensive 1D and 2D NMR spectroscopy, high-resolution mass spectrometry, and electronic circular dichroism (ECD) data analysis. Murratrines A and B (1, 2) both contain an unprecedented carbazole trimeric skeleton, and murradines A and D (3, 6) are the first natural C-1-C-3'-methyl-linked and C-6-C-3'-methyl-linked dimeric carbazole alkaloids, respectively. Compounds 4, 10, 14, 15, and 17 exhibited inhibition of nitric oxide production stimulated by lipopolysaccharide in BV-2 microglial cells with IC50 values in the range of 11.2-19.3 μM.

  17. Synthesis of Carbazole Alkaloids by Ring-Closing Metathesis and Ring Rearrangement-Aromatization.

    PubMed

    Dhara, Kalyan; Mandal, Tirtha; Das, Joydeb; Dash, Jyotirmayee

    2015-12-21

    Aprocess for the assembly of carbazole alkaloids has been developed on the basis of ring-closing metathesis (RCM) and ringrearrangement-aromatization (RRA) as the key steps. This method is based on allyl Grignard addition to isatin derivatives to provide smooth access to 2,2-diallyl 3-oxindole derivatives through a 1,2-allyl shift. The diallyl derivatives were used as RCM precursors to afford a novel class of spirocyclopentene-3-oxindole derivatives, which underwent a novel RRA reaction to afford carbazole derivatives. The synthetic sequence to carbazoles was shortened by combining the RCM and RRA steps in an orthogonal tandem catalytic process. The utility of this methodology was further demonstrated by the straightforward synthesis of carbazole alkaloids, including amukonal derivative, girinimbilol, heptaphylline, and bis(2-hydroxy-3-methylcarbazole). PMID:26768698

  18. Copper-Catalyzed Oxidative C-H Amination of Tetrahydrofuran with Indole/Carbazole Derivatives.

    PubMed

    Yang, Qingjing; Choy, Pui Ying; Fu, Wai Chung; Fan, Baomin; Kwong, Fuk Yee

    2015-11-01

    A simple α-C-H amination of cyclic ether with indole/carbazole derivatives has been accomplished by employing copper(II) chloride/bipy as the catalyst system. In the presence of the di-tert-butyl peroxide oxidant, cyclic ethers such as tetrahydrofuran, 1,4-dioxane, and tetrahydropyran successfully undergo C-H/N-H cross dehydrogenative coupling (CDC) with various carbazole or indole derivatives in good-to-excellent yields. PMID:26485515

  19. Synthesis of substituted indoline and carbazole by benzyne-mediated cyclization-functionalization.

    PubMed

    Noji, Toshiharu; Fujiwara, Hideto; Okano, Kentaro; Tokuyama, Hidetoshi

    2013-04-19

    A benzyne-mediated synthesis of substituted indolines and carbazoles was developed. The reaction includes generation of benzyne using Mg(TMP)2·2LiCl as a base, cyclization, and trapping the resulting organomagnesium intermediate with an electrophile to provide a series of substituted indolines and carbazoles in a regiospecific manner. This was applied to a concise five-pot total synthesis of heptaphylline.

  20. Characterization and Biological Potency of Mono- to Tetra-Halogenated Carbazoles.

    PubMed

    Riddell, Nicole; Jin, Un-Ho; Safe, Stephen; Cheng, Yating; Chittim, Brock; Konstantinov, Alex; Parette, Robert; Pena-Abaurrea, Miren; Reiner, Eric J; Poirier, David; Stefanac, Tomislav; McAlees, Alan J; McCrindle, Robert

    2015-09-01

    This paper deals with the characterization and aryl hydrocarbon receptor (AhR) agonist activities of a series of chlorinated, brominated, and mixed bromo/chlorocarbazoles, some of which have been identified in various environmental samples. Attention is directed here to the possibility that halogenated carbazoles may currently be emitted into the environment as a result of the production of carbazole-containing polymers present in a wide variety of electronic devices. We have found that any carbazole that is not substituted in the 1,3,6,8 positions may be lost during cleanup of environmental extracts if a multilayer column is utilized, as is common practice for polychlorinated dibenzo-p-dioxin (dioxin) and related compounds. In the present study, (1)H NMR spectral shift data for 11 relevant halogenated carbazoles are reported, along with their gas chromatographic separation and analysis by mass spectrometry. These characterization data allow for confident structural assignments and the derivation of possible correlations between structure and toxicity based on the halogenation patterns of the isomers investigated. Some halogenated carbazoles exhibit characteristics of persistent organic pollutants and their potential dioxin-like activity was further investigated. The structure-dependent induction of CYP1A1 and CYP1B1 gene expression in Ah-responsive MDA-MB-468 breast cancer cells by these carbazoles was similar to that observed for other dioxin-like compounds, and the magnitude of the fold induction responses for the most active halogenated carbazoles was similar to that observed for 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). 2,3,6,7-Tetrachlorocarbazole was one of the most active halogenated carbazoles and, like TCDD, contains 4 lateral substituents; however, the estimated relative effect potency for this compound (compared to TCDD) was 0.0001 and 0.0032, based on induction of CYP1A1 and CYP1B1 mRNA, respectively.

  1. Carbazole is a naturally occurring inhibitor of angiogenesis and inflammation isolated from antipsoriatic coal tar

    SciTech Connect

    Jack L. Arbiser; Baskaran Govindarajan; Traci E. Battle; Rebecca Lynch; David A. Frank; Masuko Ushio-Fukai; Betsy N. Perry; David F. Stern; G. Tim Bowden; Anquan Liu; Eva Klein; Pawel J. Kolodziejski; N. Tony Eissa; Chowdhury F. Hossain; Dale G. Nagle

    2006-06-15

    Coal tar is one of the oldest and an effective treatment for psoriasis. Coal tar has been directly applied to the skin, or used in combination with UV light as part of the Goeckerman treatment. The use of coal tar has caused long-term remissions in psoriasis, but has fallen out of favor because the treatment requires hospitalization and coal tar is poorly acceptable aesthetically to patients. Thus, determining the active antipsoriatic component of coal tar is of considerable therapeutic interest. We fractionated coal tar into its components, and tested them using the SVR angiogenesis inhibitor assay. Treatment of SVR endothelial cells with coal tar fractions resulted in the isolation of a single fraction with antiangiogenic activity. The active antiangiogenic compound in coal tar is carbazole. In addition to antiangiogenic activity, carbazole inhibited the production of inflammatory IL-15 by human mononuclear cells. IL-15 is elevated in psoriasis and is thought to contribute to psoriatic inflammation. Carbazole treatment also reduced activity of inducible nitric oxide synthase (iNOS), which is proinflammatory and elevated in psoriasis. The effect of carbazole on upstream pathways in human psoriasis was determined, and carbazole was shown to inhibit signal transducer and activator of transcription (stat)3-mediated transcription, which has been shown to be relevant in human psoriasis. IL-15, iNOS, and stat3 activation require the activation of the small GTPase rac for optimal activity. Carbazole was found to inhibit rac activation as a mechanism for its inhibition of downstream inflammatory and angiogenic pathways. Given its antiangiogenic and anti-inflammatory activities, carbazole is likely a major component of the antipsoriatic activity of coal tar. Carbazole and derivatives may be useful in the therapy of human psoriasis.

  2. [Environmental Behaviors and Ecotoxicology of the Emerging Contaminants Polyhalogenated Carbazoles].

    PubMed

    Lin, Kun-de; Chen, Yan-qiu; Yuan, Dong-xing

    2016-04-15

    Polyhalogenated carbazoles (PHCs), with a complex chemical structure similar to polychlorinated dibenzofurans, are a class of emerging environmental organic contaminants. There are 135 congeners for PHCs with a pure halogenation. Most of PHCs are not man-made products. Although PHCs in the environment were firstly discovered in the 1980s, these emerging halogenated compounds were not seriously considered until recent years. Recently, more than 20 PHCs have been detected in sediment and soil samples. In addition, studies have shown that PHCs exhibited dioxin-like toxicity and were persistent and bioaccumulative. Therefore, it is very important to understand the distribution, origins and ecotoxicology of PHCs for a better assessment of their environmental risks. To date, research on the environmental behaviors of PHCs is relatively limited and warrants further investigations. In this review, the environmental distribution, source, analytical methods and toxicity of PHCs were summarized and future research needs were outlined.

  3. Oegylated and cross-linking carbazole dendrons and dendrimers: Synthesis, characterization, assembly and thin film fabrication

    NASA Astrophysics Data System (ADS)

    Felipe, Mary Jane Legaspi

    2011-12-01

    Dendrimers and dendrons (fractional dendrimers) are macromolecular structures that have well-defined molecular weights and precise number of functional groups. Tailoring these structures has provided designer molecules that can be used for various applications including drug delivery, sensors, and anti-biofouling surfaces. Overall, this dissertation provides novel protocols for the understanding of molecular design, synthesis, and structure-property relationship of OEGylated and conjugated carbazole dendrons and dendrimers. In this design, the use of oligo(ethylene glycol) (OEG) allows for the fabrication of biocompatible materials and imparts hydrophilicity on the structure while the carbazole functionality allows the cross-linking of these designer molecules. Such fine-tuning of macromolecular structures leading to the fabrication of anti-biofouling thin films, nanostructuring at the air-water interface, and assembly into supramolecular superstructures are considered in this dissertation. Chapter 2 details the synthesis, characterization, and electrochemical cross-linking of OEGylated linear dendrons and "Janus-type" dendrimers. Cross-linking the carbazole moieties enables the deposition of these films on Au, indium tin oxide-coated glass, and doped silicon through cyclic voltammetry and provides films with secondary level of organization imparted by the inter- and intra-molecular interaction among the carbazole units. Chapter 3 describes the fabrication of nonspecific protein adsorption resistant surfaces through electrochemical grafting of three different dendrons on SAM carbazole-coated gold substrates. The predictable shape of each dendron and the ability to cross-link the carbazole units have enabled parametrization of OEG conformation and density on these interfaces. Chapter 4 demonstrates the fundamental architectural requirements for obtaining stable films with OEGylated linear dendron molecules providing a new architectural design of nanostructuring

  4. Biodegradation of methyl violet by Pseudomonas mendocina MCM B-402.

    PubMed

    Sarnaik, S; Kanekar, P

    1999-08-01

    Pseudomonas mendocina MCM B-402 was found to utilize a triphenylmethane dye, methyl violet as the sole source of carbon when incorporated in synthetic medium. Almost complete decolorization of methyl violet by P. mendocina was observed within 48 h of incubation at ambient temperature (28 +/- 2 degrees C) under aerated culture conditions, when the bacteria were inoculated into Davis Mingioli's synthetic medium at a concentration of 100 mg/l medium. Methyl violet was mineralized to CO2 through three unknown intermediate metabolites and phenol. The decolorization of the dye involved demethylation.

  5. Identification of alkyl carbazoles and alkyl benzocarbazoles in Brazilian petroleum derivatives.

    PubMed

    Oliveira, Eniz Conceição; Vaz de Campos, Maria Cecília; Rodrigues, Maria Regina Alves; Pérez, Valéria Flores; Melecchi, Maria Inês Soares; Vale, Maria Goreti Rodrigues; Zini, Cláudia Alcaraz; Caramão, Elina Bastos

    2006-02-10

    Carbozoles are important compounds in crude oils, as they may be used as geochemical tracers, being the major type of nitrogen compounds in petroleum. At the same time, they are regarded as undesirable due to the problems they may cause in the refining process, such as catalyst poisoning, corrosion, gum or color formation in final products. As separation and identification of carbazoles are challenging goals, this work presents a chromatographic method, made of a pre-fractionation on neutral alumina followed by the separation and identification of two classes of carbazoles using FeCl(3)/Chromossorb W and gas chromatograph with mass spectrometer (GC/MS) (SIM-single ion monitoring mode) analysis. For the first time, a series of alkyl carbazoles and alkyl benzocarbazoles were identified in heavy gas oil (HGO) and atmospheric residue of distillation (ARD) obtained from Brazilian petroleum.

  6. Persistence and dioxin-like toxicity of carbazole and chlorocarbazoles in soil.

    PubMed

    Mumbo, John; Henkelmann, Bernhard; Abdelaziz, Ahmed; Pfister, Gerd; Nguyen, Nghia; Schroll, Reiner; Munch, Jean Charles; Schramm, Karl-Werner

    2015-01-01

    Halogenated carbazoles have recently been detected in soil and water samples, but their environmental effects and fate are unknown. Eighty-four soil samples obtained from a site with no recorded history of pollution were used to assess the persistence and dioxin-like toxicity of carbazole and chlorocarbazoles in soil under controlled conditions for 15 months. Soil samples were divided into two temperature conditions, 15 and 20 °C, both under fluctuating soil moisture conditions comprising 19 and 44 drying-rewetting cycles, respectively. This was characterized by natural water loss by evaporation and rewetting to -15 kPa. Accelerated solvent extraction (ASE) and cleanup were performed after incubation. Identification and quantification were done using high-resolution gas chromatogram/mass spectrometer (HRGC/MS), while dioxin-like toxicity was determined by ethoxyresorufin-O-deethylase (EROD) induction in H4IIA rat hepatoma cells assay and multidimensional quantitative structure-activity relationships (mQSAR) modelling. Carbazole, 3-chlorocarbazole and 3,6-dichlorocarbazole were detected including trichlorocarbazole not previously reported in soils. Carbazole and 3-chlorocarbazole showed significant dissipation at 15 °C but not at 20 °C incubating conditions indicating that low temperature could be suitable for dissipation of carbazole and chlorocarbazoles. 3,6-Dichlorocarbazole was resistant at both conditions. Trichlorocarbazole however exhibited a tendency to increase in concentration with time. 3-Chlorocarbazole, 3,6-dibromocarbazole and selected soil extracts exhibited EROD activity. Dioxin-like toxicity did not decrease significantly with time, whereas the sum chlorocarbazole toxic equivalence concentrations (∑TEQ) did not contribute significantly to the soil assay dioxin-like toxicity equivalent concentrations (TCDD-EQ). Carbazole and chlorocarbazoles are persistent with the latter also toxic in natural conditions. PMID:25142342

  7. Persistence and dioxin-like toxicity of carbazole and chlorocarbazoles in soil.

    PubMed

    Mumbo, John; Henkelmann, Bernhard; Abdelaziz, Ahmed; Pfister, Gerd; Nguyen, Nghia; Schroll, Reiner; Munch, Jean Charles; Schramm, Karl-Werner

    2015-01-01

    Halogenated carbazoles have recently been detected in soil and water samples, but their environmental effects and fate are unknown. Eighty-four soil samples obtained from a site with no recorded history of pollution were used to assess the persistence and dioxin-like toxicity of carbazole and chlorocarbazoles in soil under controlled conditions for 15 months. Soil samples were divided into two temperature conditions, 15 and 20 °C, both under fluctuating soil moisture conditions comprising 19 and 44 drying-rewetting cycles, respectively. This was characterized by natural water loss by evaporation and rewetting to -15 kPa. Accelerated solvent extraction (ASE) and cleanup were performed after incubation. Identification and quantification were done using high-resolution gas chromatogram/mass spectrometer (HRGC/MS), while dioxin-like toxicity was determined by ethoxyresorufin-O-deethylase (EROD) induction in H4IIA rat hepatoma cells assay and multidimensional quantitative structure-activity relationships (mQSAR) modelling. Carbazole, 3-chlorocarbazole and 3,6-dichlorocarbazole were detected including trichlorocarbazole not previously reported in soils. Carbazole and 3-chlorocarbazole showed significant dissipation at 15 °C but not at 20 °C incubating conditions indicating that low temperature could be suitable for dissipation of carbazole and chlorocarbazoles. 3,6-Dichlorocarbazole was resistant at both conditions. Trichlorocarbazole however exhibited a tendency to increase in concentration with time. 3-Chlorocarbazole, 3,6-dibromocarbazole and selected soil extracts exhibited EROD activity. Dioxin-like toxicity did not decrease significantly with time, whereas the sum chlorocarbazole toxic equivalence concentrations (∑TEQ) did not contribute significantly to the soil assay dioxin-like toxicity equivalent concentrations (TCDD-EQ). Carbazole and chlorocarbazoles are persistent with the latter also toxic in natural conditions.

  8. Carbazole angular dioxygenation and mineralization by bacteria isolated from hydrocarbon-contaminated tropical African soil.

    PubMed

    Salam, L B; Ilori, M O; Amund, O O; Numata, M; Horisaki, T; Nojiri, H

    2014-01-01

    Four bacterial strains isolated from hydrocarbon-contaminated soils in Lagos, Nigeria, displayed extensive degradation abilities on carbazole, an N-heterocyclic aromatic hydrocarbon. Physicochemical analyses of the sampling sites (ACPP, MWO, NESU) indicate gross pollution of the soils with a high hydrocarbon content (157,067.9 mg/kg) and presence of heavy metals. Phylogenetic analysis of the four strains indicated that they were identified as Achromobacter sp. strain SL1, Pseudomonas sp. strain SL4, Microbacterium esteraromaticum strain SL6, and Stenotrophomonas maltophilia strain BA. The rates of degradation of carbazole by the four isolates during 30 days of incubation were 0.057, 0.062, 0.036, and 0.050 mg L(-1) h(-1) for strains SL1, SL4, SL6, and BA. Gas chromatographic (GC) analyses of residual carbazole after 30 days of incubation revealed that 81.3, 85, 64.4, and 76 % of 50 mg l(-1) carbazole were degraded by strains SL1, SL4, SL6, and BA, respectively. GC-mass spectrometry and high-performance liquid chromatographic analyses of the extracts from the growing and resting cells of strains SL1, SL4, and SL6 cultured on carbazole showed detection of anthranilic acid and catechol while these metabolites were not detected in strain BA under the same conditions. This study has established for the first time carbazole angular dioxygenation and mineralization by isolates from African environment.

  9. Venus in Violet and Near Infrared Light

    NASA Technical Reports Server (NTRS)

    1990-01-01

    These images of the Venus clouds were taken by Galileo's Solid State Imaging System February 13,1990, at a range of about 1 million miles. The smallest detail visible is about 20 miles. The two right images show Venus in violet light, the top one at a time six hours later than the bottom one. They show the state of the clouds near the top of Venus's cloud deck. A right to left motion of the cloud features is evident and is consistent with westward winds of about 230 mph. The two left images show Venus in near infrared light, at the same times as the two right images. Sunlight penetrates through the clouds more deeply at the near infrared wavelengths, allowing a view near the bottom of the cloud deck. The westward motion of the clouds is slower (about 150 mph) at the lower altitude. The clouds are composed of sulfuric acid droplets and occupy a range of altitudes from 30 to 45 miles. The images have been spatially filtered to bring out small scale details and de-emphasize global shading. The filtering has introduced artifacts (wiggly lines running north/south) that are faintly visible in the infrared image. The Galileo Project is managed for NASA's Office of Space Science and Applications by the Jet Propulsion Laboratory; its mission is to study Jupiter and its satellites and magnetosphere after multiple gravity assist flybys at Venus and Earth.

  10. Removal of methyl violet from aqueous solution by perlite.

    PubMed

    Doğan, Mehmet; Alkan, Mahir

    2003-11-01

    The use of perlite for the removal of methyl violet from aqueous solutions at different concentration, pH, and temperature has been investigated. Adsorption equilibrium is reached within 1 h. The capacity of perlite samples for the adsorption of methyl violet was found to increase with increasing pH and temperature and decrease with expansion and increasing acid-activation. The adsorption isotherms are described by means of the Langmuir and Freundlich isotherms. The adsorption isotherm was measured experimentally at different conditions and the experimental data were correlated reasonably well by the adsorption isotherm of Langmuir. The order of heat of adsorption corresponds to a physical reaction. It is concluded that the methyl violet is physically adsorbed onto the perlite. The removal efficiency (P) and dimensionless separation factor (R) have shown that perlite can be used for removal of methyl violet from aqueous solutions, but unexpanded perlite is more effective.

  11. Orthogonally Substituted Benzimidazole-Carbazole Benzene As Universal Hosts for Phosphorescent Organic Light-Emitting Diodes.

    PubMed

    Huang, Jau-Jiun; Hung, Yu-Hsiang; Ting, Pei-Ling; Tsai, Yu-Ning; Gao, Huan-Jie; Chiu, Tien-Lung; Lee, Jiun-Haw; Chen, Chi-Lin; Chou, Pi-Tai; Leung, Man-kit

    2016-02-19

    The novel ambipolar hosts of o-CbzBz and o-DiCbzBz contain carbazole and benzimidazole through an ortho-connection. The orthogonal conformations cause the triplet state to be confined at the carbazole units to secure efficient energy transfer. The phosphorescent organic light-emitting diodes (PhOLEDs) show a high current efficiency, power efficiency, and low efficiency roll-off. o-DiCbzBz can be used as a host for sky-blue, green, and orange-red PhOLEDs, giving 57.5, 78.4, and 60.3 cd/A, respectively. PMID:26829339

  12. Metallophyte status of violets of the section Melanium.

    PubMed

    Hermann, Bothe; Katarina, Vogel-Mikuš; Paula, Pongrac; Matevž, Likar; Neva, Stepic; Primož, Pelicon; Primož, Vavpetič; Luka, Jeromel; Marjana, Regvar

    2013-11-01

    Violets from metal-enriched soils have controversially been described as both heavy-metal accumulators and excluders in the literature. The present study solves the issue for violets of the section Melanium (zinc violets, Viola lutea ssp. calaminaria and V. lutea ssp. westfalica; hartsease or wild pansy, Viola tricolor; and mountain pansy, V. lutea). The aims were to determine the concentrations of heavy metals in the soil and in the roots and shoots of field-collected plants, to evaluate the potential impact of colonisation by arbuscular mycorrhizal fungi on heavy-metal concentrations in the plant tissues, and to quantitatively define the localisation of the elements in root cross-sections. When these violets grow in low-metal soils, higher concentrations of the heavy metals were found in the roots and shoots than in the soil, whereas the opposite was seen in samples from high-metal soils. Under all field conditions examined, the roots of all of these species were colonised by arbuscular mycorrhizal fungi. However, V. tricolor was marginally colonised when the concentrations of Zn and P were higher in the soil. Determination of the spatial distribution of the elements in root cross-sections of these violets indicates tissue-specific deposition of elements within the vascular tissue, the cortex, and the rhizodermis. These data indicate that violets of the section Melanium are heavy-metal excluders.

  13. Tuning Coordination in s-Block Carbazol-9-yl Complexes

    PubMed Central

    Ortu, Fabrizio; Moxey, Graeme J; Blake, Alexander J; Lewis, William; Kays, Deborah L

    2015-01-01

    1,3,6,8-Tetra-tert-butylcarbazol-9-yl and 1,8-diaryl-3,6-di(tert-butyl)carbazol-9-yl ligands have been utilized in the synthesis of potassium and magnesium complexes. The potassium complexes (1,3,6,8-tBu4carb)K(THF)4 (1; carb=C12H4N), [(1,8-Xyl2-3,6-tBu2carb)K(THF)]2 (2; Xyl=3,5-Me2C6H3) and (1,8-Mes2-3,6-tBu2carb)K(THF)2 (3; Mes=2,4,6-Me3C6H2) were reacted with MgI2 to give the Hauser bases 1,3,6,8-tBu4carbMgI(THF)2 (4) and 1,8-Ar2-3,6-tBu2carbMgI(THF) (Ar=Xyl 5, Ar=Mes 6). Structural investigations of the potassium and magnesium derivatives highlight significant differences in the coordination motifs, which depend on the nature of the 1- and 8-substituents: 1,8-di(tert-butyl)-substituted ligands gave π-type compounds (1 and 4), in which the carbazolyl ligand acts as a multi-hapto donor, with the metal cations positioned below the coordination plane in a half-sandwich conformation, whereas the use of 1,8-diaryl substituted ligands gave σ-type complexes (2 and 6). Space-filling diagrams and percent buried volume calculations indicated that aryl-substituted carbazolyl ligands offer a steric cleft better suited to stabilization of low-coordinate magnesium complexes. PMID:25783772

  14. Tuning coordination in s-block carbazol-9-yl complexes.

    PubMed

    Ortu, Fabrizio; Moxey, Graeme J; Blake, Alexander J; Lewis, William; Kays, Deborah L

    2015-04-27

    1,3,6,8-Tetra-tert-butylcarbazol-9-yl and 1,8-diaryl-3,6-di(tert-butyl)carbazol-9-yl ligands have been utilized in the synthesis of potassium and magnesium complexes. The potassium complexes (1,3,6,8-tBu4carb)K(THF)4 (1; carb = C12H4N), [(1,8-Xyl2-3,6-tBu2carb)K(THF)]2 (2; Xyl = 3,5-Me2C6H3) and (1,8-Mes2-3,6-tBu2carb)K(THF)2 (3; Mes = 2,4,6-Me3C6H2) were reacted with MgI2 to give the Hauser bases 1,3,6,8-tBu4carbMgI(THF)2 (4) and 1,8-Ar2-3,6-tBu2carbMgI(THF) (Ar = Xyl 5, Ar = Mes 6). Structural investigations of the potassium and magnesium derivatives highlight significant differences in the coordination motifs, which depend on the nature of the 1- and 8-substituents: 1,8-di(tert-butyl)-substituted ligands gave π-type compounds (1 and 4), in which the carbazolyl ligand acts as a multi-hapto donor, with the metal cations positioned below the coordination plane in a half-sandwich conformation, whereas the use of 1,8-diaryl substituted ligands gave σ-type complexes (2 and 6). Space-filling diagrams and percent buried volume calculations indicated that aryl-substituted carbazolyl ligands offer a steric cleft better suited to stabilization of low-coordinate magnesium complexes. PMID:25783772

  15. Facile preparation of stable palygorskite/methyl violet@SiO2 "Maya Violet" pigment.

    PubMed

    Zhang, Yujie; Zhang, Junping; Wang, Aiqin

    2015-11-01

    Maya Blue pigment has attracted considerable attention owing to their extraordinary stability. The growing interest in this field has largely expanded the study of Maya Blue-like pigments. Inspired by Maya Blue, a stable palygorskite/methyl violet@SiO2 (PAL/MV@SiO2) "Maya Violet" pigment was fabricated via adsorption of MV by PAL, and then deposition of a layer of SiO2 on the surface by polycondensation of tetraethoxysilane (TEOS) in the presence of cetyltrimethylammonium bromide (CTAB). The weight ratio of MV to PAL is as high as 10%. The pigments were characterized by scanning electron microscopy and a variety of analytical techniques, e.g., Fourier Transform infrared spectroscopy and zeta potential. The results indicate that MV molecules are fixed onto the exterior surface, the grooves and at the entrances of the channels of PAL. The PAL/MV@SiO2 pigment shows excellent stability against chemical attacks, e.g., 0.1 M HCl, 0.1 M NaOH and various organic solvents. Different from Maya Blue, grinding and heating treatment are virtually ineffective in improving stability of the PAL/MV pigment. CTAB and the SiO2 layer formed on the surface of PAL/MV contribute greatly to the improved stability of the pigment due to shielding effect. The optimal CTAB/TEOS/ammonia/H2O molar ratio for the surface modification of PAL/MV is 0.24/1/2.89/495. PMID:26196708

  16. Facile preparation of stable palygorskite/methyl violet@SiO2 "Maya Violet" pigment.

    PubMed

    Zhang, Yujie; Zhang, Junping; Wang, Aiqin

    2015-11-01

    Maya Blue pigment has attracted considerable attention owing to their extraordinary stability. The growing interest in this field has largely expanded the study of Maya Blue-like pigments. Inspired by Maya Blue, a stable palygorskite/methyl violet@SiO2 (PAL/MV@SiO2) "Maya Violet" pigment was fabricated via adsorption of MV by PAL, and then deposition of a layer of SiO2 on the surface by polycondensation of tetraethoxysilane (TEOS) in the presence of cetyltrimethylammonium bromide (CTAB). The weight ratio of MV to PAL is as high as 10%. The pigments were characterized by scanning electron microscopy and a variety of analytical techniques, e.g., Fourier Transform infrared spectroscopy and zeta potential. The results indicate that MV molecules are fixed onto the exterior surface, the grooves and at the entrances of the channels of PAL. The PAL/MV@SiO2 pigment shows excellent stability against chemical attacks, e.g., 0.1 M HCl, 0.1 M NaOH and various organic solvents. Different from Maya Blue, grinding and heating treatment are virtually ineffective in improving stability of the PAL/MV pigment. CTAB and the SiO2 layer formed on the surface of PAL/MV contribute greatly to the improved stability of the pigment due to shielding effect. The optimal CTAB/TEOS/ammonia/H2O molar ratio for the surface modification of PAL/MV is 0.24/1/2.89/495.

  17. The binding modes of carbazole derivatives with telomere G-quadruplex

    NASA Astrophysics Data System (ADS)

    Zhang, Xiu-feng; Zhang, Hui-juan; Xiang, Jun-feng; Li, Qian; Yang, Qian-fan; Shang, Qian; Zhang, Yan-xia; Tang, Ya-lin

    2010-10-01

    It is reported that carbazole derivatives can stabilize G-quadruplex DNA structure formed by human telomeric sequence, and therefore, they have the potential to serve as anti-cancer agents. In this present study, in order to further explore the binding mode between carbazole derivatives and G-quadruplex formed by human telomeric sequence, two carbazole iodides (BMVEC, MVEC) molecules were synthesized and used to investigate the interaction with the human telomeric parallel and antiparallel G-quadruplex structures by NMR, CD and molecular modeling study. Interestingly, it is the pivotal the cationic charge pendant groups of pyridinium rings of carbazole that plays an essential role in the stabilizing and binding mode of the human telomeric sequences G-quadruplex structure. It was found that BMVEC with two cationic charge pendant groups of pyridinium rings of 9-ethylcarbazole cannot only stabilize parallel G-quadruple of Hum6 by groove binding and G-tetrad stacking modes and antiparallel G-quadruplex of Hum22 by groove binding, but also induce the formation of mixed G-quadruplex of Hum22. While MVEC with one cationic charge pendant groups of pyridinium ring only can bind with the parallel G-quadruplex of Hum6 by the stacking onto the G4 G-tetrad and could not interact with the G-quadruplex of Hum22.

  18. Cytotoxic Effect of a Novel Synthesized Carbazole Compound on A549 Lung Cancer Cell Line

    PubMed Central

    Molatlhegi, Refilwe P.; Phulukdaree, Alisa; Anand, Krishnan; Gengan, Robert M.; Tiloke, Charlette; Chuturgoon, Anil A.

    2015-01-01

    Increased death rates due to lung cancer have necessitated the search for potential novel anticancer compounds such as carbazole derivatives. Carbazoles are aromatic heterocyclic compounds with anticancer, antibacterial and anti-inflammatory activity. The study investigated the ability of the novel carbazole compound (Z)-4-[9-ethyl-9aH-carbazol-3-yl) amino] pent-3-en-2-one (ECAP) to induce cytotoxicity of lung cancer cells and its mechanism of action. ECAP was synthesized as a yellow powder with melting point of 240-247 °C. The 3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT), lipid peroxidation and comet assays were used to assess the cytotoxic effect of the compound on A549 lung cancer cells. Protein expression was determined using western blots, apoptosis was measured by luminometry (caspase-3/7, -8 and -9) assay and flow cytometry was used to measure phosphatidylserine (PS) externalisation. ECAP induced a p53 mediated apoptosis of lung cancer cells due to a significant reduction in the expression of antioxidant defence proteins (Nrf2 and SOD), Hsp70 (p < 0.02) and Bcl-2 (p < 0.0006), thereby up-regulating reactive oxygen species (ROS) production. This resulted in DNA damage (p < 0.0001), up-regulation of Bax expression and caspase activity and induction of apoptosis in lung cancer cells. The results show the anticancer potential of ECAP on lung cancer. PMID:26134408

  19. Gold-Catalyzed Direct Assembly of Aryl-Annulated Carbazoles from 2-Alkynyl Arylazides and Alkynes.

    PubMed

    Li, Nan; Lian, Xiao-Lei; Li, Yu-Hui; Wang, Tian-Yi; Han, Zhi-Yong; Zhang, Liming; Gong, Liu-Zhu

    2016-09-01

    An unprecedented gold-catalyzed synthetic method for the direct assembly of aryl-annulated carbazoles from 2-alkynyl arylazides and alkynes is described. The reaction is proposed to proceed via a sequential cyclopropenation and intramolecular metal carbene/arene Friedel-Crafts-type reaction, respectively, mediated by two gold carbene intermediates. PMID:27529360

  20. 9-Ethyl-N-(3-nitro­benzyl­idene)-9H-carbazol-3-amine

    PubMed Central

    Archana, R.; Yamuna, E.; Rajendra Prasad, K. J.; Thiruvalluvar, A.; Butcher, R. J.

    2011-01-01

    The title compound, C21H17N3O2, crystallizes with two mol­ecules in the asymmetric unit. The carbazole groups show relatively small deviations from planarity [maximum displacements from the mean carbazole plane are 0.077 (7) and 0.101 (7) Å]. The dihedral angles between the 3-nitro­benzyl­idene­amine and carbazole groups are 37.9 (1) and 37.0 (1)° in the two mol­ecules. PMID:21837172

  1. Ablation of dentin by irradiation of violet diode laser

    NASA Astrophysics Data System (ADS)

    Hatayama, H.; Kato, J.; Akashi, G.; Hirai, Y.; Inoue, A.

    2006-02-01

    Several lasers have been used for clinical treatment in dentistry. Among them, diode lasers are attractive because of their compactness compared with other laser sources. Near-infrared diode lasers have been practically used for cutting soft tissues. Because they penetrate deep to soft tissues, they cause sufficiently thick coagulation layer. However, they aren't suitable for removal of carious dentin because absorption by components in dentin is low. Recently, a violet diode laser with a wavelength of 405nm has been developed. It will be effective for cavity preparation because dentin contains about 20% of collagen whose absorption coefficient at a violet wavelength is larger than that at a near-infrared wavelength. In this paper, we examined cutting performance of the violet diode laser for dentin. To our knowledge, there have been no previous reports on application of a violet laser to dentin ablation. Bovine teeth were irradiated by continuous wave violet diode laser with output powers in a range from 0.4W to 2.4W. The beam diameter on the sample was about 270μm and an irradiation time was one second. We obtained the crater ablated at more than an output power of 0.8W. The depth of crater ranged from 20μm at 0.8W to 90μm at 2.4W. Furthermore, the beam spot with an output power of 1.7W was scanned at a speed of 1mm/second corresponding to movement of a dentist's hand in clinical treatment. Grooves with the depth of more than 50μm were also obtained. From these findings, the violet diode laser has good potential for cavity preparation. Therefore, the violet diode laser may become an effective tool for cavity preparation.

  2. Violet-red discolouration of canned Palmyra palm during processing.

    PubMed

    Chamchong, Montip; Tatidin, Yuporn; Misayan, Apinya

    2016-01-01

    The objectives of the research were to investigate the causes of the violet-red discolouration during processing of canned Palmyra palm and to identify preventive methods without the use of chemical additives. Palmyra palm flesh with (13-21 %) /without some peel left on was tested for the source of violet-red discolouration during blanching. It was found that blanching in distilled water had no effect on discolouration when blanching conditions were at 75, 85, and 95 °C for 7 min but the violet-red discolouration occurred only when tap water was used for blanching at 95 °C for 7 min. Moreover, the addition of bicarbonate (NaHCO3) in distilled water to imitate higher alkalinity of tap water during blanching could contribute to the violet-red discolouration. Thus the observed cut off alkalinity of the blanching water wherein not to expect any discolouration was found to be about 100 ppm. After sterilization, there was no violet-red discolouration from Palmyra palm flesh without any peel left on even though it had a preceding treatment of blanching in highly alkaline tap water. PMID:26787982

  3. Violet-red discolouration of canned Palmyra palm during processing.

    PubMed

    Chamchong, Montip; Tatidin, Yuporn; Misayan, Apinya

    2016-01-01

    The objectives of the research were to investigate the causes of the violet-red discolouration during processing of canned Palmyra palm and to identify preventive methods without the use of chemical additives. Palmyra palm flesh with (13-21 %) /without some peel left on was tested for the source of violet-red discolouration during blanching. It was found that blanching in distilled water had no effect on discolouration when blanching conditions were at 75, 85, and 95 °C for 7 min but the violet-red discolouration occurred only when tap water was used for blanching at 95 °C for 7 min. Moreover, the addition of bicarbonate (NaHCO3) in distilled water to imitate higher alkalinity of tap water during blanching could contribute to the violet-red discolouration. Thus the observed cut off alkalinity of the blanching water wherein not to expect any discolouration was found to be about 100 ppm. After sterilization, there was no violet-red discolouration from Palmyra palm flesh without any peel left on even though it had a preceding treatment of blanching in highly alkaline tap water.

  4. Spectral characteristics and nonlinear studies of crystal violet dye.

    PubMed

    Sukumaran, V Sindhu; Ramalingam, A

    2006-03-01

    Solid-state dye-doped polymer is an attractive alternative to the conventional liquid dye solution. In this paper, the spectral characteristics and the nonlinear optical properties of the dye crystal violet are studied. The spectral characteristics of crystal violet dye doped poly(methylmethacrylate) modified with additive n-butyl acetate (nBA) are studied by recording its absorption and fluorescence spectra and the results are compared with the corresponding liquid mixture. The nonlinear refractive index of the dye in nBA and dye doped polymer film were measured using z-scan technique, by exciting with He-Ne laser. The results obtained are intercompared. Both the samples of dye crystal violet show a negative nonlinear refractive index. The origin of optical nonlinearity in the dye may be attributed due to laser-heating induced nonlinear effect.

  5. Photobiological properties of positively charged methylene violet analogs.

    PubMed

    Houghtaling, M A; Perera, R; Owen, K E; Wagner, S; Kuhn, R J; Morrison, H

    2000-01-01

    O-Methyl methylene violet (OMeMV), O-methyl bromomethylene violet (OMeBrMV) and O-methyl iodomethylene violet (OMeIMV) have been prepared in order to test their potential utility as anti-viral and anti-tumor phototoxic dyes. Rates of photosensitized toxicity of KB cells with 633 nm irradiation are (x 10(-19) photon-1): 2.4, 2.2, 1.9 and 0.17 for OMeIMV, OMeBrMV, methylene violet (MV) and OMeMV, respectively. Rates of photosensitized inactivation of Sindbis virus in phosphate-buffered saline with 633 nm irradiation are (x 10(-18) photon-1): 3.3, 1.8, 0.99, 0.15 for MV, OMeIMV, OMeBrMV and OMeMV, respectively. Quantum efficiencies for singlet oxygen formation were determined as OMeIMV, 0.64; OMeBrMV, 0.40; OMeMV, 0.054. Titration of the dyes with double-stranded (ds)DNA resulted in bathochromic shifts and hypochromic effects in the visible absorption spectra. Association constants for interaction of the methylated dyes with dsDNA of approximately 1 x 10(5) M-1 were determined by Scatchard analysis of equilibrium dialysis and UV absorption titration data. Photolysis of the halogenated dyes with DNA under argon led to covalent bond formation with the nucleic acid; there was no evidence of covalent binding in the dark.

  6. Optical mechanotransduction with carbazole-based luminescent liquid single-crystal elastomers.

    PubMed

    Garcia-Amorós, Jaume; Velasco, Dolores

    2015-04-01

    Carbazole-based liquid single-crystal elastomers (LSCEs) are valuable fluorescent flexible materials to perform optical mechanotransduction under ambient conditions. Indeed, the covalent incorporation of carbazole derivatives into nematic LSCEs allows to tune their luminescence on demand under mechanical control in a quick and reversible fashion. Specifically, the fluorescence intensity for these materials can be switched back and forth in less than a second. Moreover, such a process can be performed several times without detecting any sign of fatigue in the system. In addition, these materials show excellent resistance to aging; 2 years after their preparation they exhibit the very same mechanofluorescent behavior as when freshly prepared. In fact, the here reported fluorescent systems are highly sensitive; the application of a force of 70 mN decreases the fluorescence in the elastomeric material by 7%. Thus, mechanical forces are attractive external stimuli to modulate the fluorescence of nematic elastomers rapidly and reversibly enabling thereby mechanotransduction. PMID:25704537

  7. Crystal structure of dimethyl 9H-carbazole-2,7-di-carb-oxy-late.

    PubMed

    Lehane, Ryan L; Golen, James A; Rheingold, Arnold L; Manke, David R

    2015-10-01

    In the title compound, C16H13NO4, the carbazole ring system is almost planar with non-H atoms possessing a mean deviation from planarity of 0.037 Å. The two ester groups are orientated trans to one another and tilted slightly from the mean plane of the carbazole ring system, making dihedral angles of 8.12 (6) and 8.21 (5)°. In the crystal, mol-ecules are linked by pairs of N-H⋯O hydrogen bonds forming inversion dimers. The dimers are linked by parallel slipped π-π inter-actions, forming slabs propagating along the b-axis direction [inter-centroid distance = 3.6042 (8) Å, inter-planar distance = 3.3437 (5) Å, slippage = 1.345 Å]. PMID:26594478

  8. Carbazole Scaffold in Medicinal Chemistry and Natural Products: A Review from 2010-2015.

    PubMed

    Tsutsumi, Lissa S; Gündisch, Daniela; Sun, Dianqing

    2016-01-01

    9H-carbazole is an aromatic molecule that is tricyclic in nature, with two benzene rings fused onto a 5-membered pyrrole ring. Obtained from natural sources or by synthetic routes, this scaffold has gained much interest due to its wide range of biological activity upon modifications, including antibacterial, antimalarial, anticancer, and anti-Alzheimer properties. This review reports a survey of the literature on carbazole-containing molecules and their medicinal activities from 2010 through 2015. In particular, we focus on their in vitro and in vivo activities and summarize structure-activity relationships (SAR), mechanisms of action, and/or cytotoxicity/selectivity findings when available to provide future guidance for the development of clinically useful agents from this template.

  9. Final report on the safety assessment of Acid Violet 43.

    PubMed

    Fiume, M Z

    2001-01-01

    Acid Violet 43 is an anthraquinone color that may be used as a colorant in cosmetic formulations that are hair dyes, colors, and coloring rinses. Batches of Acid Violet 43 that are certified to meet the United States Food and Drug Administration (U.S. FDA) specifications are termed Ext. D & C Violet No. 2. Hair dyes and colors containing Acid Violet 43 are considered coal tar ingredients and, as such, routinely bear a caution statement regarding potential skin irritation and instructions for determining whether the product causes skin irritation in any given individual. Expected concentrations of use are less than or equal to 1%. Impurities include anthracenedione derivatives, p-toluidine, and p-toluidine sulfonic acid, as well as heavy metals. Based on extensive safety test data, the U.S. FDA has established specifications (including limits on impurities) for Ext. D & C Violet No. 2 that allow its use in any cosmetic. It is the certified color (Ext. D & C Violet No. 2) that has been evaluated in the following safety tests. Oral toxicity tests do not demonstrate significant acute toxicity. In a short-term dermal toxicity study using guinea pigs and a subchronic dermal toxicity study using rabbits, no signs of systemic toxicity and no significant local skin reactions were noted. This ingredient was not genotoxic in bacterial assays, nor was it carcinogenic when applied to mouse skin at a 1% concentration. Accordingly, Acid Violet 43 was determined to be safe for use in hair dye formulations, when impurities are limited as follows: < or = 18% volatile matter (at 135 degrees C) and chlorides and sulfates (calculated as sodium salts); < or = 0.4% water-insoluble matter; < or = 0.2% 1-hydroxy-9,10-anthracenedione; < or = 0.2% 1,4-dihydroxy-9,10-anthracenedione; < or = 0.1% p-toluidine; < or = 0.2% p-toluidine sulfonic acids, sodium salts; < or = 1% subsidiary colors; < or = 20 ppm lead (as Pb); < or = 3 ppm arsenic (as As); < or = 1 ppm mercury (as Hg); and with > or

  10. Solvent free selective dehydrogenation of indolic and carbazolic molecules with an iridium pincer catalyst.

    PubMed

    Brayton, Daniel F; Jensen, Craig M

    2014-06-01

    A previously known iridium POCOP pincer catalyst was found to selectively dehydrogenate the heterocyclic portion of several indolic and carbazolic molecules. These molecules were found to have an "activity window" (172-178 °C) upon which only the heterocyclic ring underwent dehydrogenation. All reactions were run solvent free, yields for selected substrates were excellent, and the products were isolated by either distillation or alumina plug filtration. PMID:24763968

  11. Palladium-catalyzed synthesis of N-arylated carbazoles using anilines and cyclic diaryliodonium salts

    PubMed Central

    Riedmüller, Stefan

    2013-01-01

    Summary The direct synthesis of N-arylated carbazoles through a palladium-catalyzed amination of cyclic iodonium salts with anilines is described. In particular, electron-poor aniline derivatives reacted smoothly with only 5 mol % of Pd(OAc)2 as catalyst to give the desired products in up to 71% yield. Furthermore, the reactivity of cyclic iodonium salts is compared with the reactivity of the corresponding cyclic bromonium analogues. PMID:23843915

  12. (S)-(+)-4-(Oxiran-2-ylmeth­oxy)-9H-carbazole

    PubMed Central

    Lu, Ding-Qiang; Chen, Jia; Wu, Wen-Yuan; Ling, Xiu-Quan; Chang, Ya-Jun

    2010-01-01

    In the title compound, C15H13NO2, all atoms of the carbazole group are coplanar (r.m.s. deviation = 0.005 Å), and the dihedral angle between this plane and C—O—C plane of oxane group is 57.1 (4)°. The crystal packing is stabilized by an N—H⋯O hydrogen bond, resulting in infinite supra­molecular chains along [001]. PMID:21588983

  13. 21 CFR 500.29 - Gentian violet for use in animal feed.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Gentian violet for use in animal feed. 500.29... § 500.29 Gentian violet for use in animal feed. The Food and Drug Administration has determined that gentian violet is not generally recognized as safe for use in animal feed and is a food additive...

  14. 21 CFR 500.30 - Gentian violet for animal drug use.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Gentian violet for animal drug use. 500.30 Section... Gentian violet for animal drug use. The Food and Drug Administration (FDA) has determined that gentian violet is not generally recognized as safe and effective for any veterinary drug use in food animals...

  15. 21 CFR 500.30 - Gentian violet for animal drug use.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Gentian violet for animal drug use. 500.30 Section... Gentian violet for animal drug use. The Food and Drug Administration (FDA) has determined that gentian violet is not generally recognized as safe and effective for any veterinary drug use in food animals...

  16. 21 CFR 500.29 - Gentian violet for use in animal feed.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Gentian violet for use in animal feed. 500.29... § 500.29 Gentian violet for use in animal feed. The Food and Drug Administration has determined that gentian violet is not generally recognized as safe for use in animal feed and is a food additive...

  17. 21 CFR 500.30 - Gentian violet for animal drug use.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Gentian violet for animal drug use. 500.30 Section... Gentian violet for animal drug use. The Food and Drug Administration (FDA) has determined that gentian violet is not generally recognized as safe and effective for any veterinary drug use in food animals...

  18. 21 CFR 500.29 - Gentian violet for use in animal feed.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Gentian violet for use in animal feed. 500.29... § 500.29 Gentian violet for use in animal feed. The Food and Drug Administration has determined that gentian violet is not generally recognized as safe for use in animal feed and is a food additive...

  19. 21 CFR 500.29 - Gentian violet for use in animal feed.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Gentian violet for use in animal feed. 500.29... § 500.29 Gentian violet for use in animal feed. The Food and Drug Administration has determined that gentian violet is not generally recognized as safe for use in animal feed and is a food additive...

  20. 21 CFR 500.29 - Gentian violet for use in animal feed.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Gentian violet for use in animal feed. 500.29... § 500.29 Gentian violet for use in animal feed. The Food and Drug Administration has determined that gentian violet is not generally recognized as safe for use in animal feed and is a food additive...

  1. 21 CFR 500.30 - Gentian violet for animal drug use.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Gentian violet for animal drug use. 500.30 Section... Gentian violet for animal drug use. The Food and Drug Administration (FDA) has determined that gentian violet is not generally recognized as safe and effective for any veterinary drug use in food animals...

  2. 21 CFR 500.30 - Gentian violet for animal drug use.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Gentian violet for animal drug use. 500.30 Section... Gentian violet for animal drug use. The Food and Drug Administration (FDA) has determined that gentian violet is not generally recognized as safe and effective for any veterinary drug use in food animals...

  3. Vascular barrier protective effects of 3-N- or 3-O-cinnamoyl carbazole derivatives.

    PubMed

    Ku, Sae-Kwang; Lee, Jee-Hyun; O, Yuseok; Lee, Wonhwa; Song, Gyu-Yong; Bae, Jong-Sup

    2015-10-01

    In this Letter, we investigated the barrier protective effects of 3-N-(MeO)n-cinnamoyl carbazoles (BS 1; n=1, BS 2; n=2, BS 3; n=3) and 3-O-(MeO)3-cinnamoyl carbazole (BS 4) against high-mobility group box 1 (HMGB1)-mediated vascular disruptive responses in human umbilical vein endothelial cells (HUVECs) and in mice for the first time. Data showed that BS 2, BS 3, and BS 4, but not BS 1, inhibited HMGB1-mediated vascular disruptive responses and transendothelial migration of human neutrophils to HUVECs. BS 2, BS3, and BS 4 also suppressed HMGB1-induced hyperpermeability and leukocyte migration in mice. Interestingly, the barrier protective effects of BS 3 and BS 4 were better than those of BS 2. These results suggest that the number of methoxy groups substituted on the cinnamamide or cinnamate moiety of the 9H-3-carbazole derivative is an important pharmacophore for the barrier protective effects of these compounds.

  4. Synthesis and antitumor activity of novel N-substituted carbazole imidazolium salt derivatives

    PubMed Central

    Liu, Lan-Xiang; Wang, Xue-Quan; Zhou, Bei; Yang, Li-Juan; Li, Yan; Zhang, Hong-Bin; Yang, Xiao-Dong

    2015-01-01

    A series of novel N-substituted carbazole imidazolium salt derivatives has been prepared and investigated for their cytotoxic activity against five human tumor cell lines by MTS assay. The results indicated that the existence of 5,6-dimethyl-benzimidazole ring, substitution of the imidazolyl-3-position with a 2-bromobenzyl or naphthylacyl group, as well as alkyl chain length between carbazole and imidazole ring were important for the antitumor activity. Compound 61, bearing a 2-bromobenzyl substituent at position-3 of the 5,6-dimethyl-benzimidazole, showed powerful inhibitory activities and was more selective to HL-60, SMMC-7721, MCF-7 and SW480 cell lines with IC50 values 0.51–2.48 μM. Mechanism of action studies revealed that this new compound could remarkably induce cell cycle arrest and apoptosis in SMMC-7721 cells. This work provides alternative novel way for future drug development based on carbazole and imidazolium salt scaffolds. PMID:26287982

  5. Dry deposition, concentration and gas/particle partitioning of atmospheric carbazole

    NASA Astrophysics Data System (ADS)

    Esen, Fatma; Tasdemir, Yücel; Cindoruk, S. Sıddık

    2010-03-01

    The atmospheric concentrations and dry deposition of carbazole were measured to present the temporal changes, gas/particle partitioning and magnitude of fluxes. Atmospheric samples were collected from July 2004 to May 2005 at four different sites in Bursa, Turkey. The average total (gas and particulate) carbazole concentrations were 7.6 ± 9.9 ng m - 3 in Gulbahce (Residential), 1.1 ± 1.2 ng m - 3 in BUTAL (Traffic), 3.3 ± 5.0 ng m - 3 in BOID (Industrial), and 1.2 ± 0.7 ng m - 3 in the Uludag University Campus (UU) (Suburban). Experimental gas/particle partition coefficient ( Kp) was determined using the study results and compared with Kp values calculated from octanol-air and soot-air + octanol partitioning models. Total dry deposition fluxes of carbazole were 290 ± 484 ng m - 2 d - 1 in BUTAL and 72 ± 67 ng m - 2 d - 1 in the UU Campus. Particulate phase dry deposition velocities were 0.81 ± 0.78 cm s - 1 and 0.90 ± 1.53 cm s - 1 for BUTAL and the UU Campus, respectively. On the other hand, gas-phase mass transfer coefficients were calculated to be 0.34 ± 0.29 cm s - 1 and 0.26 ± 0.17 cm s - 1 for BUTAL and the UU Campus, respectively.

  6. 3,6-Carbazole vs 2,7-carbazole: A comparative study of hole-transporting polymeric materials for inorganic–organic hybrid perovskite solar cells

    PubMed Central

    Li, Wei; Otsuka, Munechika; Wang, Yang; Mori, Takehiko

    2016-01-01

    Summary The ever increasing demand for clean energy has encouraged researchers to intensively investigate environmentally friendly photovoltaic devices. Inorganic–organic hybrid perovskite solar cells (PSCs) are very promising due to their potentials of easy fabrication processes and high power conversion efficiencies (PCEs). Designing hole-transporting materials (HTMs) is one of the key factors in achieving the high PCEs of PSCs. We now report the synthesis of two types of carbazole-based polymers, namely 3,6-Cbz-EDOT and 2,7-Cbz-EDOT, by Stille polycondensation. Despite the same chemical composition, 3,6-Cbz-EDOT and 2,7-Cbz-EDOT displayed different optical and electrochemical properties due to the different connectivity mode of the carbazole unit. Therefore, their performances as hole-transporting polymeric materials in the PSCs were also different. The device based on 2,7-Cbz-EDOT showed better photovoltaic properties with the PCE of 4.47% than that based on 3,6-Cbz-EDOT. This could be due to its more suitable highest occupied molecular orbital (HOMO) level and higher hole mobility. PMID:27559390

  7. 3,6-Carbazole vs 2,7-carbazole: A comparative study of hole-transporting polymeric materials for inorganic-organic hybrid perovskite solar cells.

    PubMed

    Li, Wei; Otsuka, Munechika; Kato, Takehito; Wang, Yang; Mori, Takehiko; Michinobu, Tsuyoshi

    2016-01-01

    The ever increasing demand for clean energy has encouraged researchers to intensively investigate environmentally friendly photovoltaic devices. Inorganic-organic hybrid perovskite solar cells (PSCs) are very promising due to their potentials of easy fabrication processes and high power conversion efficiencies (PCEs). Designing hole-transporting materials (HTMs) is one of the key factors in achieving the high PCEs of PSCs. We now report the synthesis of two types of carbazole-based polymers, namely 3,6-Cbz-EDOT and 2,7-Cbz-EDOT, by Stille polycondensation. Despite the same chemical composition, 3,6-Cbz-EDOT and 2,7-Cbz-EDOT displayed different optical and electrochemical properties due to the different connectivity mode of the carbazole unit. Therefore, their performances as hole-transporting polymeric materials in the PSCs were also different. The device based on 2,7-Cbz-EDOT showed better photovoltaic properties with the PCE of 4.47% than that based on 3,6-Cbz-EDOT. This could be due to its more suitable highest occupied molecular orbital (HOMO) level and higher hole mobility. PMID:27559390

  8. Carbazole-degradative IncP-7 plasmid pCAR1.2 is structurally unstable in Pseudomonas fluorescens Pf0-1, which accumulates catechol, the intermediate of the carbazole degradation pathway.

    PubMed

    Takahashi, Yurika; Shintani, Masaki; Li, Li; Yamane, Hisakazu; Nojiri, Hideaki

    2009-06-01

    We determined the effect of the host on the function and structure of the nearly identical IncP-7 carbazole-degradative plasmids pCAR1.1 and pCAR1.2. We constructed Pseudomonas aeruginosa PAO1(pCAR1.2) and P. fluorescens Pf0-1Km(pCAR1.2) and compared their growth on carbazole- and succinate-containing media with that of P. putida KT2440(pCAR1.1). We also assessed the stability of the genetic structures of the plasmids in each of the three hosts. Pf0-1Km(pCAR1.2) showed dramatically delayed growth when carbazole was supplied as the sole carbon source, while the three strains grew at nearly the same rate on succinate. Among the carbazole-grown Pf0-1Km(pCAR1.2) cells, two types of deficient strains appeared and dominated the population; such dominance was not observed in the other two strains or for succinate-grown Pf0-1Km(pCAR1.2). Genetic analysis showed that the two deficient strains possessed pCAR1.2 derivatives in which the carbazole-degradative car operon was deleted or its regulatory gene, antR, was deleted by homologous recombination between insertion sequences. From genomic information and quantitative reverse transcription-PCR analyses of the genes involved in carbazole mineralization by Pf0-1Km(pCAR1.2), we found that the cat genes on the chromosome of Pf0-1Km, which are necessary for the degradation of catechol (a toxic intermediate in the carbazole catabolic pathway), were not induced in the presence of carbazole. The resulting accumulation of catechol may have enabled the strain that lost its carbazole-degrading ability to have overall higher fitness than the wild-type strain. These results suggest that the functions of the chromosomal genes contributed to the selection of plasmid derivatives with altered structures.

  9. Carbazole-based emitting compounds: Synthesis, photophysical properties and formation of nanoparticles

    NASA Astrophysics Data System (ADS)

    Adhikari, Ravi M.

    Carbazole is a heterocyclic tricyclic aromatic organic compound consisting of two six-membered benzene rings fused on either side of a five-membered nitrogen-containing ring. A large number of carbazole derivatives have been designed and synthesized and organic electronic devices based on these derivatives such as organic light emitting diodes (OLEDs), have been investigated. Ever since Tang and VanSlyke constructed electroluminescent (EL) devices using organic materials as emitters, development of efficient and stable EL materials has taken good momentum. Carbazole derivatives are widely used as materials for EL and hole-transporting layers of OLEDs which use their high charge mobility. The optical and electrical properties of carbazoles are affected by substitution on the 2-, 3-, 6-, 7- and 9H-positions. Many carbazole derivatives have sufficiently high triplet energy to make them an efficient host where they can serve as red, green, or blue triplet emitters. Highly fluorescent and stable carbazole-based compounds were synthesized and characterized. Substitution of carbazoles at 3- and 6-position by tert-butyl group enhanced the solubility. They showed high extinction coefficients of absorption (Amax ≈ 328-353 nm) and quantum yields of fluorescence (lambdamax ≈ 386-437 nm; phiF ≈ 0.72-0.89; tauF ≈ 2.09-3.91 ns) in dichloromethane. The quantum yields of fluorescence of these compounds in the solid state were also high (lambdamax ≈ 385-422 nm; phiF ≈ 0.40-0.85). Simple synthetic procedures were developed to prepare other stable carbazoles. These compounds emit blue, green, and orange-red light. The red-shifted emission in the solid state which can be as much as 120nm relative to that in solution is highly dependent on the nature and positions of the substituents. The presence of a carbaldehyde or malononitrile on the carbazole moiety quenches fluorescence severely in solution and in the solid state. However, the effect is not the same for the

  10. Photoporation and cell transfection using a violet diode laser

    NASA Astrophysics Data System (ADS)

    Paterson, L.; Agate, B.; Comrie, M.; Ferguson, R.; Lake, T. K.; Morris, J. E.; Carruthers, A. E.; Brown, C. T. A.; Sibbett, W.; Bryant, P. E.; Gunn-Moore, F.; Riches, A. C.; Dholakia, Kishan

    2005-01-01

    The introduction and subsequent expression of foreign DNA inside living mammalian cells (transfection) is achieved by photoporation with a violet diode laser. We direct a compact 405 nm laser diode source into an inverted optical microscope configuration and expose cells to 0.3 mW for 40 ms. The localized optical power density of ~1200 MW/m2 is six orders of magnitude lower than that used in femtosecond photoporation (~104 TW/m2). The beam perforates the cell plasma membrane to allow uptake of plasmid DNA containing an antibiotic resistant gene as well as the green fluorescent protein (GFP) gene. Successfully transfected cells then expand into clonal groups which are used to create stable cell lines. The use of the violet diode laser offers a new and simple poration technique compatible with standard microscopes and is the simplest method of laser-assisted cell poration reported to date.

  11. Dichroism and birefringence of natural violet diamond crystals

    SciTech Connect

    Konstantinova, A. F. Titkov, S. V.; Imangazieva, K. B.; Evdishchenko, E. A.; Sergeev, A. M.; Zudin, N. G.; Orekhova, V. P.

    2006-05-15

    Investigation of the optical properties of natural violet diamonds from the Yakutian kimberlites is performed. A red shift of the absorption edge is revealed in the absorption spectra of these crystals. This shift is indicative of the presence of a high concentration of nitrogen in the diamonds studied. Along with the strong band at 0.550 {mu}m, weaker bands at 0.390, 0.456 and 0.496 {mu}m are revealed. It is shown that violet diamond crystals have birefringence and dichroism of about 10{sup -5} and 10{sup -6}, respectively. When a light beam propagates perpendicularly to colored lamellas, the dichroism is much larger and the birefringence is smaller than in the case where the beam direction is parallel to lamellas.

  12. Dispersive charge transport due to strong charge dipole interactions of cyano-group in the cyano-carbazole based molecular glass

    NASA Astrophysics Data System (ADS)

    Oh, Dong Keun; Hong, Sung Mok; Lee, Cheol Eui; Kim, B.-S.; Jin, J.-I.

    2005-12-01

    Using the time of flight (ToF) method, we investigated the bipolar charge transport for two glass-forming molecules containing carbazole and cyano-carbazole moiety. The enhanced electron mobility was observed in the cyano-carbazole compound. From the numerical method based the Laplace formalism, the distribution of hole trapping energy was obtained for the carbazole compound. This result was compared with the exponential distribution extracted from dispersion parameter for the cyano-carbazole material. Considering charge-dipole interactions as a reason for the disordered trapping mechanism, we discussed dispersive charge transport induced by a strong dipolar (i.e. cyano) group by comparing the distributions of hole trapping sites for two compounds.

  13. Tests and calibration on ultra violet imaging telescope (UVIT)

    NASA Astrophysics Data System (ADS)

    Kumar, Amit; Ghosh, S. K.; Kamath, P. U.; Postma, Joe; Kathiravan, S.; Mahesh, P. K.; Nagbhushana, S.; Navalgund, K. H.; Rajkumar, N.; Rao, M. N.; Sarma, K. S.; Sriram, S.; Stalin, C. S.; Tandon, S. N.

    2012-09-01

    Ultra Violet Imaging Telescope on ASTROSAT Satellite mission is a suite of Far Ultra Violet (FUV; 130 - 180 nm), Near Ultra Violet (NUV; 200 - 300 nm) and Visible band (VIS; 320-550nm) imagers. ASTROSAT is a first multi wavelength mission of INDIA. UVIT will image the selected regions of the sky simultaneously in three channels & observe young stars, galaxies, bright UV Sources. FOV in each of the 3 channels is ~ 28 arc-minute. Targeted angular resolution in the resulting UV images is better than 1.8 arc-second (better than 2.0 arc-second for the visible channel). Two identical co-aligned telescopes (T1, T2) of Ritchey-Chretien configuration (Primary mirror of ~375 mm diameter) collect the celestial radiation and feed to the detector system via a selectable filter on a filter wheel mechanism; gratings are available in the filter wheels of FUV and NUV channels for slit-less low resolution spectroscopy. The detector system for each of the 3 channels is generically identical. One telescope images in the FUV channel, and other images in NUV and VIS channels. One time open-able mechanical cover on each telescope also works as Sun-shield after deployment. We will present the optical tests and calibrations done on the two telescopes. Results on vibrations test and thermo-vacuum tests on the engineering model will also be presented.

  14. Vacuum ultra-violet and ultra-violet scintillation light detection by means of silicon photomultipliers at cryogenic temperature

    NASA Astrophysics Data System (ADS)

    Falcone, A.; Bertoni, R.; Boffelli, F.; Bonesini, M.; Cervi, T.; Menegolli, A.; Montanari, C.; Prata, M. C.; Rappoldi, A.; Raselli, G. L.; Rossella, M.; Simonetta, M.; Spanu, M.; Torti, M.; Zani, A.

    2015-07-01

    We tested the performance of two types of silicon photomultipliers, AdvanSiD ASD-NUV-SiPM3S-P and Hamamatsu 3×3 MM-50 UM VUV2, both at room (300 K) and at liquid nitrogen (77 K) temperature: breakdown voltage, quenching resistance, signal shape, gain and dark counts rate have been studied as function of temperature. The response of the devices to ultra-violet light is also studied.

  15. Photochemical Synthesis of Complex Carbazoles: Evaluation of Electronic Effects in Both UV- and Visible-Light Methods in Continuous Flow.

    PubMed

    Hernandez-Perez, Augusto C; Caron, Antoine; Collins, Shawn K

    2015-11-01

    An evaluation of both a visible-light- and UV-light-mediated synthesis of carbazoles from various triarylamines with differing electronic properties under continuous-flow conditions has been conducted. In general, triarylamines bearing electron-rich groups tend to produce higher yields than triarylamines possessing electron-withdrawing groups. The incorporation of nitrogen-based heterocycles, as well as halogen-containing arenes in carbazole skeletons, was well tolerated, and often synthetically useful complementarity was observed between the UV-light and visible-light (photoredox) methods.

  16. The thermodynamic properties of 2-aminobiphenyl (an intermediate in the carbazole/hydrogen reaction network)

    SciTech Connect

    Steele, W.V.; Chirico, R.D.; Knipmeyer, S.E.; Nguyen, A.

    1990-12-01

    Catalytic hydrodenitrogenation (HDN) is a key step in upgrading processes for conversion of heavy petroleum, shale oil, tar sands, and the products of the liquefaction of coal to economically viable products. This research program provides accurate experimental thermochemical and thermophysical properties for key organic nitrogen-containing compounds present in the range of alternative feedstocks, and applies the experimental information to thermodynamic analyses of key HDN reaction networks. This report is the first in a series that will lead to an analysis of a three-ring HDN system; the carbazole/hydrogen reaction network. 2-Aminobiphenyl is the initial intermediate in the HDN pathway for carbazole, which consumes the least hydrogen possible. Measurements leading to the calculation of the ideal-gas thermodynamic properties for 2-aminobiphenyl are reported. Experimental methods included combustion calorimetry, adiabatic heat-capacity calorimetry, comparative ebulliometry, inclined-piston gauge manometry, and differential-scanning calorimetry (d.s.c). Entropies, enthalpies, and Gibbs energies of formation were derived for the ideal gas for selected temperatures between 298.15 K and 820 K. The critical temperature and critical density were determined for 2-aminobiphenyl with the d.s.c., and the critical pressure was derived. The Gibbs energies of formation are used in thermodynamic calculations to compare the feasibility of the initial hydrogenolysis step in the carbazole/H{sub 2} network with that of its hydrocarbon and oxygen-containing analogous; i.e., fluorene/H{sub 2} and dibenzofuran/H{sub 2}. Results of the thermodynamic calculations are compared with those of batch-reaction studies reported in the literature. 57 refs., 8 figs., 18 tabs.

  17. Adsorption of methyl violet from aqueous solutions by the biochars derived from crop residues.

    PubMed

    Xu, Ren-kou; Xiao, Shuang-cheng; Yuan, Jin-hua; Zhao, An-zhen

    2011-11-01

    The adsorption of methyl violet by the biochars from crop residues was investigated with batch and leaching experiments--adsorption capacity varied with their feedstock in the following order: canola straw char>peanut straw char>soybean straw char>rice hull char. This order was generally consistent with the amount of negative charge of the biochars. Zeta potentials and Fourier transform infrared photoacoustic spectroscopy, combined with adsorption isotherms and effect of ionic strength, indicated that adsorption of methyl violet on biochars involved electrostatic attraction, specific interaction between the dye and carboxylate and phenolic hydroxyl groups on the biochars, and surface precipitation. Leaching experiments showed that 156 g of rice hull char almost completely removed methyl violet from 18.2 L of water containing 1.0 mmol/L of methyl violet. The biochars had high removal efficiency for methyl violet and could be effective adsorbents for removal of methyl violet from wastewater. PMID:21924897

  18. 21 CFR 74.2602a - Ext. D&C Violet No. 2.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false Ext. D&C Violet No. 2. 74.2602a Section 74.2602a... COLOR ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602a Ext. D&C Violet No. 2. (a) Identity. The color additive Ext. D&C Violet No. 2 is principally the monosodium salt of 2-...

  19. 21 CFR 74.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false D&C Violet No. 2. 74.1602 Section 74.1602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Drugs § 74.1602 D&C Violet No. 2. (a) Identity. (1) The color additive D&C Violet No. 2 is principally 1-hydroxy -4- -9,10-anthracenedione. (2) Color additive mixtures...

  20. 21 CFR 74.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false D&C Violet No. 2. 74.1602 Section 74.1602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Drugs § 74.1602 D&C Violet No. 2. (a) Identity. (1) The color additive D&C Violet No. 2 is principally 1-hydroxy -4- -9,10-anthracenedione. (2) Color additive mixtures...

  1. 21 CFR 82.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false D&C Violet No. 2. 82.1602 Section 82.1602 Food and... PROVISIONALLY LISTED COLORS AND SPECIFICATIONS Drugs and Cosmetics § 82.1602 D&C Violet No. 2. The color additive D&C Violet No. 2 shall conform in identity and specifications to the requirements of §...

  2. 21 CFR 74.2602a - Ext. D&C Violet No. 2.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false Ext. D&C Violet No. 2. 74.2602a Section 74.2602a... COLOR ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602a Ext. D&C Violet No. 2. (a) Identity. The color additive Ext. D&C Violet No. 2 is principally the monosodium salt of 2-...

  3. 21 CFR 74.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false D&C Violet No. 2. 74.1602 Section 74.1602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Drugs § 74.1602 D&C Violet No. 2. (a) Identity. (1) The color additive D&C Violet No. 2 is principally 1-hydroxy -4- -9,10-anthracenedione. (2) Color additive mixtures...

  4. 21 CFR 74.3602 - D&C Violet No. 2.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false D&C Violet No. 2. 74.3602 Section 74.3602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Medical Devices § 74.3602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to...

  5. 21 CFR 74.2602a - Ext. D&C Violet No. 2.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false Ext. D&C Violet No. 2. 74.2602a Section 74.2602a... COLOR ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602a Ext. D&C Violet No. 2. (a) Identity. The color additive Ext. D&C Violet No. 2 is principally the monosodium salt of 2-...

  6. 21 CFR 74.2602 - D&C Violet No. 2.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false D&C Violet No. 2. 74.2602 Section 74.2602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to the...

  7. 21 CFR 74.2602 - D&C Violet No. 2.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false D&C Violet No. 2. 74.2602 Section 74.2602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to the...

  8. 21 CFR 82.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false D&C Violet No. 2. 82.1602 Section 82.1602 Food and... PROVISIONALLY LISTED COLORS AND SPECIFICATIONS Drugs and Cosmetics § 82.1602 D&C Violet No. 2. The color additive D&C Violet No. 2 shall conform in identity and specifications to the requirements of §...

  9. 21 CFR 74.2602a - Ext. D&C Violet No. 2.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Ext. D&C Violet No. 2. 74.2602a Section 74.2602a... COLOR ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602a Ext. D&C Violet No. 2. (a) Identity. The color additive Ext. D&C Violet No. 2 is principally the monosodium salt of 2-...

  10. 21 CFR 74.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false D&C Violet No. 2. 74.1602 Section 74.1602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Drugs § 74.1602 D&C Violet No. 2. (a) Identity. (1) The color additive D&C Violet No. 2 is principally 1-hydroxy -4- -9,10-anthracenedione. (2) Color additive mixtures...

  11. 21 CFR 74.2602 - D&C Violet No. 2.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false D&C Violet No. 2. 74.2602 Section 74.2602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to the...

  12. 21 CFR 74.2602a - Ext. D&C Violet No. 2.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false Ext. D&C Violet No. 2. 74.2602a Section 74.2602a... COLOR ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602a Ext. D&C Violet No. 2. (a) Identity. The color additive Ext. D&C Violet No. 2 is principally the monosodium salt of 2-...

  13. 21 CFR 74.3602 - D&C Violet No. 2.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false D&C Violet No. 2. 74.3602 Section 74.3602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Medical Devices § 74.3602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to...

  14. 21 CFR 74.3602 - D&C Violet No. 2.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false D&C Violet No. 2. 74.3602 Section 74.3602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Medical Devices § 74.3602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to...

  15. 21 CFR 74.3602 - D&C Violet No. 2.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false D&C Violet No. 2. 74.3602 Section 74.3602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Medical Devices § 74.3602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to...

  16. 21 CFR 74.2602 - D&C Violet No. 2.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false D&C Violet No. 2. 74.2602 Section 74.2602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to the...

  17. 21 CFR 74.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false D&C Violet No. 2. 74.1602 Section 74.1602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Drugs § 74.1602 D&C Violet No. 2. (a) Identity. (1) The color additive D&C Violet No. 2 is principally 1-hydroxy -4- -9,10-anthracenedione. (2) Color additive mixtures...

  18. 21 CFR 82.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false D&C Violet No. 2. 82.1602 Section 82.1602 Food and... PROVISIONALLY LISTED COLORS AND SPECIFICATIONS Drugs and Cosmetics § 82.1602 D&C Violet No. 2. The color additive D&C Violet No. 2 shall conform in identity and specifications to the requirements of §...

  19. 21 CFR 74.2602 - D&C Violet No. 2.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false D&C Violet No. 2. 74.2602 Section 74.2602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Cosmetics § 74.2602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to the...

  20. 21 CFR 82.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false D&C Violet No. 2. 82.1602 Section 82.1602 Food and... PROVISIONALLY LISTED COLORS AND SPECIFICATIONS Drugs and Cosmetics § 82.1602 D&C Violet No. 2. The color additive D&C Violet No. 2 shall conform in identity and specifications to the requirements of §...

  1. 21 CFR 74.3602 - D&C Violet No. 2.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false D&C Violet No. 2. 74.3602 Section 74.3602 Food and... ADDITIVES SUBJECT TO CERTIFICATION Medical Devices § 74.3602 D&C Violet No. 2. (a) Identity and specifications. The color additive D&C Violet No. 2 shall conform in identity and specifications to...

  2. 21 CFR 82.1602 - D&C Violet No. 2.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false D&C Violet No. 2. 82.1602 Section 82.1602 Food and... PROVISIONALLY LISTED COLORS AND SPECIFICATIONS Drugs and Cosmetics § 82.1602 D&C Violet No. 2. The color additive D&C Violet No. 2 shall conform in identity and specifications to the requirements of §...

  3. Biodegradation of crystal violet by the white rot fungus Phanerochaete chrysosporium.

    PubMed Central

    Bumpus, J A; Brock, B J

    1988-01-01

    Biodegradation of crystal violet (N,N,N',N',N'',N''-hexamethylpararosaniline) in ligninolytic (nitrogen-limited) cultures of the white rot fungus Phanerochaete chrysosporium was demonstrated by the disappearance of crystal violet and by the identification of three metabolites (N,N,N',N',N''-pentamethylpararosaniline, N,N,N',N''-tetramethylpararosaniline, and N,N',N''-trimethylpararosaniline) formed by sequential N-demethylation of the parent compound. Metabolite formation also occurred when crystal violet was incubated with the extracellular fluid obtained from ligninolytic cultures of this fungus, provided that an H2O2-generating system was supplied. This, as well as the fact that a purified ligninase catalyzed N-demethylation of crystal violet, demonstrated that biodegradation of crystal violet by this fungus is dependent, at least in part, upon its lignin-degrading system. In addition to crystal violet, six other triphenylmethane dyes (pararosaniline, cresol red, bromphenol blue, ethyl violet, malachite green, and brilliant green) were shown to be degraded by the lignin-degrading system of this fungus. An unexpected result was the finding that substantial degradation of crystal violet also occurred in nonligninolytic (nitrogen-sufficient) cultures of P. chrysosporium, suggesting that in addition to the lignin-degrading system, another mechanism exists in this fungus which is also able to degrade crystal violet. PMID:3389809

  4. Charge transfer states in stable neutral and oxidized radical adducts from carbazole derivatives.

    PubMed

    Fajarí, Lluís; Papoular, Robert; Reig, Marta; Brillas, Enric; Jorda, José Luis; Vallcorba, Oriol; Rius, Jordi; Velasco, Dolores; Juliá, Luis

    2014-02-21

    In this paper we report the spectral properties of the stable radical adducts 1(•)-3(•), which are formed by an electron donor moiety, the carbazole ring, and an electron acceptor moiety, the polychlorotriphenylmethyl radical. The molecular structure of radical adduct 1(•) in the crystalline state shows a torsion angle of approximately 90° between the phenyl and the carbazole rings due to steric interactions. They exhibit a charge transfer band in the visible range of the electronic spectrum. All of them are chemically oxidized with copper(II) perchlorate to the respective cation species, which show a strong charge transfer band into the near-infrared region of the spectrum. Radical adducts 1(•)-3(•) and the corresponding stable oxidized species 1(+)-3(+) are real organic mixed-valence compounds due to the open-shell nature of their electronic structure. Charge transfer bands of the cation species are stronger and are bathochromically shifted with respect to those of the neutral species due to the greater acceptor ability of the positively charged central carbon atom of the triphenylmethyl moiety. The cationic species 1(+)-3(+) are diamagnetic, as shown by the absence of a signal in the EPR spectrum in acetonitrile solution at room temperature, but they show an intense and unique band in frozen solutions (183 K).

  5. Synthesis, photophysical and electrochemical properties of two novel carbazole-based dye molecules

    NASA Astrophysics Data System (ADS)

    Zhang, Qing; Zhu, Weiju; Fang, Min; Yin, Fangfang; Li, Cun

    2015-01-01

    Two carbazole-based dye molecules: 3-(6-benzothiazol-2-yl-9H-hexylcarbazole-3-yl)-2-cyano-acylic acid (D3) and 3-[5-(6-benzothiazol-2-yl-9H-hexylcarbazole-3-yl)-thiophen-2-yl]-2-cyan-acylic acid (D4) were synthesized by an approach from carbazole derivate using Vilsmeier-Haack, Suzuki cross-coupling and Knoevenagel reactions. Their physical and electrochemical properties were investigated. D3 and D4 exhibit different optical properties, such as UV absorption, photoluminescence, fluorescence quantum yield and fluorescence lifetime in different solvents. Compared with D3 without a thiophene unit, the maximum absorption wavelength of D4 red-shift obviously and its fluorescence intensity is also enhanced. A shift of the EHOMO and ELUMO is observed for D3 (EHOMO = 2.06 V, ELUMO = -1.39 V vs. NHE) and D4 (EHOMO = 1.73 V, ELUMO = -1.33 V vs. NHE). D3 and D4 can be used as dyes for dye-sensitized solar cells (DSSCs) with TiO2 nanomaterial because their EHOMO are lower than the conduction band edge of TiO2 [-0.5 V (vs. NHE)] and their ELUMO are higher than the I3-/I- redox potential [0.42 V (vs. NHE)].

  6. HPLC analysis of 5H-benzo[a]carbazole with antifungal activity.

    PubMed

    Segall, A I; Vitale, M F; Perez, V L; Pizzorno, M T

    2003-04-01

    A sensitive and simple high-performance liquid chromatographic (HPLC) method for the assay of 6,11-dihydro-2-methoxy-5H-benzo[a]carbazole (1) and 6,11-dihydro-2-methoxy-11-[2-(1-piperidinyl)]ethyl-5H-benzo[a]carbazole (2) was developed. The procedure is based on the use of the reversed-phase high-performance liquid chromatographic (RP-HPLC) method with UV detector. Each analysis required no longer than 11 min. A linear relationship between the concentration of both the drugs and the UV absorbance at 254 nm was obtained. This linearity was maintained over the concentration ranged from 5 to 80 microg/ml. The detection limits were found to be 1.6 and 0.7 ng for compounds 1 and 2. The quantitation limits were found to be 5.3 and 2.5 ng for compounds 1 and 2, respectively. For recovery studies, several determinations were carried out. Recovery values ranged from 98 to 102.1% for compound 1 and from 98.4 to 101.6% for compound 2. Method precision was also evaluated and RSD% found was less than 2%. This method was applied without any interference from degradation products.

  7. An Aminopropyl Carbazole Derivative Induces Neurogenesis by Increasing Final Cell Division in Neural Stem Cells

    PubMed Central

    Shin, Jae-Yeon; Kong, Sun-Young; Yoon, Hye Jin; Ann, Jihyae; Lee, Jeewoo; Kim, Hyun-Jung

    2015-01-01

    P7C3 and its derivatives, 1-(3,6-dibromo-9H-carbazol-9-yl)-3-(p-tolylamino)propan-2-ol (1) and N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide (2), were previously reported to increase neurogenesis in rat neural stem cells (NSCs). Although P7C3 is known to increase neurogenesis by protecting newborn neurons, it is not known whether its derivatives also have protective effects to increase neurogenesis. In the current study, we examined how 1 induces neurogenesis. The treatment of 1 in NSCs increased numbers of cells in the absence of epidermal growth factor (EGF) and fibroblast growth factor 2 (FGF2), while not affecting those in the presence of growth factors. Compound 1 did not induce astrocytogenesis during NSC differentiation. 5-Bromo-2′-deoxyuridine (BrdU) pulsing experiments showed that 1 significantly enhanced BrdU-positive neurons. Taken together, our data suggest that 1 promotes neurogenesis by the induction of final cell division during NSC differentiation. PMID:26157546

  8. Intercalative poly(carbazole) precursor electropolymerization within hybrid nanostructured titanium oxide ultrathin films.

    PubMed

    Frau, Antonio F; Estillore, Nicel C; Fulghum, Timothy M; Advincula, Rigoberto C

    2010-12-01

    A protocol for nanostructuring and electropolymerization of a hybrid semiconductor polycarbazole-titanium oxide ultrathin film is described. Ultrathin (<100 nm) films based on polycarbazole precursor polyelectrolytes and titanium oxide (TiOx) have been fabricated by combining the layer-by-layer (LbL) and surface sol-gel layering techniques. Film growth was followed and confirmed through UV-vis spectroscopy, ellipsometry and quartz crystal microbalance with dissipation (QCM-D). Subsequent anodic electrochemical oxidation of the carbazole pendant units afforded a conjugated polymer network (CPN) film within intercalating TiOx layers of cross-linked and π-conjugated carbazole units. Cyclic voltammetry (CV), UV-vis, and fluorescence spectroscopy measurements confirmed this process. The LbL-driven polyelectrolyte deposition process resulted in a quantified electrochemical response, proportional to the number of layers, while the TiOx acted as a dielectric spacer limiting electron transfer kinetics and attenuating energy transfer in fluorescence. Electro-optical properties were compared with other polycarbazole thin film materials with respect to bandgap energy (Eg). The straightforward protocol in film nanostructuring and barrier/dielectric properties of the inorganic oxide slab (denoted here as, TiOx) should enable applications in organic light-emitting diodes (OLEDs), dielectric mirrors, planar waveguides, and photovoltaic devices for these hybrid ultrathin films.

  9. A promising phosphorescent heteroleptic iridium complex with carbazole-functionalized substituent: Synthesis, photophysical and electroluminescent performances

    NASA Astrophysics Data System (ADS)

    Li, Xiao; Zang, Tienan; Yu, Lianshui; Zhang, Dongyu; Lu, Gonghao; Chi, Haijun; Xiao, Guoyong; Dong, Yan; Cui, Zheng; Zhang, Zhiqiang; Hu, Zhizhi

    2012-12-01

    A promising heteroleptic iridium complex with carbazole-functionalized substituent, i.e., (cbbt)2Ir(acac), in which cbbt was 2-(4-(4-(9H-carbazol-9-yl)butoxy)phenyl)benzo[d]thiazole and acac acetylacetonate, was designed, synthesized and structurally characterized. The complex emitted intensely orange phosphorescence upon photoexcitation with high luminescent quantum efficiency (0.30), short triplet lifetime (0.15 μs) and high decomposition temperature (310 °C). The electronic properties of (cbbt)2Ir(acac) were also examined according to the density functional theory calculations. Organic light-emitting diodes using (cbbt)2Ir(acac) as doped emitter exhibited orange electrophosphorescence with prominent performances. An extremely high brightness of 17,910 cd m-2 at a high voltage (17 V) and a maximum luminance efficiency of 25.5 cd A-1 were achieved. More importantly, those devices exhibited low efficiency roll-off of 30-35% from 10 to 100 mA cm-2, which was probably attributed to the short triplet lifetime of (cbbt)2Ir(acac).

  10. Synthesis, photophysical and electrochemical properties of two novel carbazole-based dye molecules.

    PubMed

    Zhang, Qing; Zhu, Weiju; Fang, Min; Yin, Fangfang; Li, Cun

    2015-01-25

    Two carbazole-based dye molecules: 3-(6-benzothiazol-2-yl-9H-hexylcarbazole-3-yl)-2-cyano-acylic acid (D3) and 3-[5-(6-benzothiazol-2-yl-9H-hexylcarbazole-3-yl)-thiophen-2-yl]-2-cyan-acylic acid (D4) were synthesized by an approach from carbazole derivate using Vilsmeier-Haack, Suzuki cross-coupling and Knoevenagel reactions. Their physical and electrochemical properties were investigated. D3 and D4 exhibit different optical properties, such as UV absorption, photoluminescence, fluorescence quantum yield and fluorescence lifetime in different solvents. Compared with D3 without a thiophene unit, the maximum absorption wavelength of D4 red-shift obviously and its fluorescence intensity is also enhanced. A shift of the EHOMO and ELUMO is observed for D3 (EHOMO=2.06 V, ELUMO=-1.39 V vs. NHE) and D4 (EHOMO=1.73 V, ELUMO=-1.33 V vs. NHE). D3 and D4 can be used as dyes for dye-sensitized solar cells (DSSCs) with TiO2 nanomaterial because their EHOMO are lower than the conduction band edge of TiO2 [-0.5 V (vs. NHE)] and their ELUMO are higher than the I(3-)/I(-) redox potential [0.42 V (vs. NHE)]. PMID:25104283

  11. Smart windows application of carbazole and triazine based star shaped architecture.

    PubMed

    Guzel, Merve; Soganci, Tugba; Ayranci, Rukiye; Ak, Metin

    2016-08-01

    A novel triazine-based, star shape and electroactive monomer, 2,4,6-tris(2-(9H-carbazol-9-yl)ethoxy)-1,3,5-triazine (TCZ) which contains 2,4,6-trichloro-1,3,5-triazine as the core and 2-(9H-carbazol-9-yl)ethanol as the arms, was successfully synthesized. After electrochemical polymerization of the TCZ monomer, called PTCZ, the polymer shows superior optoelectronic and thermal properties due to its unique three-dimensional shape and highly-branched structure in comparison with linear analogues. Electrochromic studies exhibited that PTCZ has turquoise color in the oxidized state and is transparent in the neutral state. Due to the fact that the redox color characteristics of PTCZ are indispensable for smart windows, a PTCZ-based electrochromic device was formed with PEDOT as complementary coloring material. A potential range of -1.5 to +1.8 V was determined to be suitable for operating the PTCZ/PEDOT device between transparent and blue colors. Characterizations of the device were performed in term of switching times, optical contrast, optical memory and redox stability. PMID:27431786

  12. Smart windows application of carbazole and triazine based star shaped architecture.

    PubMed

    Guzel, Merve; Soganci, Tugba; Ayranci, Rukiye; Ak, Metin

    2016-08-01

    A novel triazine-based, star shape and electroactive monomer, 2,4,6-tris(2-(9H-carbazol-9-yl)ethoxy)-1,3,5-triazine (TCZ) which contains 2,4,6-trichloro-1,3,5-triazine as the core and 2-(9H-carbazol-9-yl)ethanol as the arms, was successfully synthesized. After electrochemical polymerization of the TCZ monomer, called PTCZ, the polymer shows superior optoelectronic and thermal properties due to its unique three-dimensional shape and highly-branched structure in comparison with linear analogues. Electrochromic studies exhibited that PTCZ has turquoise color in the oxidized state and is transparent in the neutral state. Due to the fact that the redox color characteristics of PTCZ are indispensable for smart windows, a PTCZ-based electrochromic device was formed with PEDOT as complementary coloring material. A potential range of -1.5 to +1.8 V was determined to be suitable for operating the PTCZ/PEDOT device between transparent and blue colors. Characterizations of the device were performed in term of switching times, optical contrast, optical memory and redox stability.

  13. Crystal violet staining to quantify Candida adhesion to epithelial cells.

    PubMed

    Negri, M; Gonçalves, V; Silva, S; Henriques, M; Azeredo, J; Oliveira, R

    2010-01-01

    In vitro studies of adhesion capability are essential to characterise the virulence of Candida species. However, the assessment of adhesion by traditional methods is time-consuming. The aim of the present study is the development of a simple methodology using crystal violet staining to quantify in vitro adhesion of different Candida species to epithelial cells. The experiments are performed using Candida albicans (ATCC 90028), C. glabrata (ATCC 2001), C. parapsilosis (ATCC 22019) and C. tropicalis (ATCC 750). A human urinary bladder epithelial cell line (TCC-SUP) is used. Yeast and epithelial cells were stained with crystal violet, epithelial cells were then destained using intermediate washing, and the dye in the yeast cells was extracted with acetic acid. The method was validated for the different Candida reference species by comparison with traditional microscope observation and enumeration. The method was then used to assess Candida adhesion to epithelial cells and also to silicone. For all Candida spp. high correlation values (r2= 0.9724-0.9997) between the number of adherent yeasts (microscope enumeration) and absorbance values were obtained for an inoculum concentration >10(6) cells/mL. The proposed technique was easy to perform and reproducible, enabling the determination of adhesion ability of Candida species to an epithelial cell line. PMID:20973406

  14. Compositional changes in red and violet smoke mixes after combustion

    SciTech Connect

    Buchanan, M.V.; Rubin, I.B.; Moneyhun, J.H.

    1983-01-01

    Anthraquinone-derived dyes are commonly used in colored dye mixes prepared for signal smoke grenades. Biological studies have shown, however, that a number of these dyes exhibit bacterial mutagenicity. In addition, these dyes are similar in structure to several polycyclic aromatic hydrocarbons which are well-known carcinogens. The grenades contain not only anthraquinone-derived dyes, but also a pyrotechnic fuel and cooling and starting mixes consisting primarily of potassium chlorate and nitrate, sodium bicarbonate, and sulfur. These dyes are volatilized at temperatures up to 550/sup 0/C during the detonation of the grenade, which could subject the dyes to oxidative and pyrolytic reactions that could result in a variety of reaction by-products. As part of a program to investigate possible environmental and occupational risks of the colored smoke dyes and in signal grenades, two colored smoke mixes, red and violet, have been studied both before and after detonation to evaluate any differences in composition due to the combustion process. This report focuses primarily on the separation and identification of the components of the original and combusted red and violet smoke mixes. The conditions for the detonation of the smoke grenades and sampling of the combusted smoke mixes are also discussed.

  15. Inductive effects of diphenylphosphoryl moieties on carbazole host materials: Design rules for blue electrophosphorescent organic light-emitting devices

    SciTech Connect

    Sapochak, Linda S.; Padmaperuma, Asanga B.; Cai, Xiuyu; Male, Jonathan L.; Burrows, Paul E.

    2008-05-29

    We show that the inductive electron-withdrawing effect of diphenylphosphoryl (Ph2P=O) groups stabilizes both the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO) of a carbazole chromophore. This improves electron injection from a cathode without affecting the high triplet exciton energy (ET ~ 3.0 eV) of the host material. Three new carbazole derivatives 3,6-bis(diphenylphosphoryl)-9-ethylcarbazole (PO10), 3,6-bis(diphenylphosphoryl)-9-phenylcarbazole (PO9) and N-(4-diphenylphosphoryl phenyl) carbazole (MPO12) were investigated as host materials in blue phosphor-doped organic light-emitting devices (OLEDs). Photophysical characterization showed all three carbazole derivatives exhibit monomer UV fluorescence (367-385 nm) in solution and contributions from molecular aggregates in solid-state films (378-395 nm). The polar MPO12 derivative exhibited solvatochromism and had the highest propensity for aggregate formation in the solid-state. Testing of OLEDs using PO9, PO10 and MPO12 as host materials for the sky blue organometallic phosphor, iridium(III)bis(4,6-(di-fluorophenyl)-pyridinato-N,C2') picolinate (FIrpic) gave external quantum efficiencies (EQE) and operating voltages at a similar current density (J = 13 mA/cm2) of 6 - 8 % at < 7V. The best device performance was exhibited using MPO12 as the host when an appropriate hole blocking layer was implemented. At a brightness of 800 cd/m2 an EQE of 9.09 ± 0.12% at 4.8 V was achieved. The higher performance of MPO12 was attributed to the ambipolar charge transporting character of the polar carbazole derivative. However, exciton relaxation on nonradiative aggregate or excimer states of all host materials studied may limit further improvements in device efficiencies.

  16. Irrigation Effects on the Spread of Corynespora Leaf Spot on African Violets

    Technology Transfer Automated Retrieval System (TEKTRAN)

    African violet cultivars have had severe leaf spot epidemics caused by Corynespora cassiicola in recent years. Unfortunately, little information has been published on the relationship between African violets and C. cassiicola. Mist, drip, and ebb and flow irrigation systems were studied to determi...

  17. Experimental and Theoretical Investigation for the Level of Conjugation in Carbazole-Based Precursors and Their Mono-, Di-, and Polynuclear Pt(II) Complexes.

    PubMed

    Al-Balushi, Rayya A; Haque, Ashanul; Jayapal, Maharaja; Al-Suti, Mohammed K; Husband, John; Khan, Muhammad S; Koentjoro, Olivia F; Molloy, Kieran C; Skelton, Jonathan M; Raithby, Paul R

    2016-07-01

    A series of trimethylsilyl-protected monoalkynes (Me3SiC≡C-R) and bis-alkynes (Me3 SiC≡C-R-C≡CSiMe3) incorporating carbazole spacer groups (R = carbazole-2-yl, carbazole-3-yl, carbazole-2,7-diyl, N-(2-ethylhexyl)carbazole-2,7-diyl, carbazole-3,6-diyl, N-(2-ethylhexyl)carbazole-3,6-diyl), together with the corresponding terminal monoalkynes (H-C≡C-R) and bis-alkynes (H-C≡C-R-C≡C-H), have been synthesized and characterized. The CuI-catalyzed dehydrohalogenation reaction between trans-[(Ph)(Et3P)2PtCl], trans-[(Et3P)2PtCl2], and trans-[(P(n)Bu3)2PtCl2] and the terminal alkynes in (i)Pr2NH/CH2Cl2 affords a series of Pt(II) mono- and diynes, while the dehydrohalogenation polycondensation reactions with trans-[(P(n)Bu3)2PtCl2] under similar reaction conditions yields four Pt(II) poly-ynes of the form trans-[(P(n)Bu3)2Pt-C≡C-R-C≡C-]n. The acetylide-functionalized carbazole ligands and the mono-, di-, and polynuclear Pt(II) σ-acetylide complexes have been characterized spectroscopically, with a subset analyzed using single-crystal X-ray diffraction. The Pt(II) mono-, di-, and poly-ynes incorporating the carbazole spacers are soluble in common organic solvents, and solution absorption spectra show a consistent red-shift between the 2- and 2,7- as well as 3- and 3,6-carbazole complexes. Computational modeling is used to explain the observed spectral shifts, which are related to the enhanced electronic delocalization in the latter systems. These results also indicate that the inclusion of carbazole-2,7-diyl units into rigid-rod organometallic polymers should enhance electronic transport along the chains. PMID:27284807

  18. Photophysical properties and computational investigation on substituent effects on the structural and electronic properties of 3,6-di(thiophene-2-yl)-carbazole-based derivatives

    NASA Astrophysics Data System (ADS)

    Sriyab, Suwannee; Gleeson, Matthew Paul; Hannongbua, Supa; Suramitr, Songwut

    2016-12-01

    A series of 3,6-carbazole-based derivatives, 3,6-CzTh-(1), 3,6-CzTh-(2), 3,6-CzTh-(3) and 3,6-CzTh-(4), were synthesized to investigate the influence of structural distortion on intramolecular charge transfer (ICT) complexation between the conjugation components and carbazole core unit of the 3,6-carbazole-based derivatives. The 3,6-carbazole-based derivatives were synthesized and analysed using UV-Visible, photoluminescence spectroscopy and DFT calculations. The electron-donating substituents on the carbazole core unit, which was linked by formyl and acetyl at the 3,6-positions of the carbazole core so as to directly involve the electron-donating edge substituents in backbone, exhibited conjugation breaks in the middle of the carbazole core units. The break lead to a planar structure with an extraordinary ability to stabilize on the excited state resulting in a strong fluorescence quantum yield (Vfluo ≈ 0.6-0.7). The results of the Time-dependent density functional theory (TD-DFT) calculations were in agreement with the experimental results, and indicated that the low fluorescence of 3,6-CzTh-(1) and 3,6-CzTh-(2) is derived not only from intersystem crossing but also from internal conversion due to the proximity effect; this inference was also supported by the measurements of the photoluminescence spectra at low temperatures. In addition, factors leading efficiently to non-radiative processes were shown to be absent in 3,6-CzTh-(3) and 3,6-CzTh-(4). This work deepens our understanding of 3,6-di(thiophen-2-yl)-carbazole-based derivatives and provides insight into the future design of novel materials for improved fluorescence efficiencies and optoelectronic devices.

  19. Venus as Viewed Through Violet and Near Infrared Filters

    NASA Technical Reports Server (NTRS)

    1991-01-01

    These two Galileo images of Venus show the global structure of cloud patterns at two different depths in the upper cloud layers. The large bluish image, taken through the violet filter, shows patterns at the very top of Venus' main sulfuric acid haze layer. The subsolar point is to the right, not far from the limb; the atmospheric flow runs to the left from there. The small red image, taken through a near infrared filter, shows the cloud patterns several miles below the visible cloud tops. The colors shown are artificial; the images were enhanced at the National Optical Astronomy Observatories, Tucson, Arizona. The Galileo Project is managed for NASA by the Jet Propulsion Laboratory.

  20. The violet and ultraviolet opacity problem for carbon stars

    NASA Technical Reports Server (NTRS)

    Johnson, Hollis R.; Luttermoser, Donald G.; Faulkner, Danny R.

    1988-01-01

    The paper considers the longstanding problem of the 'violet opacity' in cool carbon stars by testing, through synthetic spectra, many new and previously suggested opacity sources, based on currently available model atmospheres for carbon stars and M giant stars. While several bound-free edges of neutral metals are important opacity sources, those of Na I at at 2413 A, Mg I at 2514 A, and particularly Ca I at 2940 A are especially significant. Collectively, thousands of atomic lines are important, and the enormous line of Mg I at 2852 A influences the spectrum well into the visible. The pseudocontinuum of C3 and the photoionization continuum of CH both play noticeable but secondary roles. Synthetic spectra form the carbon star models with and without polyatomic molecules fit nicely the collected observations of the well-observed carbon star TX Psc.

  1. Bordetella bronchiseptica phase variation induced by crystal violet.

    PubMed Central

    Ishikawa, H; Isayama, Y

    1986-01-01

    A method for effective induction of phase variation in Bordetella bronchiseptica by treatment with crystal violet (CV) is presented. When grown in CV-broth, phase I cells dissociated into three serial phases. Appearance of variant cells was observed simultaneously with the beginning of cell multiplication. The maximum effect of CV was obtained at a concentration of 8 micrograms/ml, when the proportion of variants in the population reached 100%. The main factors which affected phase variation were concentration of CV, culture age, and temperature of treatment. The phase variants obtained were phenotypically stable upon serial passages on Bordet-Gengou agar plates. By this treatment, no reversion of phase descendants to former phases was observed. Images PMID:3700613

  2. Transient transfection of mammalian cells using a violet diode laser

    NASA Astrophysics Data System (ADS)

    Torres-Mapa, Maria Leilani; Angus, Liselotte; Ploschner, Martin; Dholakia, Kishan; Gunn-Moore, Frank J.

    2010-07-01

    We demonstrate the first use of the violet diode laser for transient mammalian cell transfection. In contrast to previous studies, which showed the generation of stable cell lines over a few weeks, we develop a methodology to transiently transfect cells with an efficiency of up to ~40%. Chinese hamster ovary (CHO-K1) and human embryonic kidney (HEK293) cells are exposed to a tightly focused 405-nm laser in the presence of plasmid DNA encoding for a mitochondrial targeted red fluorescent protein. We report transfection efficiencies as a function of laser power and exposure time for our system. We also show, for the first time, that a continuous wave laser source can be successfully applied to selective gene silencing experiments using small interfering RNA. This work is a major step towards an inexpensive and portable phototransfection system.

  3. [Qualitative Determination of Organic Vapour Using Violet and Visible Spectrum].

    PubMed

    Jiang, Bo; Hu, Wen-zhong; Liu, Chang-jian; Zheng, Wei; Qi, Xiao-hui; Jiang, Ai-li; Wang, Yan-ying

    2015-12-01

    Vapours of organic matters were determined qualitatively employed with ultraviolet-visible absorption spectroscopy. Vapours of organic matters were detected using ultraviolet-visible spectrophotometer employing polyethylene film as medium, the ultraviolet and visible absorption spectra of vegetable oil vapours of soybean oil, sunflower seed oil, peanut oil, rapeseed oil, sesame oil, cotton seed oil, tung tree seed oil, and organic compound vapours of acetone, ethyl acetate, 95% ethanol, glacial acetic acid were obtained. Experimental results showed that spectra of the vegetable oil vapour and the organic compound vapour could be obtained commendably, since ultra violet and visible spectrum of polyethylene film could be deducted by spectrograph zero setting. Different kinds of vegetable oils could been distinguished commendably in the spectra since the λ(max), λ(min), number of absorption peak, position, inflection point in the ultra violet and visible spectra obtained from the vapours of the vegetable oils were all inconsistent, and the vapours of organic compounds were also determined perfectly. The method had a good reproducibility, the ultraviolet and visible absorption spectra of the vapours of sunflower seed oil in 10 times determination were absolutely the same. The experimental result indicated that polyethylene film as a kind of medium could be used for qualitative analysis of ultraviolet and visible absorption spectroscopy. The method for determination of the vapours of the vegetable oils and organic compounds had the peculiarities of fast speed analysis, well reproducibility, accuracy and reliability and low cost, and so on. Ultraviolet and visible absorption spectrum of organic vapour could provide feature information of material vapour and structural information of organic compound, and provide a novel test method for identifying vapour of compound and organic matter.

  4. [Qualitative Determination of Organic Vapour Using Violet and Visible Spectrum].

    PubMed

    Jiang, Bo; Hu, Wen-zhong; Liu, Chang-jian; Zheng, Wei; Qi, Xiao-hui; Jiang, Ai-li; Wang, Yan-ying

    2015-12-01

    Vapours of organic matters were determined qualitatively employed with ultraviolet-visible absorption spectroscopy. Vapours of organic matters were detected using ultraviolet-visible spectrophotometer employing polyethylene film as medium, the ultraviolet and visible absorption spectra of vegetable oil vapours of soybean oil, sunflower seed oil, peanut oil, rapeseed oil, sesame oil, cotton seed oil, tung tree seed oil, and organic compound vapours of acetone, ethyl acetate, 95% ethanol, glacial acetic acid were obtained. Experimental results showed that spectra of the vegetable oil vapour and the organic compound vapour could be obtained commendably, since ultra violet and visible spectrum of polyethylene film could be deducted by spectrograph zero setting. Different kinds of vegetable oils could been distinguished commendably in the spectra since the λ(max), λ(min), number of absorption peak, position, inflection point in the ultra violet and visible spectra obtained from the vapours of the vegetable oils were all inconsistent, and the vapours of organic compounds were also determined perfectly. The method had a good reproducibility, the ultraviolet and visible absorption spectra of the vapours of sunflower seed oil in 10 times determination were absolutely the same. The experimental result indicated that polyethylene film as a kind of medium could be used for qualitative analysis of ultraviolet and visible absorption spectroscopy. The method for determination of the vapours of the vegetable oils and organic compounds had the peculiarities of fast speed analysis, well reproducibility, accuracy and reliability and low cost, and so on. Ultraviolet and visible absorption spectrum of organic vapour could provide feature information of material vapour and structural information of organic compound, and provide a novel test method for identifying vapour of compound and organic matter. PMID:26964229

  5. [Markers for Immunofluorescence Analysis Based on Europium Complex with Fluorinated β-Diketones Carbazole Series].

    PubMed

    Kostryukova, T S; Ivanovskaya, N P; Zatonsky, G V; Osin, N S; Vasilev, N V

    2015-01-01

    In order to develop new markers for immunofluorescence time-resolved luminescence analysis tetraketodiester carbazole series was obtained. Compound contains methoxycarbonyl reactive groups, separated from the 1,3-dicarbonyl chelating fragment by difluoromethylene spacers (CF2)4. Complexes of this compound with the ions Eu3+ are stable in aqueous solution and possess a long-living intensive luminescence with the main peaks: emission--in the area of 615 nm and excitation--in the 380-390 nm, that distinguishes them from most used analogues. Conjugate of streptavidin to compound was obtained and its fluorescent spectral characteristics allow to use it as a universal reagent for various schemes of biological microanalysis.

  6. N-(2-Ethylhexyl)carbazole: A New Fluorophore Highly Suitable as a Monomolecular Liquid Scintillator.

    PubMed

    Montbarbon, Eva; Sguerra, Fabien; Bertrand, Guillaume H V; Magnier, Élodie; Coulon, Romain; Pansu, Robert B; Hamel, Matthieu

    2016-08-16

    The synthesis, photophysical properties, and applications in scintillation counting of N-(2-ethylhexyl)carbazole (EHCz) are reported. This molecule displays all of the required characteristics for an efficient liquid scintillator (emission wavelength, scintillation yield), and can be used without any extra fluorophores. Thus, its scintillation properties are discussed, as well as its fast neutron/gamma discrimination. For the latter application, the material is compared with the traditional liquid scintillator BC-501 A, and other liquid fluorescent molecules classically used as scintillation solvents, such as xylene, pseudocumene (PC), linear alkylbenzenes (LAB), diisopropylnaphthalene (DIN), 1-methylnaphthalene (1-MeNapht), and 4-isopropylbiphenyl (iPrBiph). For the first time, an excimeric form of a molecule has been advantageously used in scintillation counting. A moderate discrimination between fast neutrons and gamma rays was observed in bulk EHCz, with an apparent neutron/gamma discrimination potential half of that of BC-501 A. PMID:27406840

  7. Molecular engineering of carbazole functionalized ruthenium dyes for efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Nguyen, Hong Minh; Vu, Dinh Lam; Nghia Nguyen, Duc

    2011-12-01

    A new ruthenium complex, coded HMP-12, incorporating an antenna ligand composed of the sequential connection of a conjugated segment and carbazole hole-transport moiety was synthesized. This dye exhibits a lower energy metal-to-ligand charge transfer (MLCT) band centered at 536 nm with a high molar absorption coefficient of 21.43×103 M‑1 cm‑1. Nanocrystalline ZnO dye-sensitized solar cells employing HMP-12 show good conversion efficiency (4.46%). It was found that the difference in light-harvesting properties between Rut-B1, HMP-11 and HMP-12 is associated mainly with dye structure. The power conversion efficiency of solar cells based on HMP-11 is 4.11% while the Rut-B1 delivered a lower efficiency of 3.57% under the same device fabrication and measuring conditions.

  8. Understanding the domino reaction between 3-chloroindoles and methyl coumalate yielding carbazoles. A DFT study.

    PubMed

    Domingo, Luis R; Sáez, José A; Emamian, Saeed R

    2015-02-21

    The molecular mechanism of the reaction between N-methyl-3-chloroindole and methyl coumalate yielding carbazole has been studied using DFT methods at the MPWB1K/6-311G(d,p) level in toluene. This reaction is a domino process that comprises three consecutive reactions: (i) a polar Diels-Alder (P-DA) reaction between indole and methyl coumalate yielding two stereoisomeric [2 + 4] cycloadducts (CAs); (ii) the elimination of HCl from these CAs affording two stereoisomeric intermediates; and (iii) the extrusion of CO2 in these intermediates, finally yielding the carbazole. This P-DA reaction proceeds in a completely regioselective and slightly exo selective fashion. In spite of the highly polar character of this P-DA reaction, it presents a high activation enthalpy of 21.8 kcal mol(-1) due to the loss of the aromatic character of the indole during the C-C bond formation. Thermodynamic calculations suggest that the P-DA reaction is the rate-determining step of this domino reaction; in addition, the initial HCl elimination in the formal [2 + 4] CAs is kinetically favoured over the extrusion of CO2. Although the P-DA reaction is kinetically and thermodynamically very unfavourable, the easier HCl and CO2 elimination from the [2 + 4] CAs together with the strong exergonic character of the CO2 extrusion makes the P-DA reaction irreversible. An ELF topological analysis of the bonding changes along the P-DA reaction supports a two-stage one-step mechanism. An analysis of the global DFT reactivity indices at the ground state of the reagents confirms the highly polar character of this P-DA reaction. Finally, the complete regioselectivity of the studied reactions can be explained using the Parr functions. PMID:25520216

  9. Understanding the domino reaction between 3-chloroindoles and methyl coumalate yielding carbazoles. A DFT study.

    PubMed

    Domingo, Luis R; Sáez, José A; Emamian, Saeed R

    2015-02-21

    The molecular mechanism of the reaction between N-methyl-3-chloroindole and methyl coumalate yielding carbazole has been studied using DFT methods at the MPWB1K/6-311G(d,p) level in toluene. This reaction is a domino process that comprises three consecutive reactions: (i) a polar Diels-Alder (P-DA) reaction between indole and methyl coumalate yielding two stereoisomeric [2 + 4] cycloadducts (CAs); (ii) the elimination of HCl from these CAs affording two stereoisomeric intermediates; and (iii) the extrusion of CO2 in these intermediates, finally yielding the carbazole. This P-DA reaction proceeds in a completely regioselective and slightly exo selective fashion. In spite of the highly polar character of this P-DA reaction, it presents a high activation enthalpy of 21.8 kcal mol(-1) due to the loss of the aromatic character of the indole during the C-C bond formation. Thermodynamic calculations suggest that the P-DA reaction is the rate-determining step of this domino reaction; in addition, the initial HCl elimination in the formal [2 + 4] CAs is kinetically favoured over the extrusion of CO2. Although the P-DA reaction is kinetically and thermodynamically very unfavourable, the easier HCl and CO2 elimination from the [2 + 4] CAs together with the strong exergonic character of the CO2 extrusion makes the P-DA reaction irreversible. An ELF topological analysis of the bonding changes along the P-DA reaction supports a two-stage one-step mechanism. An analysis of the global DFT reactivity indices at the ground state of the reagents confirms the highly polar character of this P-DA reaction. Finally, the complete regioselectivity of the studied reactions can be explained using the Parr functions.

  10. Biodegradation of crystal violet by the white rot fungus phanerochaete chrysosporium

    SciTech Connect

    Bumpus, J.A.; Brock, B.J.

    1988-01-01

    Biodegradation of crystal violet (N,N,N',N',N',N''- hexamethylpararosaniline) in ligninolytic (nitrogen-limited) cultures of the white rot fungus Phanerochaete chrysosporium was demonstrated by the disappearance of crystal violet and by the identification of three metabolites (N,N,N',N',N'' -pentamethylpararosaniline, N,N,N',N'' -tetramethylpararosaniline, and N,N',N'' -trimethylpararosaniline) formed by sequential N-demethylation of the parent compound. Metabolite formation also occurred when crystal violet was incubated with the extracellular fluid obtained from ligninolytic cultures of this fungus, provided that an H2O2-generating system was supplied. This, as well as the fact that a purified ligninase catalyzed N-demethylation of crystal violet, demonstrated that biodegradation of crystal violet by this fungus is dependent, at least in part, upon its lignin-degrading system. In addition to crystal violet, six other triphenylmethane dyes (pararosaniline, cresol red, bromphenol blue, ethyl violet, malachite green, and brilliant green) were shown to be degraded by the lignin-degrading system of this fungus.

  11. Toxicity induced by Basic Violet 14, Direct Red 28 and Acid Red 26 in zebrafish larvae.

    PubMed

    Shen, Bing; Liu, Hong-Cui; Ou, Wen-Bin; Eilers, Grant; Zhou, Sheng-Mei; Meng, Fan-Guo; Li, Chun-Qi; Li, Yong-Quan

    2015-12-01

    Basic Violet 14, Direct Red 28 and Acid Red 26 are classified as carcinogenic dyes in the European textile ecology standard, despite insufficient toxicity data. In this study, the toxicity of these dyes was assessed in a zebrafish model, and the underlying toxic mechanisms were investigated. Basic Violet 14 and Direct Red 28 showed acute toxicity with a LC50 value at 60.63 and 476.84 µg ml(-1) , respectively, whereas the LC50 of Acid Red 26 was between 2500 and 2800 µg ml(-1) . Treatment with Basic Violet 14, Direct Red 28 and Acid Red 26 resulted in common developmental abnormalities including delayed yolk sac absorption and swimming bladder deflation. Hepatotoxicity was observed in zebrafish treated with Basic Violet 14, and cardiovascular toxicity was found in zebrafish treated with Acid Red 26 at concentrations higher than 2500 µg ml(-1) . Basic Violet 14 also caused significant up-regulation of GCLC gene expression in a dose-dependent manner whereas Acid Red 26 induced significant up-regulation of NKX2.5 and down-regulation of GATA4 at a high concentration in a dose-dependent manner. These results suggest that Basic Violet 14, Direct Red 28 and Acid Red 26 induce developmental and organ-specific toxicity, and oxidative stress may play a role in the hepatotoxicity of Basic Violet 14, the suppressed GATA4 expression may have a relation to the cardiovascular toxicity of Acid Red 26.

  12. Ferulic acid-carbazole hybrid compounds: Combination of cholinesterase inhibition, antioxidant and neuroprotection as multifunctional anti-Alzheimer agents.

    PubMed

    Fang, Lei; Chen, Mohao; Liu, Zhikun; Fang, Xubin; Gou, Shaohua; Chen, Li

    2016-02-15

    In order to search for novel multifunctional anti-Alzheimer agents, a series of ferulic acid-carbazole hybrid compounds were designed and synthesized. Ellman's assay revealed that the hybrid compounds showed moderate to potent inhibitory activity against the cholinesterases. Particularly, the AChE inhibition potency of compound 5k (IC50 1.9μM) was even 5-fold higher than that of galantamine. In addition, the target compounds showed pronounced antioxidant ability and neuroprotective property, especially against the ROS-induced toxicity. Notably, the neuroprotective effect of 5k was obviously superior to that of the mixture of ferulic acid and carbazole, indicating the therapeutic effect of the hybrid compound is better than the combination administration of the corresponding mixture.

  13. Ferulic acid-carbazole hybrid compounds: Combination of cholinesterase inhibition, antioxidant and neuroprotection as multifunctional anti-Alzheimer agents.

    PubMed

    Fang, Lei; Chen, Mohao; Liu, Zhikun; Fang, Xubin; Gou, Shaohua; Chen, Li

    2016-02-15

    In order to search for novel multifunctional anti-Alzheimer agents, a series of ferulic acid-carbazole hybrid compounds were designed and synthesized. Ellman's assay revealed that the hybrid compounds showed moderate to potent inhibitory activity against the cholinesterases. Particularly, the AChE inhibition potency of compound 5k (IC50 1.9μM) was even 5-fold higher than that of galantamine. In addition, the target compounds showed pronounced antioxidant ability and neuroprotective property, especially against the ROS-induced toxicity. Notably, the neuroprotective effect of 5k was obviously superior to that of the mixture of ferulic acid and carbazole, indicating the therapeutic effect of the hybrid compound is better than the combination administration of the corresponding mixture. PMID:26795115

  14. Determination by ultraviolet absorption spectrometry and theoretical calculation of dissociation constant of 1,2,3,9-tetrahydro-4H-carbazol-4-one.

    PubMed

    Zhang, Shufang; Zhang, Xiaoyan; Tang, Ke; Zhou, Zhengyu

    2009-08-15

    The dissociation constant of 1,2,3,9-tetrahydro-4H-carbazol-4-one was determined by ultraviolet absorption spectrometry method based on the absorption spectra of 1,2,3,9-tetrahydro-4H-carbazol-4-one at different pH in ethanol-water mixed solvents. The results show that the pK(b) was a good linear function of the volume fraction of ethanol in the concentration range studied. The dissociation constant of 1, 2, 3,9-tetrahydro-4H-carbazol-4-one in water were determined by extrapolation to be 14.04 under the condition of this experiment. The accurate pK(b) calculations of 1,2,3,9-tetrahydro-4H-carbazol-4-one have been investigated using the combination of the extended clusters-continuum model with the polarizable continuum solvation model (PCM). The calculations are performed at the B3LYP/6-31G levels. The formation of molecular clusters by means of the 1,2,3,9-tetrahydro-4H-carbazol-4-one wrapped up with water molecules leads to the weakness of the interaction between the polar solvents and the 1,2,3,9-tetrahydro-4H-carbazol-4-one, hence, the accuracy of pK(b) has been enhanced. The dissociation constant of 1,2,3,9-tetrahydro-4H-carbazol-4-one in water were calculated to be 14.10 and agreed well with experimental data.

  15. Mosaic of Jupiter's Great Red Spot (Violet Filter)

    NASA Technical Reports Server (NTRS)

    1996-01-01

    Great Red Spot of Jupiter as seen through the violet (404 nm) filter of the Galileo imaging system. The image is a mosaic of six images that have been map-projected to a uniform grid of latitude and longitude. North is at the top. The mosaic was taken over a 75 second interval beginning at universal time 4 hours, 18 minutes, 8 seconds on June 26, 1996. The Red Spot is 20,000 km long and has been followed by observers on Earth since the telescope was invented 300 years ago. It is a huge storm made visible by variations in the composition of the cloud particles. The Red Spot is not unique, but is simply the largest of a class of long-lived vortices, some of which are visible in the lower part of the image. The range is 1.76 million kilometers.

    The Jet Propulsion Laboratory, Pasadena, CA manages the mission for NASA's Office of Space Science, Washington, DC.

    This image and other images and data received from Galileo are posted on the World Wide Web, on the Galileo mission home page at URL http://galileo.jpl.nasa.gov. Background information and educational context for the images can be found at URL http://www.jpl.nasa.gov/galileo/sepo

  16. A combined resorcin-crystal violet-periodic acid-Schiff stain.

    PubMed

    Cannon, M S; Schultz, L H

    1980-02-01

    Resorcin-crystal violet followed by the periodic acid-Schiff (PAS) reaction can be used to stain elastic fibers and membranes greenish-yellow, while coloring PAS-positive materials pink to purple. Other tissue components are left unstained.

  17. Biodegradation of hazardous triphenylmethane dye methyl violet by Rhizobium radiobacter (MTCC 8161).

    PubMed

    Parshetti, Ganesh; Saratale, Ganesh; Telke, Amar; Govindwar, Sanjay

    2009-09-01

    Rhizobium radiobacter MTCC 8161 completely decolorized methyl violet (10 mg l(-1)) within 8 h both at static and shaking conditions. The decolorization time increased with increasing dye concentration. The effect of different carbon and nitrogen sources on the decolorization of methyl violet was studied. The maximum decolorization was observed in the presence of sucrose (1%) and urea (1%). UV-Visible, HPLC and FTIR analysis of extracted products confirmed biodegradation of methyl violet. The significant increase in the activities of lignin peroxidase and aminopyrine N-demethylase in the cells obtained after decolorization indicated involvement of these enzymes in the decolorization process. In addition to methyl violet, this strain also shows an ability to decolorize various industrial dyes, (red HE7B, yellow 4G, blue 2B, navy blue HE22, red M5B and red HE3B).

  18. Surface-enhanced Raman scattering from crystal violet adsorbed on a silver electrode

    NASA Astrophysics Data System (ADS)

    Watanabe, Tadashi; Pettinger, Bruno

    1982-07-01

    SERS from crystal violet (CV) on a Ag electrode was investigated under preresonance and resonance conditions. The excitation profile of the chemisorbed species is like that of dissolved molecules but intensities are ≈ 1000 times larger. The Raman enhancement is ≈ 10 8 and exhibits a specific potential dependence even in the absence of adsorption-desorption process. At potentials where reduction of CV occurs leuco crystal violet was detected.

  19. Photo Inactivation of Streptococcus mutans Biofilm by Violet-Blue light.

    PubMed

    Gomez, Grace F; Huang, Ruijie; MacPherson, Meoghan; Ferreira Zandona, Andrea G; Gregory, Richard L

    2016-09-01

    Among various preventive approaches, non-invasive phototherapy/photodynamic therapy is one of the methods used to control oral biofilm. Studies indicate that light at specific wavelengths has a potent antibacterial effect. The objective of this study was to determine the effectiveness of violet-blue light at 380-440 nm to inhibit biofilm formation of Streptococcus mutans or kill S. mutans. S. mutans UA159 biofilm cells were grown for 12-16 h in 96-well flat-bottom microtiter plates using tryptic soy broth (TSB) or TSB with 1 % sucrose (TSBS). Biofilm was irradiated with violet-blue light for 5 min. After exposure, plates were re-incubated at 37 °C for either 2 or 6 h to allow the bacteria to recover. A crystal violet biofilm assay was used to determine relative densities of the biofilm cells grown in TSB, but not in TSBS, exposed to violet-blue light. The results indicated a statistically significant (P < 0.05) decrease compared to the non-treated groups after the 2 or 6 h recovery period. Growth rates of planktonic and biofilm cells indicated a significant reduction in the growth rate of the violet-blue light-treated groups grown in TSB and TSBS. Biofilm viability assays confirmed a statistically significant difference between violet-blue light-treated and non-treated groups in TSB and TSBS. Visible violet-blue light of the electromagnetic spectrum has the ability to inhibit S. mutans growth and reduce the formation of S. mutans biofilm. This in vitro study demonstrated that violet-blue light has the capacity to inhibit S. mutans biofilm formation. Potential clinical applications of light therapy in the future remain bright in preventing the development and progression of dental caries. PMID:27278805

  20. Strong ultraviolet and violet emissions from ZnO/TiO2 multilayer thin films

    NASA Astrophysics Data System (ADS)

    Xu, Linhua; Zheng, Gaige; Wu, Hongyan; Wang, Junfeng; Gu, Fang; Su, Jing; Xian, Fenglin; Liu, Zhanhui

    2013-06-01

    ZnO/TiO2 multilayer thin films were prepared by electron beam evaporation and the influence of annealing temperature on their structural and optical properties was investigated. The analyses of X-ray diffraction (XRD) show that TiO2 in the as-deposited ZnO/TiO2 multilayer thin film as well as in that one annealed at 300 °C is amorphous. When the annealing temperature is increased up to 400 °C, the TiO2 is transformed into a brookite phase. Eventually, the TiO2 is transformed into an anatase phase with the annealing temperature rising up to 500 °C. However, ZnO in these composite films all crystallizes in a wurtzite structure and has a preferred orientation along the (0 0 2) direction whether the ZnO/TiO2 multilayer thin film is annealed or not. The photoluminescence spectra show that all the samples have two strong emission peaks including an ultraviolet (UV) peak and a violet peak. The strong UV and violet co-emissions in ZnO materials is seldom reported previously. With the increase of annealing temperature, both the UV and violet emissions are enhanced. However, the intensity of UV emission is increased faster than that of the violet emission under the same annealing temperature. The mechanism of the violet emission and the reason for the variations of the UV and violet emissions with the different annealing temperatures are analyzed.

  1. Discovery of a Carbazole-Derived Lead Drug for Human African Trypanosomiasis.

    PubMed

    Thomas, Sarah M; Purmal, Andrei; Pollastri, Michael; Mensa-Wilmot, Kojo

    2016-01-01

    The protozoan parasite Trypanosoma brucei causes the fatal illness human African trypanosomiasis (HAT). Standard of care medications currently used to treat HAT have severe limitations, and there is a need to find new chemical entities that are active against infections of T. brucei. Following a "drug repurposing" approach, we tested anti-trypanosomal effects of carbazole-derived compounds called "Curaxins". In vitro screening of 26 compounds revealed 22 with nanomolar potency against axenically cultured bloodstream trypanosomes. In a murine model of HAT, oral administration of compound 1 cured the disease. These studies established 1 as a lead for development of drugs against HAT. Pharmacological time-course studies revealed the primary effect of 1 to be concurrent inhibition of mitosis coupled with aberrant licensing of S-phase entry. Consequently, polyploid trypanosomes containing 8C equivalent of DNA per nucleus and three or four kinetoplasts were produced. These effects of 1 on the trypanosome are reminiscent of "mitotic slippage" or endoreplication observed in some other eukaryotes. PMID:27561392

  2. Inhibition of Plasmodium falciparum Hsp90 Contributes to the Antimalarial Activities of Aminoalcohol-carbazoles.

    PubMed

    Wang, Tai; Mäser, Pascal; Picard, Didier

    2016-07-14

    Malaria caused by the protozoan parasite Plasmodium falciparum (Pf) remains a major public health problem throughout the developing world. One molecular target that should receive more attention is the molecular chaperone Hsp90. It is essential and highly conserved in all eukaryotes, including in protozoan parasites. We have identified an amino-alcohol carbazole (N-CBZ) as a PfHsp90-selective inhibitor by virtually docking a large set of antimalarial compounds, previously found in a phenotypic screen, into a PfHsp90-specific pocket. By correlating the ability of 30 additional N-CBZ derivatives to bind directly to PfHsp90 with their Pf-inhibitory activity, we found that these types of compounds are more likely to inhibit Pf growth if they bind PfHsp90. For plausible targets such as PfHsp90, our workflow may help identifying the molecular target for compounds found by screening large chemical libraries for a desired biological effect and, conversely, ensuring biological effectiveness for compounds affecting a particular target. PMID:27312008

  3. Discovery of a Carbazole-Derived Lead Drug for Human African Trypanosomiasis

    PubMed Central

    Thomas, Sarah M.; Purmal, Andrei; Pollastri, Michael; Mensa-Wilmot, Kojo

    2016-01-01

    The protozoan parasite Trypanosoma brucei causes the fatal illness human African trypanosomiasis (HAT). Standard of care medications currently used to treat HAT have severe limitations, and there is a need to find new chemical entities that are active against infections of T. brucei. Following a “drug repurposing” approach, we tested anti-trypanosomal effects of carbazole-derived compounds called “Curaxins”. In vitro screening of 26 compounds revealed 22 with nanomolar potency against axenically cultured bloodstream trypanosomes. In a murine model of HAT, oral administration of compound 1 cured the disease. These studies established 1 as a lead for development of drugs against HAT. Pharmacological time-course studies revealed the primary effect of 1 to be concurrent inhibition of mitosis coupled with aberrant licensing of S-phase entry. Consequently, polyploid trypanosomes containing 8C equivalent of DNA per nucleus and three or four kinetoplasts were produced. These effects of 1 on the trypanosome are reminiscent of “mitotic slippage” or endoreplication observed in some other eukaryotes. PMID:27561392

  4. Cyclotriveratrylene-carbazole cage for self-assembly of C₆₀.

    PubMed

    Wu, Hongjuan; Zhang, Caihong; Li, Lifeng; Chao, Jianbin; Han, Yujie; Dong, Chuan; Guo, Yujing; Shuang, Shaomin

    2013-03-15

    A novel open-bowl pyramidal compound cyclotriveratrylene-carbazole (CTV-CZ) was designed and synthesized. Its absorption and emission spectroscopic properties in different organic solvents were characterized. Three absorption peaks of CTV-CZ around 235 nm, 260 nm and 290 nm were observed. The fluorescence emission peaks were at about 353 nm and 368 nm using a solution of ∼10(-7)M CTV-CZ. The intermolecular interaction between CTV-CZ and fullerene (C₆₀) was studied in detail by UV-vis absorption and fluorescence spectra. CTV-CZ could associate with C₆₀ to form supramolecular complex with 1:1 molar ratio and the binding constant was estimated to be 5.0(6) × 10(4)M(-1) by fluorimetry. The formation of inclusion complex for CTV-CZ and C₆₀ was further confirmed by (1)H NMR and cyclic voltammetry. The downfield shift of protons of CTV-CZ in its (1)H NMR spectrum and the decrease of redox currents on addition of C₆₀ showed that photo induced electron transfer (PET) occurred from the electron donor CTV and CZ units to the electron acceptor C₆₀. PMID:23598151

  5. Asymmetric energy transfer and optical diffraction in novel molecular glass with carbazole moiety

    NASA Astrophysics Data System (ADS)

    Tsutsumi, Naoto; Eguchi, Junya; Sakai, Wataru

    2006-12-01

    Asymmetric energy transfer and optical diffraction under optically interfered beams was presented in composites with novel star-shaped molecular glass end-caped by carbazole moiety, α,α',α″-tris-(4-(carbazoryl)- n-hexyloxyphenyl)-1,3,5-triisopropylbenzene (Tris). Composite consisted of Tris as host matrix, 2,4,7-trinitro-9-fluorenone (TNF) as a sensitizer, ( S)-(-)-1-(4-nitrophenyl)-2-pyrrolidine-methanol (NPP) as a nonlinear optical dye and either tricresyl phosphate (TCP), n-butyl benzyl phthalate (BBP), diphenyl phthalate (DPP), or dicyclohexyl phthalate (DCP) as a plasticizer. Asymmetric two beam coupling (asymmetric energy transfer) and beam diffraction were achieved with no external field. Glass transition temperature of the composites plays an important role for these phenomena of asymmetric energy transfer and optical diffraction with no external field. Highest net gain coefficient of 59.7 cm -1 with optical gain of 151.3 cm -1 and absorption coefficient of 91.6 cm -1 was obtained for Tris/NPP/DPP/TNF (35/20/40/5) composite. TNF anion produced by laser illumination plays a key role of beam diffraction and asymmetric two beam coupling in the composites.

  6. Neuroprotective efficacy of aminopropyl carbazoles in a mouse model of amyotrophic lateral sclerosis.

    PubMed

    Tesla, Rachel; Wolf, Hamilton Parker; Xu, Pin; Drawbridge, Jordan; Estill, Sandi Jo; Huntington, Paula; McDaniel, Latisha; Knobbe, Whitney; Burket, Aaron; Tran, Stephanie; Starwalt, Ruth; Morlock, Lorraine; Naidoo, Jacinth; Williams, Noelle S; Ready, Joseph M; McKnight, Steven L; Pieper, Andrew A

    2012-10-16

    We previously reported the discovery of P7C3, an aminopropyl carbazole having proneurogenic and neuroprotective properties in newborn neural precursor cells of the hippocampal dentate gyrus. We have further found that chemicals having efficacy in this in vivo screening assay also protect dopaminergic neurons of the substantia nigra following exposure to the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, a mouse model of Parkinson disease. Here, we provide evidence that an active analog of P7C3, known as P7C3A20, protects ventral horn spinal cord motor neurons from cell death in the G93A-SOD1 mutant mouse model of amyotrophic lateral sclerosis (ALS). P7C3A20 is efficacious in this model when administered at disease onset, and protection from cell death correlates with preservation of motor function in assays of walking gait and in the accelerating rotarod test. The prototypical member of this series, P7C3, delays disease progression in G93A-SOD1 mice when administration is initiated substantially earlier than the expected time of symptom onset. Dimebon, an antihistaminergic drug with significantly weaker proneurogenic and neuroprotective efficacy than P7C3, confers no protection in this ALS model. We propose that the chemical scaffold represented by P7C3 and P7C3A20 may provide a basis for the discovery and optimization of pharmacologic agents for the treatment of ALS.

  7. Effect of carbazole as a donor moiety on the second-order nonlinearity of organic molecules

    NASA Astrophysics Data System (ADS)

    Meshulam, Guilia; Berkovic, Garry; Kotler, Zvi; Ben-Asuly, Amos; Mazor, Royi; Shapiro, Lev; Khodorkovsky, Vladimir

    1999-10-01

    The second order nonlinearity of conjugated organic molecules involving, 1,3 indandione derivatives as an acceptor moiety has been studied. Varying the donor from dialkylamino to the chemically similar substituent, N- carbazolyl resulted in a drastic reduction of electric field induced second harmonic (beta) values. For some molecules, even a small negative value of (beta) was received. Quantum chemical calculations indicate that the decrease occurs as a result of two overlapping transitions, which contribute to (beta) with opposite signs. The charge transfer band gives a positive (beta) zzz along the molecular long axis, while a transition essentially within the carbazole moiety provides a negative (beta zzz contribution to (beta EFISH. Thus, these molecules must be described with a 2D model as opposed to the 'classical' model of 1D nonlinear optical chromophores. The prediction of the 2D model was verified experimentally by using a combination of two methods, EFISH and Hyper-Rayleigh Scattering, which probe different combination of the (beta) tensor elements.

  8. Neuroprotective efficacy of aminopropyl carbazoles in a mouse model of amyotrophic lateral sclerosis

    PubMed Central

    Tesla, Rachel; Wolf, Hamilton Parker; Xu, Pin; Drawbridge, Jordan; Estill, Sandi Jo; Huntington, Paula; McDaniel, LaTisha; Knobbe, Whitney; Burket, Aaron; Tran, Stephanie; Starwalt, Ruth; Morlock, Lorraine; Naidoo, Jacinth; Williams, Noelle S.; Ready, Joseph M.; McKnight, Steven L.; Pieper, Andrew A.

    2012-01-01

    We previously reported the discovery of P7C3, an aminopropyl carbazole having proneurogenic and neuroprotective properties in newborn neural precursor cells of the hippocampal dentate gyrus. We have further found that chemicals having efficacy in this in vivo screening assay also protect dopaminergic neurons of the substantia nigra following exposure to the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, a mouse model of Parkinson disease. Here, we provide evidence that an active analog of P7C3, known as P7C3A20, protects ventral horn spinal cord motor neurons from cell death in the G93A-SOD1 mutant mouse model of amyotrophic lateral sclerosis (ALS). P7C3A20 is efficacious in this model when administered at disease onset, and protection from cell death correlates with preservation of motor function in assays of walking gait and in the accelerating rotarod test. The prototypical member of this series, P7C3, delays disease progression in G93A-SOD1 mice when administration is initiated substantially earlier than the expected time of symptom onset. Dimebon, an antihistaminergic drug with significantly weaker proneurogenic and neuroprotective efficacy than P7C3, confers no protection in this ALS model. We propose that the chemical scaffold represented by P7C3 and P7C3A20 may provide a basis for the discovery and optimization of pharmacologic agents for the treatment of ALS. PMID:23027932

  9. Initial Conservative Management of Exomphalos Major with Gentian Violet

    PubMed Central

    Ferdous, KMN

    2012-01-01

    Aim: The purpose of the study was to assess the results of topical use of gentian violet (GV), among the babies with exomphalos major in our institute. Methods: The study was carried out retrospectively in a tertiary care hospital during the period from 2005 to 2010 inclusive. Exomphalos patients were classified as major if diameter was >5 cm and/or had liver in the sac as content. These patients were initially preferentially treated conservatively with topical 1% GV over the sac resultig a ventral hernia to be repaired later. Results: A total of 84 exomphalos patients were admitted during the study period. Among them, 37 neonates (26 males and 11 females) had exomphalos major (EM). Ten of them were prenatally diagnosed. The mean gestational age at delivery was 35 weeks, and mean birth weight was 2.1 Kg. Mean age at presentation was 3.7 days. Thirty (81%) had other associated anomalies, mostly cardiac (66.6%) and pulmonary (46.6%). Ten patients with EM needed early operation because of ruptured sac, and other anomalies. There were 2 pre-operative and 8 postoperative deaths in this subgroup. Twenty seven patients were treated conservatively, among these 4 died of overwhelming sepsis. Remaining 23 patients left the hospital with a ventral hernia planned to be repaired at 1 year of age. Overall mortality in our series was 37.83%. Conclusion: Initial conservative treatment of the sac with GV results in satisfactory outcome for infants with EM who cannot undergo immediate closure. PMID:26023410

  10. Investigation of ultra violet (UV) resistance for high strength fibers

    NASA Astrophysics Data System (ADS)

    Said, M. A.; Dingwall, Brenda; Gupta, A.; Seyam, A. M.; Mock, G.; Theyson, T.

    Ultra long duration balloons (ULDB), currently under development by the National Aeronautics and Space Administration (NASA), requires the use of high strength fibers in the selected super-pressure pumpkin design. The pumpkin shape balloon concept allows clear separation of the load transferring functions of the major structural elements of the pneumatic envelope, the tendons and the film. Essentially, the film provides the gas barrier and transfers only local pressure load to the tendons. The tendons, in the mean time, provide the global pressure containing strength. In that manner, the strength requirement for the film only depends on local parameters. The tendon is made of p-phenylene-2,6-benzobisoxazole (PBO) fibers, which is selected due to its high strength to weight ratio when compared to other high performance, commercially available, fibers. High strength fibers, however, are known to degrade upon exposure to light, particularly at short wavelengths. This paper reports the results of an investigation of the resistance of four commercial high strength fibers to ultra violet (UV) exposure. The results indicate that exposing high strength fibers in continuous yarn form to UV led to serious loss in strength of the fibers except for Spectra® fibers. The adverse changes in mechanical behavior occurred over short duration of exposure compared to the 100 day duration targeted for these missions. UV blocking finishes to improve the UV resistance of these fibers are being investigated. The application of these specially formulated coatings is expected to lead to significant improvement of the UV resistance of these high performance fibers. In this publication, we report on the mechanical behavior of the fibers pre- and post-exposure to UV, but without application of the blocking finishes.

  11. Synthesis and spectra of a kind of novel longer-wavelength benzoxazole indole styryl cyanine dye with a carbazole-bridged chain.

    PubMed

    Fei, Xuening; Gu, Yingchun; Li, Chao; Liu, Yuru; Yu, Lu

    2013-01-01

    Based on cyanine dye probe oxazole yellow (YO) and Cy(3), a series of novel styryl cyanine dyes were designed and synthesized. Carbazole was inserted into the structures of YO and Cy(3) to act as a bridge to link the benzoxazole and indole group. This modification resulted in a novel kind of benzoxazole indole styryl cyanine dye with a carbazole-bridged chain. The dyes were characterized by (1)HNMR and MS. The spectra of the novel dyes were also performed and the results showed that the maximum emission wavelength of the carbazole styryl cyanine dye was shifted red, the Stokes shift increased and the fluorescence intensity enhanced compared with those of YO and Cy(3). These results indicated that the novel dye could be used as an excellent fluorescent probe in biological labeling.

  12. Self-Assembly of Electron Donor-Acceptor-Based Carbazole Derivatives: Novel Fluorescent Organic Nanoprobes for Both One- and Two-Photon Cellular Imaging.

    PubMed

    Zhang, Jinfeng; Chen, Wencheng; Kalytchuk, Sergii; Li, King Fai; Chen, Rui; Adachi, Chihaya; Chen, Zhan; Rogach, Andrey L; Zhu, Guangyu; Yu, Peter K N; Zhang, Wenjun; Cheah, Kok Wai; Zhang, Xiaohong; Lee, Chun-Sing

    2016-05-11

    In this study, we report fluorescent organic nanoprobes with intense blue, green, and orange-red emissions prepared by self-assembling three carbazole derivatives into nanorods/nanoparticles. The three compounds consist of two or four electron-donating carbazole groups linked to a central dicyanobenzene electron acceptor. Steric hindrance from the carbazole groups leads to noncoplanar 3D molecular structures favorable to fluorescence in the solid state, while the donor-acceptor structures endow the molecules with good two-photon excited emission properties. The fluorescent organic nanoprobes exhibit good water dispersibility, low cytotoxicity, superior resistance against photodegradation and photobleaching. Both one- and two-photon fluorescent imaging were shown in the A549 cell line. Two-photon fluorescence imaging with the fluorescent probes was demonstrated to be more effective in visualizing and distinguishing cellular details compared to conventional one-photon fluorescence imaging.

  13. Concise synthesis of carbazole-1,4-quinones and evaluation of their antiproliferative activity against HCT-116 and HL-60 cells.

    PubMed

    Nishiyama, Takashi; Hatae, Noriyuki; Yoshimura, Teruki; Takaki, Sawa; Abe, Takumi; Ishikura, Minoru; Hibino, Satoshi; Choshi, Tominari

    2016-10-01

    We report a convenient synthesis of carbazole-1,4-quinone alkaloid koeniginequinones A and B using a tandem ring-closing metathesis with the dehydrogenation reaction sequence under an O2 atmosphere as an important step. Using this method, carbazole-1,4-quinones substituted at the 5-, 6-, 7-, and/or 8-positions have been synthesized. Moreover, 24 compounds, including koeniginequinones A and B, have been evaluated for their antiproliferative activity against HCT-116 and HL-60 cells, and the 6-nitro analog exhibited the most potent activity against both tumor cell types. PMID:27318980

  14. One-Pot Synthesis of N-(α-Peroxy)Indole/Carbazole via Chemoselective Three-Component Condensation Reaction in Open Atmosphere.

    PubMed

    Wang, Xinbo; Pan, Yupeng; Huang, Kuo-Wei; Lai, Zhiping

    2015-11-20

    A facile one-pot synthesis of N-(α-peroxy)indole and N-(α-peroxy)carbazole has been developed using metal-free, organo-acid-catalyzed three-component condensation reactions of indole/carbazole, aldehyde, and peroxide. Based on the reaction discovered, a new synthetic proposal for Fumitremorgin A and Verruculogen is introduced. Such a protocol could be easily handled and scaled up in an open atmosphere with a wide substrate scope, enabling the construction of a new molecule library. PMID:26541059

  15. Global Ultra-Violet Ionosphere-Thermosphere Observatory (GUVITO)

    NASA Astrophysics Data System (ADS)

    Curtis, N.; Crowley, G.; Christensen, A. B.; Paxton, L. J.; Robichaud, J.; Barry, M. A.; Bust, G. S.

    2009-12-01

    UV spectrographic imagers such as SSUSI and GUVI provide measurements of the aurora, ionospheric electron density, ionospheric bubbles, and thermospheric temperature, composition, and density. These imagers have been a key element of the Air Force DMSP program, but to accommodate new satellite concepts and maintain flexibility in the choice of new space systems and launch options, lighter weight and more capable UV instruments are needed to replace the current series of SSUSI sensors. Here we describe a technological alternative to the currently flying SSUSI sensors. It is a spectrographic imaging capability known as the “Global Ultra-Violet Ionosphere-Thermosphere Observatory” (GUVITO) sensor and associated software. GUVITO improves upon current instruments by being smaller in size, weight and power but with improved functionality. The GUVITO sensor represents an upgrade of the SSUSI and GUVI sensors in terms of scan mirror functionality and reliability, sensor functionality, mass, and power requirements. In particular, this improved functionality is expected to lead to enhanced capability in observing ionospheric bubbles, which are thought to cause scintillation and serious technological challenges for communications, navigation and surveillance systems. Initial development and risk reduction activities are currently funded by AFRL through a SBIR Phase II contract. The enhanced reliability and performance of the GUVITO sensor system is achieved with flight heritage components, concepts, software, hardware and is guided by key personnel experienced with both the SSUSI and GUVI hardware, software and operations. GUVITO would meet DoD priority requirements in ionospheric density, scintillation, and satellite drag, meet NPOESS IORD-II requirements for space environment Environmental Data Records (EDRs), maintain current DMSP capability, ensure long-term continuity of space environmental monitoring and leverage new technology development for future operational

  16. Comparison of violet diode laser with CO II laser in surgical performance of soft tissues

    NASA Astrophysics Data System (ADS)

    Hatayama, H.; Kato, J.; Inoue, A.; Akashi, G.; Hirai, Y.

    2007-02-01

    The violet diode laser (405nm) has recently begun to be studied for surgical use and authors reported the soft tissue could be effectively incised by irradiation power of even less than 1W. The wavelength of this laser is highly absorbed by hemoglobin, myoglobin or melanin pigment. Cutting or ablating soft tissues by lower irradiation power might be preferable for wound healing. The CO II laser is known to be preferable for low invasive treatment of soft tissues and widely used. The CO II laser light (10.6μm) is highly absorbed by water and proper for effective ablation of soft tissues. In this paper, we report the comparison of the violet diode laser with the CO II laser in surgical performance of soft tissues. Tuna tissue was used as an experimental sample. In the case of the violet diode laser, extensive vaporization of tissue was observed after the expansion of coagulation. Carbonization of tissue was observed after the explosion. On the other hand, consecutive vaporization and carbonization were observed immediately after irradiation in the case of CO II laser. The violet diode laser could ablate tissue equivalently with the CO II laser and coagulate larger area than the CO II laser. Therefore the violet diode laser might be expectable as a surgical tool which has excellent hemostatis.

  17. A Methoxydiphenylamine-Substituted Carbazole Twin Derivative: An Efficient Hole-Transporting Material for Perovskite Solar Cells.

    PubMed

    Gratia, Paul; Magomedov, Artiom; Malinauskas, Tadas; Daskeviciene, Maryte; Abate, Antonio; Ahmad, Shahzada; Grätzel, Michael; Getautis, Vytautas; Nazeeruddin, Mohammad Khaja

    2015-09-21

    The small-molecule-based hole-transporting material methoxydiphenylamine-substituted carbazole was synthesized and incorporated into a CH3NH3PbI3 perovskite solar cell, which displayed a power conversion efficiency of 16.91%, the second highest conversion efficiency after that of Spiro-OMeTAD. The investigated hole-transporting material was synthesized in two steps from commercially available and relatively inexpensive starting reagents. Various electro-optical measurements (UV/Vis, IV, thin-film conductivity, hole mobility, DSC, TGA, ionization potential) have been carried out to characterize the new hole-transporting material. PMID:26184563

  18. Genetic characterization and evolutionary implications of a car gene cluster in the carbazole degrader Pseudomonas sp. strain CA10.

    PubMed

    Nojiri, H; Sekiguchi, H; Maeda, K; Urata, M; Nakai, S; Yoshida, T; Habe, H; Omori, T

    2001-06-01

    The nucleotide sequences of the 27,939-bp-long upstream and 9,448-bp-long downstream regions of the carAaAaBaBbCAc(ORF7)Ad genes of carbazole-degrading Pseudomonas sp. strain CA10 were determined. Thirty-two open reading frames (ORFs) were identified, and the car gene cluster was consequently revealed to consist of 10 genes (carAaAaBaBbCAcAdDFE) encoding the enzymes for the three-step conversion of carbazole to anthranilate and the degradation of 2-hydroxypenta-2,4-dienoate. The high identities (68 to 83%) with the enzymes involved in 3-(3-hydroxyphenyl)propionic acid degradation were observed only for CarFE. This observation, together with the fact that two ORFs are inserted between carD and carFE, makes it quite likely that the carFE genes were recruited from another locus. In the 21-kb region upstream from carAa, aromatic-ring-hydroxylating dioxygenase genes (ORF26, ORF27, and ORF28) were found. Inductive expression in carbazole-grown cells and the results of homology searching indicate that these genes encode the anthranilate 1,2-dioxygenase involved in carbazole degradation. Therefore, these ORFs were designated antABC. Four homologous insertion sequences, IS5car1 to IS5car4, were identified in the neighboring regions of car and ant genes. IS5car2 and IS5car3 constituted the putative composite transposon containing antABC. One-ended transposition of IS5car2 together with the 5' portion of antA into the region immediately upstream of carAa had resulted in the formation of IS5car1 and ORF9. In addition to the insertion sequence-dependent recombination, gene duplications and presumed gene fusion were observed. In conclusion, through the above gene rearrangement, the novel genetic structure of the car gene cluster has been constructed. In addition, it was also revealed that the car and ant gene clusters are located on the megaplasmid pCAR1. PMID:11371531

  19. Radial liquid crystal alignment based on circular rubbing of a substrate coated with poly(N-vinyl carbazole) film

    NASA Astrophysics Data System (ADS)

    Chen, Yuan-Di; Ying-Guey Fuh, Andy; Liu, Cheng-Kai; Cheng, Ko-Ting

    2011-06-01

    This paper presents a simple method to produce radial liquid crystal (LC) alignment layers using circular rubbing of poly(N-vinyl carbazole) (PVK) films. The produced layer can be used for fabricating axially symmetric homogeneous-radial, homeotropic-radial and radial-radial LC alignment devices by combining a rubbed PVK-coated substrate with another one with a desired LC alignment layer. The transmittance-voltage curves of the fabricated LC devices at various positions are measured to examine the uniformity of the alignment effect. Additionally, the PVK film does not absorb visible light, and can be operated at high temperatures.

  20. N-(2,6-Dimeth­oxy­pyridin-3-yl)-9-methyl-9H-carbazole-3-sulfonamide

    PubMed Central

    Shan, Guangzhi; Li, Zhuorong; Hu, Laixing; Jiang, Jiandong; Liu, Zongying

    2013-01-01

    In the title compound, C20H19N3O4S, a novel tubulin ligand active against human cancer, the dihedral angle between the pyridine ring and the carbazole ring system is 42.87 (10)°. In the crystal, the mol­ecules are held together by N—H⋯O and C—H⋯O hydrogen bonds into layers, which are assembled into a three-dimensional network via π–π stacking inter­actions between inversion-related pyridine rings, with centroid–centroid distances of 3.5101 (12) Å. PMID:23634116

  1. Neuroprotective efficacy of aminopropyl carbazoles in a mouse model of Parkinson disease

    PubMed Central

    De Jesús-Cortés, Héctor; Xu, Pin; Drawbridge, Jordan; Estill, Sandi Jo; Huntington, Paula; Tran, Stephanie; Britt, Jeremiah; Tesla, Rachel; Morlock, Lorraine; Naidoo, Jacinth; Melito, Lisa M.; Wang, Gelin; Williams, Noelle S.; Ready, Joseph M.; McKnight, Steven L.; Pieper, Andrew A.

    2012-01-01

    We previously reported the discovery of P7C3, an aminopropyl carbazole having proneurogenic and neuroprotective properties in newborn neural precursor cells of the dentate gyrus. Here, we provide evidence that P7C3 also protects mature neurons in brain regions outside of the hippocampus. P7C3 blocks 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-mediated cell death of dopaminergic neurons in the substantia nigra of adult mice, a model of Parkinson disease (PD). Dose–response studies show that the P7C3 analog P7C3A20 blocks cell death with even greater potency and efficacy, which parallels the relative potency and efficacy of these agents in blocking apoptosis of newborn neural precursor cells of the dentate gyrus. P7C3 and P7C3A20 display similar relative effects in blocking 1-methyl-4-phenylpyridinium (MPP+)-mediated death of dopaminergic neurons in Caenorhabditis elegans, as well as in preserving C. elegans mobility following MPP+ exposure. Dimebon, an antihistaminergic drug that is weakly proneurogenic and neuroprotective in the dentate gyrus, confers no protection in either the mouse or the worm models of PD. We further demonstrate that the hippocampal proneurogenic efficacy of eight additional analogs of P7C3 correlates with their protective efficacy in MPTP-mediated neurotoxicity. In vivo screening of P7C3 analogs for proneurogenic efficacy in the hippocampus may thus provide a reliable means of predicting neuroprotective efficacy. We propose that the chemical scaffold represented by P7C3 and P7C3A20 provides a basis for optimizing and advancing pharmacologic agents for the treatment of patients with PD. PMID:23027934

  2. Neuroprotective efficacy of aminopropyl carbazoles in a mouse model of Parkinson disease.

    PubMed

    De Jesús-Cortés, Héctor; Xu, Pin; Drawbridge, Jordan; Estill, Sandi Jo; Huntington, Paula; Tran, Stephanie; Britt, Jeremiah; Tesla, Rachel; Morlock, Lorraine; Naidoo, Jacinth; Melito, Lisa M; Wang, Gelin; Williams, Noelle S; Ready, Joseph M; McKnight, Steven L; Pieper, Andrew A

    2012-10-16

    We previously reported the discovery of P7C3, an aminopropyl carbazole having proneurogenic and neuroprotective properties in newborn neural precursor cells of the dentate gyrus. Here, we provide evidence that P7C3 also protects mature neurons in brain regions outside of the hippocampus. P7C3 blocks 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-mediated cell death of dopaminergic neurons in the substantia nigra of adult mice, a model of Parkinson disease (PD). Dose-response studies show that the P7C3 analog P7C3A20 blocks cell death with even greater potency and efficacy, which parallels the relative potency and efficacy of these agents in blocking apoptosis of newborn neural precursor cells of the dentate gyrus. P7C3 and P7C3A20 display similar relative effects in blocking 1-methyl-4-phenylpyridinium (MPP(+))-mediated death of dopaminergic neurons in Caenorhabditis elegans, as well as in preserving C. elegans mobility following MPP(+) exposure. Dimebon, an antihistaminergic drug that is weakly proneurogenic and neuroprotective in the dentate gyrus, confers no protection in either the mouse or the worm models of PD. We further demonstrate that the hippocampal proneurogenic efficacy of eight additional analogs of P7C3 correlates with their protective efficacy in MPTP-mediated neurotoxicity. In vivo screening of P7C3 analogs for proneurogenic efficacy in the hippocampus may thus provide a reliable means of predicting neuroprotective efficacy. We propose that the chemical scaffold represented by P7C3 and P7C3A20 provides a basis for optimizing and advancing pharmacologic agents for the treatment of patients with PD.

  3. Post-Katrina Fecal Contamination in Violet Marsh near New Orleans

    PubMed Central

    Furey, John S.; Fredrickson, Herbert; Foote, Chris; Richmond, Margaret

    2007-01-01

    Fecal material entrained in New Orleans flood waters was pumped into the local environment. Violet Marsh received water pumped from St. Bernard Parish and the Lower Ninth Ward. Sediment core samples were collected from canals conducting water from these areas to pump stations and from locations within Violet Marsh. Viable indicator bacteria and fecal sterols were used to assess the levels of fecal material in sediment deposited after the levee failures and deeper sediments deposited before. Most of the cores had fecal coliform levels that exceed the biosolids criterion. All of the cores had fecal sterols that exceeded the suggested environmental quality criterion. Our data show both a long history of fecal contamination in Violet Marsh and an increase in fecal loading corresponding to the failure of the levee system. The work was performed as part of the Interagency Performance Evaluation Task Force investigation into the consequences of the failures of the New Orleans levee system. PMID:17617670

  4. Post-Katrina fecal contamination in Violet Marsh near New Orleans.

    PubMed

    Furey, John S; Fredrickson, Herbert; Foote, Chris; Richmond, Margaret

    2007-06-01

    Fecal material entrained in New Orleans flood waters was pumped into the local environment. Violet Marsh received water pumped from St. Bernard Parish and the Lower Ninth Ward. Sediment core samples were collected from canals conducting water from these areas to pump stations and from locations within Violet Marsh. Viable indicator bacteria and fecal sterols were used to assess the levels of fecal material in sediment deposited after the levee failures and deeper sediments deposited before. Most of the cores had fecal coliform levels that exceed the biosolids criterion. All of the cores had fecal sterols that exceeded the suggested environmental quality criterion. Our data show both a long history of fecal contamination in Violet Marsh and an increase in fecal loading corresponding to the failure of the levee system. The work was performed as part of the Interagency Performance Evaluation Task Force investigation into the consequences of the failures of the New Orleans levee system.

  5. Oxidation kinetics of crystal violet by potassium permanganate in acidic medium

    NASA Astrophysics Data System (ADS)

    Khan, Sameera Razi; Ashfaq, Maria; Mubashir; Masood, Summyia

    2016-05-01

    The oxidation kinetics of crystal violet (a triphenylmethane dye) by potassium permanganate was focused in an acidic medium by the spectrophotometric method at 584 nm. The oxidation reaction of crystal violet by potassium permanganate is carried out in an acidic medium at different temperatures ranging within 298-318 K. The kinetic study was carried out to investigate the effect of the concentration, ionic strength and temperature. The reaction followed first order kinetics with respect to potassium permanganate and crystal violet and the overall rate of the reaction was found to be second order. Thermodynamic activation parameters like the activation energy ( E a), enthalpy change (Δ H*), free energy change (Δ G*), and entropy change (Δ S*) have also been evaluated.

  6. White light emission from polystyrene under pulsed ultra violet laser irradiation

    PubMed Central

    Kim, Eunkyeom; Kyhm, Jihoon; Kim, Jung Hyuk; Lee, Gi Yong; Ko, Doo-Hyun; Han, Il Ki; Ko, Hyungduk

    2013-01-01

    This paper reports for the first time the luminescent property of polystyrene (PS), produced by pulsed ultra violet laser irradiation. We have discovered that, in air, ultra-violet (UV) irradiated PS nanospheres emit bright white light with the dominant peak at 510 nm, while in vacuum they emit in the near-blue region. From the comparison of PS nanospheres irradiated in vacuum and air, we suggest that the white luminescence is due to the formation of carbonyl groups on the surface of PS by photochemical oxidation. Our results potentially offer a new route and strategy for white light sources. PMID:24247038

  7. [N6-dipeptide derivatives of the N12-ribosyl-indolo[2,3-a]carbazole].

    PubMed

    Goryunova, O V; Zakharchuk, G M; Zhukova, O S; Fetisova, L V; Kuzmina, N E

    2014-01-01

    N6-derivatives of N12-ribosyl-indolo[2,3-a]pirrolo[3,4-c]carbazole-5,7-dione are synthesized as potential antitumor agents, in which an atom of N6-pyrrole part of heterocycle is included into the dipeptide residual of the general formula >N6-(CH2)n-CO-Ala/βAla-OMe (n = 2 or 3). These compounds are derived by reacting of 13-methyl-12-(2,3,4-three-O-acetyl-β-D-ribopyranosyl)indolo[2,3-a]furano[3,4-c] carbazole-5,7-dione with dipeptides, having an unreplaced N-amino end-group, in DMF at 130°C, wherein the nitrogen atom of peptide amino group replaces oxygen O6 in furan ring of heterocycle and is embedded in imide nitrogen atom of pyrrole N6. The ability of the obtained compounds to inhibit growth of SKOV3 human ovarian carcinoma cells was studied, only derivative with radical >N6-(CH2)3-CO-L-Ala-OMe showed cytotoxic activity with an inhibitory concentration of IC50 = 8 μM. PMID:25898719

  8. Novel Carbazole-Based Hole-Transporting Materials with Star-Shaped Chemical Structures for Perovskite-Sensitized Solar Cells.

    PubMed

    Kang, Min Soo; Sung, Sang Do; Choi, In Taek; Kim, Hyoungjin; Hong, MunPyo; Kim, Jeongho; Lee, Wan In; Kim, Hwan Kyu

    2015-10-14

    Novel carbazole-based hole-transporting materials (HTMs), including extended π-conjugated central core units such as 1,4-phenyl, 4,4'-biphenyl, or 1,3,5-trisphenylbenzene for promoting effective π-π stacking as well as the hexyloxy flexible group for enhancing solubility in organic solvent, have been synthesized as HTM of perovskite-sensitized solar cells. A HTM with 1,3,5-trisphenylbenzene core, coded as SGT-411, exhibited the highest charge conductivity caused by its intrinsic property to form crystallized structure. The perovskite-sensitized solar cells with SGT-411 exhibited the highest PCE of 13.00%, which is 94% of that of the device derived from spiro-OMeTAD (13.76%). Time-resolved photoluminescence spectra indicate that SGT-411 shows the shortest decay time constant, which is in agreement with the trends of conductivity data, indicating it having fastest charge regeneration. In this regard, a carbazole-based HTM with star-shaped chemical structure is considered to be a promising candidate HTM.

  9. Highly enantioselective construction of carbazole derivatives via [4+2] cycloaddition of silyloxyvinylindoles and β,γ-unsaturated α-ketoesters.

    PubMed

    Zhao, Xiaohu; Mei, Hongjiang; Xiong, Qian; Fu, Kai; Lin, Lili; Liu, Xiaohua; Feng, Xiaoming

    2016-08-23

    A highly efficient catalytic asymmetric [4+2] cycloaddition of silyloxyvinylindoles with β,γ-unsaturated α-ketoesters has been accomplished by an available chiral N,N'-dioxide/yttrium triflate complex. A widespread range of carbazole derivatives were obtained in 47-98% yield with 86-99% ee under mild reaction conditions. PMID:27507350

  10. Quantitative electrochemical and electrochromic behavior of terthiophene and carbazole containing conjugated polymer network film precursors: EC-QCM and EC-SPR.

    PubMed

    Taranekar, Prasad; Fulghum, Timothy; Baba, Akira; Patton, Derek; Advincula, Rigoberto

    2007-01-16

    A comparative analysis of the copolymerization behavior between an electro-active terthiophene and a carbazole moiety of a conjugated polymer precursor was investigated using electrochemical and hyphenated electrochemical methods. Five different precursor polymers were first synthesized and characterized using NMR, IR, and GPC. The polymers include homopolymers of individual electro-active groups (P3T, P-CBZ) and different compositions of 25, 50, and 75% (P3TC-25, P3TC50, and P3TC-75) with respect to the two electro-active groups. Since the oxidation potentials of terthiophene and carbazole lie very close to each other, highly cross-linked copolymer films of varying extent were produced depending on the composition. The copolymerization extent was found to be dependent primarily on the amount of the terthiophene, which in this case provided for a more efficient carbazole polymerization and copolymerization than with just carbazole alone (homopolymer). The extent of copolymerization, electrochromic properties, and viscoelastic changes was quantitatively investigated using a number of hyphenated electrochemistry techniques: spectro-electrochemistry, electrochemical quartz crystal microbalance studies (EC-QCM), and electrochemical surface plasmon resonance spectroscopy (EC-SPR). Each technique revealed a unique aspect of the electrocopolymerization behavior that was used to define structure-property relationships and the deposition/copolymerization mechanism.

  11. Structural and photophysical properties of HPPCO (4-hydroxy-5-phenyl-6H-pyrido[3,2,1-jk]carbazol-6-one) derivatives

    NASA Astrophysics Data System (ADS)

    Jeong, Yong-Kwang; Kim, Min-Ah; Lee, Hyo-Sung; Kim, Jong-Moon; Lee, Sung Woo; Kang, Jun-Gill

    2015-01-01

    Proton-substitution effects of 4-hydroxy-5-phenyl-6H-pyrido[3,2,1-jk]carbazol-6-one (HPPCO) on structural and photophysical properties were presented. HPPCO crystallized in the orthorhombic space group Pbca with an intermolecular hydrogen bonding between OH and oxygen atom of the carbonyl. The proton-substituted derivatives, 6-oxo-5-phenyl-6H-pyrido[3,2,1-jk]carbazol-4-yl acetate (OPPCA) and 6-oxo-5-phenyl-6H-pyrido[3,2,1-jk]carbazol-4-yl benzoate (OPPCB), crystallized in the monoclinic P21/c space group. For OPPCA and OPPCB, a weak interaction between carbonyl oxygen atom in the substituted group and carbon atom in the fused ring was responsible for three-dimensional arrangements. In addition, 6-oxo-5-phenyl-6H-pyrido[3,2,1-jk]carbazol-4-yl furan-2-carboxylate (OPPCF), and 6-oxo-5-phenyl-6H-pyrido[3,2,1-jk]carbazol-4-yl naphthoate (OPPCN) were also synthesized. HPPCO and the four derivatives excited by ultraviolet (UV) light produced blue emission. Proton substitution of the OH group significantly increased the radiative transitions and moderately decreased the non-radiative transitions. Consequently the luminescence quantum yields of the derivatives enhanced more than 4.6-fold, no matter what the groups were substituted. Structural and optical properties were further determined using density functional theory (DFT) and ZINDO calculations. The planar structure of the pyridocarbazole-fused ring resulted in π → π* electronic transitions within the main frame, with an additional transition from the n(O) of carbonyl to the π* of the main frame. The three excited states that arose from these transitions were responsible for the blue luminescence.

  12. Design, synthesis and biological evaluation of novel 1,2,3-triazolyl [Formula: see text]-hydroxy alkyl/carbazole hybrid molecules.

    PubMed

    Rad, Mohammad Navid Soltani; Behrouz, Somayeh; Behrouz, Marzieh; Sami, Akram; Mardkhoshnood, Mehdi; Zarenezhad, Ali; Zarenezhad, Elham

    2016-08-01

    The design, synthesis and biological study of several novel 1,2,3-triazolyl [Formula: see text]-hydroxy alkyl/carbazole hybrid molecules as a new type of antifungal agent has been described. In this synthesis, the N-alkylation reaction of carbazol-9-ide potassium salt with 3-bromoprop-1-yne afforded 9-(prop-2-ynyl)-9H-carbazole. The 'Click' Huisgen cycloaddition reaction of 9-(prop-2-ynyl)-9H-carbazole with diverse [Formula: see text]-azido alcohols in the presence of copper-doped silica cuprous sulphate led to target molecules in excellent yields. The in vitro antifungal and antibacterial activities of title compounds were screened against various pathogenic fungal strains, Gram-positive and/or Gram-negative bacteria. In particular, 1-(4-((9H-carbazol-9-yl) methyl)-1H-1,2,3-triazol-1-yl)-3-butoxypropan-2-ol (10e) proved to have potent antifungal activity against all fungal tests compared with fluconazole and clotrimazole as studied reference drugs. Our molecular docking analysis revealed an appropriate fitting and a potential powerful interaction between compound 10e and an active site of the Mycobacterium P450DM enzyme. The strong hydrogen bondings between [Formula: see text]-hydroxyl and ether groups in 10e were found to be the main factors that drive the molecule to fit in the active site of enzyme. The in silico pharmacokinetic studies were used for a better description of 10a-10n as potential lead antifungal agents for future investigations. PMID:27278443

  13. DNA rearrangement has occurred in the carbazole-degradative plasmid pCAR1 and the chromosome of its unsuitable host, Pseudomonas fluorescens Pf0-1.

    PubMed

    Shintani, Masaki; Matsumoto, Takashi; Yoshikawa, Hirofumi; Yamane, Hisakazu; Ohkuma, Moriya; Nojiri, Hideaki

    2011-12-01

    The carbazole-degradative plasmid pCAR1 carries the class II transposon Tn4676, which contains the car and ant genes, essential for conversion of carbazole into anthranilate, and anthranilate into catechol, respectively. In our previous study, DNA rearrangements in pCAR1 were frequently detected in the host Pseudomonas fluorescens Pf0-1 in the presence of carbazole, resulting in the improvement of host survivability. Several Pf0-1 mutants harbouring pCAR1 were isolated, and deletion of DNA in the plasmid ant gene was found. Here, we compared genome sequences of the parent strain Pf0-1L(pCAR1::rfp) and one of its mutants, 5EP83, to assess whether other DNA rearrangements occurred in either the plasmid or the host chromosome. We found transposition of Tn4676 into the 5EP83 chromosome. In addition, ISPre1 had transposed into the car gene intergenic region on the pCAR1-derivative plasmid of 5EP83, which inhibited car transcription. As a result of these transpositions, 5EP83 was able to metabolize carbazole due to the Tn4676 on its chromosome, although the car genes on its plasmid were non-functional. We also found that one copy of duplicate carAa genes had been deleted, and that ISPre4 had transposed into both the host chromosome and the plasmid. Our findings suggest that Pf0-1 harbouring pCAR1 is subjected to DNA rearrangements not only on the plasmid but also on its chromosome in the presence of carbazole.

  14. Violet LED light enhances the recruitment of a thrip predator in open fields.

    PubMed

    Ogino, Takumi; Uehara, Takuya; Muraji, Masahiko; Yamaguchi, Terumi; Ichihashi, Takahisa; Suzuki, Takahiro; Kainoh, Yooichi; Shimoda, Masami

    2016-01-01

    The predatory bug Orius sauteri is an indigenous natural enemy of thrips and whiteflies in Asian countries. To put these bugs to practical use in pest management, methods to attract and retain the bugs in agricultural fields are needed. We previously showed that violet light (405 nm) attracts O. sauteri selectively. Many thrips and whiteflies are attracted to UV or green light. In this study, we examined the effect of violet-LED illumination on O. sauteri in pesticide-free eggplant (Solanum melongena L.) cultivation. In three cultivation trials, the density of O. sauteri on eggplant leaves was consistently higher in the illuminated plots; at least twice that of the non-illuminated plots. Simultaneously, the density of thrips declined markedly to less than half that of the non-illuminated plots. We identified three positive effects of violet light including an "immediate-effect" on predator attraction, a "persistent-effect" on predator reproduction, and a "secondary-effect" on the food web structure. Our results showed that illumination with violet light provides a powerful tool for integrated pest management. This is the first report on the use of illumination to manipulate the behavior of natural enemies. PMID:27604315

  15. Adsorption of methyl violet in aqueous solutions by poly(acrylamide-co-acrylic acid) hydrogels

    NASA Astrophysics Data System (ADS)

    Şolpan, D.; Duran, S.; Saraydin, D.; Güven, O.

    2003-02-01

    In this study, Acrylamide(AAm)/Acrylic Acid(AAc) monomer mixtures which contain different quantities of acrylic acid have been irradiated to form hydrogels with γ-radiation. Acrylamide/Acrylic Acid (AAm/AAc) monomer mixtures which contain 15%, 20%, 30% AAm and irradiated with 8.0 kGy were used for swelling and diffusion studies in water and solutions of methyl violet. Diffusions of water and methyl violet within the hydrogels were found to be non-Fickian in character. In experiments on the adsorption of methyl violet, Type-S adsorption was found. Poly(AAm-co-AAc) hydrogel adsorbed methyl violet, while poly(AAm) hydrogel did not adsorb any dye. (Δ H) Heat of adsorption, (Δ G) Free energy of adsorption, (Δ S) Entropy of adsorption were calculated. These results show that poly(AAm-co-AAc) hydrogels can be used as a sorbent for water pollutants such as dyes and treatment of these organic contaminants from wastewater.

  16. Crystal violet reactions of fresh clinical isolates of Staphylococcus aureus from two British hospitals.

    PubMed

    Freeman, R; Hudson, S J; Burdess, D

    1990-12-01

    When 168 fresh clinical isolates of Staphylococcus aureus were examined for their reactions on a medium containing 1 part in 100,000 crystal violet 50.6% of strains produced a purple appearance, 39.3% produced a white appearance and 10.1% produced a yellow appearance. Purple-reacting isolates were significantly associated with both invasive infections (P less than 0.01) and hospital origin (P less than 0.001). There were no significant associations between the crystal violet reactions and either animal contact or other properties previously reported to be characteristic of white and yellow-reacting strains (beta haemolysin and bovine coagulase production). The results of phage typing showed associations between susceptibility to group III phages and purple-reacting strains and between phage group II susceptibility and white and yellow-reacting strains. There was also a highly significant association between white reactions on crystal violet agar and susceptibility to lysis by a combination of all three groups (that is, I + II + III) and white-reacting strains were significantly more susceptible to lysis by phages 94 and/or 96, whether as a restricted pattern or as part of a broader pattern. The purple reaction on crystal violet medium may be a reliable marker of the 'hospital staphylococcus'.

  17. Fluorescence screening of leucomalachite green and leucogentian violet residues in catfish

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The tripheylmethane dyes malachite green (MG) and gentian violet (GV) are effective fungicides, ectoparasiticides and disinfectants in aquaculture. This practice may leave toxic residues in seafood which is not allowed by FDA and many regulatory agencies worldwide. In this work, residues of their me...

  18. Violet LED light enhances the recruitment of a thrip predator in open fields

    NASA Astrophysics Data System (ADS)

    Ogino, Takumi; Uehara, Takuya; Muraji, Masahiko; Yamaguchi, Terumi; Ichihashi, Takahisa; Suzuki, Takahiro; Kainoh, Yooichi; Shimoda, Masami

    2016-09-01

    The predatory bug Orius sauteri is an indigenous natural enemy of thrips and whiteflies in Asian countries. To put these bugs to practical use in pest management, methods to attract and retain the bugs in agricultural fields are needed. We previously showed that violet light (405 nm) attracts O. sauteri selectively. Many thrips and whiteflies are attracted to UV or green light. In this study, we examined the effect of violet-LED illumination on O. sauteri in pesticide-free eggplant (Solanum melongena L.) cultivation. In three cultivation trials, the density of O. sauteri on eggplant leaves was consistently higher in the illuminated plots; at least twice that of the non-illuminated plots. Simultaneously, the density of thrips declined markedly to less than half that of the non-illuminated plots. We identified three positive effects of violet light including an “immediate-effect” on predator attraction, a “persistent-effect” on predator reproduction, and a “secondary-effect” on the food web structure. Our results showed that illumination with violet light provides a powerful tool for integrated pest management. This is the first report on the use of illumination to manipulate the behavior of natural enemies.

  19. [Active carbon from Thalia dealbata residues: its preparation and adsorption performance to crystal violet].

    PubMed

    Chu, Shu-Yi; Yang, Min; Xiao, Ji-Bo; Zhang, Jun; Zhu, Yan-Ping; Yan, Xiang-Jun; Tian, Guang-Ming

    2013-06-01

    By using phosphoric acid as activation agent, active carbon was prepared from Thalia dealbata residues. The BET specific surface area of the active carbon was 1174.13 m2 x g(-1), micropore area was 426.99 m2 x g(-1), and average pore diameter was 3.23 nm. An investigation was made on the adsorption performances of the active carbon for crystal violet from aqueous solution under various conditions of pH, initial concentration of crystal violet, contact time, and contact temperature. It was shown that the adsorbed amount of crystal violet was less affected by solution pH, and the adsorption process could be divided into two stages, i. e., fast adsorption and slow adsorption, which followed the pseudo-second-order kinetics model. At the temperature 293, 303, and 313 K, the adsorption process was more accordance with Langmuir isotherm model, and the maximum adsorption capacity was 409.83, 425.53, and 438.59 mg x g(-1), respectively. In addition, the adsorption process was spontaneous and endothermic, and the randomness of crystal violet molecules increased. PMID:24066559

  20. [Active carbon from Thalia dealbata residues: its preparation and adsorption performance to crystal violet].

    PubMed

    Chu, Shu-Yi; Yang, Min; Xiao, Ji-Bo; Zhang, Jun; Zhu, Yan-Ping; Yan, Xiang-Jun; Tian, Guang-Ming

    2013-06-01

    By using phosphoric acid as activation agent, active carbon was prepared from Thalia dealbata residues. The BET specific surface area of the active carbon was 1174.13 m2 x g(-1), micropore area was 426.99 m2 x g(-1), and average pore diameter was 3.23 nm. An investigation was made on the adsorption performances of the active carbon for crystal violet from aqueous solution under various conditions of pH, initial concentration of crystal violet, contact time, and contact temperature. It was shown that the adsorbed amount of crystal violet was less affected by solution pH, and the adsorption process could be divided into two stages, i. e., fast adsorption and slow adsorption, which followed the pseudo-second-order kinetics model. At the temperature 293, 303, and 313 K, the adsorption process was more accordance with Langmuir isotherm model, and the maximum adsorption capacity was 409.83, 425.53, and 438.59 mg x g(-1), respectively. In addition, the adsorption process was spontaneous and endothermic, and the randomness of crystal violet molecules increased.

  1. Color-Pure Violet-Light-Emitting Diodes Based on Layered Lead Halide Perovskite Nanoplates.

    PubMed

    Liang, Dong; Peng, Yuelin; Fu, Yongping; Shearer, Melinda J; Zhang, Jingjing; Zhai, Jianyuan; Zhang, Yi; Hamers, Robert J; Andrew, Trisha L; Jin, Song

    2016-07-26

    Violet electroluminescence is rare in both inorganic and organic light-emitting diodes (LEDs). Low-cost and room-temperature solution-processed lead halide perovskites with high-efficiency and color-tunable photoluminescence are promising for LEDs. Here, we report room-temperature color-pure violet LEDs based on a two-dimensional lead halide perovskite material, namely, 2-phenylethylammonium (C6H5CH2CH2NH3(+), PEA) lead bromide [(PEA)2PbBr4]. The natural quantum confinement of two-dimensional layered perovskite (PEA)2PbBr4 allows for photoluminescence of shorter wavelength (410 nm) than its three-dimensional counterpart. By converting as-deposited polycrystalline thin films to micrometer-sized (PEA)2PbBr4 nanoplates using solvent vapor annealing, we successfully integrated this layered perovskite material into LEDs and achieved efficient room-temperature violet electroluminescence at 410 nm with a narrow bandwidth. This conversion to nanoplates significantly enhanced the crystallinity and photophysical properties of the (PEA)2PbBr4 samples and the external quantum efficiency of the violet LED. The solvent vapor annealing method reported herein can be generally applied to other perovskite materials to increase their grain size and, ultimately, improve the performance of optoelectronic devices based on perovskite materials. PMID:27336850

  2. Adaptive evolutionary paths from UV reception to sensing violet light by epistatic interactions

    PubMed Central

    Yokoyama, Shozo; Altun, Ahmet; Jia, Huiyong; Yang, Hui; Koyama, Takashi; Faggionato, Davide; Liu, Yang; Starmer, William T.

    2015-01-01

    Ultraviolet (UV) reception is useful for such basic behaviors as mate choice, foraging, predator avoidance, communication, and navigation, whereas violet reception improves visual resolution and subtle contrast detection. UV and violet reception are mediated by the short wavelength–sensitive (SWS1) pigments that absorb light maximally (λmax) at ~360 nm and ~395 to 440 nm, respectively. Because of strong nonadditive (epistatic) interactions among amino acid changes in the pigments, the adaptive evolutionary mechanisms of these phenotypes are not well understood. Evolution of the violet pigment of the African clawed frog (Xenopus laevis, λmax = 423 nm) from the UV pigment in the amphibian ancestor (λmax = 359 nm) can be fully explained by eight mutations in transmembrane (TM) I–III segments. We show that epistatic interactions involving the remaining TM IV–VII segments provided evolutionary potential for the frog pigment to gradually achieve its violet-light reception by tuning its color sensitivity in small steps. Mutants in these segments also impair pigments that would cause drastic spectral shifts and thus eliminate them from viable evolutionary pathways. The overall effects of epistatic interactions involving TM IV–VII segments have disappeared at the last evolutionary step and thus are not detectable by studying present-day pigments. Therefore, characterizing the genotype-phenotype relationship during each evolutionary step is the key to uncover the true nature of epistasis. PMID:26601250

  3. Violet LED light enhances the recruitment of a thrip predator in open fields

    PubMed Central

    Ogino, Takumi; Uehara, Takuya; Muraji, Masahiko; Yamaguchi, Terumi; Ichihashi, Takahisa; Suzuki, Takahiro; Kainoh, Yooichi; Shimoda, Masami

    2016-01-01

    The predatory bug Orius sauteri is an indigenous natural enemy of thrips and whiteflies in Asian countries. To put these bugs to practical use in pest management, methods to attract and retain the bugs in agricultural fields are needed. We previously showed that violet light (405 nm) attracts O. sauteri selectively. Many thrips and whiteflies are attracted to UV or green light. In this study, we examined the effect of violet-LED illumination on O. sauteri in pesticide-free eggplant (Solanum melongena L.) cultivation. In three cultivation trials, the density of O. sauteri on eggplant leaves was consistently higher in the illuminated plots; at least twice that of the non-illuminated plots. Simultaneously, the density of thrips declined markedly to less than half that of the non-illuminated plots. We identified three positive effects of violet light including an “immediate-effect” on predator attraction, a “persistent-effect” on predator reproduction, and a “secondary-effect” on the food web structure. Our results showed that illumination with violet light provides a powerful tool for integrated pest management. This is the first report on the use of illumination to manipulate the behavior of natural enemies. PMID:27604315

  4. Consequences of Ultra-Violet Irradiation on the Mechanical Properties of Spider Silk

    PubMed Central

    Lai, Wee Loong; Goh, Kheng Lim

    2015-01-01

    The outstanding combination of high tensile strength and extensibility of spider silk is believed to contribute to the material’s toughness. Thus, there is great interest in engineering silk for biomedical products such as suture or implants. Additionally, over the years, many studies have also sought to enhance the mechanical properties of spider silk for wider applicability, e.g., by irradiating the material using ultra-violet radiation. However, the limitations surrounding the use of ultra-violet radiation for enhancing the mechanical properties of spider silk are not well-understood. Here, we have analyzed the mechanical properties of spider silk at short ultra-violet irradiation duration. Specimens of spider silk were subjected to ultra-violet irradiation (254-nm wavelength, i.e. UVC) for 10, 20, and 30 min, respectively, followed by tensile test to rupture to determine the strength (maximum stress), extensibility (rupture strain), and toughness (strain energy density to rupture). Controls, i.e., specimens that did not received UVC, were also subjected to tensile test to rupture to determine the respective mechanical properties. One-way analysis of variance reveals that these properties decrease significantly (p < 0.05) with increasing irradiation duration. Among the three mechanical parameters, the strength of the spider silk degrades most rapidly; the extensibility of the spider silk degrades the slowest. Overall, these changes correspond to the observed surface modifications as well as the bond rupture between the peptide chains of the treated silk. Altogether, this simple but comprehensive study provides some key insights into the dependence of the mechanical properties on ultra-violet irradiation duration. PMID:26378587

  5. Consequences of Ultra-Violet Irradiation on the Mechanical Properties of Spider Silk.

    PubMed

    Lai, Wee Loong; Goh, Kheng Lim

    2015-01-01

    The outstanding combination of high tensile strength and extensibility of spider silk is believed to contribute to the material's toughness. Thus, there is great interest in engineering silk for biomedical products such as suture or implants. Additionally, over the years, many studies have also sought to enhance the mechanical properties of spider silk for wider applicability, e.g., by irradiating the material using ultra-violet radiation. However, the limitations surrounding the use of ultra-violet radiation for enhancing the mechanical properties of spider silk are not well-understood. Here, we have analyzed the mechanical properties of spider silk at short ultra-violet irradiation duration. Specimens of spider silk were subjected to ultra-violet irradiation (254-nm wavelength, i.e. UVC) for 10, 20, and 30 min, respectively, followed by tensile test to rupture to determine the strength (maximum stress), extensibility (rupture strain), and toughness (strain energy density to rupture). Controls, i.e., specimens that did not received UVC, were also subjected to tensile test to rupture to determine the respective mechanical properties. One-way analysis of variance reveals that these properties decrease significantly (p < 0.05) with increasing irradiation duration. Among the three mechanical parameters, the strength of the spider silk degrades most rapidly; the extensibility of the spider silk degrades the slowest. Overall, these changes correspond to the observed surface modifications as well as the bond rupture between the peptide chains of the treated silk. Altogether, this simple but comprehensive study provides some key insights into the dependence of the mechanical properties on ultra-violet irradiation duration. PMID:26378587

  6. Identification of methyl violet 2B as a novel blocker of focal adhesion kinase signaling pathway in cancer cells

    SciTech Connect

    Kim, Hwan; Kim, Nam Doo; Lee, Jiyeon; Han, Gyoonhee; Sim, Taebo

    2013-07-26

    Highlights: •FAK signaling cascade in cancer cells is profoundly inhibited by methyl violet 2B. •Methyl violet 2B identified by virtual screening is a novel allosteric FAK inhibitor. •Methyl violet 2B possesses extremely high kinase selectivity. •Methyl violet 2B suppresses strongly the proliferation of cancer cells. •Methyl violet 2B inhibits focal adhesion, invasion and migration of cancer cells. -- Abstract: The focal adhesion kinase (FAK) signaling cascade in cancer cells was profoundly inhibited by methyl violet 2B identified with the structure-based virtual screening. Methyl violet 2B was shown to be a non-competitive inhibitor of full-length FAK enzyme vs. ATP. It turned out that methyl violet 2B possesses extremely high kinase selectivity in biochemical kinase profiling using a large panel of kinases. Anti-proliferative activity measurement against several different cancer cells and Western blot analysis showed that this substance is capable of suppressing significantly the proliferation of cancer cells and is able to strongly block FAK/AKT/MAPK signaling pathways in a dose dependent manner at low nanomolar concentration. Especially, phosphorylation of Tyr925-FAK that is required for full activation of FAK was nearly completely suppressed even with 1 nM of methyl violet 2B in A375P cancer cells. To the best of our knowledge, it has never been reported that methyl violet possesses anti-cancer effects. Moreover, methyl violet 2B significantly inhibited FER kinase phosphorylation that activates FAK in cell. In addition, methyl violet 2B was found to induce cell apoptosis and to exhibit strong inhibitory effects on the focal adhesion, invasion, and migration of A375P cancer cells at low nanomolar concentrations. Taken together, these results show that methyl violet 2B is a novel, potent and selective blocker of FAK signaling cascade, which displays strong anti-proliferative activities against a variety of human cancer cells and suppresses adhesion

  7. 21 CFR 73.3117 - 16,23-Dihydrodinaphtho[2,3-a:2′,3′-i] naphth [2′,3′:6,7] indolo [2,3-c] carbazole-5,10,15,17,22...

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ..., DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3117 16,23-Dihydrodinaphtho naphth indolo carbazole-5,10,15,17,22,24-hexone. (a)...

  8. 21 CFR 73.3117 - 16,23-Dihydrodinaphtho[2,3-a:2′,3′-i] naphth [2′,3′:6,7] indolo [2,3-c] carbazole-5,10,15,17,22...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ..., DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3117 16,23-Dihydrodinaphtho naphth indolo carbazole-5,10,15,17,22,24-hexone. (a)...

  9. Synthesis, structure and properties of zinc(II) coordination polymers with 9H-carbazole-2,7-dicarboxylic acid

    SciTech Connect

    Yi, Xiu-Chun; Xi, Fu-Gui; Wang, Kun; Su, Zhao; Gao, En-Qing

    2013-10-15

    From a new dicarboxylate ligand, 9H-carbazole-2,7-dicarboxylic acid (2,7-H{sub 2}CDC), three Zn(II) metal-organic frameworks were synthesized in the absence or presence of ditopic N-donor ligands. They are formulated as [Zn{sub 5}(μ{sub 3}-OH){sub 2}(2,7-CDC){sub 4}(DEF){sub 2}] (1) (DEF=N,N-diethylformamide), [Zn{sub 2}(2,7-CDC){sub 2}(DABCO)(H{sub 2}O)]·5DMF·H{sub 2}O (2) (DABCO=1-diaza-bicyclo[2.2.2]octane, DMF=N,N-dimethylformamide), and [Zn{sub 2}(2,7-CDC){sub 2}(bpea)]·3DMA·2 H{sub 2}O (3) (bpea=1,2-bis(4-pyridyl)ethylane, DMA=N,N-dimethylacetamide). Compounds 1 and 3 display the 3D pcu frameworks. In 1 the unusual pentanuclear [Zn{sub 5}(μ{sub 3}-OH){sub 2}(COO){sub 8}] secondary building units (SBUs) are linked by dicarboxylate ligands. Differently, in 3 the well-known paddle–wheel [Zn{sub 2}(COO){sub 4}] SBUs are linked by dicarboxylate and dipyridyl ligands. Compound 2 shows the rare self-catenated 3D alb-3,6-C2/c net topology based on the dinuclear paddle–wheel SBU and a mononuclear unit. The stability and fluorescent properties of the compounds have been studied. - Graphical abstract: A new dicarboxylate ligand, 9H-carbazole-2,7-dicarboxylic acid, was used to construct Zn(II) metal-organic frameworks, including a novel self-catenated network with the rare 3D alb-3,6-C2/c net and two pcu-type networks based on an unprecedented pentanuclear clusters and the common paddle–wheel units. The compounds show blue fluorescent properties. Display Omitted - Highlights: • MOFs with a new carbazole-based dicarboxylate ligand. • New pentanuclear [Zn{sub 5}(μ{sub 3}-OH){sub 2}(COO){sub 8}] secondary building unit. • The rare self-catenated 3D alb-3,6-C2/c net.

  10. Facile synthesis of 5H-benzo[b]carbazol-6-yl ketones via sequential reaction of Cu-catalyzed Friedel-Crafts alkylation, iodine-promoted cyclization, nucleophilic substitution and aromatization.

    PubMed

    Wu, Jing; Wang, Dongping; Wang, Haolong; Wu, Fan; Li, Xincheng; Wan, Boshun

    2014-09-21

    A convenient method to access 5H-benzo[b]carbazol-6-yl ketones via a sequential Cu-catalyzed Friedel-Crafts alkylation reaction of indoles with 2-(2-(alkynyl)benzylidene)malonates and iodine-promoted electrophilic cyclization followed by nucleophilic substitution and aromatization was developed. The products of the functional 5H-benzo[b]carbazol-6-yl ketones were obtained with up to 98% yield. PMID:25070224

  11. Albanian violets of the section Melanium, their morphological variability, genetic similarity and their adaptations to serpentine or chalk soils.

    PubMed

    Słomka, Aneta; Godzik, Barbara; Szarek-Łukaszewska, Grażyna; Shuka, Lulëzim; Hoef-Emden, Kerstin; Bothe, Hermann

    2015-02-01

    Violets of the section Melanium from Albanian serpentine and chalk soils were examined for their taxonomic affiliations, their ability to accumulate heavy metals and their colonization by arbuscular mycorrhizal fungi (AMF). The sequence analysis of the ITS1-5.8S rDNA-ITS2 region showed that all the sampled six Albanian violets grouped between Viola lutea and Viola arvensis, but not with Viola tricolor. The fine resolution of the ITS sequences was not sufficient for a further delimitation of the Albanian violets within the V. lutea-V. arvensis clade. Therefore, the Albanian violets were classified by a set of morphological characters. Viola albanica, Viola dukadjinica and Viola raunsiensis from serpentine soils as well as Viola aetolica from a chalk meadow were unambiguously identified, whereas the samples of Viola macedonica showed high morphological variability. All the violets, in both roots and shoots contained less than or similar levels of heavy metals as their harboring soils, indicating that they were heavy metal excluders. All the violets were strongly colonized by AMF with the remarkable exception of V. albanica. This violet lived as a scree creeper in shallow serpentine soil where the concentration of heavy metals was high but those of P, K and N were scarce.

  12. Violets of the section Melanium, their colonization by arbuscular mycorrhizal fungi and their occurrence on heavy metal heaps.

    PubMed

    Słomka, A; Kuta, E; Szarek-Łukaszewska, G; Godzik, B; Kapusta, P; Tylko, G; Bothe, H

    2011-07-15

    Violets of the sections Melanium were examined for their colonization by arbuscular mycorrhizal fungi (AMF). Heartsease (Viola tricolor) from several heavy metal soils was AMF-positive at many sites but not at extreme biomes. The zinc violets Viola lutea ssp. westfalica (blue zinc violet) and ssp. calaminaria (yellow zinc violet) were always AMF-positive on heavy metal soils as their natural habitats. As shown for the blue form, zinc violets germinate independently of AMF and can be grown in non-polluted garden soils. Thus the zinc violets are obligatorily neither mycotrophs nor metalophytes. The alpine V. lutea, likely ancestor of the zinc violets, was at best poorly colonized by AMF. As determined by atomic absorption spectrometry, the contents of Zn and Pb were lower in AMF colonized plants than in the heavy metal soils from where the samples had been taken. AMF might prevent the uptake of toxic levels of heavy metals into the plant organs. Dithizone staining indicated a differential deposition of heavy metals in tissues of heartsease. Leaf hairs were particularly rich in heavy metals, indicating that part of the excess of heavy metals is sequestered into these cells.

  13. Biodegradation of crystal violet using Burkholderia vietnamiensis C09V immobilized on PVA-sodium alginate-kaolin gel beads.

    PubMed

    Cheng, Ying; Lin, HongYan; Chen, Zuliang; Megharaj, Mallavarapu; Naidu, Ravi

    2012-09-01

    The strain, Burkholderia vietnamiensis C09V was immobilized on PVA-alginate-kaolin gel beads as a biomaterial to improve the degradation of crystal violet from aqueous solution. The results show that 98.6% (30 mg L(-1)) crystal violet was removed from aqueous solution using immobilized cells on PVA-alginate-kaolin gel beads, while 94.0% crystal violet was removed by free cells after degradation at the pH 5 and 30°C for 30 h. Kinetics studies show that the pseudo-second-order kinetics well described the adsorption of crystal violet on the PVA-alginate-kaolin beads. Biodegradation of crystal violet on immobilized cells was fitted well by first-order reaction kinetics, indicating that CV was adsorbed onto kaolin and followed their degradation by immobilized cells onto the the PVA-alginate-kaolin beads. Characterization with SEM shows that cells attached well to the surface of PVA-alginate-kaolin beads, leading to improved crystal violet transfer from aqueous solution to immobilized cells. In addition, UV-vis show that the absorption peak at 588 nm was reduced by the degraded N-bond linkages, as well as the formation of degrading products were observed by Fourier transform infrared (FTIR). These results suggest that crystal violet was biodegraded to N,N-dimethylaminophenol and Michler's Ketone prior to these intermediates being further degraded. PMID:22789742

  14. Biodegradation of crystal violet using Burkholderia vietnamiensis C09V immobilized on PVA-sodium alginate-kaolin gel beads.

    PubMed

    Cheng, Ying; Lin, HongYan; Chen, Zuliang; Megharaj, Mallavarapu; Naidu, Ravi

    2012-09-01

    The strain, Burkholderia vietnamiensis C09V was immobilized on PVA-alginate-kaolin gel beads as a biomaterial to improve the degradation of crystal violet from aqueous solution. The results show that 98.6% (30 mg L(-1)) crystal violet was removed from aqueous solution using immobilized cells on PVA-alginate-kaolin gel beads, while 94.0% crystal violet was removed by free cells after degradation at the pH 5 and 30°C for 30 h. Kinetics studies show that the pseudo-second-order kinetics well described the adsorption of crystal violet on the PVA-alginate-kaolin beads. Biodegradation of crystal violet on immobilized cells was fitted well by first-order reaction kinetics, indicating that CV was adsorbed onto kaolin and followed their degradation by immobilized cells onto the the PVA-alginate-kaolin beads. Characterization with SEM shows that cells attached well to the surface of PVA-alginate-kaolin beads, leading to improved crystal violet transfer from aqueous solution to immobilized cells. In addition, UV-vis show that the absorption peak at 588 nm was reduced by the degraded N-bond linkages, as well as the formation of degrading products were observed by Fourier transform infrared (FTIR). These results suggest that crystal violet was biodegraded to N,N-dimethylaminophenol and Michler's Ketone prior to these intermediates being further degraded.

  15. Synthesis, spectroscopic characterization and structural investigations of new adduct compound of carbazole with picric acid: DNA binding and antimicrobial studies

    NASA Astrophysics Data System (ADS)

    Saravanabhavan, Munusamy; Sathya, Krishnan; Puranik, Vedavati G.; Sekar, Marimuthu

    2014-01-01

    Carbazole picrate (CP), a new organic compound has been synthesized, characterized by various analytical and spectroscopic technique such as FT-IR, UV-Vis, 1H and 13C NMR spectroscopy. An orthorhombic geometry was proposed based on single crystal XRD study. The thermal stability of the crystal was studied by using thermo-gravimetric and differential thermal analyses and found that it was stable up to 170 °C. Further, the newly synthesized title compound was tested for its in vitro antibacterial and antifungal activity against various bacterial and fungal species. Also, the compound was tested for its binding activity with Calf thymus (CT) DNA and the results show a considerable interaction between CP and CT-DNA.

  16. Spectroscopic studies on 9H-carbazole-9-(4-phenyl) boronic acid pinacol ester by DFT method

    NASA Astrophysics Data System (ADS)

    Sas, E. B.; Kurt, M.; Can, M.; Horzum, N.; Atac, A.

    2016-08-01

    9H-Carbazole-9-(4-phenyl) boronic acid pinacol ester (9-CPBAPE) molecule was investigated by FT-IR, Raman, UV-vis, 1H and 13C NMR spectra. FT-IR, FT-Raman and dispersive Raman spectra were recorded in the solid phase. 1H, 13C NMR and UV-vis spectra were recorded in dimethyl sulfoxide (DMSO) solution. The results of theoretical calculations for the spectra of the title molecule were compared with the experimental spectra. The highest occupied molecular orbital (HOMO) the lowest unoccupied molecular orbital (LUMO) and molecular electrostatic potential (MEP) analyses were performed. The theoretical calculations for the molecular structure and spectroscopic studies were performed with DFT (B3LYP) and 6-311G (d,p) basis set calculations using the Gaussian 09 program. The total (TDOS), partial (PDOS) density of state and overlap population density of state (OPDOS) diagrams analyses were performed using GaussSum 2.2 program.

  17. Specific indolo[3,2,1-jk]carbazole conducting thin-film materials production by selective substitution.

    PubMed

    Henry, John B; Wharton, Stuart I; Wood, Elanor R; McNab, Hamish; Mount, Andrew R

    2011-06-01

    Selectively substituted indolo[3,2,1-jk] carbazole (IC) molecules have been synthesized through flash vacuum pyrolysis (FVP) and then electro-oxidized, resulting in the formation of redox-active and electronically conducting thin films consisting exclusively of three highly luminescent dimer species, the 2,2'-, 2,10'-, and 10,10'-coupled dimers. DFT calculation has enabled both the accurate calculation of monomer oxidation potentials and the prediction of the nature of the resulting dimers through consideration of the coupling of the oxidized monomer radical cations. This demonstrates that substituted ICs represent a class of molecules able to form redox-active and conducting dimer films of controlled composition upon oxidation and that DFT calculations can be used to inform the synthesis of specific IC monomers most likely to both produce electronically conducting thin-film materials and yield specific luminescent dimers with desirable materials properties.

  18. Microfluidic Biosensor Array with Integrated Poly(2,7-Carbazole)/Fullerene-Based Photodiodes for Rapid Multiplexed Detection of Pathogens

    PubMed Central

    Pires, Nuno Miguel Matos; Dong, Tao

    2013-01-01

    A multiplexed microfluidic biosensor made of poly(methylmethacrylate) (PMMA) was integrated into an array of organic blend heterojunction photodiodes (OPDs) for chemiluminescent detection of pathogens. Waterborne Escherichia coli O157:H7, Campylobacter jejuni and adenovirus were targeted in the PMMA chip, and detection of captured pathogens was conducted by poly(2,7-carbazole)/fullerene OPDs which showed a responsivity over 0.20 A/W at 425 nm. The limits of chemiluminescent detection were 5 × 105 cells/mL for E. coli, 1 × 105 cells/mL for C. jejuni, and 1 × 10−8 mg/mL for adenovirus. Parallel analysis for all three analytes in less than 35 min was demonstrated. Further recovery tests illustrated the potential of the integrated biosensor for detecting bacteria in real water samples. PMID:24287522

  19. Indolo[3,2-a]carbazoles from a Deep-Water Sponge of the Genus Asteropus

    PubMed Central

    2013-01-01

    Two new indolo[3,2-a]carbazoles (1, 2) were isolated from a deep-water collection of a sponge of the genus Asteropus. The structures of 1 and 2 were determined through the analysis of spectroscopic data including mass spectrometry and 2D-NMR. Compound 1 showed minimum inhibitory concentrations of 25 μg/mL against the fungal pathogen Candida albicans and 50 μg/mL against methicillin-resistant Staphylococcus aureus (MRSA). Compounds 1 and 2 showed no cytotoxicity against the PANC1 human pancreatic carcinoma and NCI/ADR-RES ovarian adenocarcinoma cell lines at our standard test concentration of 5 μg/mL. PMID:24063539

  20. Crystal structure of 9-butyl-6-[2-(pyridin-4-yl)ethen­yl]carbazol-3-amine

    PubMed Central

    Zhang, Ping; Bai, Xiang-Yang; Zhang, Ting

    2015-01-01

    The asymmetric unit of the title compound, C23H23N3, consists of two mol­ecules, A and B, with different conformations. In mol­ecule A, the dihedral angle between the carbazole ring system (r.m.s. deviation = 0.028 Å) and the pyridine ring is 20.28 (9)° and the N—C—C—C torsion angle of the butyl side chain is −63.4 (3)°. The equivalent data for mol­ecule B are 0.065 Å, 48.28 (11)° and 61.0 (3)°, respectively. In the crystal, the components are connected by weak N—H⋯N hydrogen bonds, generating [030] C(14) chains of alternating A and B mol­ecules. PMID:25995940

  1. Crystal structure of 9-butyl-6-[2-(pyridin-4-yl)ethen-yl]carbazol-3-amine.

    PubMed

    Zhang, Ping; Bai, Xiang-Yang; Zhang, Ting

    2015-05-01

    The asymmetric unit of the title compound, C23H23N3, consists of two mol-ecules, A and B, with different conformations. In mol-ecule A, the dihedral angle between the carbazole ring system (r.m.s. deviation = 0.028 Å) and the pyridine ring is 20.28 (9)° and the N-C-C-C torsion angle of the butyl side chain is -63.4 (3)°. The equivalent data for mol-ecule B are 0.065 Å, 48.28 (11)° and 61.0 (3)°, respectively. In the crystal, the components are connected by weak N-H⋯N hydrogen bonds, generating [030] C(14) chains of alternating A and B mol-ecules.

  2. Four new carbazole alkaloids from Murraya koenigii that display anti-inflammatory and anti-microbial activities.

    PubMed

    Nalli, Yedukondalu; Khajuria, Vidushi; Gupta, Shilpa; Arora, Palak; Riyaz-Ul-Hassan, Syed; Ahmed, Zabeer; Ali, Asif

    2016-03-28

    In our present study, four new, designated as murrayakonine A-D (), along with 18 known carbazole alkaloids were isolated from CHCl3 : MeOH (1 : 1) crude extracts of the stems and leaves of Murraya koenigii (Linn.) Spreng. The structures of the all isolated compounds were characterized by analysis of HR-ESI-MS and NMR (1D and 2D spectroscopy) results, and comparison of their data with the literature data. For the first time, all the isolates were evaluated for their anti-inflammatory activities, using both in vitro and in vivo experiments, against the key inflammatory mediators TNF-α and IL-6. The new compound murrayakonine A (), O-methylmurrayamine A () and mukolidine () were proven to be the most active, efficiently inhibiting TNF-α and IL-6 release in a dose-dependent manner and showing decreased LPS induced TNF-α and IL-6 production in human PBMCs. Furthermore, all the isolates were screened for their antimicrobial potential, and the compounds girinimbine () (IC50 3.4 μM) and 1-hydroxy-7-methoxy-8-(3-methylbut-2-en-1-yl)-9H-carbazole-3-carbaldehyde () (IC50 10.9 μM) displayed potent inhibitory effects against Bacillus cereus. Furthermore, compounds murrayamine J () (IC50 11.7 μM) and koenimbine () (IC50 17.0 μM) were active against Staphylococcus aureus. However, none of the compounds were found to be active against Escherichia coli or Candida albicans. PMID:26947457

  3. PbBr-Based Layered Perovskite Organic-Inorganic Superlattice Having Carbazole Chromophore; Hole-Mobility and Quantum Mechanical Calculation.

    PubMed

    Era, Masanao; Yasuda, Takeshi; Mori, Kento; Tomotsu, Norio; Kawano, Naoki; Koshimizu, Masanori; Asai, Keisuke

    2016-04-01

    We have successfully evaluated hole mobility in a spin-coated film of a lead-bromide based layered perovskite having carbazole chromophore-linked ammonium molecules as organic layer by using FET measurement. The values of hole mobility, threshold voltage and on/off ratio at room temperature were evaluated.to.be 1.7 x 10(-6) cm2 V-1 s-1, 27 V and 28 V, respectively. However, the spin-coated films on Si substrates were not so uniform compared with those on fused quartz substrates. To improve the film uniformity, we examined the relationship between substrate temperature during spin-coating and film morphology in the layered perovskite spin-coated films. The mean roughness of the spin-coated films on Si substrates was dependent on the substrate temperature. At 353 K, the mean roughness was minimized and the carrier mobility was enhanced by one order of magnitude; the values of hole mobility and threshold voltage were .estimated to be 3.4 x 10(-5) cm2 V-1 s-1, and 22 V at room temperature in a preliminary FET evaluation, respectively. In addition, we determined a crystal structure of the layered perovskite by X-ray diffraction analysis. To gain a better understanding of the observed hole transports, we conducted quantum mechanical calculations using the obtained crystal structure information. The calculated band structure of the layered organic perovskite showed that the valence band is composed of the organic carbazole layer, which confirms that.the measured hole mobility is mainly derived from the organic part of the layered perovskite. Band and hopping transport mechanisms were discussed by calculating the effective masses and transfer integrals for the 2D periodic system of the organic layer in isolation. PMID:27451598

  4. Theoretical investigation of the broad one-photon absorption line-shape of a flexible symmetric carbazole derivative.

    PubMed

    Liu, Yanli; Cerezo, Javier; Santoro, Fabrizio; Rizzo, Antonio; Lin, Na; Zhao, Xian

    2016-08-17

    The one-photon absorption spectrum of a carbazole derivative has been studied by employing density functional response theory combined with a mixed quantum/classical (QC) approach to simulate the spectral shape. In a first step of our analysis we employed the vertical gradient (VG) vibronic model to investigate the role of Franck-Condon (FC) profiles of the first ten electronic excited states of the system, underlying most of the range of the experimental spectrum. We then focussed on the first six excited states covering the low-energy region of the spectrum, and investigated the effect of inter-state electronic couplings on the spectral shapes within Herzberg-Teller (HT) theory. Furthermore, in order to introduce the broadening effects due to the two inter-ring torsions, we employed a QC approach, adopting VG vibronic models for high-frequency modes and computing the contribution of the torsions to the spectrum from the distribution of the excitation energies along a two-dimensional relaxed potential energy. Finally, we estimated the solvent inhomogeneous broadening by computing the solvent reorganization energy using a polarizable continuum model. Our calculations allow us to obtain a non-phenomenological description of the low-energy part of the spectrum in semi-quantitative agreement with experiment and to dissect the relative importance of solvent, torsional flexibility, FC vibronic progressions, and inter-state couplings in determining its broad spectral shapes and the modulation of its intensity. Our analysis also clearly highlights that the investigated carbazole represents a big challenge for available methodologies due to the existence of many close-lying excited electronic states coupled by internal low-frequency and high-frequency motions and by solvent fluctuations. The study of their impact on the spectra at the HT level is only approximate and more refined treatments would require a fully quantum-dynamical calculation on the manifold of the coupled

  5. Contrasting photophysical properties of rhenium(i) tricarbonyl complexes having carbazole groups attached to the polypyridine ligand.

    PubMed

    Ramos, L D; Sampaio, R N; de Assis, F F; de Oliveira, K T; Homem-de-Mello, P; Patrocinio, A O T; Frin, K P M

    2016-07-19

    In the present work, new rhenium(i) polypyridyl compounds, fac-[Re(L)(CO)3(cbz2phen)](+/0) where cbz2phen = 4,7-di(9H-carbazol-9-yl)-1,10-phenanthroline and L = Cl(-), pyridine (py) or 2-aminomethylpyridine (ampy) were synthesized and characterized by (1)H NMR, UV-Vis and IR spectroscopy combined with theoretical calculations using time-dependent density functional theory (TD-DFT). Their photophysical properties were investigated by steady state and time-resolved emission spectroscopy. These compounds show a strong and broad absorption band around 350-500 nm that, also by TD-DFT, corresponds to the carbazol → phenanthroline intraligand charge transfer transition, (1)ILCTcbz2phen, with some contribution of the Re(i) → phenanthroline metal-to-ligand charge transfer transition, (1)MLCTRe→cbz2phen. In contrast to typical Re(i) polypyridyl complexes, cbz2phen-based Re(i) compounds exhibit two emission maxima in CH3CN solution and relatively low emission quantum yields, 10(-3)-10(-2). Solution phase time-resolved photoluminescence and excited state quenching experiments provided meaningful information on the presence of multiple emitter states after light excitation, which were identified as an (1)ILCTcbz2phen excited state deactivation at higher energies and a long-lived phosphorescence attributed to the (3)MLCTRe→cbz2phen excited state. When embedded into a PMMA matrix, the radiative decay from the singlet state is inhibited and the contribution of both (3)MLCT and (3)ILCTcbz2phen to the luminescence is observed. The photophysics of these Re(i) compounds reported herein provide new insights into the understanding of substitutional groups on the polypyridyl ligands that are relevant to practical and fundamental development of photo-induced molecular devices. PMID:27192346

  6. Adsorption of Basic Violet 14 in aqueous solutions using KMnO4-modified activated carbon.

    PubMed

    Shi, Qianqian; Zhang, Jian; Zhang, Chenglu; Nie, Wei; Zhang, Bo; Zhang, Huayong

    2010-03-01

    In this paper, an activated carbon was prepared from Typha orientalis and then treated with KMnO(4) and used for the removal of Basic Violet 14 from aqueous solutions. KMnO(4) treatment influenced the physicochemical properties of the carbon and improved its adsorption capacity. Adsorption experiments were then conducted with KMnO(4)-modified activated carbon to study the effects of carbon dosage (250-1500 mg/L), pH (2-10), ion strength (0-0.5 mol/L), temperature, and contact time on the adsorption of Basic Violet 14 from aqueous solutions. The equilibrium data were analyzed by the Langmuir and Freundlich isotherms and fitted well with the Langmuir model. The pseudo-first-order, pseudo-second-order, and intraparticle diffusion models were used to evaluate the kinetic data and the pseudo-second-order kinetics was the best with good correlation.

  7. Structure-activity relationships of carboline and carbazole derivatives as a novel class of ATP-competitive kinesin spindle protein inhibitors.

    PubMed

    Takeuchi, Tomoki; Oishi, Shinya; Watanabe, Toshiaki; Ohno, Hiroaki; Sawada, Jun-ichi; Matsuno, Kenji; Asai, Akira; Asada, Naoya; Kitaura, Kazuo; Fujii, Nobutaka

    2011-07-14

    The kinesin spindle protein (KSP) is a mitotic kinesin involved in the establishment of a functional bipolar mitotic spindle during cell division. It is considered to be an attractive target for cancer chemotherapy with reduced side effects. Based on natural product scaffold-derived fused indole-based inhibitors and known biphenyl-type KSP inhibitors, various carboline and carbazole derivatives were synthesized and biologically evaluated. β-Carboline and lactam-fused carbazole derivatives exhibited remarkably potent KSP inhibitory activity and mitotic arrest in prometaphase with formation of an irregular monopolar spindle. The planar tri- and tetracyclic analogs inhibited KSP ATPase in an ATP-competitive manner just like biphenyl-type inhibitors.

  8. Conjugated polymer network films of poly(p-phenylene vinylene) with hole-transporting carbazole pendants: dual photoluminescence and electrochromic behavior.

    PubMed

    Ponnapati, Ramakrishna; Felipe, Mary Jane; Muthalagu, Vetrichelvan; Puno, Katherine; Wolff, Birte; Advincula, Rigoberto

    2012-03-01

    A series of poly(p-phenylene vinylene) (PPV) copolymers functionalized with hole-transport and electrochemically active carbazole units as pendant moieties is reported. These polymers exhibit photoluminescence properties by virtue of the PPV analogous backbone. They were also designed as precursor polymer bearing the electroactive carbazole group to form conjugated polymer network (CPN) films by electrodeposition. The electrochemical polymerization of the pendant units eventually lead to a dual property electro-optically active thin film - photoluminescence (PL) behavior that can be attenuated with CPN formation, and a reversible doping and dedoping processes at controlled potentials that lead to an electrochromic behavior. This reveals the ability to incorporate complementary optical and electro-optical properties within the same film using the CPN approach. It should be possible to design and synthesize other PPV π-conjugated polymers with efficient pendant hole-transport groups exhibiting tunable PL and electrochromism with cross-linking. PMID:22329863

  9. Conjugated polymer network films of poly(p-phenylene vinylene) with hole-transporting carbazole pendants: dual photoluminescence and electrochromic behavior.

    PubMed

    Ponnapati, Ramakrishna; Felipe, Mary Jane; Muthalagu, Vetrichelvan; Puno, Katherine; Wolff, Birte; Advincula, Rigoberto

    2012-03-01

    A series of poly(p-phenylene vinylene) (PPV) copolymers functionalized with hole-transport and electrochemically active carbazole units as pendant moieties is reported. These polymers exhibit photoluminescence properties by virtue of the PPV analogous backbone. They were also designed as precursor polymer bearing the electroactive carbazole group to form conjugated polymer network (CPN) films by electrodeposition. The electrochemical polymerization of the pendant units eventually lead to a dual property electro-optically active thin film - photoluminescence (PL) behavior that can be attenuated with CPN formation, and a reversible doping and dedoping processes at controlled potentials that lead to an electrochromic behavior. This reveals the ability to incorporate complementary optical and electro-optical properties within the same film using the CPN approach. It should be possible to design and synthesize other PPV π-conjugated polymers with efficient pendant hole-transport groups exhibiting tunable PL and electrochromism with cross-linking.

  10. A violet emission in ZnS:Mn,Eu: Luminescence and applications for radiation detection

    SciTech Connect

    Ma, Lun; Chen, Wei; Jiang, Ke; Liu, Xiao-tang

    2014-03-14

    We prepared manganese and europium co-doped zinc sulfide (ZnS:Mn,Eu) phosphors and used them for radiation detection. In addition to the red fluorescence at 583 nm due to the d-d transition of Mn ions, an intense violet emission at 420 nm is newly observed in ZnS:Mn,Eu phosphors. The emission is related to Eu{sup 2+} doping but only appears at certain Eu{sup 2+} concentrations. It is found that the intensity of the 420 nm violet fluorescence is X-ray does-dependent, while the red fluorescence of 583 nm is not. The ratio of fluorescence intensities at 420 nm and 583 nm has been monitored as a function of X-ray doses that exposed upon the ZnS:Mn,Eu phosphors. Empirical formulas are provided to estimate the doses of applied X-ray irradiation. Finally, possible mechanisms of X-ray irradiation induced fluorescence quenching are discussed. The intense 420 nm emission not only provides a violet light for solid state lighting but also offers a very sensitive method for radiation detection.

  11. Broadband Photoreceptors Are Involved in Violet Light Preference in the Parasitoid Fly Exorista Japonica

    PubMed Central

    Tokushima, Yoshiaki; Uehara, Takuya; Yamaguchi, Terumi; Arikawa, Kentaro; Kainoh, Yooichi

    2016-01-01

    Phototaxis has been described in many insects, which are often attracted to specific wavelengths of light. However, little is known about phototaxis in parasitoid insect species that are potentially useful for integrated pest management. In this study, we investigated the wavelength dependency of the phototactic behavior of the parasitoid fly Exorista japonica and its possible mechanism. Multiple-choice tests with six monochromatic stimuli revealed that the flies were specifically attracted to violet light peaking at 405 nm, which was unexpected because insects are generally attracted to ultraviolet or green light. We measured the spectral sensitivity of the compound eye, and found that the sensitivity peaked at 340 nm, as in other brachyceran flies. We used statistical modeling and optimization of the process parameters to predict the type of photoreceptor contributing to the violet preference. The analysis revealed that the wavelength preference could be explained by linear models of the quanta received by photoreceptors, including the R1-6 broadband receptors. The broadband receptors appear to contribute positively, whereas the R7-8 narrowband receptors contribute negatively to achieve the violet preference; i.e., spectral opponency might be involved. PMID:27532635

  12. Evolutionary relationships, interisland biogeography, and molecular evolution in the Hawaiian violets (Viola: Violaceae).

    PubMed

    Havran, J Christopher; Sytsma, Kenneth J; Ballard, Harvey E

    2009-11-01

    The endemic Hawaiian flora offers remarkable opportunities to study the patterns of plant morphological and molecular evolution. The Hawaiian violets are a monophyletic lineage of nine taxa distributed across six main islands of the Hawaiian archipelago. To describe the evolutionary relationships, biogeography, and molecular evolution rates of the Hawaiian violets, we conducted a phylogenetic study using nuclear rDNA internal transcribed spacer sequences from specimens of each species. Parsimony, maximum likelihood (ML), and Bayesian inference reconstructions of island colonization and radiation strongly suggest that the Hawaiian violets first colonized the Maui Nui Complex, quickly radiated to Kaua'i and O'ahu, and recently dispersed to Hawai'i. The lineage consists of "wet" and "dry" clades restricted to distinct precipitation regimes. The ML and Bayesian inference reconstructions of shifts in habitat, habit, and leaf shape indicate that ecologically analogous taxa have undergone parallel evolution in leaf morphology and habit. This parallel evolution correlates with shifts to specialized habitats. Relative rate tests showed that woody and herbaceous sister species possess equal molecular evolution rates. The incongruity of molecular evolution rates in taxa on younger islands suggests that these rates may not be determined by growth form (or lifespan) alone, but may be influenced by complex dispersal events.

  13. Surface-enhanced Raman scattering of crystal violets from periodic array of gold nanocylinders

    NASA Astrophysics Data System (ADS)

    Bi, Gang; Wang, Li; Cai, Chunfeng; Ueno, Kosei; Misawa, Hiroaki; Qiu, Jianrong

    2014-09-01

    The periodic arrays of gold nanocylinder with 121 nm in diameter, 6.3 nm in gap, and 34 nm in thickness are fabricated on glass by electron-beam lithography and lift-off techniques. Some crystal violet molecules are coated on the array by using the dipping and drawing method. In addition, the surface-enhanced Raman scattering (SERS) spectra of these samples with and without gold nanocylinder arrays are characterized specifically. The largest enhancement factor is obtained when the excitation wavelength corresponds to the peak wavelength of localized surface plasmon resonance (LSPR). The density functional theory and the finite-difference time-domain method are used for the calculations of the extinction spectrum of the arrays and Raman spectra of the crystal violet, respectively. These results unambiguously demonstrate that the periodic arrays of gold nanocylinder have good and effective surface-enhanced properties for Raman scattering of crystal violets, and they also show that the excitation wavelength corresponding to the peak one of the LSPR is one of the major reasons causing SERS.

  14. Sensitive detection of malachite green and crystal violet by nonlinear laser wave mixing and capillary electrophoresis.

    PubMed

    Maxwell, Eric J; Tong, William G

    2016-05-01

    An ultrasensitive label-free antibody-free detection method for malachite green and crystal violet is presented using nonlinear laser wave-mixing spectroscopy and capillary zone electrophoresis. Wave-mixing spectroscopy provides a sensitive absorption-based detection method for trace analytes. This is accomplished by forming dynamic gratings within a sample cell, which diffracts light to create a coherent laser-like signal beam with high optical efficiency and high signal-to-noise ratio. A cubic dependence on laser power and square dependence on analyte concentration make wave mixing sensitive enough to detect molecules in their native form without the use of fluorescent labels for signal enhancement. A 532 nm laser and a 635 nm laser were used for malachite green and crystal violet sample excitation. The use of two lasers of different wavelengths allows the method to simultaneously detect both analytes. Selectivity is obtained through the capillary zone electrophoresis separation, which results in characteristic migration times. Measurement in capillary zone electrophoresis resulted in a limit of detection of 6.9 × 10(-10)M (2.5 × 10(-19) mol) for crystal violet and 8.3 × 10(-11)M (3.0 × 10(-20) mol) for malachite green at S/N of 2.

  15. Sensitive detection of malachite green and crystal violet by nonlinear laser wave mixing and capillary electrophoresis.

    PubMed

    Maxwell, Eric J; Tong, William G

    2016-05-01

    An ultrasensitive label-free antibody-free detection method for malachite green and crystal violet is presented using nonlinear laser wave-mixing spectroscopy and capillary zone electrophoresis. Wave-mixing spectroscopy provides a sensitive absorption-based detection method for trace analytes. This is accomplished by forming dynamic gratings within a sample cell, which diffracts light to create a coherent laser-like signal beam with high optical efficiency and high signal-to-noise ratio. A cubic dependence on laser power and square dependence on analyte concentration make wave mixing sensitive enough to detect molecules in their native form without the use of fluorescent labels for signal enhancement. A 532 nm laser and a 635 nm laser were used for malachite green and crystal violet sample excitation. The use of two lasers of different wavelengths allows the method to simultaneously detect both analytes. Selectivity is obtained through the capillary zone electrophoresis separation, which results in characteristic migration times. Measurement in capillary zone electrophoresis resulted in a limit of detection of 6.9 × 10(-10)M (2.5 × 10(-19) mol) for crystal violet and 8.3 × 10(-11)M (3.0 × 10(-20) mol) for malachite green at S/N of 2. PMID:26998858

  16. 10-W CW blue-violet diode laser array on the micro-channel cooler

    NASA Astrophysics Data System (ADS)

    Suzuki, Nobuyasu; Morimoto, Kiyoshi

    2012-03-01

    Improved light output power of blue-violet laser diodes (BVLDs) is necessary in order to use them as a light source for crystallization of amorphous silicon (a-Si) thin films to fabricate thin film transistors (TFTs). A multi-emitter BVLD array is a promising solution to obtain high light output power. For realization of the high power blue-violet laser source, we carried out a thermal design using the finite element method (FEM). Because conventional packaging is significantly affected by heat dissipation, we mounted the multi-emitter BVLD array on micro-channel coolers (MCCs). A steady thermal analysis using FEM revealed that the direct-mounted BVLD array with appropriate emitter pitch had a flatshaped transverse temperature distribution across the array. In contrast, a convex-shaped distribution was obtained when a highly thermal conductive sub-mounts, such as a diamond-composite, was inserted between the array and the MCCs. The local temperature rise in the center emitter of the direct-mounted laser array was suppressed due to their relatively shorter heat transfer paths. The flat-shaped temperature distribution should contribute to achieving high optical output power. Therefore, the BVLD arrays were directly mounted on coefficient of thermal expansion (CTE) controlled MCCs using AuSn hard solder. Under continuous wave (CW) operation, we achieved an output over 10 W with a ten-emitter BVLD array, which is the highest reported output power for a blue-violet laser source.

  17. Preparation of vinylogous 2-sulfonylindolines by the palladium-catalyzed heteroannulation of o-iodoanilines with dienyl sulfones and their further transformation to indoles and carbazoles.

    PubMed

    Back, T G; Bethell, R J; Parvez, M; Taylor, J A

    2001-12-14

    The palladium-catalyzed heteroannulation of o-iodoanilines with dienyl sulfones provides a convenient route to vinylogous 2-sulfonylindolines 3. The reaction proceeds in DMF/water in the presence of potassium carbonate and catalytic palladium(II) acetate and is compatible with both electron-donating and -withdrawing substituents in the para position of the aniline, and with an alkyl substituent at C-2 of the dienyl sulfone. The indolines underwent oxidation with DDQ to afford the corresponding indoles 4. The latter were then employed as dienes in Diels-Alder reactions with dimethyl acetylenedicarboxylate (DMAD), methyl propiolate, or methyl acrylate. In the case of the latter two dienophiles, the cycloadditions were highly regioselective, affording the corresponding 1,3-products (with respect to the relative positions of the sulfone and ester groups), exclusively. The cycloadducts from acetylenic dienophiles were converted to the corresponding carbazoles by elimination of the sulfone moiety with DBU, and that from methyl acrylate was subjected to reductive desulfonylation and oxidation to the corresponding carbazole with DDQ. The method thus provides access to carbazoles with various substituents at the 3-, 4-, and 6-positions. PMID:11735543

  18. BC3EE2,9B, a synthetic carbazole derivative, upregulates autophagy and synergistically sensitizes human GBM8901 glioblastoma cells to temozolomide.

    PubMed

    Chen, Chien-Min; Syu, Jhih-Pu; Way, Tzong-Der; Huang, Li-Jiau; Kuo, Sheng-Chu; Lin, Chung-Tien; Lin, Chih-Li

    2015-11-01

    Glioblastoma multiforme (GBM) is the most fatal form of human brain cancer. Although temozolomide (TMZ), an oral alkylating chemotherapeutic agent, improves the survival rate, the prognosis of patients with GBM remains poor. Naturally occurring carbazole alkaloids isolated from curry leaves (Murraya koenigii Spreng.) have been shown to possess a wide range of anticancer properties. However, the effects of carbazole derivatives on glioblastoma cells remain poorly understood. In the present study, anti‑glioblastoma profiles of a series of synthetic carbazole derivatives were evaluated in vitro. The most promising derivative in this series was BC3EE2,9B, which showed significant anti‑proliferative effects in GBM8401 and GBM8901 cells. BC3EE2,9B also triggered cell‑cycle arrest, most prominently at the G1 stage, and suppressed glioblastoma cell invasion and migration. Furthermore, BC3EE2,9B induced autophagy‑mediated cell death and synergistically sensitized GBM cells to TMZ cytotoxicity. The possible mechanism underlying BC3EE2,9B‑induced autophagy may involve activation of adenosine monophosphate-activated protein kinase and the attenuation of the Akt and mammalian target of the rapamycin downstream signaling pathway. Taken together, the present results provide molecular evidence for the mode of action governing the ability of BC3EE2,9B to sensitize drug‑resistant glioblastoma cells to the chemotherapeutic agent TMZ.

  19. BC3EE2,9B, a synthetic carbazole derivative, upregulates autophagy and synergistically sensitizes human GBM8901 glioblastoma cells to temozolomide

    PubMed Central

    CHEN, CHIEN-MIN; SYU, JHIH-PU; WAY, TZONG-DER; HUANG, LI-JIAU; KUO, SHENG-CHU; LIN, CHUNG-TIEN; LIN, CHIH-LI

    2015-01-01

    Glioblastoma multiforme (GBM) is the most fatal form of human brain cancer. Although temozolomide (TMZ), an oral alkylating chemotherapeutic agent, improves the survival rate, the prognosis of patients with GBM remains poor. Naturally occurring carbazole alkaloids isolated from curry leaves (Murraya koenigii Spreng.) have been shown to possess a wide range of anticancer properties. However, the effects of carbazole derivatives on glioblastoma cells remain poorly understood. In the present study, anti-glioblastoma profiles of a series of synthetic carbazole derivatives were evaluated in vitro. The most promising derivative in this series was BC3EE2,9B, which showed significant anti-proliferative effects in GBM8401 and GBM8901 cells. BC3EE2,9B also triggered cell-cycle arrest, most prominently at the G1 stage, and suppressed glioblastoma cell invasion and migration. Furthermore, BC3EE2,9B induced autophagy-mediated cell death and synergistically sensitized GBM cells to TMZ cytotoxicity. The possible mechanism underlying BC3EE2,9B-induced autophagy may involve activation of adenosine monophosphate-activated protein kinase and the attenuation of the Akt and mammalian target of the rapamycin downstream signaling pathway. Taken together, the present results provide molecular evidence for the mode of action governing the ability of BC3EE2,9B to sensitize drug-resistant glioblastoma cells to the chemotherapeutic agent TMZ. PMID:26329365

  20. Effect of Self-Assembled Monolayer Modification on Indium-Tin Oxide Surface for Surface-Initiated Vapor Deposition Polymerization of Carbazole Thin Films

    NASA Astrophysics Data System (ADS)

    Yuya Umemoto,; Seong-Ho Kim,; Rigoberto C. Advincula,; Kuniaki Tanaka,; Hiroaki Usui,

    2010-04-01

    With the aim of controlling the interface between an inorganic electrode and an organic layer, a surface-initiated vapor deposition polymerization method was employed to prepare carbazole polymer thin films that are chemically bound to an indium-tin oxide (ITO) surface. A self-assembled monolayer (SAM) that has an azo initiator as a terminal group was prepared on an ITO surface, on which carbazole acrylate monomers were evaporated under ultraviolet (UV) irradiation. The surface morphological characteristics of the films prepared with/without UV irradiation and with/without the SAM were compared. It was found that the UV irradiation leads to the polymerization of carbazole monomers irrespective of the type of substrate used. On the other hand, the surface morphological characteristics were largely dependent on the existence of the SAM. Uniform and smooth polymer thin films were obtained only when the monomers were evaporated on the SAM-modified surface under UV irradiation. A comparison of film growth characteristics on a UV-ozone-treated ITO surface suggested that the formation of uniform films was made possible not by the modification of surface energy but by the growth of the polymers chemically bound to the substrate surface.

  1. Synthesis, biological evaluation and molecular modeling study of novel tacrine-carbazole hybrids as potential multifunctional agents for the treatment of Alzheimer's disease.

    PubMed

    Thiratmatrakul, Supatra; Yenjai, Chavi; Waiwut, Pornthip; Vajragupta, Opa; Reubroycharoen, Prasert; Tohda, Michihisa; Boonyarat, Chantana

    2014-03-21

    New tacrine-carbazole hybrids were developed as potential multifunctional anti-Alzheimer agents for their cholinesterase inhibitory and radical scavenging activities. The developed compounds showed high inhibitory activity on acetylcholinesterase (AChE) with IC50 values ranging from 0.48 to 1.03 μM and exhibited good inhibition selectivity against AChE over butyrylcholinesterase (BuChE). Molecular modeling studies revealed that these tacrine-carbazole hybrids interacted simultaneously with the catalytic active site (CAS) and the peripheral anionic site (PAS) of AChE. The derivatives containing methoxy group showed potent ABTS radical scavenging activity. Considering their neuroprotection, our results indicate that these derivatives can reduce neuronal death induced by oxidative stress and β-amyloid (Aβ). Moreover, S1, the highest potency for both radical scavenging and AChE inhibitory activity, exhibited an ability to improve both short-term and long-term memory deficit in mice induced by scopolamine. Overall, tacrine-carbazole derivatives can be considered as a candidate with potential impact for further pharmacological development in Alzheimer's therapy.

  2. Fast analysis of malachite green, leucomalachite green, crystal violet and leucocrystal violet in fish tissue based on a modified QuEChERS procedure.

    PubMed

    Zhu, Chengyun; Wei, Jie; Dong, Xuefang; Guo, Zhimou; Liu, Mingyang; Liang, Xinmiao

    2014-04-01

    Triphenylmethane dyes malachite green (MG) and crystal violet (CV) have been used as antimicrobial, antiparasitic and antiseptic agents in aquaculture. However, MG and CV, as well as their metabolites leucomalachite green (LMG) and leucocrystal violet (LCV) are potential mutagens and carcinogens. Thus, the efficient determination of dye residues is of great concern. Considering the complexity of the aquatic products, the sample pretreatment is significant for decreasing matrix interference and improving detection sensitivity. In this study, a simple and rapid QuEChERS procedure was developed and combined with HPLC analysis for the simultaneous determination of the four dyes in fish tissue. An XCharge C18 column was applied in HPLC analysis to achieve good peak shape and selectivity. The pretreatment method involved the extraction of dyes from fish tissue and further clean-up with dispersive solid phase extraction (d-SPE) material. The extraction volume, extraction time as well as d-SPE materials were systematically optimized. The results indicated that reversed-phase/strong anion exchange (C18SAX) adsorbent in the d-SPE procedure could effectively improve the recovery compared with conventional C18 or C18 incorporated with primary secondary amine (PSA) material. Under optimized conditions, good linearity was achieved in the concentration range of 0.5-100 mg/L with R2 greater than 0. 998. The recoveries were 73%-91% and the precisions were 0.66%-5.41%. The results demonstrated the feasibility and efficiency of QuEChERS procedure incorporated with HPLC for dye monitoring.

  3. Fast analysis of malachite green, leucomalachite green, crystal violet and leucocrystal violet in fish tissue based on a modified QuEChERS procedure.

    PubMed

    Zhu, Chengyun; Wei, Jie; Dong, Xuefang; Guo, Zhimou; Liu, Mingyang; Liang, Xinmiao

    2014-04-01

    Triphenylmethane dyes malachite green (MG) and crystal violet (CV) have been used as antimicrobial, antiparasitic and antiseptic agents in aquaculture. However, MG and CV, as well as their metabolites leucomalachite green (LMG) and leucocrystal violet (LCV) are potential mutagens and carcinogens. Thus, the efficient determination of dye residues is of great concern. Considering the complexity of the aquatic products, the sample pretreatment is significant for decreasing matrix interference and improving detection sensitivity. In this study, a simple and rapid QuEChERS procedure was developed and combined with HPLC analysis for the simultaneous determination of the four dyes in fish tissue. An XCharge C18 column was applied in HPLC analysis to achieve good peak shape and selectivity. The pretreatment method involved the extraction of dyes from fish tissue and further clean-up with dispersive solid phase extraction (d-SPE) material. The extraction volume, extraction time as well as d-SPE materials were systematically optimized. The results indicated that reversed-phase/strong anion exchange (C18SAX) adsorbent in the d-SPE procedure could effectively improve the recovery compared with conventional C18 or C18 incorporated with primary secondary amine (PSA) material. Under optimized conditions, good linearity was achieved in the concentration range of 0.5-100 mg/L with R2 greater than 0. 998. The recoveries were 73%-91% and the precisions were 0.66%-5.41%. The results demonstrated the feasibility and efficiency of QuEChERS procedure incorporated with HPLC for dye monitoring. PMID:25069333

  4. Magnetic solid-phase extraction for determination of the total malachite green, gentian violet and leucomalachite green, leucogentian violet in aquaculture water by high-performance liquid chromatography with fluorescence detection.

    PubMed

    Zhao, Jiao; Wei, Daqiao; Yang, Yaling

    2016-06-01

    In this study, magnetic multi-walled carbon nanotube nanoparticles were synthesized and used as the adsorbent for the sums of malachite green, gentian violet and leucomalachite green, leucogentian violet in aquaculture water samples followed by high performance liquid chromatography with fluorescence detection. This method was based on in situ reduction of chromic malachite green, gentian violet to colorless leucomalachite green, leucogentian violet with potassium borohydride, respectively. The obtained adsorbent combines the advantages of carbon nanotubes and Fe3 O4 nanoparticles in one material for separation and preconcentration of the reductive dyes in aqueous media. The structure and properties of the prepared nanoparticles were characterized by transmission and scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. The main parameters affecting the adsorption recoveries were investigated and optimized, including reducing agent concentration, type and amount of sorbent, sample pH, and eluting conditions. Under the optimum conditions, the limits of detection in this method were 0.22 and 0.09 ng/mL for malachite green and gentian violet, respectively. Product recoveries ranged from 87.0 to 92.8% with relative standard deviations from 4.6 to 5.9%. The results indicate that the sorbent is a suitable material for the removal and concentration of triphenylmethane dyes from polluted environmental samples. PMID:27120413

  5. Magnetic solid-phase extraction for determination of the total malachite green, gentian violet and leucomalachite green, leucogentian violet in aquaculture water by high-performance liquid chromatography with fluorescence detection.

    PubMed

    Zhao, Jiao; Wei, Daqiao; Yang, Yaling

    2016-06-01

    In this study, magnetic multi-walled carbon nanotube nanoparticles were synthesized and used as the adsorbent for the sums of malachite green, gentian violet and leucomalachite green, leucogentian violet in aquaculture water samples followed by high performance liquid chromatography with fluorescence detection. This method was based on in situ reduction of chromic malachite green, gentian violet to colorless leucomalachite green, leucogentian violet with potassium borohydride, respectively. The obtained adsorbent combines the advantages of carbon nanotubes and Fe3 O4 nanoparticles in one material for separation and preconcentration of the reductive dyes in aqueous media. The structure and properties of the prepared nanoparticles were characterized by transmission and scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. The main parameters affecting the adsorption recoveries were investigated and optimized, including reducing agent concentration, type and amount of sorbent, sample pH, and eluting conditions. Under the optimum conditions, the limits of detection in this method were 0.22 and 0.09 ng/mL for malachite green and gentian violet, respectively. Product recoveries ranged from 87.0 to 92.8% with relative standard deviations from 4.6 to 5.9%. The results indicate that the sorbent is a suitable material for the removal and concentration of triphenylmethane dyes from polluted environmental samples.

  6. Selective removal of the violet color produced by anthocyanins in procyanidin-rich unfermented cocoa extracts.

    PubMed

    Wallace, Taylor C; Giusti, M Monica

    2011-09-01

    Cacao (Theobroma cacao L.) is rich in procyanidins, a large portion of which degrades during the natural fermentation process of producing cocoa powder. Recent advances in technology have enabled scientists to produce unfermented cocoa powder, preserving the original profile of procyanidins present in cocoa and allowing for the development of highly concentrated procyanidin-rich extracts. During this process, the anthocyanins naturally present in unfermented cocoa remain intact, producing a violet color in the final extract. The objective of this study was to selectively remove the violet color in procyanidin-rich extracts produced from unfermented cocoa powder, while maintaining the stability and composition of procyanidins present in the matrix. Several processing parameters, including pH fluctuations, enzymatic treatments, and the addition of potassium meta-bisulfite, were explored to influence the color of procyanidin-rich extracts throughout a 60-d shelf life study. The addition of potassium meta-bisulfite (500 ppm) was found to be the most effective means of removing the violet color present in the treated extracts (L*= 71.39, a*= 8.44, b*= 9.61, chroma = 12.79, and hue = 48.8˚) as compared to the control (L*= 52.84, a*= 11.08, b*= 2.24, chroma = 11.28, and hue = 11.4˚). The use of potassium meta-bisulfite at all treatment levels (200, 500, and 1000 ppm) did not show any significant detrimental effects on the stability, composition, or amount of procyanidins present in the extracts over the shelf life period as monitored by UV-Vis spectrophotometry and HPLC-MS. This research will enable the food industry to incorporate highly concentrated procyanidin-rich extracts in food products without influencing the color of the final product.

  7. Aqueous photofate of crystal violet under simulated and natural solar irradiation: Kinetics, products, and pathways.

    PubMed

    Li, Yong; Yang, Shaogui; Sun, Cheng; Wang, Lianhong; Wang, Qingeng

    2016-01-01

    In this work photodegradation rates and pathways of an illegal veterinary drug, crystal violet, were studied under simulated and solar irradiation with the goal of assessing the potential of photolysis as a removal mechanism in the aquatic environment. Factors influencing the photodegradation process under simulated sunlight were investigated, including pH, humic acid, Fe(2+), Ca(2+), [Formula: see text] , and [Formula: see text] , of which favorable conditions were optimized by the orthogonal array design. The degradation processes of crystal violet conformed to pseudo first-order kinetics, with different rate constants under different conditions. Reactive oxygen species such as hydroxyl radical, singlet oxygen, and superoxide anion participated in the indirect photolysis process, leading to much higher decolorization efficiencies than those of direct photolysis and hydrolysis. Contrasting to simulated irradiation, solar irradiation led to complete decolorization. Sixty-four products were identified by high resolution liquid chromatography-time-of-flight mass spectrometry and gas chromatography-mass spectrometry, elucidating relatively complete mineralization through photolysis. Based on the analyses of the degradation products and calculations of the frontier electron density, transformation pathways were proposed as singlet oxygen addition, N-demethylation, hydroxyl addition, decomposition of conjugated structure, the removal of benzene ring and the ring-opening reaction. As a result, small products generated as carboxylic acids, alcohols and amines, which were not likely to cause severe hazards to the environment. This study provided both a reference for photodegradation of crystal violet and future safety applications and predictions of decontamination of related triphenylmethane veterinary drug under environmental conditions.

  8. Adsorption of Crystal violet on raw and acid-treated montmorillonite, K10, in aqueous suspension.

    PubMed

    Sarma, Gautam Kumar; Sen Gupta, Susmita; Bhattacharyya, Krishna G

    2016-04-15

    Crystal violet is used as a dye in cotton and silk textiles, paints and printing ink. The dye is hazardous and exposure to it may cause permanent injury to the cornea and conjunctiva including permanent blindness, and in severe cases, may lead to respiratory and kidney failure. The present work describes removal of Crystal violet from aqueous solution by adsorption on raw and acid-treated montmorillonite, K10. The clay mineral was treated with 0.25 and 0.50 M sulfuric acid and the resulting materials were characterized by XRD, zeta potential, SEM, FTIR, cation exchange capacity, BET surface area and pore volume measurements. The influences of pH, interaction time, adsorbent amount, and temperature on adsorption were monitored and explained on the basis of physico-chemical characteristics of the materials. Basic pH generally favors adsorption but considerable removal was possible even under neutral conditions. Adsorption was very rapid and equilibrium could be attained in 180 min. The kinetics conformed to second order model. Langmuir monolayer adsorption capacity of raw montmorillonite K10 was 370.37 mg g(-1) whereas 0.25 M and 0.50 M acid treated montmorillonite K10 had capacities of 384.62 and 400.0 mg g(-1) respectively at 303 K. Adsorption was exothermic and decreased in the temperature range of 293-323 K. Thermodynamically, the process was spontaneous with Gibbs energy decreasing with rise in temperature. The results suggest that montmorillonite K10 and its acid treated forms would be suitable for removing Crystal violet from aqueous solution.

  9. Jupiter's Belt-Zone Boundary in Near-Infrared and Violet Light

    NASA Technical Reports Server (NTRS)

    1997-01-01

    Mosaics of a belt-zone boundary near Jupiter's equator in violet (top panel) and near-infrared (bottom panel) light. The four images that make up each of these mosaics were taken within a few minutes of each other. Sunlight at 757 nanometers (near-infrared) penetrates deep into Jupiter's troposphere before being absorbed or scattered by clouds to the Galileo spacecraft. This wavelength reveals the features of the lower visible cloud deck. Sunlight at 415 nanometers (violet) is a scattered or absorbed to varying degrees in different parts of Jupiter's atmosphere depending on the types and concentrations of cloud particles and chemicals that color Jupiter's atmosphere. The near-infrared mosaic primarily shows cloud features. The violet mosaic has three distinct regions: it is brightest at the latitude of the jet (horizontally across the center of the mosaic), moderately bright north of the jet, and dark and patchy south of the jet.

    North is at the top. The mosaic covers latitudes -13 to +3 degrees and is centered at longitude 282 degrees West. The smallest resolved features are tens of kilometers in size. These images were taken on November 5th, 1996, at a range of 1.2 million kilometers by the Solid State Imaging system aboard NASA's Galileo spacecraft.

    The Jet Propulsion Laboratory, Pasadena, CA manages the mission for NASA's Office of Space Science, Washington, DC.

    This image and other images and data received from Galileo are posted on the World Wide Web, on the Galileo mission home page at URL http://galileo.jpl.nasa.gov. Background information and educational context for the images can be found at URL http://www.jpl.nasa.gov/galileo/sepo

  10. Semi-quantitative analysis of gentian violet by surface-enhanced Raman spectroscopy using silver colloids.

    PubMed

    Liu, Fangfang; Gu, Huaimin; Yuan, Xiaojuan; Dong, Xiao

    2010-11-01

    The viability of the application of surface-enhanced Raman spectroscopy (SERS) to the semi-quantitative analysis of the triphenylmethane dye gentian violet was examined by using activated borohydride-reduced silver colloids. Raman and SERS spectra of aqueous solutions of gentian violet at different pH values were acquired for the first time and equally intense SERS signals were obtained at both acidic and alkaline pH values. Two maxima intensities observed in the pH profile revealed the presence of different ionization states of the dye. The pH conditions for SERS were optimized over the pH range 1 to 12 and the biggest enhancement for SERS of this charged dye was found to be at pH 2.0; thus, this condition was used for semi-quantitative analysis. A good linear correlation was observed for the dependence of the signal intensities of the SERS bands at 1620 cm(-1) (R = 0.999) and 1370 cm(-1) (R = 0.952) on dye concentration over the range 10(-6) to 10(-4) mol/L, using laser excitation at 514.5 nm. At concentrations of dye above 10(-2) mol/L, the concentration dependence of the SERS signals is nonlinear. This is explained as due to the precipitation of metallic silver as well as due to saturation caused by complete coverage of the SERS substrate. A series of intensities of the band at 1620 cm(-1) measured from dye molecules proved that the single-molecule limit of gentian violet is attained at the concentration of 10(-9) mol/L.

  11. Aqueous photofate of crystal violet under simulated and natural solar irradiation: Kinetics, products, and pathways.

    PubMed

    Li, Yong; Yang, Shaogui; Sun, Cheng; Wang, Lianhong; Wang, Qingeng

    2016-01-01

    In this work photodegradation rates and pathways of an illegal veterinary drug, crystal violet, were studied under simulated and solar irradiation with the goal of assessing the potential of photolysis as a removal mechanism in the aquatic environment. Factors influencing the photodegradation process under simulated sunlight were investigated, including pH, humic acid, Fe(2+), Ca(2+), [Formula: see text] , and [Formula: see text] , of which favorable conditions were optimized by the orthogonal array design. The degradation processes of crystal violet conformed to pseudo first-order kinetics, with different rate constants under different conditions. Reactive oxygen species such as hydroxyl radical, singlet oxygen, and superoxide anion participated in the indirect photolysis process, leading to much higher decolorization efficiencies than those of direct photolysis and hydrolysis. Contrasting to simulated irradiation, solar irradiation led to complete decolorization. Sixty-four products were identified by high resolution liquid chromatography-time-of-flight mass spectrometry and gas chromatography-mass spectrometry, elucidating relatively complete mineralization through photolysis. Based on the analyses of the degradation products and calculations of the frontier electron density, transformation pathways were proposed as singlet oxygen addition, N-demethylation, hydroxyl addition, decomposition of conjugated structure, the removal of benzene ring and the ring-opening reaction. As a result, small products generated as carboxylic acids, alcohols and amines, which were not likely to cause severe hazards to the environment. This study provided both a reference for photodegradation of crystal violet and future safety applications and predictions of decontamination of related triphenylmethane veterinary drug under environmental conditions. PMID:26497275

  12. Nitrogen-containing microporous conjugated polymers via carbazole-based oxidative coupling polymerization: preparation, porosity, and gas uptake.

    PubMed

    Chen, Qi; Liu, De-Peng; Luo, Min; Feng, Li-Juan; Zhao, Yan-Chao; Han, Bao-Hang

    2014-01-29

    Facile preparation of microporous conjugated polycarbazoles via carbazole-based oxidative coupling polymerization is reported. The process to form the polymer network has cost-effective advantages such as using a cheap catalyst, mild reaction conditions, and requiring a single monomer. Because no other functional groups such as halo groups, boric acid, and alkyne are required for coupling polymerization, properties derived from monomers are likely to be fully retained and structures of final polymers are easier to characterize. A series of microporous conjugated polycarbazoles (CPOP-2-7) with permanent porosity are synthesized using versatile carbazolyl-bearing 2D and 3D conjugated core structures with non-planar rigid conformation as building units. The Brunauer-Emmett-Teller specific surface area values for these porous materials vary between 510 and 1430 m(2) g(-1) . The dominant pore sizes of the polymers based on the different building blocks are located between 0.59 and 0.66 nm. Gas (H2 and CO2 ) adsorption isotherms show that CPOP-7 exhibits the best uptake capacity for hydrogen (1.51 wt% at 1.0 bar and 77 K) and carbon dioxide (13.2 wt% at 1.0 bar and 273 K) among the obtained polymers. Furthermore, its high CH4 /N2 and CO2 /N2 adsorption selectivity gives polymer CPOP-7 potential application in gas separation.

  13. Charge carrier mobility in conjugated organic polymers: simulation of an electron mobility in a carbazole-benzothiadiazole-based polymer

    NASA Astrophysics Data System (ADS)

    Li, Yaping; Lagowski, Jolanta B.

    2011-08-01

    Inorganic (mostly silicon based) solar cells are important devices that are used to solve the world energy and environmental needs. Now days, organic solar cells are attracting considerable attention in the field of photovoltaic cells because of their low cost and processing flexibility. Often conjugated polymers are used in the construction of the organic solar cells. We study the conjugated polymers' charge transport using computational approach that involves the use of the density functional theory (DFT), semiempirical (ZINDO), and Monte Carlo (MC) theoretical methods in order to determine their transfer integrals, reorganization energies, transfer rates (with the use of Marcus-Hush equation) and mobilities. We employ the experimentally determined three dimensional (3D) structure of poly(9,9'-di-n-octylfluorene-alt-benzothiadiazole) (F8BT) to estimate the electron mobility in a similar co-alternating polymer consisting of carbazole and benzothiadiazole units (C8BT). In agreement with our previous work, we found that including an orientational disorder in the crystal reduces the electron mobility in C8BT. We hope that the proposed computational approach can be used to predict charge mobility in organic materials that are used in solar cells.

  14. Photoconductivity in the Poly(2,7-Carbazole) Copolymer PCDTBT, and in Bulk Heterojunction Composites with PC70BM

    NASA Astrophysics Data System (ADS)

    Coates, Nelson; Tong, Minghong; Moses, Daniel; Heeger, Alan; Beaupré, Serge; Leclerc, Mario

    2010-03-01

    We have studied the carrier generation in an alternating donor-acceptor low bandgap copolymer and in composites of that polymer with a soluble fullerene derivative, using steady-state and transient photoconductivity. The Poly(2,7-Carbazole) copolymer PCDTBT we studied represents a class of donor-acceptor copolymers that hold promise for photovoltaic applications because of the ability to tune the electronic energy levels. Photovoltaic devices fabricated from PCDTBT with the soluble fullerene derivative [6,6]-phenyl C70-butyric acid methyl ester (PC70BM) have exhibited a higher solar cell power conversion efficiency than has been achieved in P3HT based devices. In PCDTBT, the absorption extends out to 1.75 eV, with two distinct but broad absorption bands that are centered at ˜2 eV and ˜3 eV. We have used steady-state and transient photoconductivity to investigate the carrier generation and collection efficiency of PCDTBT and its composite with PC70BM after photoexcitation at each of its distinct absorption bands.

  15. Synthesis, structure and properties of zinc(II) coordination polymers with 9H-carbazole-2,7-dicarboxylic acid

    NASA Astrophysics Data System (ADS)

    Yi, Xiu-Chun; Xi, Fu-Gui; Wang, Kun; Su, Zhao; Gao, En-Qing

    2013-10-01

    From a new dicarboxylate ligand, 9H-carbazole-2,7-dicarboxylic acid (2,7-H2CDC), three Zn(II) metal-organic frameworks were synthesized in the absence or presence of ditopic N-donor ligands. They are formulated as [Zn5(μ3-OH)2(2,7-CDC)4(DEF)2] (1) (DEF=N,N-diethylformamide), [Zn2(2,7-CDC)2(DABCO)(H2O)]·5DMF·H2O (2) (DABCO=1-diaza-bicyclo[2.2.2]octane, DMF=N,N-dimethylformamide), and [Zn2(2,7-CDC)2(bpea)]·3DMA·2 H2O (3) (bpea=1,2-bis(4-pyridyl)ethylane, DMA=N,N-dimethylacetamide). Compounds 1 and 3 display the 3D pcu frameworks. In 1 the unusual pentanuclear [Zn5(μ3-OH)2(COO)8] secondary building units (SBUs) are linked by dicarboxylate ligands. Differently, in 3 the well-known paddle-wheel [Zn2(COO)4] SBUs are linked by dicarboxylate and dipyridyl ligands. Compound 2 shows the rare self-catenated 3D alb-3,6-C2/c net topology based on the dinuclear paddle-wheel SBU and a mononuclear unit. The stability and fluorescent properties of the compounds have been studied.

  16. Optical biosensor with poly[N-nonyl-3,6-bis(ethylenedioxythiophene)carbazole] matrix for monitoring of phenol derivatives

    NASA Astrophysics Data System (ADS)

    Jedrychowska, Agnieszka; Malecha, Karol; Cabaj, Joanna; Sołoducho, Jadwiga

    2014-08-01

    The aim of the research was to develop an enzymatic, optical biosensor which provides quick and convenient determination of phenolic compounds in aqueous solutions. The biosensing strategy concerns design, fabrication and testing of a miniature ceramic-based biosensor which is destined for in-situ substrate monitoring. The base of the measuring system was fabricated using low temperature co-fired ceramics (LTCC) technology. The biocatalyst - laccase- was immobilized on the thin film of poly[N-nonyl-3,6-bis(ethylenedioxythiophene)carbazole] which provided good binding of the enzyme to the substrate and positively affected on the catalytic activity of the protein. In order to evaluate properties of the designed biosensor, its response for various concentrations of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diamonnium sal (ABTS) was measured. The optical biosensor produced by presented method could find applications in many fields, i.e. for detection of phenolic compounds in food products and beverages, in industry for control of technological processes or for environmental monitoring

  17. Characterization of a novel cometabolic degradation carbazole pathway by a phenol-cultivated Arthrobacter sp. W1.

    PubMed

    Shi, Shengnan; Qu, Yuanyuan; Zhou, Hao; Ma, Qiao; Ma, Fang

    2015-10-01

    Arthrobacter sp. W1 was used to characterize the pathways involved in cometabolic degradation of carbazole (CA) with phenol as the primary substrate. To clarify the upper pathway of cometabolic degradation CA, Escherichia coli strain BL21 expressing phenol hydroxylase from strain W1 (PHIND) was investigated to degrade CA. Firstly, CA was initially monohydroxylated at C-2 and C-4 positions to produce 2- and 4-hydroxycarbazole, followed by successively hydroxylated to the corresponding 1,2- and 3,4-dihydroxycarbazole, of which 3,4-dihydroxycarbazole was unequivocally identified for the first time. To characterize the downstream cometabolic degradation CA pathway, purified 3,4-dihydroxycarbazole was used as the substrate for phenol-grown W1, and a series of novel indole derivatives were identified. These results suggested that a novel pathway of CA catabolism was employed by strain W1 via a successive hydroxylation and meta-cleavage pathway. These findings provide new insights into the cometabolic degradation CA process and have potential applications in biotechnology and bioremediation.

  18. Bioremediation of coking wastewater containing carbazole, dibenzofuran, dibenzothiophene and naphthalene by a naphthalene-cultivated Arthrobacter sp. W1.

    PubMed

    Shi, Shengnan; Qu, Yuanyuan; Ma, Fang; Zhou, Jiti

    2014-07-01

    A naphthalene-utilizing bacterium, Arthrobacter sp. W1, was used to investigate the cometabolic degradation of carbazole (CA), dibenzofuran (DBF) and dibenzothiophene (DBT) using naphthalene as the primary substrate. Both the growing and washed cells of strain W1 could degrade CA, DBF, DBT, and naphthalene simultaneously and quickly. Inhibition kinetics confirmed that the presence of CA, DBF and DBT in the growing system would inhibit the cells growth and biodegradability of strain W1. The relationship between ln(C/C0) and time, and specific degradation rate and CA, DBF and DBT concentration could be described well by First-order and Michaelis-Menten kinetics. The treatment of real coking wastewater containing high concentration of phenol, naphthalene, CA, DBF, DBT and NH3-N was shown to be highly efficient by naphthalene-grown W1 coupling with activation zeolite. Toxicity assessment indicated the treatment of the coking wastewater by strain W1 coupling with activation led to less toxicity than untreated wastewater.

  19. Tissue-specific DNA adduct formation in mice treated with the environmental carcinogen, 7H-dibenzo[c,g]carbazole.

    PubMed

    Schurdak, M E; Randerath, K

    1985-09-01

    Covalent adduction of DNA by chemical agents is commonly thought to be an essential part of the initiation of chemical carcinogenesis. Until recently, assays of DNA damage by covalent binding of chemicals have been restricted mostly to substances that are available in radiolabeled form, which excludes many environmental compounds with carcinogenic potential. In this paper, the binding of non-radioactive 7H-dibenzo[c,g]carbazole (DBC), a known environmental carcinogen, to DNA in female CD-1 mice after s.c. injection of 44 mumol/kg of the compound has been investigated using a 32P-postlabeling assay. DBC showed strong hepatic specificity with a mean total level of 107 adducts per 10(7) nucleotides at 24 h, while much lower levels of binding were seen in kidney, lung, spleen, skin and brain with 4.3, 2.1, 1.3, 0.4 and 0.04 adducts, respectively, per 10(7) nucleotides. Proportions of individual DBC adducts also varied considerably between tissues. The degree of hepatic preference displayed by DBC is not seen with other polycyclic aromatic carcinogens such as benzo[a]pyrene and 2-acetylaminofluorene. The DNA-binding data, together with other hepatotoxic effects of the compound, may be causally related to the known hepatocarcinogenicity of DBC.

  20. Extreme ultra-violet movie camera for imaging microsecond time scale magnetic reconnection

    SciTech Connect

    Chai, Kil-Byoung; Bellan, Paul M.

    2013-12-15

    An ultra-fast extreme ultra-violet (EUV) movie camera has been developed for imaging magnetic reconnection in the Caltech spheromak/astrophysical jet experiment. The camera consists of a broadband Mo:Si multilayer mirror, a fast decaying YAG:Ce scintillator, a visible light block, and a high-speed visible light CCD camera. The camera can capture EUV images as fast as 3.3 × 10{sup 6} frames per second with 0.5 cm spatial resolution. The spectral range is from 20 eV to 60 eV. EUV images reveal strong, transient, highly localized bursts of EUV radiation when magnetic reconnection occurs.

  1. Can Ultra-violet Mie Lidar Be an Effective Instrument During High Pollution Episode?

    NASA Astrophysics Data System (ADS)

    Liu, Qiaojun; Wang, Zhangjun; Du, Libin; Cheng, Andrew Yuk Sun; Meng, Xiangqian; Chen, Chao; Li, Xianxin; Liu, Xingtao

    2016-06-01

    Vertical profiles of particulates were measured by a 355 nm Mie scattering lidar during a dust-storm event. A high energy pulse laser was employed as the light source to detect the extinction coefficient in the altitude up to 6 km in the day and 9 km at night. The extinction profiles showed layers of high aerosol concentrations in good agreement with ground-based pollution measurements, which indicated that such ultra-violet lidar is a very useful remote sensing instrument for monitoring extinction profiles during extreme high aerosol loading and low visibility atmospheric conditions when low energy lidar systems cannot obtain effective results.

  2. High light extraction efficiency in bulk-GaN based volumetric violet light-emitting diodes

    SciTech Connect

    David, Aurelien Hurni, Christophe A.; Aldaz, Rafael I.; Cich, Michael J.; Ellis, Bryan; Huang, Kevin; Steranka, Frank M.; Krames, Michael R.

    2014-12-08

    We report on the light extraction efficiency of III-Nitride violet light-emitting diodes with a volumetric flip-chip architecture. We introduce an accurate optical model to account for light extraction. We fabricate a series of devices with varying optical configurations and fit their measured performance with our model. We show the importance of second-order optical effects like photon recycling and residual surface roughness to account for data. We conclude that our devices reach an extraction efficiency of 89%.

  3. Nanostructural Analysis of a GaN-BASED Violet Laser Diode

    NASA Astrophysics Data System (ADS)

    Yang, J. R.; Tsai, H. L.; Wang, T. Y.; Yen, H. W.; Chen, C. Y.; Li, W. C.; Chen, H. R.

    The nanostructure of p-type AlGaN/GaN strained-layer superlattice (SLS) cladding in a GaN-based violet laser diode (LD) has been investigated by high-angle annular dark-field (HAADF) scanning-transmission electron microscopy (STEM). The pairs of the AlGaN and GaN layers in SLS cladding are observed, where the AlGaN and GaN layers appear as dark and bright bands. It is also found that the threading dislocations disappeared within the SLS; this evidence manifests the role of SLS in suppressing threading dislocation propagation.

  4. Exploring the temporally resolved electron density evolution in extreme ultra-violet induced plasmas

    NASA Astrophysics Data System (ADS)

    van der Horst, R. M.; Beckers, J.; Nijdam, S.; Kroesen, G. M. W.

    2014-07-01

    We measured the electron density in an extreme ultra-violet (EUV) induced plasma. This is achieved in a low-pressure argon plasma by using a method called microwave cavity resonance spectroscopy. The measured electron density just after the EUV pulse is 2.6 × 1016 m-3. This is in good agreement with a theoretical prediction from photo-ionization, which yields a density of 4.5 × 1016 m-3. After the EUV pulse the density slightly increases due to electron impact ionization. The plasma (i.e. electron density) decays in tens of microseconds.

  5. Defect-engineered GaN:Mg nanowire arrays for overall water splitting under violet light

    SciTech Connect

    Kibria, M. G.; Chowdhury, F. A.; Zhao, S.; Mi, Z.; Trudeau, M. L.; Guo, H.

    2015-03-16

    We report that by engineering the intra-gap defect related energy states in GaN nanowire arrays using Mg dopants, efficient and stable overall neutral water splitting can be achieved under violet light. Overall neutral water splitting on Rh/Cr{sub 2}O{sub 3} co-catalyst decorated Mg doped GaN nanowires is demonstrated with intra-gap excitation up to 450 nm. Through optimized Mg doping, the absorbed photon conversion efficiency of GaN nanowires reaches ∼43% at 375–450 nm, providing a viable approach to extend the solar absorption of oxide and non-oxide photocatalysts.

  6. Kinetic spectrophotometric determination of trace manganese (II) with dahlia violet in nonionic microemulsion medium.

    PubMed

    Wei, Qin; Yan, Liangguo; Chang, Guohua; Ou, Qingyu

    2003-02-01

    A new catalytic kinetic spectrophotometric method has been developed for the determination of trace amount of manganese (II) in nonionic microemulsion medium. The method is based on the catalytic effect of manganese (II) on the oxidation of dahlia violet by potassium periodate with nitrilotriacetic acid as an activitor in the presence of nonionic microemulsion. Under the optimum conditions, the calibration graph is linear in the range of 0.0004-0.0056 mug ml(-1) of manganese (II) at 580 nm. The detection limit achieved is 3.75x10(-5) mug ml(-1). Manganese (II) in foodstuff samples was determined with satisfactory results. PMID:18968906

  7. Oxidation preventative capping layer for deep-ultra-violet and soft x-ray multilayers

    DOEpatents

    Prisbrey, Shon T.

    2004-07-06

    The invention uses iridium and iridium compounds as a protective capping layer on multilayers having reflectivity in the deep ultra-violet to soft x-ray regime. The iridium compounds can be formed in one of two ways: by direct deposition of the iridium compound from a prepared target or by depositing a thin layer (e.g., 5-50 angstroms) of iridium directly onto an element. The deposition energy of the incoming iridium is sufficient to activate the formation of the desired iridium compound. The compounds of most interest are iridium silicide (IrSi.sub.x) and iridium molybdenide (IrMo.sub.x).

  8. Multi walled carbon nanotubes as sorbent for removal of crystal violet.

    PubMed

    Kumar, Sandeep; Bhanjana, Gaurav; Dilbaghi, Neeraj; Umar, Ahmad

    2014-09-01

    Carbon nanotubes (CNTs) possess high surface active site to volume ratio as well as controlled pore size distribution that make them high profile material with an exceptional sorption capability and high sorption efficiency compared to conventional adsorbents. In the present paper, multi walled carbon nanotubes were synthesized by chemical vapor deposition (CVD) method and were further used for the removal of dye crystal violet. Microscopic and spectroscopic techniques were used for characterization. The systematic assessments of the pH and effect of adsorbent on different concentrations of dye with respect to contact time were examined. Langmuir and Temkin models were used to describe the isotherm studies. PMID:25924370

  9. Combination of photoreactor and packed bed bioreactor for the removal of ethyl violet from wastewater.

    PubMed

    Chen, Chih-Yu; Yen, Shao-Hsiung; Chung, Ying-Chien

    2014-12-01

    An efficient treatment system that combines a photoreactor and packed bed bioreactor (PBR) was developed and evaluated for treating ethyl violet (EV)-containing wastewater. Initial experiments demonstrated that the optimal operating parameters for the photoreactor in treating EV-containing wastewater were 2h reaction time, pH of 7, and 2 min liquid retention time. Under these conditions, the photocatalytic reaction achieved a 61% EV removal efficiency and resulted in a significant BOD/COD increase in the solution. The results displayed by the coupled photobiological system achieved a removal efficiency of 85% and EC50 of the solution increased by 19 times in a semi-continuous mode when the EV concentration was <150 mg +L(-)(1). The effect of shock loading on the EV removal was temporary but coexisting substrate (glucose and crystal violet) at specific levels would affect the EV removal efficiency of the PBR. Phylogenetic analysis in the PBR indicated that the major bacteria species were Bdellovibrio bacteriovorus, Ralstonia pickettii, Stenotrophomonas maltophilia, and Comamonas sp. Furthermore, the possible degrading mechanisms of this coupled system were demethylation, deethylation, aromatic ring opening, nitrification, and carbon oxidation. The intermediates were characterized using gas chromatography-mass spectrometry analysis. These results indicated that the coupled photobiological system provides an effective method of EV removal. PMID:25259784

  10. Liquid phase adsorption of Crystal violet onto activated carbons derived from male flowers of coconut tree.

    PubMed

    Senthilkumaar, S; Kalaamani, P; Subburaam, C V

    2006-08-25

    Adsorption of Crystal violet, a basic dye onto phosphoric and sulphuric acid activated carbons (PAAC and SAAC), prepared from male flowers coconut tree has been investigated. Equilibrium data were successfully applied to study the kinetics and mechanism of adsorption of dye onto both the carbons. The kinetics of adsorption was found to be pseudo second order with regard to intraparticle diffusion. The pseudo second order is further supported by the Elovich model, which in turn intensifies the fact of chemisorption of dye onto both the carbons. Quantitative removal of dye at higher initial pH of dye solution reveals the basic nature of the Crystal violet and acidic nature of the activated carbons. Influence of temperature on the removal of dye from aqueous solution shows the feasibility of adsorption and its endothermic nature. Mass transfer studies were also carried out. The adsorption capacities of both the carbons were found to be 60.42 and 85.84 mg/g for PAAC and SAAC, respectively. Langmuir's isotherm data were used to design single-stage batch adsorption model.

  11. Chemical characterization and toxicologic evaluation of airborne mixtures: chemical characterization of combusted inventory red and violet smoke mixes

    SciTech Connect

    Rubin, I.B.; Buchanan, M.V.; Moneyhun, J.H.

    1982-10-01

    Red and violet smoke grenades (Grenade, Hand, Smoke, M18) were combusted within canvas tents and the combustion products were sampled and analyzed. Uncombusted red and violet smoke mixes from the same lots used to fill the combusted grenades were also analyzed. Approximately ten percent of the major dye component of the red smoke mix, methylaminoanthraquinone (MAA) was converted to aminoanthraquinones (1-AA and 2-AA). The violet smoke mix was formulated to contain 1,4-diamino-2,3-dihydroanthraquinone (DAA) and MAA. Upon combustion the DAA was converted almost completely to diaminoanthraquinone (DAA) which was a minor constituent of the uncombusted mix. As in the combusted red smoke mix, it was found that MAA was partially converted to aminoanthraquinones.

  12. Evolution and biogeography of the woody Hawaiian violets (Viola, Violaceae): arctic origins, herbaceous ancestry and bird dispersal.

    PubMed

    Ballard, H E; Sytsma, K J

    2000-10-01

    Specialists studying the genus Viola have consistently allied the Hawaiian violets comprising section Nosphinium--most of which are subshrubs or treelets--with putatively primitive subshrubs in certain South American violet groups. Hawaiian violets also possess inflorescences, a floral disposition otherwise found only in other genera of the Violaceae, thus strengthening the hypothesis of a very ancient origin for the Hawaiian species. A survey of phylogenetic relationships among infrageneric groups of Viola worldwide using nuclear rDNA internal transcribed spacer (ITS) sequences revealed a dramatically different biogeographic origin for the Hawaiian violets: A monophyletic Hawaiian clade was placed in a close sister relationship with the amphi-Beringian tundra violet, V. langsdorffii s. 1., in a highly derived position. This remarkable and unforeseen relationship received strong clade support values across analyses, and monophyly of the Hawaiian lineage was further indicated by a unique 26-base-pair deletion in section Nosphinium. The high polyploid base chromosome number (n approximately equal to 40) in the Hawaiian violets relates them to Alaskan and eastern Siberian populations in the polyploid V. langsdorffii complex. More than 50 species of the 260 allochthonous birds wintering in the Hawaiian Islands are found to breed in the Arctic, occupying habitats in which individual birds might have encountered ancestral V. langsdorffii populations and served as dispersers to the central Pacific region. Acquisition of derived morphological traits (e.g., arborescence and inflorescences), significance of a confirmed Arctic origin for a component of the Hawaiian flora, and the likelihood of other "cryptic" Arctic elements in the Hawaiian flora deserving independent molecular phylogenetic corroboration are discussed.

  13. More stable and more efficient alternatives of Z-907: carbazole-based amphiphilic Ru(II) sensitizers for dye-sensitized solar cells.

    PubMed

    Cheema, Hammad; Islam, Ashraful; Younts, Robert; Gautam, Bhoj; Bedja, Idriss; Gupta, Ravindra Kumar; Han, Liyuan; Gundogdu, Kenan; El-Shafei, Ahmed

    2014-12-28

    Here we report two novel amphiphilic Ru(II) heteroleptic bipyridyl complexes, HD-14 and HD-15, compared to previously reported NCSU-10. We have combined the strong electron donor characteristics of carbazole and the hydrophobic nature of different long alkyl chains, C7, C18 and C2 (NCSU-10), tethered to N-carbazole to study their influence on photocurrent, photovoltage and long term stability for dye-sensitized solar cells. Photon harvesting efficiency and electron donating characteristics of carbazole-based ancillary ligands were found to be unaffected by different alkyl chain lengths. However, a slight drop in the Voc of HD-14 and HD-15 was observed compared to that of NCSU-10. It was found by nanosecond flash photolysis transient absorption (TA) measurements that the faster the dye regeneration the higher the photocurrent density response, and the dye regeneration time was found to be 2.6, 3.6, and 3.7 μs for HD-14, HD-15, and N719 dyes, respectively. The difference in the amplitude of the transient absorption (TA) signal of the oxidized dye as measured by femtosecond TA studies is in excellent agreement with the photocurrent generated, which was in the following order HD-14 > HD-15 > N719. Under 1000 h light soaking conditions, HD-15 maintained up to 98% (only 2% loss) of the initial power conversion efficiency compared to 8% loss for HD-14 and 22% loss in the power conversion efficiency for NCSU-10. HD-15 was strikingly stable to light soaking conditions when employed in the presence of an ionic liquid electrolyte, which paves the way for widespread applications of dye-sensitized solar cells with long term stability. The total power conversion efficiency (η) was 9.27% for HD-14 and 9.17% for HD-15 compared to 8.92% for N719.

  14. A novel violet/blue light-emitting device based on Ce2Si2O7

    PubMed Central

    Li, Ling; Wang, Shenwei; Mu, Guangyao; Yin, Xue; Ou, Kai; Yi, Lixin

    2015-01-01

    Rare-earth silicates are highly efficient materials for silicon-based light sources. Here we report a novel light-emitting device based on Ce2Si2O7. Intense violet/blue electroluminescence was observed, with a turn-on voltage of about 13 V. The violet/blue emission is attributed to 4f–5d transitions of the Ce3+ ions in Ce2Si2O7, which are formed by interfacial reaction of CeO2 and Si. Electroluminescence and photoluminescence mechanisms of the Ce2Si2O7 light-emitting device are also discussed. PMID:26564241

  15. Red, violet and upconversion luminescence of Eu/Sm codoped sol gel SiO2-TiO2

    NASA Astrophysics Data System (ADS)

    Azzouz, I. M.; Klein, Lisa C.

    2012-12-01

    Rare earth (Eu/Sm) doped silica-titania composite systems were sensitized by sol-gel method in solid and powder forms. The crystalline phase has been identified for the annealed samples at 1000 °C by X-ray diffraction (XRD). The bonding formation of the host matrix was examined by Fourier transform infrared (FTIR). The fingerprint transition lines of Eu3+ ions, with the main emission line at 616 nm, are recorded for the samples. Improvement in Eu3+ luminescence has been recorded by adding Sm3+ and by samples. Violet emission is observed under UV irradiation. Violet-blue upconversion luminescence is recorded at room temperature.

  16. A novel violet/blue light-emitting device based on Ce2Si2O7.

    PubMed

    Li, Ling; Wang, Shenwei; Mu, Guangyao; Yin, Xue; Ou, Kai; Yi, Lixin

    2015-01-01

    Rare-earth silicates are highly efficient materials for silicon-based light sources. Here we report a novel light-emitting device based on Ce2Si2O7. Intense violet/blue electroluminescence was observed, with a turn-on voltage of about 13 V. The violet/blue emission is attributed to 4f-5d transitions of the Ce(3+) ions in Ce2Si2O7, which are formed by interfacial reaction of CeO2 and Si. Electroluminescence and photoluminescence mechanisms of the Ce2Si2O7 light-emitting device are also discussed. PMID:26564241

  17. Synthesis of Cyclo[b]fused Carbazoles via SnCl4-Mediated Domino Reaction of 2-Indolylmethylpivalates with Arenes and Heteroarenes.

    PubMed

    Saravanan, Velu; Mageshwaran, Thiyagarajan; Mohanakrishnan, Arasambattu K

    2016-09-16

    A straightforward synthesis of aryl and heteroaryl-annulated cyclo[b]carbazoles has been developed via SnCl4-mediated one-pot arylation, cyclization and aromatization reaction sequence from 3-acetyl/aroyl-2-pivaloyloxymethylindoles. The starting material is easily accessible from commercially available 2-methylindole via Friedel-Crafts acylation, bromination and pivaloylation. Remarkably, electron withdrawing/donating aroyl units including heterocyclic systems are well tolerated in the present domino reaction protocol. Furthermore, this methodology could be extended to the synthesis of dibenzofurocarbazole via bis-annulation of 2,5-bis(2-pivaloyloxymethyl)pyrrole. PMID:27564513

  18. Diversity oriented convergent access for collective total synthesis of bioactive multifunctional carbazole alkaloids: synthesis of carbazomycin A, carbazomycin B, hyellazole, chlorohyellazole, and clausenaline D.

    PubMed

    Markad, Shivaji B; Argade, Narshinha P

    2014-10-17

    Facile syntheses of imperative carbazole alkaloids carbazomycin A, carbazomycin B, hyellazole, chlorohyellazole, and clausenaline D have been demonstrated starting from readily available Boc-protected 3-formylindole and dimethyl maleate. The suitably substituted aromatic rings have been designed comprising three/four significant C-C bond forming reactions. The competent Wittig reaction, selective monoalkylations, one-pot regioselective Weinreb amide formation and Boc-deprotection, well designed Grignard reactions, dehydrative intramolecular cyclizations, and Baeyer-Villiger rearrangement of aromatic aldehydes were the main features. PMID:25296703

  19. Crystal structure of 3-(9H-carbazol-9-yl)-N′-[(E)-4-chloro­benzyl­idene]propano­hydrazide

    PubMed Central

    Akkurt, Mehmet; Jasinski, Jerry P.; Mohamed, Shaaban K.; El-Emary, Talaat I.; Albayati, Mustafa R.

    2015-01-01

    In the title compound, C22H18ClN3O, the carbazole ring system is essentially planar (r.m.s deviation = 0.003 Å), and makes a dihedral angle of 9.01 (8)° with the plane of the chloro­phenyl ring. In the crystal, neighbouring mol­ecules are linked into centrosymmetric R 2 2(8) dimers by pairs of N—H⋯O inter­actions and into a three-dimensional network by C—H⋯π inter­actions. The dimers are arranged into layers parallel to (010). PMID:26870537

  20. 2,2-Dimethyl-2,3-dihydro­pyrano[2,3-a]carbazol-4(11H)-one

    PubMed Central

    Sridharan, Makuteswaran; Prasad, Karnam J. Rajendra; Ngendahimana, Aimable; Zeller, Matthias

    2008-01-01

    The title compound, C17H15NO2, was prepared from 1-hydroxy­carbazole and 3,3-dimethyl­acrylic acid with a mixture of AlCl3 and POCl3 as the cyclization catalyst. Owing to the presence of the –CMe2– group, the mol­ecule is not quite planar. In the crystal structre, strong N—H⋯O hydrogen bonds and weaker C—H⋯π inter­actions occur, and a slipped π–π stacking inter­action [centroid–centroid separation = 3.8425 (8) Å] is also observed. PMID:21581015

  1. Morphological, dielectric and electrical conductivity characteristics of clay-containing nanohybrids of poly(N-vinyl carbazole) and polypyrrole.

    PubMed

    Haldar, Ipsita; Biswas, Mukul; Nayak, Arabinda; Ray, Suprakas Sinha

    2012-10-01

    Poly(N-vinyl carbazole) (PNVC) and polypyrrole (PPY)-montmorillonite (MMT) clay hybrids were prepared by mechanical grinding of the respective monomers with MMT followed by subsequent standard processing methods. Fourier transform infrared spectroscopic studies confirmed the inclusion of the polymers in the composites. The morphologies of the hybrids were investigated by transmission electron microscopic techniques, which suggested the formation of intercalated structures. X-ray diffraction analyses indicated the enhancement of 'd001' values in MMT implying intercalation of the polymers into the nano-interlamellar spaces of MMT. The dielectric constants of PNVC-MMT hybrids were improved (60-180) relative to the homopolymer (3-6) in the frequency range 0.1-25 kHz. PPY-MMT hybrid also showed significantly higher values of dielectric constant (2000-4000) relative to the corresponding base polymers. These variations were dependent on the MMT/polymer feed ratio in the frequency range (1-25 kHz). This feature could manifest from the characteristic differences in the interfaces between the grains and grain boundaries of the composites, which control the dielectric properties of the system. Relaxation behavior for the composites was explained by considering the Maxwell-Wagner two-layered dielectric models. The ac conductivity was found to be dependent on frequency in the entire frequency range of study (100 Hz to 25 kHz), which indicated that the composites had few free charges for conduction, and frequency dependent conductivity was due to trapped charges in the grain boundary.

  2. Effects of bis-carbazole based D-π-A sensitizers on solar energy capture in DSSCs.

    PubMed

    Kim, Bo Hyung; Freeman, Harold S

    2013-03-01

    A new series of molecular engineered dyes having a carbazole (CA) based bulky donor was synthesized and compared to a previously studied set of dyes having a diphenyl amine (DP) donor for their use in dye sensitized solar cells. In this work, their photophysical, electrochemical, and kinetic properties were measured and molecular modeling methods were used to predict their electronic and physical properties. Regarding the latter, TDDFT studies adopting different exchange correlation functionals were performed to predict solar capture behavior of these sensitizers. The calculated electronic energies showed that the introduction of the bulky CA donor gave a greater negative shift on E(HOMO) rather than E(LUMO), imparting the CA series of dyes a red shifted absorption. On the other hand, tuning of the spacer unit by using different heterocylic rings was sensitive to the shift of E(LUMO) shift. Better light absorption and driving force of devices based on the CA series were counteracted with negative effects related to the electron injection yield and electron recombination lifetime. The origin of the lower efficiency of the CA dye based devices was investigated in terms of dye load, charge recombination lifetime, in tandem with modeling studies. Results from assessing the effects of different heterocyclic rings, as a π conjugation unit on photovoltaic performance showed that the thiophene unit gave the highest current. On the other hand, CA- and DP-based dyes having an N-methyl pyrrole unit afforded the highest V(oc). The best DSSC performance in the CA series was achieved by the thiophene derivative, where η = 3.05% with J(sc) = 6.29 mA cm(-2), V(oc) = 673 mV and FF = 0.72 under 100 mW m(-2) irradiation. PMID:23149843

  3. Microbial Manganese Oxidation in Saltmarsh Surface Sediments Using a Leuco Crystal Violet Manganese Oxide Detection Technique

    NASA Astrophysics Data System (ADS)

    Spratt, Henry G.; Siekmann, Ellen C.; Hodson, Robert E.

    1994-01-01

    Microbial manganese (Mn) oxide production in surface sediments of a Georgia saltmarsh was directly measured using an assay involving the oxidation of 4,4',4″-methylidynetris (N,N-dimethylaniline), leuco crystal violet (LCV), by Mn oxides to produce crystal violet. The assay exhibits high specificity for Mn oxides without interference by Mn(II) and is sufficiently sensitive to determine rates of Mn oxidation in surface sediment or saltmarsh creek water suspensions. Sample salinity affects crystal violet absorbance in the 0-25 salinity range and must be corrected for in Mn oxide determinations for estuarine samples of variable salinity. Other oxidants found to oxidize LCV slowly included Cl(I), Cr(III), I(V), Fe(III), and Mn(III), although the sensitivity of the assay for Mn(IV) oxides was found to be seven times greater than for Mn(III), and at least 100 times greater than for any of the other oxidants. Rates of abiotic Mn oxide production in sediment suspensions treated with either sodium azide or formalin, or autoclaved, were much slower than rates determined for untreated sediments. Sodium azide (7·7 mM) inhibited Mn oxide production in these sediment suspensions to rates between 5 and 10% of the rates of Mn oxidation determined for unamended suspensions. Manganese oxidation was highly temperature dependent, with maximal rates on a dry weight basis (8·9 nmol mg dwt -1 h -1), occurring at 60°C, and negligible activity at 100 and 0°C. Rates were also dependent on sample pH, with maximal rates at pH 6·7, decreasing to near 0 as the pH was lowered to approximately 3·0. For Mn(II) concentrations ranging from 9 to 91 μM, rates of Mn oxide production were independent of Mn(II) concentration, while Mn oxide production was inhibited at concentrations greater than 91 μM (e.g. by 25-40% at 450 μM). Rates of microbial Mn oxide production in surface sediment/saltmarsh creek water suspensions incubated under natural conditions of temperature, pH, and Mn

  4. Field response of some asparagus varieties to rust, Fusarium crown root rot, and violet root rot.

    PubMed

    Fiume, F; Fiume, G

    2003-01-01

    Research was carried out to evaluate the behaviour of some asparagus genotypes against three most important fungal diseases: 1) asparagus rust caused by Puccinia asparagi D.C.; 2) Fusarium crown and root rot caused by Fusarium oxysporum (Schlecht.) f.sp. asparagi (Cohen & Heald) and Fusarium proliferatum (Matstush.) Nirenberg; 3) violet root rot caused by Rhizoctonia violacea Tul. The object of this research was also to found an eventual correlation between the plant susceptibility to asparagus rust and the sensibility to Fusarium crown root rot and violet root rot attacks. Resistant genotypes to rust should be less susceptible to attacks from F. oxysporum f.sp. asparagi, F. proliferatum and R. violacea, a fungal complex causing the plant decline. Asparagus genotypes were compared in a randomized complete block experiment design, replicated four times, in order to search that ones showing the best behaviour to escape the diseases. Phytopathological observations were carried out on November when the control plots showed 100% infected plants. The pathogens were isolated and identified. The diseased plants were registered. According to symptom evaluation scales, all the plants were grouped into infection classes, calculating frequency and McKinney index. Wishing to learn something about the infection trend of F. oxysporum f.sp. asparagi or R. violacea in relation to P. asparagi attack, the relative curvilinear regressions were calculated. The Italian cultivars "Marte" and "Grande" showed significantly the best behaviour in terms of resistance to asparagus rust, exhibiting 37% and 42% of diseased plants. The McKinney index was 9.1% and 15.6%, respectively. The susceptible plots showed 100% of infected plants and different McKinney index: 46% for "Eros", about 60% for "H 519", "Atlas" and "Golia", over 70% for the remainder. "Marte" and "Grande" showed good tolerance to F. oxysporum f.sp. asparagi and to R. violacea exhibiting up to 100% of healthy plants. The

  5. Detection of biological warfare agents using ultra violet-laser induced fluorescence LIDAR.

    PubMed

    Joshi, Deepti; Kumar, Deepak; Maini, Anil K; Sharma, Ramesh C

    2013-08-01

    This review has been written to highlight the threat of biological warfare agents, their types and detection. Bacterial biological agent Bacillus anthracis (bacteria causing the disease anthrax) which is most likely to be employed in biological warfare is being discussed in detail. Standoff detection of biological warfare agents in aerosol form using Ultra violet-Laser Induced Fluorescence (UV-LIF) spectroscopy method has been studied. Range-resolved detection and identification of biological aerosols by both nano-second and non-linear femto-second LIDAR is also discussed. Calculated received fluorescence signal for a cloud of typical biological agent Bacillus globigii (Simulants of B. anthracis) at a location of ~5.0 km at different concentrations in presence of solar background radiation has been described. Overview of current research efforts in internationally available working UV-LIF LIDAR systems are also mentioned briefly. PMID:23719340

  6. Analysis of observational data from Extreme Ultra-Violet Camera onboard Chang'E-3 mission

    NASA Astrophysics Data System (ADS)

    Yan, Yan; Wang, Hua-Ning; He, Han; He, Fei; Chen, Bo; Feng, Jian-Qing; Ping, Jin-Song; Shen, Chao; Xu, Rong-Lan; Zhang, Xiao-Xin

    2016-02-01

    The Extreme Ultra-Violet Camera (hereafter EUVC) is a scientific payload onboard the lander of the Chang'E-3 (hereafter CE-3) mission launched on December 1st, 2013. Centering on a spectral band around 30.4 nm, EUVC provides the global images of the Earth's plasmasphere from the meridian view, with a spatial resolution of 0.1 R_{oplus} in 150 × 150 pixels and a cadence of 10 minutes. Along with the data being publicly released online, some unsettled issues in the early stage have been clarified, including the geometrical preparations, the refined approach on the coefficient K for the background, and the alignment among the images. A demo of data after all the above processes is therefore presented as a guidance for users who are studying the structure and dynamics of the plasmasphere.

  7. Acylated anthocyanins from the blue-violet flowers of Anemone coronaria.

    PubMed

    Saito, Norio; Toki, Kenjiro; Moriyama, Hidekazu; Shigihara, Atsushi; Honda, Toshio

    2002-06-01

    Five polyacylated anthocyanins were isolated from blue-violet flowers of Anemone coronaria 'St. Brigid'. They were identified as delphinidin 3-O-[2-O-(2-O-(trans-caffeoyl)-beta-D-glucopyranosyl)-6-O-(malonyl)-beta-D-galactopyranoside]-7-O-[6-O-(trans-caffeoyl)-beta-D-glucopyranoside]-3'-O-[beta-D-glucuronopyranoside], and its demalonylated form, delphinidin 3-O-[2-O-(2-O-(trans-caffeoyl)-beta-D-glucopyranosyl)-6-O-(2-O-tartaryl)malonyl)-beta-D-galactopyranoside]-7-O-[6-O-(trans-caffeoyl)-beta-D-glucopyranoside]-3'-O-[beta-D-glucuronopyranoside], and its cyanidin analog as well as delphinidin 3-O-[2-O-(2-O-(trans-caffeoyl)-beta-D-glucopyranosyl)-6-O-(2-O-(tartaryl)malonyl)-beta-D-galactopyranoside]-7-O-[6-O-(trans-caffeoyl)-beta-D-glucopyranoside].

  8. Enhanced biodegradation of Reactive Violet 5R manufacturing wastewater using down flow fixed film bioreactor.

    PubMed

    Sheth, Niraj; Dave, Shailesh

    2010-11-01

    The present study emphasizes on the development of bioprocess for biodegradation and bioremediation of Reactive Violet 5R (RV5) manufacturing industry's wastewater in laboratory scale indigenously designed down flow fixed film bioreactor (DFFR). Process was investigated in DFFR, packed with furnace charcoal as a support material. During the batch and continuous operation of DFFR more than 95% degradation, 88% COD reduction and 99% copper remediation was obtained in less than 8h of contact time. Continuous mode treatment gave degradation of more than 2500mg dye in only 1h of contact time. Addition of 0.25% peptone enhanced biodegradation rate more than three-fold. The biologically treated wastewater was found to stimulate the growth of selected soil bacteria. Degradation of major components of the wastewater was confirmed by HPTLC. DFFR was operated successfully for 750d continuously, during which 716 cycles of batch treatment were operated.

  9. Bias Selectable Dual Band AlGaN Ultra-violet Detectors

    NASA Technical Reports Server (NTRS)

    Yan, Feng; Miko, Laddawan; Franz, David; Guan, Bing; Stahle, Carl M.

    2007-01-01

    Bias selectable dual band AlGaN ultra-violet (UV) detectors, which can separate UV-A and UV-B using one detector in the same pixel by bias switching, have been designed, fabricated and characterized. A two-terminal n-p-n photo-transistor-like structure was used. When a forward bias is applied between the top electrode and the bottom electrode, the detectors can successfully detect W-A and reject UV-B. Under reverse bias, they can detect UV-B and reject UV-A. The proof of concept design shows that it is feasible to fabricate high performance dual-band UV detectors based on the current AlGaN material growth and fabrication technologies.

  10. True covariance simulation of the EUVE (extreme ultra violet explorer) update filter

    NASA Technical Reports Server (NTRS)

    Bar-Itzhack, I. Y.; Harman, R. R.

    1990-01-01

    This paper presents a covariance analysis of the performance and sensitivity of the attitude determination Extended Kalman Filter (EKF) used by the onboard computer (OBC) of the Extreme Ultra Violet Explorer (EUVE) spacecraft. The linearized dynamics and measurement equations of the error states are used in formulating the 'truth model' describing the order of the systems involved. The 'design model' used by the OBC EKF is then obtained by reducing the order of the truth model. The covariance matrix of the EKF which uses the reduced order model is not the correct covariance of the EKF estimation error. A 'true covariance analysis' has to be carried out in order to evaluate the correct accuracy of the OBC generated estimates. The results of such analysis are presented which indicate both the performance and the sensitivity of the OBC EKF.

  11. Gentian Violet: A 19th Century Drug Re-Emerges in the 21st Century

    PubMed Central

    Maley, Alexander M.; Arbiser, Jack L.

    2013-01-01

    Gentian violet (GV) has a long and varied history as a medicinal agent. Historically used as an anti-bacterial and anti-fungal, recent reports have shown its utility as an anti-typranosomal, anti-viral and anti-angiogenic agent. The objective of this paper is to summarize evidence regarding the efficacy, and safety of GV use in dermatology. Recent discoveries have found novel targets of GV, namely NADPH oxidase in mammalian cells and thioredoxin reductase 2 in bacterial, fungal, and parasitic cells. These discoveries have expanded the use of GV in the 21st century. Given that GV is well tolerated, effective and inexpensive, its use in dermatology is predicted to increase. PMID:24118276

  12. Kinetics of Crystal Violet Fading in the Presence of TX-100, DTAB and SDS.

    PubMed

    Samiey, Babak; Ashoori, Fatemeh

    2011-06-01

    The rate constant of alkaline fading of crystal violet (CV+) was measured in the presence of non ionic (TX-100), cationic (DTAB) and anionic (SDS) surfactants. This reaction was studied at 283-303 K. The rate of reaction showed remarkable dependence on the electrical charge of the used surfactants. It was observed that the reaction rate constant increased in the presence of TX-100 and DTAB and decreased in the presence of SDS. Binding constants of CV+ with TX-100 and DTAB and the related thermodynamic parameters were obtained by classical (or stoichiometric) model. The results show that binding of CV+ to TX-100 is endothermic and binding of CV+ to DTAB and SDS is exothermic in the used concentration range of surfactants.

  13. Detection of biological warfare agents using ultra violet-laser induced fluorescence LIDAR.

    PubMed

    Joshi, Deepti; Kumar, Deepak; Maini, Anil K; Sharma, Ramesh C

    2013-08-01

    This review has been written to highlight the threat of biological warfare agents, their types and detection. Bacterial biological agent Bacillus anthracis (bacteria causing the disease anthrax) which is most likely to be employed in biological warfare is being discussed in detail. Standoff detection of biological warfare agents in aerosol form using Ultra violet-Laser Induced Fluorescence (UV-LIF) spectroscopy method has been studied. Range-resolved detection and identification of biological aerosols by both nano-second and non-linear femto-second LIDAR is also discussed. Calculated received fluorescence signal for a cloud of typical biological agent Bacillus globigii (Simulants of B. anthracis) at a location of ~5.0 km at different concentrations in presence of solar background radiation has been described. Overview of current research efforts in internationally available working UV-LIF LIDAR systems are also mentioned briefly.

  14. Insight into biosorption equilibrium, kinetics and thermodynamics of crystal violet onto Ananas comosus (pineapple) leaf powder

    NASA Astrophysics Data System (ADS)

    Chakraborty, Sagnik; Chowdhury, Shamik; Saha, Papita Das

    2012-06-01

    Biosorption performance of pineapple leaf powder (PLP) for removal of crystal violet (CV) from its aqueous solutions was investigated. To this end, the influence of operational parameters such as pH, biosorbent dose, initial dye concentration and temperature were studied employing a batch experimental setup. The biosorption process followed the Langmuir isotherm model with high correlation coefficients ( R 2 > 0.99) at different temperatures. The maximum monolayer biosorption capacity was found to be 78.22 mg g-1 at 293 K. The kinetic data conformed to the pseudo-second-order kinetic model. The activation energy of the system was calculated as 58.96 kJ mol- 1 , indicating chemisorption nature of the ongoing biosorption process. A thermodynamic study showed spontaneous and exothermic nature of the biosorption process. Owing to its low cost and high dye uptake capacity, PLP has potential for application as biosorbent for removal of CV from aqueous solutions.

  15. Detection of biological warfare agents using ultra violet-laser induced fluorescence LIDAR

    NASA Astrophysics Data System (ADS)

    Joshi, Deepti; Kumar, Deepak; Maini, Anil K.; Sharma, Ramesh C.

    This review has been written to highlight the threat of biological warfare agents, their types and detection. Bacterial biological agent Bacillus anthracis (bacteria causing the disease anthrax) which is most likely to be employed in biological warfare is being discussed in detail. Standoff detection of biological warfare agents in aerosol form using Ultra violet-Laser Induced Fluorescence (UV-LIF) spectroscopy method has been studied. Range-resolved detection and identification of biological aerosols by both nano-second and non-linear femto-second LIDAR is also discussed. Calculated received fluorescence signal for a cloud of typical biological agent Bacillus globigii (Simulants of B. anthracis) at a location of ˜5.0 km at different concentrations in presence of solar background radiation has been described. Overview of current research efforts in internationally available working UV-LIF LIDAR systems are also mentioned briefly.

  16. Extreme Ultra-Violet Spectroscopy of the Lower Solar Atmosphere During Solar Flares (Invited Review)

    NASA Astrophysics Data System (ADS)

    Milligan, Ryan O.

    2015-12-01

    The extreme ultra-violet (EUV) portion of the solar spectrum contains a wealth of diagnostic tools for probing the lower solar atmosphere in response to an injection of energy, particularly during the impulsive phase of solar flares. These include temperature- and density-sensitive line ratios, Doppler-shifted emission lines, nonthermal broadening, abundance measurements, differential emission measure profiles, continuum temperatures and energetics, among others. In this article I review some of the recent advances that have been made using these techniques to infer physical properties of heated plasma at footpoint and ribbon locations during the initial stages of solar flares. I primarily focus on studies that have utilised spectroscopic EUV data from Hinode/EUV Imaging Spectrometer (EIS) and Solar Dynamics Observatory/EUV Variability Experiment (SDO/EVE), and I also provide some historical background and a summary of future spectroscopic instrumentation.

  17. Removal of Basic Violet 14 from aqueous solution using sulphuric acid activated materials.

    PubMed

    Suresh, S

    2016-01-01

    In this study the adsorption of Basic Violet, 14 from aqueous solution onto sulphuric acid activated materials prepared from Calophyllum inophyllum (CS) and Theobroma cacao (TS) shells were investigated. The experimental data were analysed by Langmuir, Freundlich and Temkin isotherm models. The results showed that CS has a superior adsorption capacity compared to the TS. The adsorption capacity was found to be 1416.43 mg/g for CS and 980.39 mg/g for TS. The kinetic data results at different concentrations were analysed using pseudo first-order and pseudo-second order model. Boyd plot indicates that the dye adsorption onto CS and TS is controlled by film diffusion. The adsorbents were characterised by scanning electron microscopy. The materials used in this study were economical waste products and hence can be an attractive alternative to costlier adsorbents for dye removal in industrial wastewater treatment processes. PMID:27330899

  18. Complementary ion and extreme ultra-violet spectrometer for laser-plasma diagnosis

    SciTech Connect

    Ter-Avetisyan, S.; Ramakrishna, B.; Doria, D.; Sarri, G.; Zepf, M.; Borghesi, M.; Ehrentraut, L.; Stiel, H.; Steinke, S.; Schnuerer, M.; Nickles, P. V.; Sandner, W.; Priebe, G.

    2009-10-15

    Simultaneous detection of extreme ultra-violet (XUV) and ion emission along the same line of sight provides comprehensive insight into the evolution of plasmas. This type of combined spectroscopy is applied to diagnose laser interaction with a spray target. The use of a micro-channel-plate detector assures reliable detection of both XUV and ion signals in a single laser shot. The qualitative analysis of the ion emission and XUV spectra allows to gain detailed information about the plasma conditions, and a correlation between the energetic proton emission and the XUV plasma emission can be suggested. The measured XUV emission spectrum from water spray shows efficient deceleration of laser accelerated electrons with energies up to keV in the initially cold background plasma and the collisional heating of the plasma.

  19. Frequency Up-Conversion to the Vacuum Ultra-Violet in Coherently Prepared Media

    NASA Astrophysics Data System (ADS)

    Marangos, J. P.; Kuçukkara, I.; Anscombe, M.

    In this contribution we discuss recent work that has demonstrated that electromagnetically induced transparency (EIT) can greatly increase the intensity of coherent vacuum ultra-violet (VUV) radiation (at wavelengths shorter than 130nm) generated in resonant four-wave mixing schemes. We will start by introducing the basic concept of EIT enhanced resonant four-wave mixing, comparing it briefly with other coherently enhanced non-linear frequency up-conversion schemes. Experiments proving this concept in atomic hydrogen in the mid-1990's will be summarised. Our own recent work on EIT enhanced four-wave mixing in Kr will be presented and recent results demonstrating high conversion efficiencies into the VUV, and the limits placed on this process at high density-length products, will be discussed.

  20. Terrific Trichomes (and Other Specialised Cells) in African Violets: How to Get a Lot from One Plant in the Classroom

    ERIC Educational Resources Information Center

    Cottrell, Vicki M.

    2013-01-01

    African violet (genus "Saintpaulia") was identified as a particularly suitable genus for the study of specialised plant cells in the classroom using microscopes. The techniques described here involve simple preparation without staining. The cells and structures that can be investigated include: trichomes (hairs); stomata; guard cells and…

  1. Anthocyanins, colour and antioxidant properties of eggplant (Solanum melongena L.) and violet pepper (Capsicum annuum L.) peel extracts.

    PubMed

    Sadilova, Eva; Stintzing, Florian C; Carle, Reinhold

    2006-01-01

    Acetone extracts from eggplant (Solanum melongena L.) and violet pepper (Capsicum annuum L.) peels both belonging to the Solanaceae plant family were characterized with respect to their anthocyanin profiles, colour qualities and antioxidant capacities. According to HPLC-DAD-MS3 analyses the major anthocyanin in eggplant was delphinidin-3-rutinoside, while the predominant pigment in violet pepper was assigned to delphinidin-3-trans-coumaroylrutinoside-5-glucoside. Since virtually all anthocyanins were delphinidin-based, the effect of acylation and glycosylation patterns on colour stability and antioxidant capacity could be assessed. Application of two in vitro-assays for antioxidant capacity assessment revealed that eggplant generally exhibited higher values compared to violet pepper which was ascribed to 3,5-diglycosylated structures predominating in the latter. The higher extent of acylation in violet pepper was reflected by a more purplish colour shade of the extracts, but did not translate into a higher stability against fading which again was attributed to additional glycosyl substitution at C5. These findings support the relevance of structure-related activities of anthocyanins both for understanding food colour and their particular nutritional value.

  2. Violet diode laser-induced chlorophyll fluorescence: a tool for assessing mosaic disease severity in cassava (Manihot esculenta Crantz) cultivars.

    PubMed

    Anderson, Benjamin; Eghan, Moses J; Asare-Bediako, Elvis; Buah-Bassuah, Paul K

    2012-01-01

    Violet diode laser-induced chlorophyll fluorescence was used in agronomical assessment (disease severity and average yield per plant). Because cassava (Manihot esculenta Crantz) is of economic importance, improved cultivars with various levels of affinity for cassava mosaic disease were investigated. Fluorescence data correlated with cassava mosaic disease severity levels and with the average yield per plant.

  3. HPLC Determination and MS Confirmation of Malachite Green, Gentian Violet, and Their Leuco Metabolites in Catfish Muscle

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Residues of malachite green (MG), gentian violet (GV), and their leuco metabolites in catfish muscle were individually determined by HPLC using visible and fluorescence detectors. This detection scheme obviated a PbO2 column that converts leuco forms to chromatic forms for visible detection, thus el...

  4. Anthocyanins, colour and antioxidant properties of eggplant (Solanum melongena L.) and violet pepper (Capsicum annuum L.) peel extracts.

    PubMed

    Sadilova, Eva; Stintzing, Florian C; Carle, Reinhold

    2006-01-01

    Acetone extracts from eggplant (Solanum melongena L.) and violet pepper (Capsicum annuum L.) peels both belonging to the Solanaceae plant family were characterized with respect to their anthocyanin profiles, colour qualities and antioxidant capacities. According to HPLC-DAD-MS3 analyses the major anthocyanin in eggplant was delphinidin-3-rutinoside, while the predominant pigment in violet pepper was assigned to delphinidin-3-trans-coumaroylrutinoside-5-glucoside. Since virtually all anthocyanins were delphinidin-based, the effect of acylation and glycosylation patterns on colour stability and antioxidant capacity could be assessed. Application of two in vitro-assays for antioxidant capacity assessment revealed that eggplant generally exhibited higher values compared to violet pepper which was ascribed to 3,5-diglycosylated structures predominating in the latter. The higher extent of acylation in violet pepper was reflected by a more purplish colour shade of the extracts, but did not translate into a higher stability against fading which again was attributed to additional glycosyl substitution at C5. These findings support the relevance of structure-related activities of anthocyanins both for understanding food colour and their particular nutritional value. PMID:16989312

  5. New Treatment for Percutaneous Sites in Patients with a Ventricular Assist Device: Nihon University Crystal Violet Method

    PubMed Central

    Niino, Tetsuya; Osaka, Shunji; Yaoita, Hiroko; Arimoto, Munehito; Hata, Hiroaki; Shiono, Motomi

    2016-01-01

    Background: Infection of the percutaneous site of a ventricular assist device (VAD) is a challenging complication. We report our experience with crystal violet Solbase (Nihon University crystal violet method) for prevention of driveline or cannula infections in VAD patients. Patients and Methods: The crystal violet method was used in 10 patients (prophylaxis in nine and treatment in one). Eight patients had an extracorporeal VAD (Nipro) and two had an implantable VAD (Heart Mate II). Results: The infection-free period was 4–623 days (mean: 144.2 ± 222.9 days). All eight patients with an extracorporeal VAD died, while the two patients with an implantable VAD (Heart Mate II) survived. Infection was improved in a patient with MRSA, and the results of bacteriological examination were always negative in the patients receiving prophylaxis. The two patients with an implantable VAD had no infection for 2 and 20 months after implantation. Conclusion: These findings suggest that the Nihon University crystal violet method is effective for prevention and treatment of driveline or cannula infections in patients with a VAD. PMID:27086670

  6. Theoretical investigation of the two-photon absorption properties of 3,6-bis(4-vinylpyridinium) carbazole derivatives--new biological fluorescent probes.

    PubMed

    Sun, Ying; Zhao, Yang; Liu, Xiao-Ting; Ren, Ai-Min; Feng, Ji-Kang; Yu, Xiao-Qiang

    2012-06-01

    The present study focuses on a series of carbazole derivatives, which are being investigated as potential two-photon fluorescent probes (TFP) for DNA detection and two-photon bioimaging. The geometric structures, electronic structures, and the one-photon (OPA) and two-photon (TPA) absorption properties of 3,6-bis(1-methyl-4-vinylpyridinium) carbazole (BMVC) derivatives, as well as their dications and diiodized derivatives, were studied using density functional theory (DFT) and Zerner's intermediate neglect of differential overlap (ZINDO) method. The results showed that the TPA spectra of the diiodized BMVC derivatives and their dications are all found in the near-infrared region (NIR). At the same time, the diiodized BMVC derivatives presented larger TPA cross-sections than the neutral BMVC derivatives and the dications. These theoretically derived values were also in good agreement with their corresponding experimentally observed values, and they indicated that the diiodized BMVC may be the form of this TFP that combines with DNA. The diiodized BMVC derivatives and the dications have the potential to be excellent TPA materials, especially when used as TFPs in nucleic acid imaging applications.

  7. Indolo[3,2-b]carbazole-based multi-donor-π-acceptor type organic dyes for highly efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Qian, Xing; Shao, Li; Li, Hongmei; Yan, Rucai; Wang, Xiaoying; Hou, Linxi

    2016-07-01

    Four novel indolo[3,2-b]carbazole-based multi-donor-π-acceptor type organic dyes QX01-04 have been designed, synthesized, and applied for dye-sensitized solar cells. These dyes consist of an indolo[3,2-b]carbazole core acting as the main donor group, a couple of groups such as ethylbenzene, N,N-diethylaniline, ethyloxylbenzene, and octyloxylbenzene acting as the secondary donors. The photophysical, electrochemical, and theoretical studies indicate that the four dyes are all capable as the photosensitizers. When introducing N,N-diethylaniline as the secondary donor, QX02 exhibits a broader absorption region and significantly improved IPCE values, which ensured a good light-harvesting ability and a high Jsc of 15.2 mA cm-2. Finally, QX02-based cell achieved a high efficiency of 8.09% which is very close to that of the commercial N719-based cell (8.26%) under 100 mW cm-2 irradiation.

  8. OFF-ON-OFF Dual Emission at Visible and UV Wavelengths from Carbazole Functionalized β-Diketonate Europium(III) Complex.

    PubMed

    Imai, Yuki; Kawai, Tsuyoshi; Yuasa, Junpei

    2016-06-23

    This work demonstrates dual emission "OFF-ON-OFF" switching at visible and UV wavelengths of a carbazole functionalized β-diketone (LH) by a simple change of a europium(III) ion (Eu(3+)) concentration in the submicromolar concentration range. In the presence of 0.25 equiv of Eu(3+) (5 μM), LH forms a luminescent 4:1 complex ([Eu(3+)(L(-))4](-)) exhibiting dual emission at 357 and 613 nm resulting from the local excitation of the carbazole ring and ligand-sensitized luminescence from the Eu(3+)-β-diketonate unit, respectively. The 4:1 complex begins to convert into a 2:1 complex ([Eu(3+)(L(-))2](+)) via a 3:1 complex [Eu(3+)(L(-))3] above a molar ratio ([Eu(3+)]/[LH]) of 0.25, which provides the opportunity for binding of solvent methanol molecules to the vacant site of the Eu(3+) ion in the complex ([Eu(3+)(L(-))2(MeOH)n](+)). The OH oscillators of coordinated methanol molecules facilitate the nonradiative pathway of the Eu(3+) emission; hence the emission at 613 nm almost disappears above the 0.50 equivalent of Eu(3+) (11 μM), while the UV emission at 357 nm remains mostly constant over the whole concentration range. PMID:27241957

  9. Synthesis, photophysical and charge-transporting properties of a novel asymmetric indolo [3,2-b]carbazole derivative containing benzothiazole and diphenylamino moieties

    NASA Astrophysics Data System (ADS)

    Shi, Heping; Yuan, Jiandong; Dong, Xiuqing; Cheng, Fangqin

    2014-12-01

    A novel asymmetric donor-π-donor-π-acceptor compound, 2-benzothiazolyl-8-diphenylamino-5,11-dihexylindolo[3,2-b]carbazole (BDDAICZ), has been successfully synthesized by introducing a benzothiazole moiety (as an electron-acceptor) and a diphenylamino moiety (as an electron-donor) to 2-position and 8-position of indolo[3,2-b]carbazole moiety (as a skeleton and an electron-donor), and characterized by elemental analysis, 1H NMR, 13C NMR and MS. The thermal, electrochemical properties of BDDAICZ were characterized by thermogravimetric analysis combined with electrochemistry. The absorption and emission spectra of BDDAICZ was experimentally determined in several solvents and computed using density functional theory (DFT) and time-dependent density functional theory (TDDFT). The calculated absorption and emission wavelengths are coincident with the measured data. The ionization potential (IP), the electron affinity (EA) and reorganization energy of BDDAICZ were also investigated using density functional theory (DFT). Charge-transporting properties of BDDAICZ were characterized by OLEDs devices fabricated by using it as charge-transport layers. The results show that BDDAICZ has excellent thermal stability, electrochemical stability and hole-transporting properties, indicating its potential application as a hole-transporting material in OLEDs devices.

  10. Photoassociation and photoinduced charge transfer in bridged diaryl compounds. 6. Intramolecular triplet excimers of dicarbazolylalkanes and their comparison to an intermolecular triplet excimer of carbazole

    SciTech Connect

    Cai, J.; Lim, E.C. )

    1994-03-10

    A time-resolved emission study of intramolecular triplet excimer formation has been carried out for dicarbazolylmethane (DCM) and dicarbazolylpropane (DCP) in fluid solution at room temperature. The triplet excimer formation was deduced from the comparison of the phosphorescence with the corresponding emission from the intermolecular triplet excimer of carbazole. It has been found that whereas the triplet excimer formation in DCP is evident in both polar and nonpolar solvents, the excimer formation in DCM is observed only in polar solvents at longer delay times. The result indicates that the conformation favored by the triplet excimer is more readily attainable in DCP than in DCM. The enhancement of the triplet excimer formation by polar solvent, which is also observed for carbazole, suggests that the triplet excimers are stabilized (at least in part) by charge resonance interactions. Comparison of the temporal characteristics of the normal delayed fluorescence of DCP with those of the corresponding excimer phosphorescence suggests that the delayed fluorescence at long delay times is produced by bimolecular annihilation of the intramolecular triplet excimers. This in turn implies that the excited singlet-state species produced by bimolecular annihilation of the triplet excimers is unstable and rearranges into monomeric (i.e., non-interacting) conformation prior to its decay by emission of radiation. 16 refs., 7 figs.

  11. Enhanced violet photoemission of nanocrystalline fluorine doped zinc oxide (FZO) thin films

    NASA Astrophysics Data System (ADS)

    Anusha, Muthukumar; Arivuoli, D.; Manikandan, E.; Jayachandran, M.

    2015-09-01

    Highly stable fluorine doped nanocrystalline zinc oxide thin films were prepared on corning glass substrates by aerosol assisted chemical vapor deposition (AACVD) at variable deposition temperature of 360 °C, 380 °C and 420 °C. Especially, the optimum deposition temperature was investigated for high intense violet emission. The film crystallinity improved with the increasing deposition temperature and highly textured film was obtained at 420 °C. The films exhibited surface morphology variation from spherical to platelets due to deposition temperature effect, analyzed by field emission scanning electron microscope (FE-SEM). Higher growth rate observed at 420 °C which leads larger grains and lowest resistivity of ∼5.77 Ω cm among the deposited films which may be due to reduction in zinc vacancies and grain boundary area. Zinc vacancies are acts as electron killer centres. UV-visible spectra indicated higher transmittance (83-90%) in the visible region. Red shift of optical absorption edges associated with the increase in particle size consistent well with the XRD results. Reduced E2(high) intensity was observed in Raman spectra, for the film deposited at 380 °C which indicates decreased oxygen incorporation confirmed by PL spectra. Especially, enhanced violet emission observed at 3.06 eV for the films deposited at 380 °C due to electronic transition from the defect level of zinc vacancies to the conduction band, probably attributed to enhanced incorporation of 'F' into 'O' sites associated with increased Zn vacancies and also decreased oxygen incorporation consistent with the electrical and Raman analyses.

  12. Surface microstructural features of scales in relation to toxic stress of Basic Violet-1.

    PubMed

    Kaur, Kirandeep; Kaur, Ramandeep; Kaur, Arvinder

    2016-01-01

    The present work deals with scanning electron microscopic (SEM) studies of the scales of Labeo rohita on exposure to lethal and sublethal doses of Basic Violet-1 (an important textile and hair colorant). The dye induced loosening of the scales and caused breakage and disorganization of lepidonts. Erosion of lepidonts occurred mostly in the fish exposed to 0.20 and 0.40 mg/L dye, during acute exposure and to 0.0225 and 0.045 mg/L dye, during the subchronic exposure. However, lepidonts were sloughed off from their sockets in 0.60 and 0.80 mg/L dye during acute exposure and in 0.09 mg/L dye during the subchronic exposure. Circuli, the base that provides anchorage to the lepidonts, got damaged, and tubercles responsible for coloration of a fish became atrophied with an increase in the duration of exposure. The results of the present investigation clearly indicated that exposure to Basic Violet-1 (BV-1) even at a concentration as low as 0.0225 mg was responsible for deleterious changes in the scale morphology of the test fish after 150 days of exposure. Similar changes were observed in the scales of the dead fish also. It can thus be suggested that this noninvasive technique is very helpful for evaluating the health status of an aquatic body. At the same time, the changes in ultramorphology of scales can act as an early indicator of the stress of very minute doses of dyes and even the scales of a dead fish can act as indicators of the untoward changes that would have occurred in the environment of the fish before death.

  13. Radiochromic leuco dye micelle hydrogels: II. Low diffusion rate leuco crystal violet gel.

    PubMed

    Babic, Steven; Battista, Jerry; Jordan, Kevin

    2009-11-21

    Radiation-sensitive hydrogels offer the capability of verifying intricate dose distributions in three-dimensional (3D) space conveniently in a single measurement with sub-millimetre spatial resolution. In this study, a new radiochromic hydrogel called leuco crystal violet (LCV) micelle gel is introduced. Upon irradiation, LCV converts to crystal violet (CV(+)). Triton X-100 micelles are used to provide the required hybrid-interfacing environment to dissolve LCV. The diffusion coefficient of the LCV gel has been measured to be 0.036 +/- 0.001 mm(2) h(-1), which is a factor of 25 times less than the standard radiochromic ferrous xylenol-orange (FX) gel; LCV gels without Triton X-100 micelles have a diffusion coefficient of 0.33 +/- 0.02 mm(2) h(-1). The LCV gel formulation contains: 1 mM LCV, 25 mM trichloroacetic acid, 4 mM Triton X-100 and 4% w/w gelatin. The primary innovative feature of this 3D hydrogel is that the radiation-induced CV(+) dye is more soluble in the Triton X-100 micelles than in the surrounding water which consequently leads to more stable post-irradiation dose distributions. A dosimetric characterization revealed that the dose response is reproducible to within 1% over three separate batches, independent of energy, dose rate and dose fractionation but is affected by the temperature ( approximately 4% per degree C) during irradiation. LCV micelle gels scanned optically with a yellow light source are a promising system for 3D dose verification. They may prove to be, especially, useful for scanning large volume dosimeters (i.e. 20 cm) since they are easily manufactured, transparent and near colourless prior to irradiation.

  14. Radiochromic leuco dye micelle hydrogels: II. Low diffusion rate leuco crystal violet gel

    NASA Astrophysics Data System (ADS)

    Babic, Steven; Battista, Jerry; Jordan, Kevin

    2009-11-01

    Radiation-sensitive hydrogels offer the capability of verifying intricate dose distributions in three-dimensional (3D) space conveniently in a single measurement with sub-millimetre spatial resolution. In this study, a new radiochromic hydrogel called leuco crystal violet (LCV) micelle gel is introduced. Upon irradiation, LCV converts to crystal violet (CV+). Triton X-100 micelles are used to provide the required hybrid-interfacing environment to dissolve LCV. The diffusion coefficient of the LCV gel has been measured to be 0.036 ± 0.001 mm2 h-1, which is a factor of 25 times less than the standard radiochromic ferrous xylenol-orange (FX) gel; LCV gels without Triton X-100 micelles have a diffusion coefficient of 0.33 ± 0.02 mm2 h-1. The LCV gel formulation contains: 1 mM LCV, 25 mM trichloroacetic acid, 4 mM Triton X-100 and 4% w/w gelatin. The primary innovative feature of this 3D hydrogel is that the radiation-induced CV+ dye is more soluble in the Triton X-100 micelles than in the surrounding water which consequently leads to more stable post-irradiation dose distributions. A dosimetric characterization revealed that the dose response is reproducible to within 1% over three separate batches, independent of energy, dose rate and dose fractionation but is affected by the temperature (~4% per °C) during irradiation. LCV micelle gels scanned optically with a yellow light source are a promising system for 3D dose verification. They may prove to be, especially, useful for scanning large volume dosimeters (i.e. 20 cm) since they are easily manufactured, transparent and near colourless prior to irradiation.

  15. Determination of crystal violet in water by direct solid phase spectrophotometry after rotating disk sorptive extraction.

    PubMed

    Manzo, Valentina; Navarro, Orielle; Honda, Luis; Sánchez, Karen; Inés Toral, M; Richter, Pablo

    2013-03-15

    The microextraction of crystal violet (CV) from water samples into polydimethylsiloxane (PDMS) using the rotating disk sorptive extraction (RDSE) technique was performed. The extracting device was a small Teflon disk that had an embedded miniature magnetic stirring bar and a PDMS (560 μL) film attached to one side of the disk using double-sided tape. The extraction involves a preconcentration of CV into the PDMS, where the analyte is then directly quantified using solid phase spectrophotometry at 600 nm. Different chemical and extraction device-related variables were studied to achieve the best sensitivity for the determination. The optimum extraction was performed at pH 14 because under this condition, CV is transformed to the neutral and colorless species carbinol, which can be quantitatively transferred to the PDMS phase. Although the colorless species is the chemical form extracted in the PDMS, an intense violet coloration appeared in the phase because the -OH bond in the carbinol molecule is weakened through the formation of hydrogen bonds with the oxygen atoms of the PDMS, allowing the resonance between the three benzene rings to compensate for the charge deficit on the central carbon atom of the molecule. The accuracy and precision of the method were evaluated in river water samples spiked with 10 and 30 μg L(-1) of CV, yielding a relative standard deviation of 6.2% and 8.4% and a recovery of 98.4% and 99.4%, respectively. The method detection limit was 1.8 μg L(-1) and the limit of quantification was 5.4 μg L(-1), which can be decreased if the sample volume is increased.

  16. Surface microstructural features of scales in relation to toxic stress of Basic Violet-1.

    PubMed

    Kaur, Kirandeep; Kaur, Ramandeep; Kaur, Arvinder

    2016-01-01

    The present work deals with scanning electron microscopic (SEM) studies of the scales of Labeo rohita on exposure to lethal and sublethal doses of Basic Violet-1 (an important textile and hair colorant). The dye induced loosening of the scales and caused breakage and disorganization of lepidonts. Erosion of lepidonts occurred mostly in the fish exposed to 0.20 and 0.40 mg/L dye, during acute exposure and to 0.0225 and 0.045 mg/L dye, during the subchronic exposure. However, lepidonts were sloughed off from their sockets in 0.60 and 0.80 mg/L dye during acute exposure and in 0.09 mg/L dye during the subchronic exposure. Circuli, the base that provides anchorage to the lepidonts, got damaged, and tubercles responsible for coloration of a fish became atrophied with an increase in the duration of exposure. The results of the present investigation clearly indicated that exposure to Basic Violet-1 (BV-1) even at a concentration as low as 0.0225 mg was responsible for deleterious changes in the scale morphology of the test fish after 150 days of exposure. Similar changes were observed in the scales of the dead fish also. It can thus be suggested that this noninvasive technique is very helpful for evaluating the health status of an aquatic body. At the same time, the changes in ultramorphology of scales can act as an early indicator of the stress of very minute doses of dyes and even the scales of a dead fish can act as indicators of the untoward changes that would have occurred in the environment of the fish before death. PMID:26432273

  17. Metallo-hydrazone complexes immobilized in zeolite Y: Synthesis, identification and acid violet-1 degradation

    NASA Astrophysics Data System (ADS)

    Ahmed, Ayman H.; Thabet, M. S.

    2011-12-01

    Copper(II), cobalt(II) and nickel(II) complexes of hydrazone ligand (SAPH) derived from salicylaldehyde and phenylhydrazine have been encapsulated in zeolite-Y super cages via ship-in-a-bottle synthesis. Detailed characterization of the intrazeolitic complexes were performed by elemental analysis, spectral (FT-IR, UV-Vis.) studies, magnetic measurements and X-ray diffraction. Furthers, surface texture and thermal analysis (TG, DTG, DTA) have provided further evidence for successful immobilization of the metal complexes inside zeolite Y. Investigation of the stereochemistry of these incorporated chelates pointed out that, SAPH ligand is capable to coordinate with the central metal through the (C dbnd N), phenolic (OH) and (NH) groups forming polynuclear structures. The involvement of zeolite oxygen in coordination was postulated in the hybrid materials. The intrazeolitic copper, cobalt and nickel-SAPH complexes have distorted tetrahedral, octahedral and square-pyramidal configurations, respectively. The zeolite encapsulated complexes are thermally stable up to 800 °C except Cu(II) sample which is thermally stable up to midpoint 428 °C. The assessment of the catalytic activity was performed by the use of the photo-degradation of acid violet-1 dye as a probe reaction in presence of H 2O 2 as an oxidant. Decolorization of acid violet-1 dye was examined under the same conditions whereas the unpromoted zeolite and Cu II, Co II, Ni II-hydrazone complexes supported on zeolite showed 13% and 76%, 53%, 43% color removal, respectively. The results revealed that, the zeolite encapsulated Cu(II) complex generally exhibited better catalytic efficiency (76%) compared with other investigated zeolite encapsulated metal-hydrazone samples.

  18. 21 CFR 73.3117 - 16,23-Dihydrodinaphtho[2,3-a:2′,3′-i] naphth [2′,3′:6,7] indolo [2,3-c] carbazole-5,10,15,17,22...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... Federal Food, Drug, and Cosmetic Act with respect to the contact lens in which the color additive is used... 21 Food and Drugs 1 2010-04-01 2010-04-01 false 16,23-Dihydrodinaphtho naphth indolo carbazole-5,10,15,17,22,24-hexone. 73.3117 Section 73.3117 Food and Drugs FOOD AND DRUG...

  19. COMPARISON OF BLOOD PROTEIN AND TARGET ORGAN DNA AND PROTEIN BINDING FOLLOWING TOPICAL APPLICATION OF BENZO[A]PYRENE AND 7H-DIBENZO[C,G]CARBAZOLE TO MICE

    EPA Science Inventory

    7H-Dibenzo[c,g]carbazole (DBC) induces skin and liver tumors in mice following topical application, whereas benzo[a]pyrene (BP) induces only skin tumors. DBC also binds to liver DNA to a much greater extent than does BP. The present study examined factors that might account for t...

  20. Evidence from action and fluorescence spectra that UV-induced violet-blue-green fluorescence enhances leaf photosynthesis.

    PubMed

    Mantha, S V; Johnson, G A; Day, T A

    2001-03-01

    We assessed the contribution of UV-induced violet-blue-green leaf fluorescence to photosynthesis in Poa annua, Sorghum halepense and Nerium oleander by measuring UV-induced fluorescence spectra (280-380 nm excitation, 400-550 nm emission) from leaf surfaces and determining the monochromatic UV action spectra for leaf photosynthetic O2-evolution. Peak fluorescence emission wavelengths from leaf surfaces ranged from violet (408 nm) to blue (448 nm), while excitation peaks for these maxima ranged from 333 to 344 nm. Action spectra were developed by supplementing monochromatic radiation from 280 to 440 nm, in 20 nm increments, to a visible nonsaturating background of 500 mumol m-2 s-1 photosynthetically active radiation and measuring photosynthetic O2-evolution rates. Photosynthetic rates tended to be higher with the 340 nm supplement than with higher or lower wavelength UV supplements. Comparing photosynthetic rates with the 340 nm supplement to those with the 400 nm supplement, the percentage enhancement in photosynthetic rates at 340 nm ranged from 7.8 to 9.8%. We suspect that 340 nm UV improves photosynthetic rates via fluorescence that provides violet-blue-green photons for photosynthetic energy conversion because (1) the peak excitation wavelength (340 nm) for violet-blue-green fluorescence from leaves was also the most effective UV wavelength at enhancing photosynthetic rates, and (2) the magnitude of photosynthetic enhancements attributable to supplemental 340 nm UV was well correlated (R2 = 0.90) with the apparent intensity of 340 nm UV-induced violet-blue-green fluorescence emission from leaves.

  1. Molecular topology tuning of bipolar host materials composed of fluorene-bridged benzimidazole and carbazole for highly efficient electrophosphorescence.

    PubMed

    Mondal, Ejabul; Hung, Wen-Yi; Chen, Yang-Huei; Cheng, Ming-Hung; Wong, Ken-Tsung

    2013-08-01

    Two new molecules, CzFCBI and CzFNBI, have been tailor-made to serve as bipolar host materials to realize high-efficiency electrophosphorescent devices. The molecular design is configured with carbazole as the hole-transporting block and N-phenylbenzimidazole as the electron-transporting block hybridized through the saturated bridge center (C9) and meta-conjugation site (C3) of fluorene, respectively. With structural topology tuning of the connecting manner between N-phenylbenzimidazole and the fluorene core, the resulting physical properties can be subtly modulated. Bipolar host CzFCBI with a C connectivity between phenylbenzimidazole and the fluorene bridge exhibited extended π conjugation; therefore, a low triplet energy of 2.52 eV was observed, which is insufficient to confine blue phosphorescence. However, the monochromatic devices indicate that the matched energy-level alignment allows CzFCBI to outperform its N-connected counterpart CzFNBI while employing other long-wavelength-emitting phosphorescent guests. In contrast, the high triplet energy (2.72 eV) of CzFNBI imparted by the N connectivity ensures its utilization as a universal bipolar host for blue-to-red phosphors. With a common device configuration, CzFNBI has been utilized to achieve highly efficient and low-roll-off devices with external quantum efficiency as high as 14 % blue, 17.8 % green, 16.6 % yellowish-green, 19.5 % yellow, and 18.6 % red. In addition, by combining yellowish-green with a sky-blue emitter and a red emitter, a CzFNBI-hosted single-emitting-layer all-phosphor three-color-based white electrophosphorescent device was successfully achieved with high efficiencies (18.4 %, 36.3 cd A(-1) , 28.3 lm W(-1) ) and highly stable chromaticity (CIE x=0.43-0.46 and CIE y=0.43) at an applied voltage of 8 to 12 V, and a high color-rendering index of 91.6.

  2. Endoscopic diagnosis of invasion depth for early colorectal carcinomas: a prospective comparative study of narrow-band imaging, acetic acid, and crystal violet.

    PubMed

    Zhang, Jing-Jing; Gu, Li-Yang; Chen, Xiao-Yu; Gao, Yun-Jie; Ge, Zhi-Zheng; Li, Xiao-Bo

    2015-02-01

    Several studies have validated the effectiveness of narrow-band imaging (NBI) in estimating invasion depth of early colorectal cancers. However, comparative diagnostic accuracy between NBI and chromoendoscopy remains unclear. Other than crystal violet, use of acetic acid as a new staining method to diagnose deep submucosal invasive (SM-d) carcinomas has not been extensively evaluated. We aimed to assess the diagnostic accuracy and interobserver agreement of NBI, acetic acid enhancement, and crystal violet staining in predicting invasion depth of early colorectal cancers. A total of 112 early colorectal cancers were prospectively observed by NBI, acetic acid, and crystal violet staining in sequence by 1 expert colonoscopist. All endoscopic images of each technique were stored and reassessed. Finally, 294 images of 98 lesions were selected for evaluation by 3 less experienced endoscopists. The accuracy of NBI, acetic acid, and crystal violet for real-time diagnosis was 85.7%, 86.6%, and 92.9%, respectively. For image evaluation by novices, NBI achieved the highest accuracy of 80.6%, compared with that of 72.4% by acetic acid, and 75.8% by crystal violet. The kappa values of NBI, acetic acid, and crystal violet among the 3 trainees were 0.74 (95% CI 0.65-0.83), 0.68 (95% CI 0.59-0.77), and 0.70 (95% CI 0.61-0.79), respectively. For diagnosis of SM-d carcinoma, NBI was slightly inferior to crystal violet staining, when performed by the expert endoscopist. However, NBI yielded higher accuracy than crystal violet staining, in terms of less experienced endoscopists. Acetic acid enhancement with pit pattern analysis was capable of predicting SM-d carcinoma, comparable to the traditional crystal violet staining.

  3. Mouse model of intraluminal MCAO: cerebral infarct evaluation by cresyl violet staining.

    PubMed

    Rousselet, Estelle; Kriz, Jasna; Seidah, Nabil G

    2012-01-01

    volume, staining with 2,3,5-triphenyltetrazolium chloride (TTC) was usually performed. Herein, we used cresyl violet staining since it offers the opportunity to test many critical markers by immunohistochemistry. In this video, we report the MCAO procedure; neurological scores and the evaluation of the infarct volume by cresyl violet staining.

  4. Measuring the Photocatalytic Breakdown of Crystal Violet Dye using a Light Emitting Diode Approach

    NASA Technical Reports Server (NTRS)

    Ryan, Robert E.; Underwood, Lauren W.; O'Neal, Duane; Pagnutti, Mary; Davis, Bruce A.

    2009-01-01

    A simple method to estimate the photocatalytic reactivity performance of spray-on titanium dioxide coatings for transmissive glass surfaces was developed. This novel technique provides a standardized method to evaluate the efficiency of photocatalytic material systems over a variety of illumination levels. To date, photocatalysis assessments have generally been conducted using mercury black light lamps. Illumination levels for these types of lamps are difficult to vary, consequently limiting their use for assessing material performance under a diverse range of simulated environmental conditions. This new technique uses an ultraviolet (UV) gallium nitride (GaN) light emitting diode (LED) array instead of a traditional black light to initiate and sustain photocatalytic breakdown. This method was tested with a UV-resistant dye (crystal violet) applied to a titanium dioxide coated glass slide. Experimental control is accomplished by applying crystal violet to both titanium dioxide coated slides and uncoated control slides. A slide is illuminated by the UV LED array, at various light levels representative of outdoor and indoor conditions, from the dye side of the slide. To monitor degradation of the dye over time, a temperature-stabilized white light LED, whose emission spectrum overlaps with the dye absorption spectrum, is used to illuminate the opposite side of the slide. Using a spectrometer, the amount of light from the white light LED transmitted through the slide as the dye degrades is monitored as a function of wavelength and time and is subsequently analyzed. In this way, the rate of degradation for photocatalytically coated versus uncoated slide surfaces can be compared. Results demonstrate that the dye absorption decreased much more rapidly on the photocatalytically coated slides than on the control uncoated slides, and that dye degradation is dependent on illumination level. For photocatalytic activity assessment purposes, this experimental configuration and

  5. Covalent anthocyanin-flavonol complexes from the violet-blue flowers of Allium 'Blue Perfume'.

    PubMed

    Saito, Norio; Nakamura, Maiko; Shinoda, Koichi; Murata, Naho; Kanazawa, Toshinari; Kato, Kazuhisa; Toki, Kenjiro; Kasai, Hiroko; Honda, Toshio; Tatsuzawa, Fumi

    2012-08-01

    Three covalent anthocyanin-flavonol complexes (pigments 1-3) were extracted from the violet-blue flower of Allium 'Blue Perfume' with 5% acetic acid-MeOH solution, in which pigment 1 was the dominant pigment. These three pigments are based on delphinidin 3-glucoside as their deacylanthocyanin and were acylated with malonyl kaempferol 3-sophoroside-7-glucosiduronic acid or malonyl-kaempferol 3-p-coumaroyl-tetraglycoside-7-glucosiduronic acid in addition to acylation with acetic acid. By spectroscopic and chemical methods, the structures of these three pigments 1-3 were determined to be: pigment 1, (6(I)-O-(delphinidin 3-O-(3(I)-O-(acetyl)-β-glucopyranoside(I))))(2(VI)-O-(kaempferol 3-O-(2(II)-O-(3(III)-O-(β-glucopyranosyl(V))-β-glucopyranosyl(III))-4(II)-O-(trans-p-coumaroyl)-6(II)-O-(β-glucopyranosyl(IV))-β-glucopyranoside(II))-7-O-(β-glucosiduronic acid(VI)))) malonate; pigment 2, (6(I)-O-(delphinidin 3-O-(3(I)-O-(acetyl)-β-glucopyranoside(I))))(2(VI)-O-(kaempferol 3-O-(2(II)-O-β-glucopyranosyl(III))-β-glucopyranoside(II))-7-O-(β-glucosiduronic acid(VI)))); and pigment 3, (6(I)-O-(delphinidin 3-O-(3(I)-O-(acetyl)-β-glucopyranoside(I))))(2(VI)-O-(kaempferol 3-O-(2(II)-O-(3(III)-O-(β-glucopyranosyl(V))-β-glucopyranosyl(III))-4(II)-O-(cis-p-coumaroyl)-6(II)-O-(β-glucopyranosyl(IV))-β-glucopyranoside(II))-7-O-(β-glucosiduronic acid(VI)))) malonate. The structure of pigment 2 was analogous to that of a covalent anthocyanin-flavonol complex isolated from Allium schoenoprasum where delphinidin was observed in place of cyanidin. The three covalent anthocyanin-flavonol complexes (pigment 1-3) had a stable violet-blue color with three characteristic absorption maxima at 540, 547 and 618nm in pH 5-6 buffer solution. From circular dichroism measurement of pigment 1 in the pH 6.0 buffer solution, cotton effects were observed at 533 (+), 604 (-) and 638 (-) nm. Based on these results, these covalent anthocyanin-flavonol complexes were presumed to maintain a

  6. Use of hydrogen peroxide treatment and crystal violet agar plates for selective recovery of bacteriophages from natural environments

    SciTech Connect

    Asghari, A.; Farrah, S.R.; Bitton, G. )

    1992-04-01

    Hydrogen peroxide inactivated bacteriophages and bacteria at different rates. A concentration of 0.1% hydrogen peroxide reduced the numbers of several bacteria by an average of 94% but caused an average of 25% inactivation in the numbers of bacteriophages tested. Treating natural samples with hydrogen peroxide selectively reduced the indigenous bacterial flora and permitted better visualization of plaques of lawns of Escherichia coli C-3000. In some cases indigenous gram-positive bacteria were relatively resistant to hydrogen peroxide, but their growth could be limited by incorporation of crystal violet into the bottom agar used for plaque assays. The use of hydrogen peroxide treatment and crystal violet-containing plates permitted recovery of more phages from natural samples than did other procedures, such as chloroform pretreatment or the use of selective plating agar such as EC medium.

  7. Bioremoval of Basic Violet 3 and Acid Blue 93 by Pseudomonas putida and its adsorption isotherms and kinetics.

    PubMed

    Arunarani, A; Chandran, Preethy; Ranganathan, B V; Vasanthi, N S; Sudheer Khan, S

    2013-02-01

    Basic Violet 3 and Acid Blue 93 are the most important group of synthetic colourants extensively used in textile industries for dyeing cotton, wool, silk and nylon. Release of these dye pollutants in to the environment adversely affects the human health and aquatic organisms. The present study we used Pseudomonas putida MTCC 4910 for the adsorptive removal of Basic Violet 3 and Acid Blue 93 from the aqueous solutions. The pH (4-9) and NaCl concentrations (1mM-1M) did not influence the adsorption process. The equilibrium adsorption process fitted well to Freundlich model than Langmuir model. The kinetics of adsorption fitted well by pseudo-second-order. Thus in the present study an attempt has been made to exploit the dye removal capability of P. putida MTCC 4910, and it was found to be an efficient microbe that could be used for bio removal of dyes from textile effluents.

  8. Novel conjugated polymers based on dithieno[3,2-b:6,7-b]carbazole for solution processed thin-film transistors.

    PubMed

    Chen, Yagang; Liu, Chengfang; Tian, Hongkun; Bao, Cheng; Zhang, Xiaojie; Yan, Donghang; Geng, Yanhou; Wang, Fosong

    2012-10-26

    Two conjugated polymers (CPs) P-tCzC12 and P-tCzC16 comprising alternating dithieno[3,2-b:6,7-b]carbazole and 4,4'-dihexadecyl-2,2'-bithiophene units have been designed and synthesized. Upon thermal annealing, they can form ordered thin films in which the polymer backbones dominantly adopted an edge-on orientation respective to the substrate with a lamellar spacing of ≈24 Å and a π-stacking distance of ≈3.7 Å. Organic thin-film transistors (OTFTs) were fabricated by solution casting. A hole mobility of 0.39 cm(2) V(-1) s(-1) has been demonstrated with P-tCzC16. This value is the highest among the CPs containing heteroacenes larger than 4 rings.

  9. Synthesis and biological evaluation of novel N-substituted 1H-dibenzo[a,c]carbazole derivatives of dehydroabietic acid as potential antimicrobial agents.

    PubMed

    Gu, Wen; Qiao, Chao; Wang, Shi-Fa; Hao, Yun; Miao, Ting-Ting

    2014-01-01

    A series of new N-substituted 1H-dibenzo[a,c]carbazole derivatives were synthesized from dehydroabietic acid, and their structures were characterized by IR, (1)H NMR and HRMS spectral data. All compounds were evaluated for their antibacterial and antifungal activities against four bacteria (Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas fluorescens) and three fungi (Candida albicans, Candida tropicalis and Aspergillus niger) by serial dilution technique. Some of the synthesized compounds displayed pronounced antimicrobial activity against tested strains with low MIC values ranging from 0.9 to 15.6μg/ml. Among them, compounds 6j and 6r exhibited potent inhibitory activity comparable to reference drugs amikacin and ketoconazole. PMID:24300736

  10. Synthesis, spectral and third-order nonlinear optical properties of terpyridine Zn(II) complexes based on carbazole derivative with polyether group

    NASA Astrophysics Data System (ADS)

    Kong, Ming; Liu, Yanqiu; Wang, Hui; Luo, Junshan; Li, Dandan; Zhang, Shengyi; Li, Shengli; Wu, Jieying; Tian, Yupeng

    2015-01-01

    Four novel Zn(II) terpyridine complexes (ZnLCl2, ZnLBr2, ZnLI2, ZnL(SCN)2) based on carbazole derivative group were designed, synthesized and fully characterized. Their photophysical properties including absorption and one-photon excited fluorescence, two-photon absorption (TPA) and optical power limiting (OPL) were further investigated systematically and interpreted on the basis of theoretical calculations (TD-DFT). The influences of different solvents on the absorption and One-Photon Excited Fluorescence (OPEF) spectral behavior, quantum yields and the lifetime of the chromophores have been investigated in detail. The third-order nonlinear optical (NLO) properties were investigated by open/closed aperture Z-scan measurements using femtosecond pulse laser in the range from 680 to 1080 nm. These results revealed that ZnLCl2 and ZnLBr2 exhibited strong two-photon absorption and ZnLCl2 showed superior optical power limiting property.

  11. Biocompatibility of the vital dye Acid Violet-17 on retinal pigment epithelial cells

    PubMed Central

    Tura, Ayşegül; Alt, Aizhan; Lüke, Julia; Grisanti, Salvatore; Haritoglou, Christos; Meyer, Carsten H; Nassar, Khaled; Lüke, Matthias

    2016-01-01

    Purpose To examine the viability and differentiation of retinal pigment epithelial (RPE) cells after exposure to the vital dye Acid Violet-17 (AV-17). Methods Bovine RPE cells were incubated with AV-17 (0.0625–0.5 mg/mL) for 30 seconds or 5 minutes. Viability was determined by live/dead staining, cleaved CASP3 immunostainings, and MTT test. Actin cytoskeleton was visualized by Alexa 488-phalloidin. Immunocytochemistry was performed to determine the levels of ZO-1, CTNNB1, and KRT19. Results Exposure to AV-17 at the concentrations of 0.25–0.5 mg/mL resulted in a dose-dependent decrease in viability, the loss of ZO-1 from tight junctions, translocation of CTNNB1 into the cytoplasm and nucleus, disarrangement of the actin cytoskeleton, and a slight increase in KRT19. Conclusion AV-17 at a concentration <0.125 mg/mL is likely to be well tolerated by the RPE cells, whereas the concentrations from 0.25 mg/mL onward can reduce viability and induce dedifferentiation particularly after long-term exposure. PMID:27536056

  12. Planar super-oscillatory lens for sub-diffraction optical needles at violet wavelengths

    PubMed Central

    Yuan, Guanghui; Rogers, Edward T. F.; Roy, Tapashree; Adamo, Giorgio; Shen, Zexiang; Zheludev, Nikolay I.

    2014-01-01

    Planar optical lenses are fundamental elements of miniaturized photonic devices. However, conventional planar optical lenses are constrained by the diffraction limit in the optical far-field due to the band-limited wavevectors supported by free-space and loss of high-spatial-frequency evanescent components. As inspired by Einstein's radiation ‘needle stick', electromagnetic energy can be delivered into an arbitrarily small solid angle. Such sub-diffraction optical needles have been numerically investigated using diffractive optical elements (DOEs) together with specially polarized optical beams, but experimental demonstration is extremely difficult due to the bulky size of DOEs and the required alignment precision. Planar super-oscillatory lenses (SOLs) were proposed to overcome these constraints and demonstrated that sub-diffraction focal spots can actually be formed without any evanescent waves, making far-field, label-free super-resolution imaging possible. Here we extend the super-oscillation concept into the vectorial-field regime to work with circularly polarized light, and experimentally demonstrate, for the first time, a circularly polarized optical needle with sub-diffraction transverse spot size (0.45λ) and axial long depth of focus (DOF) of 15λ using a planar SOL at a violet wavelength of 405 nm. This sub-diffraction circularly polarized optical needle has potential applications in circular dichroism spectroscopy, super-resolution imaging, high-density optical storage, heat-assisted magnetic recording, nano-manufacturing and nano-metrology. PMID:25208611

  13. Effect of Montmorillonite Modification on Ultra Violet Radiation Cured Nanocomposite Filled with Glycidyl Methacrylate Modified Kenaf

    NASA Astrophysics Data System (ADS)

    Rozyanty, A. R.; Rozman, H. D.; Zhafer, S. F.; Musa, L.; Zuliahani, A.

    2016-06-01

    In this study nanocomposite cured by ultra violet radiation, were produced using modified montmorillonite (MMT) as reinforcing agent, chemically modified kenaf bast fiber as filler and unsaturated polyester as the matrix. Kenaf bast fiber was chemically modified with glycidyl methacrylate (GMA) whilst MMT were modified with cetyl trimethyl ammonium bromide (CTAB) and glycidyl methacrylate (GMA). Fixed 12 percent of GMA modified kenaf bast fiber with different percentage (i.e., 1, 3 and 5) of unmodified and modified MMT loading was used to produce the composite. The performed of GMA reaction with hydroxyl group of cellulose in kenaf bast fiber was evaluated using Fourier Transform infrared (FTIR) spectroscopy. GMA-MMT filled composite showed higher mechanical properties than MMT and CTAB-MMT filled composite. However, the increase of MMT, CTAB-MMT and GMA- MMT loading resulted in the reduction of mechanical properties. Scanning electron microscopy (SEM) analysis showed the evidence of compatibility enhancement between MMT and kenaf bast fiber with unsaturated polyester matrix.

  14. Genotoxic and antibutyrylcholinesterasic activities of acid violet 7 and its biodegradation products.

    PubMed

    Mansour, Hedi Ben; Mosrati, Ridha; Limem, Ilef; Corroler, David; Ghedira, Kamel; Barillier, Daniel; Chekir-Ghedira, Leila

    2009-01-01

    Acid violet 7, a sulfonated azo dye was degraded by Pseudomonas putida mt-2 in mineral medium at concentrations up to 200 mg/L. The genotoxicity of AV7 and its biodegradation extracts was evaluated by using the DNA-strand scission assay. No genotoxicity was observed, even with or without exposition to UV irradiation, for biodegradation under shaking conditions, but increased significantly after biodegradation under static conditions. In addition, the ability of tested compounds to reduce human plasma butyrylcholinesterase (BuChE) activity was evaluated in vitro. Genotoxicity and anti-BuChE activity generated by the azoreduction products [4'-aminoacetanilid (4'-AA) and 5-acetamido-2-amino-1-hydroxy-3,6-naphtalene disulfonic acid (5-ANDS)] were assessed and compared with that of the parent unsubstituted amines. 4'-AA exhibited a strong genotoxicity, which was imputed to the presence of the acetoxy (COCH3) substituent on the aromatic amine; however, the presence of sulphonic groups in 5-ANDS seems to be responsible for its BuChE inhibition activity. The present study demonstrates that P. putida mt-2, incubated under aerobic conditions, has a catabolism that enables it to degrade AV7 and, especially, to detoxify the dye mixtures.

  15. Genetic structure among and within peripheral and central populations of three endangered floodplain violets.

    PubMed

    Eckstein, R L; O'neill, R A; Danihelka, J; Otte, A; Köhler, W

    2006-08-01

    Understanding the partitioning of genetic variance in peripheral and central populations may shed more light on the effects of genetic drift and gene flow on population genetic structure and, thereby, improve attempts to conserve genetic diversity. We analysed genetic structure of peripheral and central populations of three insect-pollinated violets (Viola elatior, Viola pumila, Viola stagnina) to evaluate to what extent these patterns can be explained by gene flow and genetic drift. Amplified fragment length polymorphism was used to analyse 930 individuals of 50 populations. Consistent with theoretical predictions, peripheral populations were smaller and more isolated, differentiation was stronger, and genetic diversity and gene flow lower in peripheral populations of V. pumila and V. stagnina. In V. elatior, probably historic fragmentation effects linked to its specific habitat type were superimposed on the plant geographic (peripheral-central) patterns, resulting in lower relative importance of gene flow in central populations. Genetic variation between regions (3-6%), among (30-37%) and within populations (60-64%) was significant. Peripheral populations lacked markers that were rare and localized in central populations. Loss of widespread markers in peripheral V. stagnina populations indicated genetic erosion. Autocorrelation within populations was statistically significant up to a distance of 10-20 m. Higher average genetic similarity in peripheral populations than in central ones indicated higher local gene flow, probably owing to management practices. Peripheral populations contributed significantly to genetic variation and contained unique markers, which made them valuable for the conservation of genetic diversity.

  16. Theoretical study of the dissociation energy and the red and violet band systems of CN

    NASA Technical Reports Server (NTRS)

    Bauschlicher, Charles W., Jr.; Langhoff, Stephen R.; Taylor, Peter R.

    1987-01-01

    The dissociation energy (D sub O) of CN is determined to be 7.65 + or - 0.06 eV. This corresponds to delta H sub f (CN) = 105.3 + or - 1.5 kcal/mole, in excellent agreement with Engleman and Rouse (1975), but considerably larger than the recent value deduced from shock-tube studies by Colket (1984). The result is obtained not only from extensive ab initio MRCI calculations using a very large Gaussian basis set, but also from extrapolation of the directly computed value by comparison of computed and experimental results fo NO, C2, and N2. As an additional calibration of the methods, the D sub O value for CN was computed from the corresponding value for CN(-) using the experimental electron affinity data. The lifetime of the nu prime = 0 level of the violet (B 2 sigma + yields X 2 sigma +) system was computed to be 62.4 ns, in good agreement with both experiment and previous calculations. Lifetimes for the red (A 2 pi yields X 2 sigma +) system decrease with increasing nu prime, which is consistent both with the recent experiment and calculations. While the computed lifetimes are significantly longer that those obtained from the experiment, they are shorter than those deduced from an analysis of the solar spectrum. However the D sub O and f (sub OO) are consistent with Lambert's model for the solar spectrum.

  17. Epigenetic differentiation and relationship to adaptive genetic divergence in discrete populations of the violet Viola cazorlensis.

    PubMed

    Herrera, Carlos M; Bazaga, Pilar

    2010-08-01

    *In plants, epigenetic variations based on DNA methylation are often heritable and could influence the course of evolution. Before this hypothesis can be assessed, fundamental questions about epigenetic variation remain to be addressed in a real-world context, including its magnitude, structuring within and among natural populations, and autonomy in relation to the genetic context. *Extent and patterns of cytosine methylation, and the relationship to adaptive genetic divergence between populations, were investigated for wild populations of the southern Spanish violet Viola cazorlensis (Violaceae) using the methylation-sensitive amplified polymorphism (MSAP) technique, a modification of the amplified fragment length polymorphism method (AFLP) based on the differential sensitivity of isoschizomeric restriction enzymes to site-specific cytosine methylation. *The genome of V. cazorlensis plants exhibited extensive levels of methylation, and methylation-based epigenetic variation was structured into distinct between- and within- population components. Epigenetic differentiation of populations was correlated with adaptive genetic divergence revealed by a Bayesian population-genomic analysis of AFLP data. Significant associations existed at the individual genome level between adaptive AFLP loci and the methylation state of methylation-susceptible MSAP loci. *Population-specific, divergent patterns of correlated selection on epigenetic and genetic individual variation could account for the coordinated epigenetic-genetic adaptive population differentiation revealed by this study.

  18. Red/violet contrast reversal on Mars - Significance for eolian sediments

    NASA Technical Reports Server (NTRS)

    Thomas, P.; Veverka, J.

    1986-01-01

    Viking Orbiter images of Mars are analyzed to define relationships between the observed contrast reversals (CR) and specific surface features. The link between CR phenomena and surface composition was first detected in contrast comparisons between UV and visible wavelength Mariner 9 data. Viking data, taken through red and violet filters, showed that the CRs occurred only with crater splotches and splotch-related streaks and in bright depositional and dark erosional streaks, both being low-albedo markings presumably caused by eolian forces. The splotch phenomena is confined mainly to the Oxia Palus region, although there are other regions where splotches and streaks commingle. Laboratory tests to mimic the CR characteristics showed that CRs are a common phenomena of different size fractions of iron oxides, e.g., goethite, where particles under 5 microns have been removed. The splotches, including dune formations, are therefore believed to indicate the presence of particles in the 100-800 microns diam range. Finer particles ride on the tops of the dust storms, and are continually removed from the surface by saltation.

  19. Determination of malachite green and crystal violet in processed fish products.

    PubMed

    Lee, Jun Bae; Kim, Hee Yun; Jang, Young Mi; Song, Ji Young; Woo, Sung Min; Park, Mi Sun; Lee, Hyun Sook; Lee, Soon Kyu; Kim, Meehye

    2010-07-01

    This paper presents analysis of malachite green (MG) and crystal violet (CV) residues in processed fish products. Samples were homogenized and extracted with ammonium acetate buffer and acetonitrile. The extracted residues were partitioned into dichloromethane, in situ oxidized to chromic forms with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, and cleaned up on neutral alumina and propylsulfonic acid cation-exchange solid-phase extraction (SPE) cartridges. MG and CV were determined at 618 and 588 nm using HPLC with a visible detector (LC-VIS) and confirmed by LC-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). The recoveries were as follows: MG (74.8-83.8%), LMG (80.0-88.4%), CV (68.6-73.9%), and LCV (85.5-90.0%). The method modified in this study has been evaluated by application in-house to a survey of 253 processed fish products. As a result of monitoring, MG and CV were positive in one shrimp and one eel sample, respectively. Our results showed that regular monitoring of these antibiotic residues is recommended for protection of public health. PMID:20544455

  20. Synthesis of CarAlg/MMt nanocomposite hydrogels and adsorption of cationic crystal violet.

    PubMed

    Mahdavinia, Gholam Reza; Aghaie, Huriyeh; Sheykhloie, Hossein; Vardini, Mohammad Taghi; Etemadi, Hossein

    2013-10-15

    CarAlg/MMt nanocomposite hydrogels composed of kappa-carrageenan (Car) and sodium alginate (Alg) biopolymers were synthesized by incorporation of sodium montmorillonite (Na-MMt) nanoclay. Acrylamide (AAm), methylenebisacrylamide (MBA), and ammonium persulfate (APS) were used as monomer, crosslinker, and initiator, respectively. The structure and morphology of nanocomposites were characterized by XRD, SEM, and TEM techniques. The XRD results showed exfoliated MMt nanoclay and exfoliation of MMt was confirmed by TEM graph. The resulting nanocomposites were evaluated to remove cationic crystal violet (CV) dye from water. According to data, the adsorption capacity of nanocomposites was enhanced as the clay content was increased. The experimental data were analyzed according to both Langmuir and Freundlich models and experimental maximum adsorption capacity was obtained 88.8 mg g(-1). By studying the effect of pH on the dye adsorption capacity of nanocomposites, it was revealed that the adsorption capacity of nanocomposites was enhanced at acidic pHs as the Na-MMt nanoclay and kappa-carrageenan components were increased.

  1. Evaluation of Plasma Temperature from the OH Violet Molecular Emission System

    NASA Astrophysics Data System (ADS)

    Nassar, Hossein; Aoude, Ouloum

    2015-09-01

    The violet OH system (A2Σ+ - X2Πi) molecular emission spectrum is frequently observed in plasma sources containing water it is a good tool for diagnosing plasmas containing this molecule. We have simulated the spectrum of (0,0) band of this system from 3064 Å for different rotational temperature. The method proposed permit to evaluate, by comparing point to point a real spectrum with the simulated one, temperature and apparatus function, approximated by the gauss function (the half-width at 1/e height). Moreover, it is shown, by noised spectra simulation, the influence of noise to signal ratio at the calculated temperature values. If the noise to signal ratio is about 10% we found an error of 6% at temperature 3000 K and 10% at 6000 K. This method has been used to determine the combustion temperature from a real spectrum recording in Polymethyl methacrylate rocket plume taken 0 mm from the nozzle of fuel grain. The rotational temperature of about 3000 +/- 350 K, has been found and noise to signal ratio is about 20%.

  2. Use of pyrocatechol violet as an effective redox additive for highly promoting the supercapacitor performances

    NASA Astrophysics Data System (ADS)

    Wang, Qian; Nie, Yong Fu; Chen, Xiang Ying; Xiao, Zheng Hui; Zhang, Zhong Jie

    2016-08-01

    In present work, we demonstrate a simple but effective redox additive of pyrocatechol violet (abbr. PCV) to largely promote the capacitive performances especially when carried out in three different kinds of electrolytes (H2SO4, Na2SO4 and KOH), mostly due to its fast electron and proton transfer occurring in the electrode/electrolyte interface. It reveals that the PCV dosage incorporated into electrolyte plays a crucial role in the determination of capacitive performance. When conducted in a two-electrode system, incorporating 0.06 mol L-1 PCV into 1 mol L-1 H2SO4 can achieve large capacitance up to 200 F g-1, which is almost 2.06 times than the one without the addition of PCV; besides, the corresponding energy density is of 28 Wh kg-1 (also increasing 2 times). What's more, PCV has been extended as the redox additive in other electrolytes such as Na2SO4 and KOH, and remarkable promotion in capacitance and energy density also occur, well evincing the high efficiency and universal applicability of PCV for the large promotion of supercapacitors' performances due to its prominent electrochemical reversibility and high solubility.

  3. Leuco-crystal-violet micelle gel dosimeters: II. Recipe optimization and testing

    NASA Astrophysics Data System (ADS)

    Nasr, A. T.; Alexander, K. M.; Olding, T.; Schreiner, L. J.; McAuley, K. B.

    2015-06-01

    In this study, recipe optimization of Leuco Crystal Violet (LCV) micelle gels made with the surfactant Cetyl Trimethyl Ammonium Bromide (CTAB) and the chemical sensitizer 2,2,2-trichloroethanol (TCE) was aided by a two-level three-factor designed experiment. The optimized recipe contains 0.75 mM LCV, 17.0 mM CTAB, 120 mM TCE, 25.0 mM tri-chloro acetic acid (TCAA), 4 wt% gelatin and ~96 wt% water. Dose sensitivity of the optimized gel is 1.5 times higher than that of Jordan’s standard LCV micelle gel. Spatial integrity of the 3D dose distribution information in 1L phantoms filled with this recipe is maintained for  >120 d. Unfortunately, phantoms made using the optimized recipe showed dose-rate dependence (14% difference in optical attenuation at the peak dose using electron beam irradiations at 100 and 400 MU min-1). Further testing suggests that the surfactant CTAB is the cause of this dose rate behaviour.

  4. Determination of malachite green and crystal violet in processed fish products.

    PubMed

    Lee, Jun Bae; Kim, Hee Yun; Jang, Young Mi; Song, Ji Young; Woo, Sung Min; Park, Mi Sun; Lee, Hyun Sook; Lee, Soon Kyu; Kim, Meehye

    2010-07-01

    This paper presents analysis of malachite green (MG) and crystal violet (CV) residues in processed fish products. Samples were homogenized and extracted with ammonium acetate buffer and acetonitrile. The extracted residues were partitioned into dichloromethane, in situ oxidized to chromic forms with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, and cleaned up on neutral alumina and propylsulfonic acid cation-exchange solid-phase extraction (SPE) cartridges. MG and CV were determined at 618 and 588 nm using HPLC with a visible detector (LC-VIS) and confirmed by LC-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). The recoveries were as follows: MG (74.8-83.8%), LMG (80.0-88.4%), CV (68.6-73.9%), and LCV (85.5-90.0%). The method modified in this study has been evaluated by application in-house to a survey of 253 processed fish products. As a result of monitoring, MG and CV were positive in one shrimp and one eel sample, respectively. Our results showed that regular monitoring of these antibiotic residues is recommended for protection of public health.

  5. Leuco-crystal-violet micelle gel dosimeters: I. Influence of recipe components and potential sensitizers.

    PubMed

    Nasr, A T; Alexander, K; Schreiner, L J; McAuley, K B

    2015-06-21

    Radiochromic leuco crystal violet (LCV) micelle gel dosimeters are promising three-dimensional radiation dosimeters because of their spatial stability and suitability for optical readout. The effects of surfactant type and surfactant concentration on dose sensitivity of LCV micelle gels are tested, demonstrating that dose sensitivity and initial colour of the gel increases with increasing Triton x-100 (Tx100) concentration. Using Cetyl Trimethyl Ammonium Bromide (CTAB) in place of Tx100 produces gels that are nearly colourless prior to irradiation, but reduces the dose sensitivity. The separate effects of Tri-chloro acetic acid concentration and pH are investigated, revealing that controlling the pH near 3.6 is crucial for achieving high dose sensitivity. The sensitizing effect of chlorinated species on dose sensitivity is tested using 2,2,2-trichloroethanol (TCE), chloroform, and 1,1,1-trichloro-2-methyl-2-propanol hemihydrate. TCE gives the largest improvement in dose sensitivity and is recommended for use in micelle gel dosimeters because it is less volatile and safer to use than chloroform. Preliminary experiments on a new gel containing CTAB as the surfactant and TCE show that this new gel gives a dose sensitivity that is 24% higher than that of previous LCV micelle gels and is nearly colourless prior to irradiation. PMID:26020840

  6. Leuco-crystal-violet micelle gel dosimeters: II. Recipe optimization and testing.

    PubMed

    Nasr, A T; Alexander, K M; Olding, T; Schreiner, L J; McAuley, K B

    2015-06-21

    In this study, recipe optimization of Leuco Crystal Violet (LCV) micelle gels made with the surfactant Cetyl Trimethyl Ammonium Bromide (CTAB) and the chemical sensitizer 2,2,2-trichloroethanol (TCE) was aided by a two-level three-factor designed experiment. The optimized recipe contains 0.75 mM LCV, 17.0 mM CTAB, 120 mM TCE, 25.0 mM tri-chloro acetic acid (TCAA), 4 wt% gelatin and ~96 wt% water. Dose sensitivity of the optimized gel is 1.5 times higher than that of Jordan's standard LCV micelle gel. Spatial integrity of the 3D dose distribution information in 1L phantoms filled with this recipe is maintained for >120 d. Unfortunately, phantoms made using the optimized recipe showed dose-rate dependence (14% difference in optical attenuation at the peak dose using electron beam irradiations at 100 and 400 MU min(-1)). Further testing suggests that the surfactant CTAB is the cause of this dose rate behaviour. PMID:26020119

  7. Adsorption of crystal violet with diatomite earth&carbon by a modification of hydrothermal carbonization process.

    PubMed

    Zhang, Yanzhuo; Li, Jun; Chen, Guanghui; Bian, Wei; Lu, Yun; Li, Wenjing; Zheng, Zhaoming; Cheng, Xiaojie

    2016-01-01

    The high colority and difficulty of decolorization are the most important tasks on printing and dyeing wastewater. This study investigates the ability of diatomite earth&carbon (DE&C) as an adsorbent to removal crystal violet (CV) from aqueous solutions. Fourier transform infrared spectroscopy results indicate the importance of functional groups during the adsorption of CV. The obtained N2 adsorption-desorption isotherm values accord with well IUPAC type II. Our calculations determined a surface area of 73.15 m(2) g(-1) for DE&C and an average pore diameter of 10.56 nm. Equilibrium data of the adsorption process fitted very well to the Langmuir model (R(2) > 0.99). The results of kinetics study showed that the pseudo-second-order model fitted to the experimental data well. The thermodynamic parameters were also evaluated. ΔH° <0, ΔS° > 0 and ΔG° < 0 demonstrated that the adsorption process was spontaneous and exothermic for dye. Furthermore the positive value of ΔS° reflected good affinity of the CV dye. PMID:27003089

  8. Combinatorial fabrication and studies of intense efficient ultraviolet--violet organic light-emitting device arrays

    SciTech Connect

    Zou, L.; Savvate'ev, V.; Booher, J.; Kim, C.-H.; Shinar, J.

    2001-10-01

    Arrays of ultraviolet--violet (indium tin oxide)/[copper phthalocyanine (CuPc)]/[4,4'-bis(9-carbazolyl)biphenyl (CBP)]/[2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4oxadiazole (Bu-PBD)]/CsF/Al organic light-emitting devices, fabricated combinatorially using a sliding shutter technique, are described. Comparison of the OLED electroluminescence and CBP photoluminescence spectra indicates that the emission originates from the bulk of that layer. In arrays of devices in which the thickness of the CuPc and Bu--PBD were varied, but that of CBP was fixed at 50 nm, the optimal radiance R was obtained at CuPc and Bu--PBD thicknesses of 15 and 18 nm, respectively. At 10 mA/cm{sup 2}, R was 0.38 mW/cm{sup 2}, i.e., the external quantum efficiency was 1.25%; R increased to {approx}1.2 mW/cm{sup 2} at 100 mA/cm{sup 2}.

  9. Buried graphene electrodes on GaN-based ultra-violet light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Kim, Byung-Jae; Lee, Chongmin; Mastro, Michael A.; Hite, Jennifer K.; Eddy, Charles R.; Ren, Fan; Pearton, Stephen J.; Kim, Jihyun

    2012-07-01

    We report that the oxidation of graphene-based highly transparent conductive layers to AlGaN/GaN/AlGaN ultra-violet (UV) light-emitting diodes (LEDs) was suppressed by the use of SiNX passivation layers. Although graphene is considered to be an ideal candidate as the transparent conductive layer to UV-LEDs, oxidation of these layers at high operating temperatures has been an issue. The oxidation is initiated at the un-saturated carbon atoms at the edges of the graphene and reduces the UV light intensity and degrades the current-voltage (I-V) characteristics. The oxidation also can occur at defects, including vacancies. However, GaN-based UV-LEDs deposited with SiNX by plasma-enhanced chemical vapor deposition showed minimal degradation of light output intensity and I-V characteristics because the graphene-based UV transparent conductive layers were shielded from the oxygen molecules. This is a simple and effective approach for maintaining the advantages of graphene conducting layers as electrodes on UV-LEDs.

  10. Studies on plant regeneration and somaclonal variation in Saintpaulia ionantha Wendl. (African violet).

    PubMed

    Daud, Norhayati; Taha, Rosna Mat; Hasbullah, Nor Azlina

    2008-05-01

    Efficient plant regeneration of Saintpaulia ionantha (African violet) has been obtained in the present study. MS medium supplemented with 1.0 mg L(-1) IAA and 2.0 mg L(-1) Zeatin resulted in 100% shoot regeneration and induced the highest number of shoots (average 15.0 +/- 0.8 shoots per explant) after being cultured for 8 weeks. The above hormone combination was optimum for shoot regeneration. Most of Saintpaulia ionantha plantlets derived from tissue culture system could be hardened and transferred to the greenhouse conditions with 84.0 +/- 1.6% success rate. However, regenerated plantlets of Saintpaulia ionantha (even after 12-months-old) failed to flower. Morphological characters of regenerated plantlets of Saintpaulia ionantha were observed and compared with in vivo (intact) plants. Regenerated plantlets showed some differences in morphological characters, such as height and leaf size, texture and colour, but the plantlets showed no variation in leaf arrangement and leaf margin. However, the morphological characters of the regenerated plantlets were found to be unstable. PMID:18819532

  11. Carbon deposition on multi-layer mirrors by extreme ultra violet ray irradiation

    NASA Astrophysics Data System (ADS)

    Matsunari, S.; Aoki, T.; Murakami, K.; Gomei, Y.; Terashima, S.; Takase, H.; Tanabe, M.; Watanabe, Y.; Kakutani, Y.; Niibe, M.; Fukuda, Y.

    2007-03-01

    Organic gases cause carbon depositions on the multi-layer mirrors by Extreme Ultra Violet (EUV) light irradiations in EUV lithography tool. The dependences on organic gas species, organic gas pressure and EUV light intensity in the carbon deposition were researched in order to understand this reaction. EUV light was irradiated on a (Si/Mo) multilayer mirror sample injecting organic gas like buthane, buthanol, methyl propionate, hexane, perfluoro octane, decane, decanol, methyl nonanoate, diethyl benzene, dimethyl phthalate and hexadecane. X-ray photoelectron spectroscopy measurements revealed that organic gases with heavier molecule weight or higher boiling temperature caused faster carbon deposition rates. Carbon deposition rates increased linearly with organic gas pressures. Dependence on EUV light intensity was estimated from comparisons between an EUV light profile and carbon distributions on irradiated samples. Carbon deposition rates increased rapidly, but became saturated at higher EUV light intensities. Three chemical reactions, an adsorption, a desorption and a carbon deposition by EUV light irradiation, were taken into account to explain the behavior of the carbon deposition. Electron irradiation on a mirror sample revealed that photoelectrons emitting from the mirror surface played an important role in carbon deposition.

  12. Planar super-oscillatory lens for sub-diffraction optical needles at violet wavelengths.

    PubMed

    Yuan, Guanghui; Rogers, Edward T F; Roy, Tapashree; Adamo, Giorgio; Shen, Zexiang; Zheludev, Nikolay I

    2014-01-01

    Planar optical lenses are fundamental elements of miniaturized photonic devices. However, conventional planar optical lenses are constrained by the diffraction limit in the optical far-field due to the band-limited wavevectors supported by free-space and loss of high-spatial-frequency evanescent components. As inspired by Einstein's radiation 'needle stick', electromagnetic energy can be delivered into an arbitrarily small solid angle. Such sub-diffraction optical needles have been numerically investigated using diffractive optical elements (DOEs) together with specially polarized optical beams, but experimental demonstration is extremely difficult due to the bulky size of DOEs and the required alignment precision. Planar super-oscillatory lenses (SOLs) were proposed to overcome these constraints and demonstrated that sub-diffraction focal spots can actually be formed without any evanescent waves, making far-field, label-free super-resolution imaging possible. Here we extend the super-oscillation concept into the vectorial-field regime to work with circularly polarized light, and experimentally demonstrate, for the first time, a circularly polarized optical needle with sub-diffraction transverse spot size (0.45λ) and axial long depth of focus (DOF) of 15λ using a planar SOL at a violet wavelength of 405 nm. This sub-diffraction circularly polarized optical needle has potential applications in circular dichroism spectroscopy, super-resolution imaging, high-density optical storage, heat-assisted magnetic recording, nano-manufacturing and nano-metrology.

  13. Planar super-oscillatory lens for sub-diffraction optical needles at violet wavelengths

    NASA Astrophysics Data System (ADS)

    Yuan, Guanghui; Rogers, Edward T. F.; Roy, Tapashree; Adamo, Giorgio; Shen, Zexiang; Zheludev, Nikolay I.

    2014-09-01

    Planar optical lenses are fundamental elements of miniaturized photonic devices. However, conventional planar optical lenses are constrained by the diffraction limit in the optical far-field due to the band-limited wavevectors supported by free-space and loss of high-spatial-frequency evanescent components. As inspired by Einstein's radiation `needle stick', electromagnetic energy can be delivered into an arbitrarily small solid angle. Such sub-diffraction optical needles have been numerically investigated using diffractive optical elements (DOEs) together with specially polarized optical beams, but experimental demonstration is extremely difficult due to the bulky size of DOEs and the required alignment precision. Planar super-oscillatory lenses (SOLs) were proposed to overcome these constraints and demonstrated that sub-diffraction focal spots can actually be formed without any evanescent waves, making far-field, label-free super-resolution imaging possible. Here we extend the super-oscillation concept into the vectorial-field regime to work with circularly polarized light, and experimentally demonstrate, for the first time, a circularly polarized optical needle with sub-diffraction transverse spot size (0.45λ) and axial long depth of focus (DOF) of 15λ using a planar SOL at a violet wavelength of 405 nm. This sub-diffraction circularly polarized optical needle has potential applications in circular dichroism spectroscopy, super-resolution imaging, high-density optical storage, heat-assisted magnetic recording, nano-manufacturing and nano-metrology.

  14. Removal of crystal violet from water by magnetically modified activated carbon and nanomagnetic iron oxide.

    PubMed

    Hamidzadeh, Soheila; Torabbeigi, Marzieh; Shahtaheri, Seyed Jamaleddin

    2015-01-01

    Magnetically modified activated carbon, which synthesized by nanomagnetic iron oxide, was used for fast and effective removal of Crystal Violet from aqueous solutions. The scanning electron microscopy (SEM) images of nano-adsorbent showed that the average sizes of adsorbent are less than 100 nm. The various parameters, affecting on adsorption process, were examined including pH and temperature of dye solution, dose of adsorbent, and contact time. Then, thermodynamic parameters of sorption were calculated. Langmuir and Freundlich isotherms were used to fit the resulting data. Adsorption kinetics was consistent with a pseudo second order equation. Thermodynamic parameters of adsorption, ∆H(0), and ∆S(0) were calculated. Also, for further investigations, nano magnetic iron oxides was synthesized and used as adsorbent. Sorption capacities were depending on the temperature varied from 44.7 to 67.1 mg/g and from 12.7 to 16.5 mg/g for magnetically modified activated carbon and nanomagnetic iron oxide, respectively. PMID:25699186

  15. The complete mitochondrial genome of the Violet-spotted reef lobster Enoplometopus debelius (Crustacea, Astacidea, Enoplometopidae).

    PubMed

    Ahn, Dong-Ha; Min, Gi-Sik; Park, Joong-Ki; Kim, Sanghee

    2016-05-01

    The violet-spotted reef lobster Enoplometopus debelius Holthuis, 1983 (Decapoda, Astacidea, Enoplometopidae) is found in the tropical reef areas of the Indo-Pacific region, and is a highly prized and very popular species in the aquarium trade industry. The complete mitochondrial genome of E. debelius has 15,641 base pairs consisting of 13 protein-coding genes, 22 transfer RNAs, 2 ribosomal RNAs, and a control region of 746 bp. The base composition of E. debelius is 36.4% A, 35.3% T, 18.1% C, 10.3% G, and the species has an AT content of 71.7%. The E. debelius mitogenome was found to have a gene arrangement and transcriptional polarity identical to that of the Homarus americanus mitogenome, a representative of the arthropod ground pattern. Here, we present the complete mitogenome sequence of E. debelius, which is the first in the superfamily Enoplometopoidea. These data will provide a useful molecular resource for the phylogenetic study of the infraorder Astacidea/order Decapoda.

  16. Leuco-crystal-violet micelle gel dosimeters: I. Influence of recipe components and potential sensitizers

    NASA Astrophysics Data System (ADS)

    Nasr, A. T.; Alexander, K.; Schreiner, L. J.; McAuley, K. B.

    2015-06-01

    Radiochromic leuco crystal violet (LCV) micelle gel dosimeters are promising three-dimensional radiation dosimeters because of their spatial stability and suitability for optical readout. The effects of surfactant type and surfactant concentration on dose sensitivity of LCV micelle gels are tested, demonstrating that dose sensitivity and initial colour of the gel increases with increasing Triton x-100 (Tx100) concentration. Using Cetyl Trimethyl Ammonium Bromide (CTAB) in place of Tx100 produces gels that are nearly colourless prior to irradiation, but reduces the dose sensitivity. The separate effects of Tri-chloro acetic acid concentration and pH are investigated, revealing that controlling the pH near 3.6 is crucial for achieving high dose sensitivity. The sensitizing effect of chlorinated species on dose sensitivity is tested using 2,2,2-trichloroethanol (TCE), chloroform, and 1,1,1-trichloro-2-methyl-2-propanol hemihydrate. TCE gives the largest improvement in dose sensitivity and is recommended for use in micelle gel dosimeters because it is less volatile and safer to use than chloroform. Preliminary experiments on a new gel containing CTAB as the surfactant and TCE show that this new gel gives a dose sensitivity that is 24% higher than that of previous LCV micelle gels and is nearly colourless prior to irradiation.

  17. Synthesis of CarAlg/MMt nanocomposite hydrogels and adsorption of cationic crystal violet.

    PubMed

    Mahdavinia, Gholam Reza; Aghaie, Huriyeh; Sheykhloie, Hossein; Vardini, Mohammad Taghi; Etemadi, Hossein

    2013-10-15

    CarAlg/MMt nanocomposite hydrogels composed of kappa-carrageenan (Car) and sodium alginate (Alg) biopolymers were synthesized by incorporation of sodium montmorillonite (Na-MMt) nanoclay. Acrylamide (AAm), methylenebisacrylamide (MBA), and ammonium persulfate (APS) were used as monomer, crosslinker, and initiator, respectively. The structure and morphology of nanocomposites were characterized by XRD, SEM, and TEM techniques. The XRD results showed exfoliated MMt nanoclay and exfoliation of MMt was confirmed by TEM graph. The resulting nanocomposites were evaluated to remove cationic crystal violet (CV) dye from water. According to data, the adsorption capacity of nanocomposites was enhanced as the clay content was increased. The experimental data were analyzed according to both Langmuir and Freundlich models and experimental maximum adsorption capacity was obtained 88.8 mg g(-1). By studying the effect of pH on the dye adsorption capacity of nanocomposites, it was revealed that the adsorption capacity of nanocomposites was enhanced at acidic pHs as the Na-MMt nanoclay and kappa-carrageenan components were increased. PMID:23987355

  18. New Twist on an Old Favorite: Gentian Violet and Methylene Blue Antibacterial Foams

    PubMed Central

    Edwards, Karen

    2016-01-01

    Significance: Absorptive antibacterial dressings that assist in controlling bioburden without risks of cytotoxicity or residual absorption can be effectively used for prolonged periods throughout the wound healing continuum. Recent Advances: Until recently, gentian violet and methylene blue (GV/MB) antibacterial dressings have been commercially available only in polyvinyl alcohol (PVA) foam; polyurethane (PU) foam bonded with GV and MB with thin film backing is now commercially available. GV/MB PU foam does not require hydration or a necessary secondary dressing. GV/MB PVA and PU foam dressings were recently granted FDA clearance as antibacterial dressings, as opposed to bacteriostatic dressings as previously classified. Within the class of antibacterial dressings, GV/MB foam dressings are of lower cost alternative to silver- or iodine-based antibacterial dressings with no risk of absorption of any of the foam components into the tissues. Critical Issues: Control of wound bioburden levels by antibacterial agents and absorption of excess exudate are crucial in preventing infections that drastically increase the price of wound care. Use of GV/MB dressings may improve wound healing outcomes and decrease overall costs through super absorption, promotion of autolytic debridement, bioburden reduction, ease of use, and decreased dressing change frequency. Future Directions: Evolution in resistant bacterial strains will drive continual changes in advanced wound care products. Demand will increase for economically priced, versatile wound care dressings that assist in debridement, maintain a moist wound environment, absorb and trap bacterial debris, and decrease dressing change frequency. PMID:26858911

  19. Ultra-violet and visible absorption characterization of explosives by differential reflectometry

    NASA Astrophysics Data System (ADS)

    Dubroca, Thierry; Moyant, Kyle; Hummel, Rolf E.

    2013-03-01

    This study presents some optical properties of TNT (2,4,6-trinitrotoluene), RDX, HMX and tetryl, specifically their absorption spectra as a function of concentration in various solvents in the ultraviolet and visible portion of the electromagnetic spectrum. We utilize a standoff explosives detection method, called differential reflectometry (DR). TNT was diluted in six different solvents (acetone, acetonitrile, ethanol, ethyl acetate, methanol, and toluene), which allowed for a direct comparison of absorption features over a wide range of concentrations. A line-shape analysis was adopted with great accuracy (R2 > 0.99) to model the absorption features of TNT in differential reflectivity spectra. We observed a blue shift in the pertinent absorption band with decreasing TNT concentration for all solvents. Moreover, using this technique, it was found that for all utilized solvents the concentration of TNT as well as of RDX, HMX, and tetryl, measured as a function of the transition wavelength of the ultra-violet absorption edge in differential reflectivity spectra shows three distinct regions. A model is presented to explain this behavior which is based on intermolecular hydrogen bonding of explosives molecules with themselves (or lack thereof) at different concentrations. Other intermolecular forces such as dipole-dipole interactions, London dispersion forces and π-stacking contribute to slight variations in the resulting spectra, which were determined to be rather insignificant in comparison to hydrogen bonding. The results are aimed towards a better understanding of the DR spectra of explosives energetic materials.

  20. Effect of different EBL structures on deep violet InGaN laser diodes performance

    NASA Astrophysics Data System (ADS)

    Alahyarizadeh, Gh.; Amirhoseiny, M.; Hassan, Z.

    2016-01-01

    Some specific designs on band structure near the active region, including the modifications of the material and thickness of the electron blocking layer (EBL), in the deep violet InGaN laser diodes (LDs) are investigated numerically with the ISE TCAD software. The analyses focus on electron and hole carrier injection efficiency, carrier distributions, electron leakage, and radiative recombination, subsequently, optical material gain, and optical intensity. The results indicate that for the ternary AlGaN EBL, the lowest threshold current and the highest output power, slope efficiency, and DQE have been obtained for the 15 nm EBL thickness with 0.22 Al mole fraction. In addition, a comparative study has been conducted on the performance characteristics of the LD structures with a ternary AlGaN EBL and a quaternary AlInGaN EBL with an output emission wavelength at 390 nm. The simulation results showed that the using quaternary AlInGaN EBL effectively improves the LD performance characteristics.

  1. Blue-violet photoluminescence of 4-isopropyl-pyridine hydroxide crystals.

    PubMed

    Vaganova, Evgenia; Wachtel, Ellen; Leitus, Gregory; Danovich, David; Popov, Inna; Dubnikova, Faina; Yitzchaik, Shlomo

    2014-05-01

    There is continuing interest in determining essential structural features of polymer gels, which display photoelectric and/or thermoelectric behavior. One such gel is the blend, poly(4-vinylpyridine-co-butyl methacrylate)/poly(4-vinylpyridine), dissolved in liquid pyridine. Following extended aeration of a three-component mixture, which serves as a model for the gel side chain interactions, crystallization of a new molecule, 4-isopropylpyridine hydroxide (IPPOH), occurs. X-ray diffraction, DFT modeling, and spectroscopy were used to determine the structural, electronic, and luminescent properties of the crystal. The crystal structure reveals molecules forming head-to-tail, hydrogen-bonded chains without base stacking or marked interchain interaction. The molecular chains are characterized by moderately long-lived, blue-violet luminescence excited in the near-UV. Because these photoluminescent properties resemble those of the gel from which the crystals are derived, we may posit similar structural features in the gel for which direct structural analysis is not available.

  2. Biodegradation of Basic Violet 3 by Candida krusei isolated from textile wastewater.

    PubMed

    Deivasigamani, Charumathi; Das, Nilanjana

    2011-11-01

    Basic Violet 3 (BV) belongs to the most important group of synthetic colorants and is used extensively in textile industries. It is considered as xenobiotic compound which is recalcitrant to biodegradation. As Candida krusei could not use BV as sole carbon source, experiments were conducted to study the effect of cosubstrates on decolorization of BV in semi synthetic medium using glucose, sucrose, lactose, maltose, yeast extract, peptone, urea and ammonium sulphate. Maximum decolorization (74%) was observed in media supplemented with sucrose. Use of sugarcane bagasse extract as sole nutrient source showed 100% decolorization of BV within 24 h under optimized condition. UV-visible, FTIR spectral analysis and HPLC analysis confirmed the biodegradation of BV. Six degradation products were isolated and identified. We propose the biodegradation pathway for BV which occurs via stepwise reduction and demethylation process to yield mono-, di-, tri-, tetra-, penta- and hexa-demethylated BV species which was degraded completely. The study of the enzymes responsible for decolorization showed the activities of lignin peroxidase, lacasse, tyrosinase, NADH-DCIP reductase, MG reductase and azoreductase in cells before and after decolorization. A significant increase in activities of NADH-DCIP reductase and laccase was observed in the cells after decolorization. The yeast C. krusei could show the ability to decolorize the textile dye BV using inexpensive source like sugarcane bagasse extract for decolorization.

  3. Adsorption of crystal violet with diatomite earth&carbon by a modification of hydrothermal carbonization process.

    PubMed

    Zhang, Yanzhuo; Li, Jun; Chen, Guanghui; Bian, Wei; Lu, Yun; Li, Wenjing; Zheng, Zhaoming; Cheng, Xiaojie

    2016-01-01

    The high colority and difficulty of decolorization are the most important tasks on printing and dyeing wastewater. This study investigates the ability of diatomite earth&carbon (DE&C) as an adsorbent to removal crystal violet (CV) from aqueous solutions. Fourier transform infrared spectroscopy results indicate the importance of functional groups during the adsorption of CV. The obtained N2 adsorption-desorption isotherm values accord with well IUPAC type II. Our calculations determined a surface area of 73.15 m(2) g(-1) for DE&C and an average pore diameter of 10.56 nm. Equilibrium data of the adsorption process fitted very well to the Langmuir model (R(2) > 0.99). The results of kinetics study showed that the pseudo-second-order model fitted to the experimental data well. The thermodynamic parameters were also evaluated. ΔH° <0, ΔS° > 0 and ΔG° < 0 demonstrated that the adsorption process was spontaneous and exothermic for dye. Furthermore the positive value of ΔS° reflected good affinity of the CV dye.

  4. The complete mitochondrial genome of the Violet-spotted reef lobster Enoplometopus debelius (Crustacea, Astacidea, Enoplometopidae).

    PubMed

    Ahn, Dong-Ha; Min, Gi-Sik; Park, Joong-Ki; Kim, Sanghee

    2016-05-01

    The violet-spotted reef lobster Enoplometopus debelius Holthuis, 1983 (Decapoda, Astacidea, Enoplometopidae) is found in the tropical reef areas of the Indo-Pacific region, and is a highly prized and very popular species in the aquarium trade industry. The complete mitochondrial genome of E. debelius has 15,641 base pairs consisting of 13 protein-coding genes, 22 transfer RNAs, 2 ribosomal RNAs, and a control region of 746 bp. The base composition of E. debelius is 36.4% A, 35.3% T, 18.1% C, 10.3% G, and the species has an AT content of 71.7%. The E. debelius mitogenome was found to have a gene arrangement and transcriptional polarity identical to that of the Homarus americanus mitogenome, a representative of the arthropod ground pattern. Here, we present the complete mitogenome sequence of E. debelius, which is the first in the superfamily Enoplometopoidea. These data will provide a useful molecular resource for the phylogenetic study of the infraorder Astacidea/order Decapoda. PMID:25264838

  5. Ultra-violet and visible absorption characterization of explosives by differential reflectometry.

    PubMed

    Dubroca, Thierry; Moyant, Kyle; Hummel, Rolf E

    2013-03-15

    This study presents some optical properties of TNT (2,4,6-trinitrotoluene), RDX, HMX and tetryl, specifically their absorption spectra as a function of concentration in various solvents in the ultraviolet and visible portion of the electromagnetic spectrum. We utilize a standoff explosives detection method, called differential reflectometry (DR). TNT was diluted in six different solvents (acetone, acetonitrile, ethanol, ethyl acetate, methanol, and toluene), which allowed for a direct comparison of absorption features over a wide range of concentrations. A line-shape analysis was adopted with great accuracy (R(2)>0.99) to model the absorption features of TNT in differential reflectivity spectra. We observed a blue shift in the pertinent absorption band with decreasing TNT concentration for all solvents. Moreover, using this technique, it was found that for all utilized solvents the concentration of TNT as well as of RDX, HMX, and tetryl, measured as a function of the transition wavelength of the ultra-violet absorption edge in differential reflectivity spectra shows three distinct regions. A model is presented to explain this behavior which is based on intermolecular hydrogen bonding of explosives molecules with themselves (or lack thereof) at different concentrations. Other intermolecular forces such as dipole-dipole interactions, London dispersion forces and π-stacking contribute to slight variations in the resulting spectra, which were determined to be rather insignificant in comparison to hydrogen bonding. The results are aimed towards a better understanding of the DR spectra of explosives energetic materials.

  6. Ampliative medicament allergy: concomitant sensitivity to multiple medicaments including yellow soft paraffin, white soft paraffin, gentian violet and Span 20.

    PubMed

    Lawrence, C M; Smith, A G

    1982-07-01

    A patient developed multiple rare medicament contact allergies including sensitivities to gentian violet, yellow and white soft paraffin, and Span 20 (sorbitan monolaurate). Nickel sensitivity antedated these medicament allergies. The possibility that nickel sensitivity is a marker of predilection to develop multiple medicament allergies was tested. We were unable to demonstrate an increased incidence of nickel sensitivity in a group of patients with 2 or more medicament allergies.

  7. Substituent effects in nitro derivatives of carbazoles investigated by comparison of low-temperature crystallographic studies with density functional theory (DFT) calculations.

    PubMed

    Gajda, Katarzyna; Zarychta, Bartosz; Kopka, Katarzyna; Daszkiewicz, Zdzisław; Ejsmont, Krzysztof

    2014-10-01

    The crystal structure of 9H-carbazole, C12H9N, (I), has been redetermined at low temperature for use as a reference structure in a comparative study with the structures of 1-nitro-9H-carbazole, C12H8N2O2, (II), and 9-nitrocarbazole, C12H8N2O2, (III). The molecule of (I) has crystallographically imposed mirror symmetry (Z' = 0.5). All three solid-state structures are slightly nonplanar, the dihedral angles between the planes of the arene and pyrrole rings ranging from 0.40 (7)° in (III) to 1.82 (18)° in (II). Nevertheless, a density functional theory (DFT) study predicts completely planar conformations for the isolated molecules. To estimate the influence of nitro-group substitution on aromaticity, the HOMA (harmonic oscillator model of aromaticity) descriptor of π-electron delocalization has been calculated in each case. The HOMA indices for the isolated and solid-state molecules are relatively consistent and decrease in value for aromatic rings that are substituted with a π-electron-withdrawing nitro group. Substitution of the arene ring influences the π-electron delocalization in the ring only weakly, showing strong resistance to a perturbation of its geometry, contrary to what is observed for nitro substitution of the five-membered heterocyclic pyrrole ring. In (II), the molecules are arranged in near-planar dimers connected to each other by strong N-H···O hydrogen bonds that stack parallel to the crystallographic b axis. A similar stacking arrangement is observed in (III), although here the stacked structure is formed by stand-alone molecules.

  8. Photophysics and non-linear absorption of Au(I) and Pt(II) acetylide complexes of a thienyl-carbazole chromophore.

    PubMed

    Goswami, Subhadip; Wicks, Geoffrey; Rebane, Aleksander; Schanze, Kirk S

    2014-12-21

    In order to understand the photophysics and non-linear optical properties of carbazole containing π-conjugated oligomers of the type ET-Cbz-TE (E = ethynylene, T = 2,5-thienylene, Cbz = 3,6-carbazole), a detailed investigation was carried out on a series of oligomers that feature Au(i) or Pt(ii) acetylide "end groups", as well as a Pt(ii)-acetylide linked polymer (CBZ-Au-1 and CBZ-Pt-1, CBZ-Poly-Pt). These organometallic chromophores were characterized by UV-visible absorption and variable temperature photoluminescence spectroscopy, nanosecond transient absorption spectroscopy, open aperture nanosecond z-scan and two photon absorption (2PA) spectroscopy. The Au(i) and Pt(ii) oligomers and polymer exhibit weak fluorescence in fluid solution at room temperature. Efficient phosphorescence is observed from the Pt(ii) systems below 150 K in a solvent glass; however, the Au(i) oligomer exhibits only weak phosphorescence at 77 K. Taken together, the emission results indicate that the intersystem crossing efficiency for the Pt(ii) chromophores is greater than for the Au(i) oligomer. Nonetheless, nanosecond transient absorption indicates that direct excitation affords moderately long-lived triplet states for all of the chromophores. Open aperture z-scan measurement shows effective optical attenuation can be achieved by using these materials. The 2PA cross section in the degenerate S0→S1 transition region was in the range 10-100 GM, and increased monotonically toward shorter wavelengths, reaching 800-1000 GM at 550 nm.

  9. Experimental and DFT studies on the vibrational and electronic spectra of 9-p-tolyl-9H-carbazole-3-carbaldehyde.

    PubMed

    Wang, Yiwei; Zhang, Yu; Ni, Haiwei; Meng, Nana; Ma, Kuirong; Zhao, Jianying; Zhu, Dunru

    2015-01-25

    The compound 9-p-tolyl-9H-carbazole-3-carbaldehyde (HCCD) was synthesized and characterized by X-ray diffraction, FT-IR, FT-Raman and UV-Vis spectra. The X-ray diffraction study showed that HCCD has a Z-configuration. The benzene ring including methyl is twisted from the mean plane of the carbazole group by 59.7(3)°, which is comparable with the calculated result 65° for B3LYP/6-311++G(d, p) method. Vibrational spectra and electronic spectra measurements were made for the compound. Optimized geometrical structure and harmonic vibrational frequencies were computed with B-based DFT (BLYP, B3LYP and cam-B3LYP) methods, and WB-based DFT (WB97, WB97X and WB97XD) methods and ab initio RHF method using 6-311++G(d, p) basis set. Assignments of the observed spectra were proposed. The equilibrium geometries computed by all of the methods were compared with X-ray diffraction results. The absorption spectra of the title compound were computed both in gas phase and in DMF solution using TD-(cam)B3LYP/6-311++G(d, p) and PCM-(cam)B3LYP/6-311++G(d, p) approaches, respectively. The calculated results provide good descriptions of the bands maxima in the observed electronic spectrum. Temperature dependence of thermodynamic parameters in the range of 100-1000 K was determined. The natural atomic hybrids were calculated and discussed.

  10. Isolation and Characterization of Paracoccus sp. GSM2 Capable of Degrading Textile Azo Dye Reactive Violet 5

    PubMed Central

    Bheemaraddi, Mallikarjun C.; Shivannavar, Channappa T.; Gaddad, Subhashchandra M.

    2014-01-01

    A potential bacterial strain GSM2, capable of degrading an azo dye Reactive Violet 5 as a sole source of carbon, was isolated from textile mill effluent from Solapur, India. The 16S rDNA sequence and phenotypic characteristics indicated an isolated organism as Paracoccus sp. GSM2. This strain exhibited complete decolorization of Reactive Violet 5 (100 mg/L) within 16 h, while maximally it could decolorize 800 mg/L of dye within 38 h with 73% decolorization under static condition. For color removal, the most suitable pH and temperature were pH 6.0–9.0 and 25–40°C, respectively. The isolate was able to decolorize more than 70% of five structurally different azo dyes within 38 h. The isolate is salt tolerant as it can bring out more than 90% decolorization up to a salt concentration of 2% (w/v). UV-Visible absorption spectra before and after decolorization suggested that decolorization was due to biodegradation and was further confirmed by FT-IR spectroscopy. Overall results indicate the effectiveness of the strain GSM2 explored for the treatment of textile industry effluents containing various azo dyes. To our knowledge, this could be the first report on biodegradation of Reactive Violet 5 by Paracoccus sp. GSM2. PMID:24883397

  11. Brain transcriptome of the violet-eared waxbill Uraeginthus granatina and recent evolution in the songbird genome

    PubMed Central

    Balakrishnan, Christopher N.; Chapus, Charles; Brewer, Michael S.; Clayton, David F.

    2013-01-01

    Songbirds are important models for the study of social behaviour and communication. To complement the recent genome sequencing of the domesticated zebra finch, we sequenced the brain transcriptome of a closely related songbird species, the violet-eared waxbill (Uraeginthus granatina). Both the zebra finch and violet-eared waxbill are members of the family Estrildidae, but differ markedly in their social behaviour. Using Roche 454 RNA sequencing, we generated an assembly and annotation of 11 084 waxbill orthologues of 17 475 zebra finch genes (64%), with an average transcript length of 1555 bp. We also identified 5985 single nucleotide polymorphisms (SNPs) of potential utility for future population genomic studies. Comparing the two species, we found evidence for rapid protein evolution (ω) and low polymorphism of the avian Z sex chromosome, consistent with prior studies of more divergent avian species. An intriguing outlier was putative chromosome 4A, which showed a high density of SNPs and low evolutionary rate relative to other chromosomes. Genome-wide ω was identical in zebra finch and violet-eared waxbill lineages, suggesting a similar demographic history with efficient purifying natural selection. Further comparisons of these and other estrildid finches may provide insights into the evolutionary neurogenomics of social behaviour. PMID:24004662

  12. Quenching of fluorescence by crystal violet and its use to differentiate between surface-bound and internalized bacteria

    NASA Astrophysics Data System (ADS)

    Mathew, S.; Lim, Y. C.; Kishen, A.

    2008-06-01

    Phagocytosis is a complex process involving attachment, ingestion and intracellular processing of bacteria by phagocytes. A great difficulty in the evaluation of this process is to differentiate between attachment of the particles to the cell surface and internalization of the particles by the cells. Various techniques have been used to differentiate internalized and surface-attached bacteria in cultured cells, but only a few permit differentiations between surface-bound and internalized bacteria. In this study the quenching of fluorescence by crystal violet on acridine orange stained bacterial biofilm and planktonic bacterial cells is used to differentiate between surface-bound and internalized bacteria within macrophages. Method: One week old Enterococcus faecalis biofilm was grown on perspex and glass substrates in All-Culture medium (nutrient-rich condition) and phosphate buffered saline (nutrient-deprived condition). As model systems, human monocytic (THP-1) and histiocytic (U937) cell lines were used. These cell lines were incubated with the biofilm bacteria for 4 hrs in CO II incubator at 37 °C. The cells and bacteria were stained with acridine orange and quenched with crystal violet to distinguish between surface-bound and internalized bacteria. Results: The presence of green-fluorescing internalized bacteria was detected within the macrophages under the planktonic, nutrient-rich and nutrient-deprived biofilm conditions. All infecting bacteria take up acridine orange and fluoresced green, crystal violet quenched the fluorescence of extra-cellular adhering bacteria so that only fluorescent intracellular bacteria would be visible under fluorescent light microscopy.

  13. Intense, stable and excitation wavelength-independent photoluminescence emission in the blue-violet region from phosphorene quantum dots.

    PubMed

    Ge, Shuaipeng; Zhang, Lisheng; Wang, Peijie; Fang, Yan

    2016-01-01

    Nanoscale phosphorene quantum dots (PQDs) with few-layer structures were fabricated by pulsed laser ablation of a bulk black phosphorus target in diethyl ether. An intense and stable photoluminescence (PL) emission of the PQDs in the blue-violet wavelength region is clearly observed for the first time, which is attributed to electronic transitions from the lowest unoccupied molecular orbital (LUMO) to the highest occupied molecular orbital (HOMO) and occupied molecular orbitals below the HOMO (H-1, H-2), respectively. Surprisingly, the PL emission peak positions of the PQDs are not red-shifted with progressively longer excitation wavelengths, which is in contrast to the cases of graphene and molybdenum disulphide quantum dots. This excitation wavelength-independence is derived from the saturated passivation on the periphery and surfaces of the PQDs by large numbers of electron-donating functional groups which cause the electron density on the PQDs to be dramatically increased and the band gap to be insensitive to the quantum size effect in the PQDs. This work suggests that PQDs with intense, stable and excitation wavelength-independent PL emission in the blue-violet region have a potential application as semiconductor-based blue-violet light irradiation sources. PMID:27265198

  14. Intense, stable and excitation wavelength-independent photoluminescence emission in the blue-violet region from phosphorene quantum dots

    PubMed Central

    Ge, Shuaipeng; Zhang, Lisheng; Wang, Peijie; Fang, Yan

    2016-01-01

    Nanoscale phosphorene quantum dots (PQDs) with few-layer structures were fabricated by pulsed laser ablation of a bulk black phosphorus target in diethyl ether. An intense and stable photoluminescence (PL) emission of the PQDs in the blue-violet wavelength region is clearly observed for the first time, which is attributed to electronic transitions from the lowest unoccupied molecular orbital (LUMO) to the highest occupied molecular orbital (HOMO) and occupied molecular orbitals below the HOMO (H-1, H-2), respectively. Surprisingly, the PL emission peak positions of the PQDs are not red-shifted with progressively longer excitation wavelengths, which is in contrast to the cases of graphene and molybdenum disulphide quantum dots. This excitation wavelength-independence is derived from the saturated passivation on the periphery and surfaces of the PQDs by large numbers of electron-donating functional groups which cause the electron density on the PQDs to be dramatically increased and the band gap to be insensitive to the quantum size effect in the PQDs. This work suggests that PQDs with intense, stable and excitation wavelength-independent PL emission in the blue-violet region have a potential application as semiconductor-based blue-violet light irradiation sources. PMID:27265198

  15. Isolation and characterization of Paracoccus sp. GSM2 capable of degrading textile azo dye Reactive Violet 5.

    PubMed

    Bheemaraddi, Mallikarjun C; Patil, Santosh; Shivannavar, Channappa T; Gaddad, Subhashchandra M

    2014-01-01

    A potential bacterial strain GSM2, capable of degrading an azo dye Reactive Violet 5 as a sole source of carbon, was isolated from textile mill effluent from Solapur, India. The 16S rDNA sequence and phenotypic characteristics indicated an isolated organism as Paracoccus sp. GSM2. This strain exhibited complete decolorization of Reactive Violet 5 (100 mg/L) within 16 h, while maximally it could decolorize 800 mg/L of dye within 38 h with 73% decolorization under static condition. For color removal, the most suitable pH and temperature were pH 6.0-9.0 and 25-40 °C, respectively. The isolate was able to decolorize more than 70% of five structurally different azo dyes within 38 h. The isolate is salt tolerant as it can bring out more than 90% decolorization up to a salt concentration of 2% (w/v). UV-Visible absorption spectra before and after decolorization suggested that decolorization was due to biodegradation and was further confirmed by FT-IR spectroscopy. Overall results indicate the effectiveness of the strain GSM2 explored for the treatment of textile industry effluents containing various azo dyes. To our knowledge, this could be the first report on biodegradation of Reactive Violet 5 by Paracoccus sp. GSM2.

  16. Intense, stable and excitation wavelength-independent photoluminescence emission in the blue-violet region from phosphorene quantum dots

    NASA Astrophysics Data System (ADS)

    Ge, Shuaipeng; Zhang, Lisheng; Wang, Peijie; Fang, Yan

    2016-06-01

    Nanoscale phosphorene quantum dots (PQDs) with few-layer structures were fabricated by pulsed laser ablation of a bulk black phosphorus target in diethyl ether. An intense and stable photoluminescence (PL) emission of the PQDs in the blue-violet wavelength region is clearly observed for the first time, which is attributed to electronic transitions from the lowest unoccupied molecular orbital (LUMO) to the highest occupied molecular orbital (HOMO) and occupied molecular orbitals below the HOMO (H-1, H-2), respectively. Surprisingly, the PL emission peak positions of the PQDs are not red-shifted with progressively longer excitation wavelengths, which is in contrast to the cases of graphene and molybdenum disulphide quantum dots. This excitation wavelength-independence is derived from the saturated passivation on the periphery and surfaces of the PQDs by large numbers of electron-donating functional groups which cause the electron density on the PQDs to be dramatically increased and the band gap to be insensitive to the quantum size effect in the PQDs. This work suggests that PQDs with intense, stable and excitation wavelength-independent PL emission in the blue-violet region have a potential application as semiconductor-based blue-violet light irradiation sources.

  17. Intense, stable and excitation wavelength-independent photoluminescence emission in the blue-violet region from phosphorene quantum dots.

    PubMed

    Ge, Shuaipeng; Zhang, Lisheng; Wang, Peijie; Fang, Yan

    2016-06-06

    Nanoscale phosphorene quantum dots (PQDs) with few-layer structures were fabricated by pulsed laser ablation of a bulk black phosphorus target in diethyl ether. An intense and stable photoluminescence (PL) emission of the PQDs in the blue-violet wavelength region is clearly observed for the first time, which is attributed to electronic transitions from the lowest unoccupied molecular orbital (LUMO) to the highest occupied molecular orbital (HOMO) and occupied molecular orbitals below the HOMO (H-1, H-2), respectively. Surprisingly, the PL emission peak positions of the PQDs are not red-shifted with progressively longer excitation wavelengths, which is in contrast to the cases of graphene and molybdenum disulphide quantum dots. This excitation wavelength-independence is derived from the saturated passivation on the periphery and surfaces of the PQDs by large numbers of electron-donating functional groups which cause the electron density on the PQDs to be dramatically increased and the band gap to be insensitive to the quantum size effect in the PQDs. This work suggests that PQDs with intense, stable and excitation wavelength-independent PL emission in the blue-violet region have a potential application as semiconductor-based blue-violet light irradiation sources.

  18. 75 FR 79339 - Notice of Scope Rulings

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-20

    ... Rulings, 75 FR 52311 (August 25, 2010). This current notice covers all scope rulings and anticircumvention...-892: Carbazole Violet Pigment 23 From India and the People's Republic of China Requestor: Nation Ford Chemical Co., and Sun Chemical Corp.; whether finished carbazole violet pigment exported from Japan...

  19. 75 FR 52311 - Notice of Scope Rulings

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-25

    ... Rulings, 75 FR 38081 (July 1, 2010). This current notice covers all scope rulings and anticircumvention...-570-892: Carbazole Violet Pigment 23 from India and the People's Republic of China. Requestor: Nation Ford Chemical Co., and Sun Chemical Corp.; whether finished carbazole violet pigment exported...

  20. Solar-energy production and energy-efficient lighting: photovoltaic devices and white-light-emitting diodes using poly(2,7-fluorene), poly(2,7-carbazole), and poly(2,7-dibenzosilole) derivatives.

    PubMed

    Beaupré, Serge; Boudreault, Pierre-Luc T; Leclerc, Mario

    2010-02-23

    World energy needs grow each year. To address global warming and climate changes the search for renewable energy sources with limited greenhouse gas emissions and the development of energy-efficient lighting devices are underway. This Review reports recent progress made in the synthesis and characterization of conjugated polymers based on bridged phenylenes, namely, poly(2,7-fluorene)s, poly(2,7-carbazole)s, and poly(2,7-dibenzosilole)s, for applications in solar cells and white-light-emitting diodes. The main strategies and remaining challenges in the development of reliable and low-cost renewable sources of energy and energy-saving lighting devices are discussed.

  1. An LED Approach for Measuring the Photocatalytic Breakdown of Crystal Violet Dye

    NASA Technical Reports Server (NTRS)

    Ryan, Robert E.; Underwood, Lauren W.; ONeal, Duane; Pagnutti, Mary; Davis, Bruce A.

    2009-01-01

    A simple technique to assess the reactivity of photocatalytic coatings sprayed onto transmissive glass surfaces was developed. This new method uses ultraviolet (UV) gallium nitride (GaN) light-emitting diodes (LEDs) to drive a photocatalytic reaction (the photocatalytic breakdown of a UV-resistant dye applied to a surface coated with the semiconductor titanium dioxide); and then a combination of a stabilized white light LED and a spectrometer to track the dye degradation as a function of time. Simple, standardized evaluation techniques that assess photocatalytic materials over a variety of environmental conditions, including illumination level, are not generally available and are greatly needed prior to in situ application of photocatalytic technologies. To date, much research pertaining to this aspect of photocatalysis has been limited and has focused primarily on laboratory experiments using mercury lamps. Mercury lamp illumination levels are difficult to control over large ranges and are temporally modulated by line power, limiting their use in helping to understand and predict how photocatalytic materials will behave in natural environmental settings and conditions. The methodology described here, using steady-state LEDs and time series spectroradiometric techniques, is a novel approach to explore the effect of UV light on the photocatalytic degradation of a UV resistant dye (crystal violet). GaN UV LED arrays, centered around 365 nm with an adjustable DC power supply, are used to create a small, spatially uniform light field where the steady state light level can be varied over three to four orders of magnitude. For this study, a set of glass microscope slides was custom coated with a thinly sprayed layer of photocatalytic titanium dioxide. Crystal violet was then applied to these titanium-dioxide coated slides and to uncoated control slides. The slides were then illuminated at various light levels from the dye side of the slide by the UV LED array. To monitor

  2. Ion pairs of crystal violet in sodium bis(2-ethylhexyl)sulfosuccinate reverse micelles.

    PubMed

    Oliveira, Carla S; Bastos, Erick L; Duarte, Evandro L; Itri, Rosangela; Baptista, Mauricio S

    2006-10-10

    The interfacial localization and the ion pair formation of the positively charged dye crystal violet (CV) in sodium bis(2-ethylhexyl)sulfosuccinate reverse micelles (AOT RMs) were studied by several structural and spectroscopic techniques and by quantum chemical calculations. The size and shape of the AOT RMs in the presence of CV were investigated by small-angle X-ray scattering, showing that CV does not significantly change the RM structure. CV localization as a function of the water to surfactant molar ratio (w(0)) was characterized by H(1) and (13)C NMR, indicating the close proximity of CV to the sulfosuccinate group of AOT at small and large w(0) values. These results were confirmed by calculation of magnetic shielding constants using the gauge-independent atomic orbital method with the HF/6-31G(d) basis set. Two different types of ion pairs between AOT and CV, i.e., contact ion pair (CIPs) and solvent-separated ion pair (SSIPs), were characterized by UV-vis spectroscopy and quantum chemical calculations using the semiempirical ZINDO-CI method. In nonpolar isotropic solvents CIPs are formed with an association constant (K(ASSOC)) of 2 x 10(4) mol(-1) L in isooctane and 750 mol(-1) L in chloroform. In AOT RMs at low w(0), CV-AOT CIPs are also formed. By increasing w(0), there is a sharp decrease in the CIP association free energy, and SSIPs are formed. (CV(+))(H(2)O)(AOT(-)) SSIPs are stable in the AOT RM up to the largest w(0) tested (w(0) = 33). PMID:17014109

  3. Effects of sonochemical parameters and inorganic ions during the sonochemical degradation of crystal violet in water.

    PubMed

    Guzman-Duque, Fernando; Pétrier, Christian; Pulgarin, Cesar; Peñuela, Gustavo; Torres-Palma, Ricardo A

    2011-01-01

    This work deals with the ultrasonic degradation (800 kHz) of crystal violet (CV) under different experimental conditions. The effects of saturating gas (argon, carbon dioxide and air), CV concentration (2.45-1225 μmol L(-1)), pH (3-9) and power (20-80 W) were evaluated. The best performances were obtained at 80 W with argon as a saturating gas. The pH had no significant effect. The influence of several water matrices containing anions (chloride, sulphate and bicarbonate) and cations (Fe(2+)) on the sonolytic degradation of CV was also investigated. Significant differences were not observed with the presence of chloride and sulphate. However, at relatively low pollutant concentration (2.45 μmol L(-1)) bicarbonate showed a particular effect: a high bicarbonate concentration (350 mmol L(-1)) produced a detrimental effect, while a low bicarbonate concentration (3 mmol L(-1)) increased the efficiency of the process. The presence of Fe(2+) (1 mmol L(-1)) also increased the CV (49 μmol L(-1)) degradation by 32% after 180 min. Analyses of intermediates by GC-MS led to the identification of several sonochemical by-products: N,N-dimethylaminobenzene, 4-(N,N-dimethylamino)-4'-(N',N'-dimethylamino)benzophenone, and N,N,N',N'-tetramethyl-4,4'-diaminodiphenylmethane. The presence of these aromatic structures showed that the main ultrasonic CV degradation pathway is linked to the reaction with *OH radicals. At the end of the treatment, these early products were converted into biodegradable organic by-products which could be easily treated in a subsequent biological treatment. PMID:20797896

  4. Adsorption dynamics of methyl violet onto granulated mesoporous carbon: Facile synthesis and adsorption kinetics.

    PubMed

    Kim, Yohan; Bae, Jiyeol; Park, Hosik; Suh, Jeong-Kwon; You, Young-Woo; Choi, Heechul

    2016-09-15

    A new and facile one-step synthesis method for preparing granulated mesoporous carbon (GMC) with three-dimensional spherical mesoporous symmetry is prepared to remove large molecular weight organic compounds in aqueous phase. GMC is synthesized in a single step using as-synthesized mesoporous carbon particles and organic binders through a simple and economical synthesis approach involving a simultaneous calcination and carbonization process. Characterization results obtained from SEM, XRD, as well as surface and porosity analysis indicate that the synthesized GMC has similar physical properties to those of the powdered mesoporous carbon and maintains the Brunauer-Emmett-Teller (BET) surface area and pore volume because the new synthesis method prevents the collapse of the pores during the granulation process. Batch adsorption experiments revealed GMC showed a substantial adsorption capacity (202.8 mg/g) for the removal of methyl violet as a target large molecular contaminant in aqueous phase. The mechanisms and dynamics modeling of GMC adsorption were also fully examined, which revealed that surface diffusion was rate limiting step on adsorption process of GMC. Adsorption kinetics of GMC enables 3 times faster than that of granular activated carbon in terms of surface diffusion coefficient. This is the first study, to the best of our knowledge, to synthesize GMC as an adsorbent for water purification by using facile granulation method and to investigate the adsorption kinetics and characteristics of GMC. This study introduces a new and simple method for the synthesis of GMC and reveals its adsorption characteristics for large molecular compounds in a water treatment.

  5. Jupiter's Equatorial Region in the Near-Infrared and Violet (Time set 2)

    NASA Technical Reports Server (NTRS)

    1997-01-01

    Mosaics of an equatorial 'hotspot' on Jupiter at 756 nanometers (top) and 410 nanometers (bottom). The mosaics cover an area of 34,000 kilometers by 11,000 kilometers. The dark region near the center of each mosaic is an equatorial 'hotspot' similar to the Galileo Probe entry site. These features are holes in the bright, reflective, equatorial cloud layer where warmer thermal emission from Jupiter's deep atmosphere can pass through. The circulation patterns observed here along with the composition measurements from the Galileo Probe suggest that dry air may be converging and sinking over these regions, maintaining their cloud-free appearance.

    The 756 nanometer (nm) near-infrared continuum filter shows the features of Jupiter's main visible cloud deck. Light at 410 nm is affected by the sizes and compositions of cloud particles, as well as the trace chemicals that give Jupiter's clouds their colors. Near-infrared continuum images are used to study cloud patterns and motions. Violet images contain additional information about cloud color and cloud particles.

    North is at the top. The mosaics cover latitudes 1 to 10 degrees and are centered at longitude 336 degrees West. The smallest resolved features are tens of kilometers in size. These images were taken on December 17, 1996, at a range of 1.5 million kilometers by the Solid State Imaging system aboard NASA's Galileo spacecraft.

    The Jet Propulsion Laboratory, Pasadena, CA manages the mission for NASA's Office of Space Science, Washington, DC.

    This image and other images and data received from Galileo are posted on the World Wide Web, on the Galileo mission home page at URL http://galileo.jpl.nasa.gov. Background information and educational context for the images can be found at URL http://www.jpl.nasa.gov/galileo/sepo

  6. The alpine violet, Viola biflora, is a rich source of cyclotides with potent cytotoxicity.

    PubMed

    Herrmann, Anders; Burman, Robert; Mylne, Joshua S; Karlsson, Gustav; Gullbo, Joachim; Craik, David J; Clark, Richard J; Göransson, Ulf

    2008-02-01

    The cyclotides are currently the largest known family of head-to-tail cyclic proteins. The complex structure of these small plant proteins, which consist of approximately 30 amino acid residues, contains both a circular peptide backbone and a cystine knot, the combination of which produces the cyclic cystine knot motif. To date, cyclotides have been found in plants from the Rubiaceae, Violaceace and Cucurbitaceae families, and are believed to be part of the host defence system. In addition to their insecticidal effect, cyclotides have also been shown to be cytotoxic, anti-HIV, antimicrobial and haemolytic agents. In this study, we show that the alpine violet Viola biflora (Violaceae) is a rich source of cyclotides. The sequences of 11 cyclotides, vibi A-K, were determined by isolation and MS/MS sequencing of proteins and screening of a cDNA library of V. biflora in parallel. For the cDNA screening, a degenerate primer against a conserved (AAFALPA) motif in the cyclotide precursor ER signal sequence yielded a series of predicted cyclotide sequences that were correlated to those of the isolated proteins. There was an apparent discrepancy between the results of the two strategies as only one of the isolated proteins could be identified as a cDNA clone. Finally, to correlate amino acid sequence to cytotoxic potency, vibi D, E, G and H were analysed using a fluorometric microculture cytotoxicity assay using a lymphoma cell line. The IC(50)-values of the bracelet cyclotides vibi E, G and H ranged between 0.96 and 5.0 microM while the Möbius cyclotide vibi D was not cytotoxic at 30 microM.

  7. An Ultra-Violet Tolerant Wild-Type Strain of Melanin-Producing Bacillus thuringiensis

    PubMed Central

    Sansinenea, Estibaliz; Salazar, Francisco; Ramirez, Melanie; Ortiz, Aurelio

    2015-01-01

    Background: Bacillus thuringiensis is the most successful biological control agent used in agriculture, forestry and mosquito control. However, the insecticidal activity of the B. thuringiensis formulation is not very stable and rapidly loses its biological activity under field conditions, due to the ultraviolet radiation in sunlight. Melanin is known to absorb radiation therefore photo protection of B. thuringiensis based on melanin has been extensively studied. Objectives: The aim of this study was to find a wild type strain of naturally melanin-producing B. thuringiensis to avoid any mutation or manipulation that can affect the Cry protein content. Materials and Methods: Bacillus thuringiensis strains were isolated from soils of different States of Mexico and pigment extraction was followed by lowering the pH to 2 using 1N HCl. Pigment was characterized by some chemical tests based on its solubility, bleaching by H2O2 and flocculation with FeCl3, and using an Infrared (IR) spectrum. Ultraviolet (UV) irradiation experiment was performed to probe the melanin efficacy. Results: ELI52 strain of B. thuringiensis was confirmed to naturally produce melanin. The Cry protein analysis suggested that ELI52 is probably a B. thuringiensis subsp. israelensis strain with toxic activity against the Diptera order of insects. Ultra Violet protection efficacy of melanin was probed counting total viable colonies after UV radiation and comparing the results with the non-producing melanin strain L-DOPA (L-3, 4-dihydroxyphenylalanine) was also detected in the culture. ELI52 strain showed an antagonistic effect over some common bacteria from the environment. Conclusions: ELI52 wild-type strain of B. thuringiensis is a good bio-insecticide that produces melanin with UV-resistance that is probably toxic against the Diptera order of insects and can inhibit the growth of other environmental bacteria. PMID:26421136

  8. Tunable light source with GaN-based violet laser diode

    NASA Astrophysics Data System (ADS)

    Omori, Masaki; Mori, Naoki; Dejima, Norihiro

    2013-03-01

    GaN based violet Laser Diode has been applying for the industrial market with unique high potential characters. It has possibility Replacing Gas lasers, Dye Lasers, SHG lasers and Solid-state Lasers and more. Diode based laser extreme small and low costs at the high volume range. In addition GaN Laser has high quality with long lifetime and has possibility to cover the wide wavelength range as between 375 to 520nm. However, in general, diode based laser could only lase with Longitudinal Multi Mode. Therefore applicable application field should be limited and it was difficult to apply for the analysis. Recently, Single Longitudinal Mode laser with GaN diode has also be accomplished with external cavity by Nichia Corporation. External cavity laser achieved at least much higher than 20dB SMSR. The feature of installing laser is that Laser on the front facet with AR coating to avoid chip mode lasing. In general, external cavity laser has been required precision of mechanical assembly and Retention Capability. Nichia has gotten rid of the issue with Intelligence Cavity and YAG Laser welding assembly technique. This laser has also been installed unique feature that the longitudinal mode could be maintained to Single Mode lasing with installing internal functional sensors in the tunable laser.*1,*2 This tunable laser source could lock a particular wavelength optionally between 390 to 465nm wavelength range. As the results, researcher will have benefit own study and it will be generated new market with the laser in the near future.

  9. Two Types of Aurora on Mars as Observed by MAVEN's Imaging UltraViolet Spectrograph

    NASA Astrophysics Data System (ADS)

    Schneider, N. M.; Deighan, J.; Jain, S.; Stiepen, A.; Stewart, I. F.; Larson, D. E.; Mitchell, D. L.; Mazelle, C. X.; Lee, C.; Lillis, R. J.; Evans, J. S.; Brain, D. A.; Stevens, M. H.; McClintock, W. E.; Chaffin, M.; Crismani, M. M. J.; Holsclaw, G. M.; Lefèvre, F.; Lo, D.; Clarke, J. T.; Montmessin, F.; Jakosky, B. M.

    2015-12-01

    The Imaging UltraViolet Spectrograph (IUVS) on the MAVEN spacecraft has detected two distinct types of auroral emission on Mars. First, we report the discovery of a low altitude, diffuse aurora spanning much of Mars' northern hemisphere coincident with a solar energetic particle outburst. IUVS observed northerly latitudes during late December 2014, detecting auroral emission in virtually all nightside observations for ~5 days spanning virtually all geographic longitudes. The vertical profile showed emission down to ~70 km altitude (1 microbar), deeper than confirmed at any other planet. The onset and duration of emission coincide with the observed arrival of solar energetic particles up to 200 keV precipitating directly and deeply into the atmosphere. Preliminary modeling of the precipitation, energy deposition and spectral line emission yields good matches to the observations. These observations represent a new class of planetary auroras produced in the Martian middle atmosphere. Given minimal magnetic fields over most of the planet, Mars is likely to exhibit aurora more globally than Earth. Second, we confirm the existence of small patches of discrete aurora near crustal magnetic fields in Mars' southern hemisphere, as observed previously by SPICAM on Mars Express (Bertaux et al., Nature, 435, 790-794 (2005)). IUVS observed southern latitudes in July and August 2015, detecting discrete auroral emission in ~1% of suitable observations. Limb scans resolved both vertically and along-slit indicate this type of auroral emission was patchy on the scale of ~40 km, and located at higher altitudes ~140 km. The higher altitudes imply a lower energy of precipitating particles. The mix of spectral emissions also differed signficiantly from the discrete aurora, indicating different excitation and quenching processes. We will discuss the observed properties of the aurora and associated charged particle precipitation, as well as the broader implications of this high

  10. Two Types of Aurora on Mars as Observed by MAVEN's Imaging UltraViolet Spectrograph

    NASA Astrophysics Data System (ADS)

    Schneider, Nicholas M.; Deighan, J.; Jain, S. K.; Stiepen, A.; Larson, D.; Mitchell, D. L.; Lee, C. O.; Lillis, R.; Brain, D.; McClintock, W. E.; Chaffin, M. S.; Crismani, M.; Holsclaw, G. M.; Jakosky, B. M.; Mazelle, C.; Evans, J. S.; Stewart, A. I. F.; Stevens, M. H.; Clarke, J. T.; Montmessin, F.; Lefevre, F.; Lo, D.

    2015-11-01

    The Imaging UltraViolet Spectrograph (IUVS) on the MAVEN spacecraft has detected two distinct types of auroral emission on Mars. First, we report the discovery of a low altitude, diffuse aurora spanning much of Mars’ northern hemisphere coincident with a solar energetic particle outburst. IUVS observed northerly latitudes during late December 2014, detecting auroral emission in virtually all nightside observations for ~5 days spanning virtually all geographic longitudes. The vertical profile showed emission down to ~70 km altitude (1 microbar), deeper than confirmed at any other planet. The onset and duration of emission coincide with the observed arrival of solar energetic particles up to 200 keV precipitating directly and deeply into the atmosphere. Preliminary modeling of the precipitation, energy deposition and spectral line emission yields good matches to the observations. These observations represent a new class of planetary auroras produced in the Martian middle atmosphere. Given minimal magnetic fields over most of the planet, Mars is likely to exhibit aurora more globally than Earth.Second, we confirm the existence of small patches of discrete aurora near crustal magnetic fields in Mars' southern hemisphere, as observed previously by SPICAM on Mars Express (Bertaux et al., Nature, 435, 790-794 (2005)). IUVS observed southern latitudes in July and August 2015, detecting discrete auroral emission in ~1% of suitable observations. Limb scans resolved both vertically and along-slit indicate this type of auroral emission was patchy on the scale of ~40 km, and located at higher altitudes ~140 km. The higher altitudes imply a lower energy of precipitating particles. The mix of spectral emissions also differed signficiantly from the diffuse aurora, indicating different excitation and quenching processes.We will discuss the observed properties of the aurora and associated charged particle precipitation, as well as the broader implications of this high

  11. Indirect differential pulse voltammetric determination of aluminum by a pyrocatechol violet-modified electrode

    SciTech Connect

    Chen, G.; Bi, S.; Dai, L.; Cao, M.; Chen, Y. Wang, X.

    1999-03-01

    Aluminum is one of the abundant elements in the earth`s crust. It has been considered to be a causative agent for various neurological disorders such as Alzheimer Senile, presenile dementia and amyotrophic lateral sclerosis. It is also very harmful to plants and aquatic organisms. Therefore, the determination of Al is very important. A Pyrocatechol Violet (PCV) modified electrode for the voltammetric determination of aluminum is reported. The modified electrode is simply prepared by dip-coating a pyrolytic graphite electrode in a NaAc-HAc buffer solution of PCV. Optimum experimental conditions for aluminum determination include a 0.2 mol/L NaAc-HAc buffer solution of pH 4.8, a PCV concentration of 0.02 mol/L used to modify the electrode and the use of differential-pulse mode for measurement. The peak currents of differential pulse voltammograms (DPV) decrease with the addition of Al into the buffer solution while the peak potentials remain the same. The decreasing value of peak current {Delta}i{sub p} is linear with Al concentration in the range of 1{times}10{sup {minus}8} to 1{times}10{sup {minus}7} mol/L and 1{times}10{sup {minus}7} to 1{times}10{sup {minus}6} mol/L. The detection limit is 5{times}10{sup {minus}9} mol/L and the relative standard deviation for 4{times}10{sup {minus}8} mol/L Al is 2.9% (n=8). The stability of this electrode is satisfactory. No serious interference is found. This method has been applied to determine Al in drinking water samples.

  12. Urinary Concentrations of Benzophenone-Type Ultra Violet Light Filters and Semen Quality

    PubMed Central

    Buck Louis, Germaine M.; Chen, Zhen; Kim, Sungduk; Sapra, Katherine J.; Bae, Jisuk; Kannan, Kurunthachalam

    2015-01-01

    Objective To assess benzophenone-type ultra violet (UV) filter concentrations, chemicals used in sunscreen and personal care products, and semen endpoints. Design Cohort. Setting 16 counties in Michigan and Texas Participants 413 men provided semen and urine samples, 2005–2009. Five UV filters were quantified (ng/mL) in urine using liquid chromatography-triple-quadrupole mass spectrometry: BP-1 (2,4-dihydroxybenzophenone), BP-2 (2,2′,4,4′-tetrahydroxybenzophenone), BP-3 (2-hydroxy-4-methoxybenzophenone), BP-8 (2,2′-dihydroxy-4-methoxybenzophenone), and 4-OH-BP (4-hydroxybenzophenone). Using linear regression, beta coefficients (β) and 95% confidence intervals (CIs) for each chemical dichotomized at the 75th percentile and Box-Cox transformed semen endpoint were estimated, after adjusting for age, BMI, cotinine, season, and site. Interventions None. Main Outcome Measures 35 semen endpoints. Results BP-2 was associated with diminished sperm concentration (β=−0.74; 95% CI −1.41, −0.08), straight (β=−4.57; 95% CI −8.95, −0.18) and linear movement (β=−3.15; 95% CI −6.01, −0.30), more immature (β=0.38; 95% CI 0.15, 0.62) sperm, and a decreased percentage of other tail abnormalities (β=−0.16; 95% CI −0.31, −0.01). BP-8 was associated with decreased hypo-osmotic swelling (β=−2.57; 95% CI −4.86, −0.29) and higher acrosome area (β=1.14; 95% CI 0.01, 2.26). No associations were observed for BP-1, BP-3 or 4OH-BP. Conclusion The findings suggest that specific UV filters may be associated with some aspects of semen endpoints, but await future corroboration. PMID:26253817

  13. Blue-Violet Laser Modification of Titania Treated Titanium: Antibacterial and Osteo-Inductive Effects

    PubMed Central

    Kawano, Takanori; Prananingrum, Widyasri; Ishida, Yuichi; Goto, Takaharu; Naito, Yoshihito; Watanabe, Megumi; Tomotake, Yoritoki; Ichikawa, Tetsuo

    2013-01-01

    Background Many studies on surface modifications of titanium have been performed in an attempt to accelerate osseointegration. Recently, anatase titanium dioxide has been found to act as a photocatalyst that expresses antibiotic properties and exhibits hydrophilicity after ultraviolet exposure. A blue-violet semiconductor laser (BV-LD) has been developed as near-ultraviolet light. The purpose of this study was to investigate the effects of exposure to this BV-LD on surface modifications of titanium with the goal of enhancing osteoconductive and antibacterial properties. Methods The surfaces of pure commercial titanium were polished with #800 waterproof polishing papers and were treated with anatase titania solution. Specimens were exposed using BV-LD (λ = 405 nm) or an ultraviolet light-emitting diode (UV-LED, λ = 365 nm) at 6 mW/cm2 for 3 h. The surface modification was evaluated physically and biologically using the following parameters or tests: surface roughness, surface temperature during exposure, X-ray diffraction (XRD) analysis, contact angle, methylene blue degradation tests, adherence of Porphyromonas gingivalis, osteoblast and fibroblast proliferation, and histological examination after implantation in rats. Results No significant changes were found in the surface roughness or XRD profiles after exposure. BV-LD exposure did not raise the surface temperature of titanium. The contact angle was significantly decreased, and methylene blue was significantly degraded. The number of attached P. gingivalis organisms was significantly reduced after BV-LD exposure compared to that in the no exposure group. New bone was observed around exposed specimens in the histological evaluation, and both the bone-to-specimen contact ratio and the new bone area increased significantly in exposed groups. Conclusions This study suggested that exposure of titanium to BV-LD can enhance the osteoconductivity of the titanium surface and induce antibacterial properties, similar to

  14. Adsorption dynamics of methyl violet onto granulated mesoporous carbon: Facile synthesis and adsorption kinetics.

    PubMed

    Kim, Yohan; Bae, Jiyeol; Park, Hosik; Suh, Jeong-Kwon; You, Young-Woo; Choi, Heechul

    2016-09-15

    A new and facile one-step synthesis method for preparing granulated mesoporous carbon (GMC) with three-dimensional spherical mesoporous symmetry is prepared to remove large molecular weight organic compounds in aqueous phase. GMC is synthesized in a single step using as-synthesized mesoporous carbon particles and organic binders through a simple and economical synthesis approach involving a simultaneous calcination and carbonization process. Characterization results obtained from SEM, XRD, as well as surface and porosity analysis indicate that the synthesized GMC has similar physical properties to those of the powdered mesoporous carbon and maintains the Brunauer-Emmett-Teller (BET) surface area and pore volume because the new synthesis method prevents the collapse of the pores during the granulation process. Batch adsorption experiments revealed GMC showed a substantial adsorption capacity (202.8 mg/g) for the removal of methyl violet as a target large molecular contaminant in aqueous phase. The mechanisms and dynamics modeling of GMC adsorption were also fully examined, which revealed that surface diffusion was rate limiting step on adsorption process of GMC. Adsorption kinetics of GMC enables 3 times faster than that of granular activated carbon in terms of surface diffusion coefficient. This is the first study, to the best of our knowledge, to synthesize GMC as an adsorbent for water purification by using facile granulation method and to investigate the adsorption kinetics and characteristics of GMC. This study introduces a new and simple method for the synthesis of GMC and reveals its adsorption characteristics for large molecular compounds in a water treatment. PMID:27262123

  15. Crystallization and preliminary X-ray diffraction analyses of the redox-controlled complex of terminal oxygenase and ferredoxin components in the Rieske nonhaem iron oxygenase carbazole 1,9a-dioxygenase

    SciTech Connect

    Matsuzawa, Jun; Aikawa, Hiroki; Umeda, Takashi; Ashikawa, Yuji; Suzuki-Minakuchi, Chiho; Kawano, Yoshiaki; Fujimoto, Zui; Okada, Kazunori; Yamane, Hisakazu; Nojiri, Hideaki

    2014-09-25

    A crystal was obtained of the complex between reduced terminal oxygenase and oxidized ferredoxin components of carbazole 1,9a-dioxygenase. The crystal belonged to space group P2{sub 1} and diffracted to 2.25 Å resolution. The initial reaction in bacterial carbazole degradation is catalyzed by carbazole 1,9a-dioxygenase, which consists of terminal oxygenase (Oxy), ferredoxin (Fd) and ferredoxin reductase components. The electron-transfer complex between reduced Oxy and oxidized Fd was crystallized at 293 K using the hanging-drop vapour-diffusion method with PEG 3350 as the precipitant under anaerobic conditions. The crystal diffracted to a maximum resolution of 2.25 Å and belonged to space group P2{sub 1}, with unit-cell parameters a = 97.3, b = 81.6, c = 116.2 Å, α = γ = 90, β = 100.1°. The V{sub M} value is 2.85 Å{sup 3} Da{sup −1}, indicating a solvent content of 56.8%.

  16. Study of Surface Enhanced Raman Scattering of Alizarin and Crystal Violet Dyes

    NASA Astrophysics Data System (ADS)

    Gopal, Ram; Swarnkar, Raj Kumar

    2010-06-01

    Surface enhanced Raman scattering (SERS) plays a vital role in analytical chemistry to characterize ultra trace quantity of organic compounds and biological samples. Two mechanisms have been considered to explain the SERS effect. The main contribution arises from a huge enhancement of the local electromagnetic field close to surface roughness of the metal structures, due to the excitation of a localized surface plasmon, while a further enhancement can be observed for molecules adsorbed onto specific sites when resonant charge transfer occurs. SERS signals have been observed from adsorbates on many metallic surfaces like Ag, Au, Ni, Cu etc. Additionally, metal oxide nanoparticles also show SERS signals It has now been established that SERS of analyte material is highly dependent on the type of substrate involved. Many types of nanostructures like nanofilms, nanorods, nanospheres etc. show highly efficient SERS signals. In particular, there are two routes available for the synthesis of these nanomaterials: the chemical route and the physical route. Chemical route involves many types of reducing agents and capping agents which can interfere in origin and measurement of these signals. The physical route avoids these anomalies and therefore it is suitable for the study of SERS phenomenon. Pulsed laser ablation in liquid medium is an excellent top down technique to produce colloidal solution of nanoparticles with desired shape and size having surface free from chemical contamination, which is essential requirement for surface application of nanoparticles. The present work deals with the study of SERS of Crystal violet dye and Alizarin group dye on Cu@ Cu_2O and Ag colloidal nanoparticles synthesized by pulsed laser ablation. M. Fleishchmann, P. J. Hendra, and A. J. McQuillian Chem. Phys. Lett., 26, 163, 1974. U. Wenning, B. Pettinger, and H. Wetzel Chem. Phys. Lett., 70, 49, 1980. S. C. Singh, R. K. Swarnkar, P. Ankit, M. C. Chattopadhyaya, and R. Gopal AIP Conf. Proc

  17. The solar extreme ultra-violet corona: Resolved loops and the unresolved active region corona

    NASA Astrophysics Data System (ADS)

    Cirtain, Jonathan Wesley

    In this work, physical characteristics of the solar corona as observed in the Extreme Ultra-Violet (EUV) regime are investigated. The focus will be the regions of intense EUV radiation generally found near the locations of sunspots. These regions are commonly called active regions. Multiple space- based observing platforms have been deployed in the last decade; it is possible to use several of these observatories in combination to develop a more complete picture of the solar corona. Joint Observing Program 146 was created to collect spectroscopic intensities using the Coronal Diagnostic Spectrometer on Solar and Heliospheric Observatory and EUV images using NASA's Transition Region and Coronal Explorer. The emission line intensities are analyzed to develop an understanding of the temperature and density of the active region coronal plasma. However, the performance of the CDS instrument in the spatial and temporal domains is limited and to compensate for these limitations, data collected by the TRACE instrument provide a high spatial and temporal resolution set of observations. One of the most exciting unsolved problems in solar astrophysics is to understand why the corona maintains a temperature roughly two orders of magnitude higher than the underlying material. A detailed investigation of the coronal emission has provided constraints on models of the heating mechanism, since the temperature, density and evolution of emission rates for multiple ionic species are indicative of the mechanism(s) working to heat the corona. The corona appears to consist of multiple unresolved structures as well as resolved active region structures, called coronal loops. The purpose of the present work is to determine the characteristics of the unresolved background corona. Using the characterizations of the coronal unresolved background, results for loops after background subtraction are also presented. This work demonstrates the magnitude of the unresolved coronal emission with

  18. Tuning emission in violet, blue, green and red in cubic GaN/InGaN/GaN quantum wells

    NASA Astrophysics Data System (ADS)

    Orozco Hinostroza, I. E.; Avalos-Borja, M.; Compeán García, V. D.; Zamora, C. Cuellar; Rodríguez, A. G.; López Luna, E.; Vidal, M. A.

    2016-02-01

    Light emission in the three primary colors was achieved in cubic GaN/InGaN/GaN heterostructures grown by molecular beam epitaxy on MgO substrates in a single growth process. A heterostructure with four quantum wells with a width of 10 nm was grown; this quantum wells width decrease the segregation effect of In. Photoluminescence emission produced four different emission signals: violet, blue, green-yellow and red. Thus, we were able to tune energy transitions in the visible spectrum modifying the In concentration in cubic InxGa1-xN ternary alloy.

  19. Crystal Violet Lactone Salicylaldehyde Hydrazone Zn(II) Complex: a Reversible Photochromic Material both in Solution and in Solid Matrix

    PubMed Central

    Li, Kai; Li, Yuanyuan; Tao, Jing; Liu, Lu; Wang, Lili; Hou, Hongwei; Tong, Aijun

    2015-01-01

    Crystal violet lactone (CVL) is a classic halochromic dye which has been widely used as chromogenic reagent in thermochromic and piezochromic systems. In this work, a very first example of CVL-based reversible photochromic compound was developed, which showed distinct color change upon UV-visible light irradiation both in solution and in solid matrix. Moreover, metal complex of CVL salicylaldehyde hydrozone was facilely synthesized, exhibiting reversible photochromic properties with good fatigue resistance. It was served as promising solid material for photo-patterning. PMID:26412101

  20. Theoretical investigations of the electronic structures of carbazole-based triphenylphosphine oxide derivatives, potential bipolar host materials in blue-phosphorescent devices.

    PubMed

    Sun, Huili; Shen, Wei; Zhang, Xiaguang; Zhang, Dongmei; Li, Ming

    2015-12-01

    Density functional theory calculations were performed to investigate the electronic structures of bipolar host materials comprising a backbone of linked acceptor moieties where each acceptor was also linked to a pendant donor moiety. The acceptor was triphenylphosphine oxide with two of its phenyls substituted with fluorine atoms or nitrile groups (CN). The donor was carbazole (CZ) substituted, or not, with t-butyl groups. The HOMO and LUMO energy levels of these host molecules were mainly influenced by their respective hole- and electron-transport units. The t-butyl substituents on the CZ moieties had an adverse effect on the triplet energies (E T) of the host molecules, especially for molecules where the phenyls of the backbone chain were substituted with CN groups. While introducing CN substituents onto the backbone chain decreased the energy difference between the lowest singlet and triplet excited states (ΔE ST), it also caused the energy gap between the HOMO and LUMO to narrow. Among the host molecules investigated, that in which one of the phenyls in the acceptor moiety was linked to the donor while the other two phenyls in the acceptor were substituted with CN substituents exhibited the highest E T, balanced charge transport, a low charge-injection barrier, and a small ΔE ST, and is therefore a promising candidate host material for use in blue-phosphorescent devices. Graphical Abstract Density functional theory calculations were performed to explore the electronic properties of bipolar host materials comprising a backbone of linked acceptor moieties where each acceptor was also linked to a pendant donor moiety. All of the designed molecules with high triplet energies were found to be suitable for use as host materials when matched with a blue-light guest material. The results demonstrate that the host molecule in which one of the phenyls in the triphenylphosphine oxide acceptor moiety was linked to the carbazole donor while the other two phenyls in the

  1. Modeling of nonequilibrium CO Fourth-Positive and CN Violet emission in CO2-N2 gases

    NASA Astrophysics Data System (ADS)

    Johnston, C. O.; Brandis, A. M.

    2014-12-01

    This work develops a chemical kinetic rate model for simulating nonequilibrium radiation from CO2-N2 gases, representative of Mars or Venus entry shock layers. Using recent EAST shock tube measurements of nonequilibrium CO 4th Positive and CN Violet emission at pressures and velocities ranging from 0.10 to 1.0 Torr and 6 to 8 km/s, the rate model is developed through an optimization procedure that minimizes the disagreement between the measured and simulated nonequilibrium radiance profiles. Only the dissociation rates of CO2, CO, and NO, along with the CN + O and CO + N rates were treated as unknown in this optimization procedure, as the nonequilibrium radiance was found to be most sensitive to them. The other rates were set to recent values from the literature. Increases in over a factor of 5 in the CO dissociation rate relative to the previous widely used value were found to provide the best agreement with measurements, while the CO2 rate was not changed. The developed model is found to capture the measured nonequilibrium radiance of CO 4th Positive and CN Violet within error bars of ±30%.

  2. Reproductive biology of the violet-chested hummingbird in Venezuela and comparisons with other tropical and temperate hummingbirds

    USGS Publications Warehouse

    Fierro-Calderon, K.; Martin, T.E.

    2007-01-01

    We provide details on the breeding biology of the Violet-chested Hummingbird (Sternoclyta cyanopectus) based on 67 nests studied in Yacambu?? National Park, Venezuela, from 2002 through 2006. Clutch size was two white eggs, usually laid every other day. Fresh egg mass (0.95 ?? 0.14 g) was 15% of female mass. Incubation and nestling periods were 20.4 ?? 0.3 and 26.0 ?? 0.4 days, respectively. Nest attentiveness increased from 60% in early incubation to 68% in late incubation. The female spent 50% of her time brooding young nestlings, but ceased brooding by 13 days of age. Only the female fed the young, with a low rate of nest visitation (3.3 trips per hour) that did not increase with age of the young. Growth rate based on nestling mass (K = 0.28) was slow. Daily predation rates decreased across stages and were 0.064 ?? 0.044, 0.033 ?? 0.008, and 0.020 ?? 0.006 during the egg-laying, incubation, and nestling periods, respectively. Most, but not all, life history traits of the Violet-chested Hummingbird were similar to those reported for other tropical and temperate hummingbirds, providing further evidence that this family shows a relatively narrow range of life history variation. ?? The Cooper Ornithological Society 2007.

  3. Blue-violet light irradiation dose dependently decreases carotenoids in human skin, which indicates the generation of free radicals.

    PubMed

    Vandersee, Staffan; Beyer, Marc; Lademann, Juergen; Darvin, Maxim E

    2015-01-01

    In contrast to ultraviolet and infrared irradiation, which are known to facilitate cutaneous photoaging, immunosuppression, or tumour emergence due to formation of free radicals and reactive oxygen species, potentially similar effects of visible light on the human skin are still poorly characterized. Using a blue-violet light irradiation source and aiming to characterize its potential influence on the antioxidant status of the human skin, the cutaneous carotenoid concentration was measured noninvasively in nine healthy volunteers using resonance Raman spectroscopy following irradiation. The dose-dependent significant degradation of carotenoids was measured to be 13.5% and 21.2% directly after irradiation at 50 J/cm² and 100 J/cm² (P < 0.05). The irradiation intensity was 100 mW/cm². This is above natural conditions; the achieved doses, though, are acquirable under natural conditions. The corresponding restoration lasted 2 and 24 hours, respectively. The degradation of cutaneous carotenoids indirectly shows the amount of generated free radicals and especially reactive oxygen species in human skin. In all volunteers the cutaneous carotenoid concentration dropped down in a manner similar to that caused by the infrared or ultraviolet irradiations, leading to the conclusion that also blue-violet light at high doses could represent a comparably adverse factor for human skin.

  4. Exposure to Crystal Violet, Its Toxic, Genotoxic and Carcinogenic Effects on Environment and Its Degradation and Detoxification for Environmental Safety.

    PubMed

    Mani, Sujata; Bharagava, Ram Naresh

    2016-01-01

    Crystal Violet (CV), a triphenylmethane dye, has been extensively used in human and veterinary medicine as a biological stain, as a textile dye in textile processing industries and also used to provide a deep violet color to paints and printing ink. CV is also used as a mutagenic and bacteriostatic agent in medical solutions and antimicrobial agent to prevent the fungal growth in poultry feed. Inspite of its many uses, CV has been reported as a recalcitrant dye molecule that persists in environment for a long period and pose toxic effects in environment. It acts as a mitotic poison, potent carcinogen and a potent clastogene promoting tumor growth in some species of fish. Thus, CV is regarded as a biohazard substance. Although, there are several physico-chemical methods such as adsorption, coagulation and ion-pair extraction reported for the removal of CV, but these methods are insufficient for the complete removal of CV from industrial wastewaters and also produce large quantity of sludge containing secondary pollutants. However, biological methods are regarded as cost-effective and eco-friendly for the treatment of industrial wastewaters, but these methods also have certain limitations. Therefore, there is an urgent need to develop such eco-friendly and cost-effective biological treatment methods, which can effectively remove the dye from industrial wastewaters for the safety of environment, as well as human and animal health. PMID:26613989

  5. Evaluation of crystal violet decolorization assay for minimal inhibitory concentration detection of primary antituberculosis drugs against Mycobacterium tuberculosis isolates*

    PubMed Central

    Coban, Ahmet Yilmaz; Akbal, Ahmet Ugur; Uzun, Meltem; Cayci, Yeliz Tanriverdi; Birinci, Asuman; Durupinar, Belma

    2016-01-01

    In this study we evaluated the crystal violet decolorization assay (CVDA) for detection of minimum inhibitory concentration (MIC) of antituberculosis drugs. 53 isolates were tested in this study and 13 of them were multidrug resistant (MDR) isolates. The antibiotics concentrations were 2-0.06 mg/L for isoniazid (INH) and rifampicin (RIF) and were 16-0.25 mg/L for streptomycin (STM) and ethambutol (EMB). Crystal violet (CV-25 mg/L) was added into the microwells on the seventh day of incubation and incubation was continued until decolorization. Decolorization of CV was the predictor of bacterial growth. Overall agreements for four drugs were detected as 98.1%, and the average time was detected as 9.5 ± 0.89 day after inoculation. One isolate for INH and two isolates for STM were determined resistant in the reference method, but susceptible by the CVDA. One isolate was susceptible to EMB by the reference method, but resistant by the CVDA. All results were concordant for RIF. This study shows that CVDA is a rapid, reliable and suitable for determination of MIC values of Mycobacterium tuberculosis. And it can be used easily especially in countries with limited-sources. PMID:27304025

  6. Evaluation of crystal violet decolorization assay for minimal inhibitory concentration detection of primary antituberculosis drugs against Mycobacterium tuberculosis isolates.

    PubMed

    Coban, Ahmet Yilmaz; Akbal, Ahmet Ugur; Uzun, Meltem; Cayci, Yeliz Tanriverdi; Birinci, Asuman; Durupinar, Belma

    2016-06-10

    In this study we evaluated the crystal violet decolorization assay (CVDA) for detection of minimum inhibitory concentration (MIC) of antituberculosis drugs. 53 isolates were tested in this study and 13 of them were multidrug resistant (MDR) isolates. The antibiotics concentrations were 2-0.06 mg/L for isoniazid (INH) and rifampicin (RIF) and were 16-0.25 mg/L for streptomycin (STM) and ethambutol (EMB). Crystal violet (CV-25 mg/L) was added into the microwells on the seventh day of incubation and incubation was continued until decolorization. Decolorization of CV was the predictor of bacterial growth. Overall agreements for four drugs were detected as 98.1%, and the average time was detected as 9.5 ± 0.89 day after inoculation. One isolate for INH and two isolates for STM were determined resistant in the reference method, but susceptible by the CVDA. One isolate was susceptible to EMB by the reference method, but resistant by the CVDA. All results were concordant for RIF. This study shows that CVDA is a rapid, reliable and suitable for determination of MIC values of Mycobacterium tuberculosis. And it can be used easily especially in countries with limited-sources. PMID:27304025

  7. Blue-Violet Light Irradiation Dose Dependently Decreases Carotenoids in Human Skin, Which Indicates the Generation of Free Radicals

    PubMed Central

    Vandersee, Staffan; Beyer, Marc; Lademann, Juergen; Darvin, Maxim E.

    2015-01-01

    In contrast to ultraviolet and infrared irradiation, which are known to facilitate cutaneous photoaging, immunosuppression, or tumour emergence due to formation of free radicals and reactive oxygen species, potentially similar effects of visible light on the human skin are still poorly characterized. Using a blue-violet light irradiation source and aiming to characterize its potential influence on the antioxidant status of the human skin, the cutaneous carotenoid concentration was measured noninvasively in nine healthy volunteers using resonance Raman spectroscopy following irradiation. The dose-dependent significant degradation of carotenoids was measured to be 13.5% and 21.2% directly after irradiation at 50 J/cm² and 100 J/cm² (P < 0.05). The irradiation intensity was 100 mW/cm². This is above natural conditions; the achieved doses, though, are acquirable under natural conditions. The corresponding restoration lasted 2 and 24 hours, respectively. The degradation of cutaneous carotenoids indirectly shows the amount of generated free radicals and especially reactive oxygen species in human skin. In all volunteers the cutaneous carotenoid concentration dropped down in a manner similar to that caused by the infrared or ultraviolet irradiations, leading to the conclusion that also blue-violet light at high doses could represent a comparably adverse factor for human skin. PMID:25741404

  8. Using violet laser-induced chlorophyll fluorescence emission spectra for crop yield assessment of cowpea (Vigna unguiculata (L) Walp) varieties

    NASA Astrophysics Data System (ADS)

    Anderson, Benjamin; Buah-Bassuah, Paul K.; Tetteh, Jonathan P.

    2004-07-01

    The use of violet laser-induced chlorophyll fluorescence (LICF) emission spectra to monitor the growth of five varieties of cowpea in the University of Cape Coast Botanical Garden is presented. Radiation from a continuous-wave violet laser diode emitting at 396 nm through a fibre is closely incident on in vivo leaves of cowpea to excite chlorophyll fluorescence, which is detected by an integrated spectrometer with CCD readout. The chlorophyll fluorescence spectra with peaks at 683 and 731 nm were used for growth monitoring of the cowpea plants over three weeks and analysed using Gaussian spectral functions with curve fitted parameters to determine the peak positions, area under the spectral curve and the intensity ratio F683/F731. The variation in the intensity ratio of the chlorophyll bands showed sensitive changes indicating the photosynthetic activity of the cowpea varieties. A discussion of the fluorescence result as compared to conventional assessment is presented with regard to discrimination between the cowpea varieties in terms of crop yield performance.

  9. Exposure to Crystal Violet, Its Toxic, Genotoxic and Carcinogenic Effects on Environment and Its Degradation and Detoxification for Environmental Safety.

    PubMed

    Mani, Sujata; Bharagava, Ram Naresh

    2016-01-01

    Crystal Violet (CV), a triphenylmethane dye, has been extensively used in human and veterinary medicine as a biological stain, as a textile dye in textile processing industries and also used to provide a deep violet color to paints and printing ink. CV is also used as a mutagenic and bacteriostatic agent in medical solutions and antimicrobial agent to prevent the fungal growth in poultry feed. Inspite of its many uses, CV has been reported as a recalcitrant dye molecule that persists in environment for a long period and pose toxic effects in environment. It acts as a mitotic poison, potent carcinogen and a potent clastogene promoting tumor growth in some species of fish. Thus, CV is regarded as a biohazard substance. Although, there are several physico-chemical methods such as adsorption, coagulation and ion-pair extraction reported for the removal of CV, but these methods are insufficient for the complete removal of CV from industrial wastewaters and also produce large quantity of sludge containing secondary pollutants. However, biological methods are regarded as cost-effective and eco-friendly for the treatment of industrial wastewaters, but these methods also have certain limitations. Therefore, there is an urgent need to develop such eco-friendly and cost-effective biological treatment methods, which can effectively remove the dye from industrial wastewaters for the safety of environment, as well as human and animal health.

  10. Thidiazuron induces shoot organogenesis at low concentrations and somatic embryogenesis at high concentrations on leaf and petiole explants of African violet (Saintpaulia ionantha Wendl).

    PubMed

    Mithila, J; Hall, J C; Victor, J M R; Saxena, P K

    2003-01-01

    Regeneration via shoot organogenesis and somatic embryogenesis was observed from thidiazuron (TDZ)-treated leaf and petiole explants of greenhouse- and in vitro-grown African violet plants. The response of cultures to other growth regulators over a range of 0.5 microM to 10 microM was 50% less than that observed with TDZ. A comparative study among several cultivars of African violet indicated that "Benjamin" and "William" had the highest regeneration potential. In "Benjamin", higher frequencies of shoot organogenesis (twofold) and somatic embryogenesis (a 50% increase) were observed from in vitro- and greenhouse-grown plants, respectively. At concentrations lower than 2.5 microM, TDZ induced shoot organogenesis, whereas at higher doses (5-10 microM) somatic embryos were formed. These findings provide the first report of simultaneous shoot organogenesis and somatic embryogenesis of African violet explants in response to TDZ. PMID:12789442

  11. An alternative staining method for counting red-eared slider turtle (Trachemys scripta) blood cells using crystal violet in cells diluted with 0.45% sodium chloride.

    PubMed

    Tsai, Chyong-Ying; Yu, Jane-Fang; Wang, Yu-Wen; Fan, Pei-Chia; Cheng, Ting-Yu; Wang, Lih-Chiann

    2014-09-01

    Various staining methods are available for reptilian species blood cell quantification. However, these methods have shown inaccurate differentiation limitations. The current study evaluates staining effects and blood cell counting results using an alternative method, counting blood cells diluted with 0.45% sodium chloride solution and stained with crystal violet. Blood samples from 8 red-eared slider turtles (Trachemys scripta) were collected. Red and white blood cell counts were performed using different methods: the unstained method, the Unopette method, Liu stain, and crystal violet method using blood cells diluted in various sodium chloride solution osmolarities. The staining properties and blood cell count results were compared. The crystal violet method using blood cells diluted in 0.45% sodium chloride solution delivered the best staining and counting results among all of the tested methods, with the lowest average coefficient of variance. The proposed method can easily be performed, serving as a feasible method for blood cell counting in chelonians.

  12. Steady-State and Transient Photoconductivity in the Poly(2,7-Carbazole) Copolymer PCDTBT, and in Bulk Heterojunction Composites with PC70BM

    NASA Astrophysics Data System (ADS)

    Coates, Nelson; Tong, Minghong; Moses, Daniel; Heeger, Alan; Beaupré, Serge; Leclerc, Mario; Gaudiana, Russell

    2009-11-01

    We have studied the nature of carrier generation in an alternating donor-acceptor low bandgap copolymer and in composites of that polymer with a soluble fullerene derivative, using steady-state and transient photoconductivity. The Poly(2,7-Carbazole) copolymer PCDTBT that we studied represents a class of donor-acceptor copolymers that hold promise for photovoltaic applications because of the ability to tune the electronic energy levels by changing the acceptor unit (see Blouin, N.; Michaud, A.; Leclerc, M. Adv. Mater. 2007, 19, 2295 - 2300). Photovoltaic devices fabricated from PCDTBT in composites with the soluble fullerene derivative [6,6]-phenyl C70-butyric acid methyl ester (PC70BM) have exhibited a higher solar cell power conversion efficiency than has been achieved in P3HT based devices. In PCDTBT, the absorption extends out to 700 nm, with two distinct but broad absorption bands that are centered at ˜400 nm and ˜600 nm. We have used steady-state and transient photoconductivity to investigate the carrier generation and collection efficiency of PCDTBT and its composite with PC70BM after photoexcitation at each of its distinct absorption bands.

  13. The tryptophan-derived endogenous arylhydrocarbon receptor ligand 6-formylindolo[3,2-b]carbazole (FICZ) is a nanomolar UVA-photosensitizer in epidermal keratinocytes

    PubMed Central

    Williams, Joshua D.; Cabello, Christopher M.; Qiao, Shuxi; Wondrak, Georg T.

    2014-01-01

    Endogenous UVA-chromophores may act as sensitizers of oxidative stress underlying cutaneous photoaging and photocarcinogenesis, but the molecular identity of non-DNA key chromophores displaying UVA-driven photodyamic activity in human skin remains largely undefined. Here we report that 6-formylindolo[3,2-b]carbazole (FICZ), a tryptophan photoproduct and endogenous high affinity aryl hydrocarbon receptor (AhR) agonist, acts as a nanomolar photosensitizer potentiating UVA-induced oxidative stress irrespective of AhR ligand activity. In human HaCaT and primary epidermal keratinocytes, photodynamic induction of apoptosis was elicited by the combined action of solar simulated UVA and FICZ, whereas exposure to the isolated action of UVA or FICZ did not impair viability. In a human epidermal tissue reconstruct, FICZ/UVA-cotreatment caused pronounced phototoxicity inducing keratinocyte cell death, and FICZ photodynamic activity was also substantiated in a murine skin exposure model. Array analysis revealed pronounced potentiation of cellular heat shock, ER stress, and oxidative stress response gene expression observed only upon FICZ/UVA-cotreatment. FICZ photosensitization caused intracellular oxidative stress, and comet analysis revealed introduction of formamidopyrimidine-DNA glycosylase (FPG)-sensitive oxidative DNA lesions suppressible by antioxidant cotreatment. Taken together, our data demonstrate that the endogenous AhR ligand FICZ displays nanomolar photodynamic activity representing a molecular mechanism of UVA-induced photooxidative stress potentially operative in human skin. PMID:25431849

  14. D-π-A-π-A Strategy to Design Benzothiadiazole-carbazole-based Conjugated Polymer with High Solar Cell Voltage and Enhanced Photocurrent.

    PubMed

    Zhou, Manxi; Wang, Min; Zhu, Lei; Yang, Zhenqing; Jiang, Chao; Cao, Dapeng; Li, Qifang

    2015-12-01

    The theoretical calculations are used to find that D-π-A-π-A style conjugated polymer PC-TBTBT is more efficient for solar cells application than the D-π-A analog PC-TBT because the D-π-A-π-A structure has a narrower band gap and higher molar absorption coefficient and redshift spectrum. Motivated by the theoretical prediction, 5,6-bis(octyloxy)-2,1,3-benzothiadiazole and 2,7-carbazole are adopted to synthesize the D-π-A-π-A style PC-TBTBT (M(w) = 31.1 kDa) and D-π-A analog PC-TBT (M(w) = 87.5 kDa) by Suzuki coupling reaction. Experimental results confirm that D-π-A-π-A PC-TBTBT-based solar cell shows a power conversion efficiency (PCE) of 4.74% with high V(OC) of 0.99 V and enhanced J(SC) of 9.70 mA cm(-2). The PCE and J(SC) achieve improvements of 17% and 26%, respectively, compared to the D-π-A PC-TBT-based solar cell. PMID:26469185

  15. Carboxylate ligands induced structural diversity of zinc(II) coordination polymers based on 3,6-bis(imidazol-1-yl)carbazole: Syntheses, structures and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Cheng, Hong-Jian; Tang, Hui-Xiang; Shen, Ya-Li; Xia, Nan-Nan; Yin, Wen-Yu; Zhu, Wei; Tang, Xiao-Yan; Ma, Yun-Sheng; Yuan, Rong-Xin

    2015-12-01

    Solvothermal reactions of Zn(NO3)2·6H2O with 3,6-bis(1-imidazolyl)carbazole (3,6-bmcz) and 1,4-benzenedicarboxylic acid (1,4-H2bdc), p-phenylenediacetic acid (p-H2pda), benzophenone-4,4-dicarboxylic acid (H2bpda) afforded three coordination polymers [Zn(1,4-bdc)(3,6-bmcz)]n (1), {[Zn(p-pda)(3,6-bmcz)]·1.5H2O}n (2) and {[Zn(bpda)(3,6-bmcz)]·0.25H2O}n (3). Complexes 1-3 were characterized by elemental analysis, IR, powder X-ray diffraction, and single-crystal X-ray diffraction. Complex 1 shows 3D structure with 2D nets inclined polycatenation. Complexes 2 and 3 possess an extended 3D supramolecular architecture based on their respective 2D layers through hydrogen-bonding interactions and the π···π stacking interactions. The solid state luminescent and optical properties of 1-3 at ambient temperature were also investigated. A comparative study on their photocatalytic activity toward the degradation of methylene blue in polluted water was explored.

  16. D-π-A-π-A Strategy to Design Benzothiadiazole-carbazole-based Conjugated Polymer with High Solar Cell Voltage and Enhanced Photocurrent.

    PubMed

    Zhou, Manxi; Wang, Min; Zhu, Lei; Yang, Zhenqing; Jiang, Chao; Cao, Dapeng; Li, Qifang

    2015-12-01

    The theoretical calculations are used to find that D-π-A-π-A style conjugated polymer PC-TBTBT is more efficient for solar cells application than the D-π-A analog PC-TBT because the D-π-A-π-A structure has a narrower band gap and higher molar absorption coefficient and redshift spectrum. Motivated by the theoretical prediction, 5,6-bis(octyloxy)-2,1,3-benzothiadiazole and 2,7-carbazole are adopted to synthesize the D-π-A-π-A style PC-TBTBT (M(w) = 31.1 kDa) and D-π-A analog PC-TBT (M(w) = 87.5 kDa) by Suzuki coupling reaction. Experimental results confirm that D-π-A-π-A PC-TBTBT-based solar cell shows a power conversion efficiency (PCE) of 4.74% with high V(OC) of 0.99 V and enhanced J(SC) of 9.70 mA cm(-2). The PCE and J(SC) achieve improvements of 17% and 26%, respectively, compared to the D-π-A PC-TBT-based solar cell.

  17. The Role of Porphyrin-Free-Base in the Electronic Structures and Related Properties of N-Fused Carbazole-Zinc Porphyrin Dye Sensitizers

    PubMed Central

    Li, Xing-Yu; Zhang, Cai-Rong; Wu, You-Zhi; Zhang, Hai-Min; Wang, Wei; Yuan, Li-Hua; Yang, Hua; Liu, Zi-Jiang; Chen, Hong-Shan

    2015-01-01

    Dye sensitizers can significantly affect power conversion efficiency of dye-sensitized solar cells (DSSCs). Porphyrin-based dyes are promising sensitizers due to their performances in DSSCs. Here, based upon a N-fused carbazole-zinc porphyrin-free-base porphyrin triad containing an ethynyl-linkage (coded as DTBC), the novel porphyrin dyes named DTBC-MP and DTBC-TP were designed by varying the porphyrin-free-base units in the π conjugation of DTBC in order to study the effect of porphyrin-free-base in the modification of electronic structures and related properties. The calculated results indicate that, the extension of the conjugate bridge with the porphyrin-free-base unit results in elevation of the highest occupied molecular orbital (HOMO) energies, decrease of the lowest unoccupied molecular orbital (LUMO) energies, reduction of the HOMO-LUMO gap, red-shift of the absorption bands, and enhancement of the absorbance. The free energy changes demonstrate that introducing more porphyrin-free-base units in the conjugate bridge induces a faster rate of electron injection. The transition properties and molecular orbital characters suggest that the different transition properties might lead to a different electron injection mechanism. In terms of electronic structure, absorption spectra, light harvesting capability, and free energy changes, the designed DTBC-TP is a promising candidate dye sensitizer for DSSCs. PMID:26610469

  18. Electronic and optical properties of novel carbazole-based donor-acceptor compounds for applications in blue-emitting organic light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Legaspi, Christian M.; Stubbs, Regan E.; Yaron, David J.; Peteanu, Linda A.; Sfeir, Matthew Y.; Kemboi, Abraham; Picker, Jesse; Fossum, Eric

    2015-08-01

    Organic light-emitting diodes (OLEDs) have received a significant attention over the past decade due to their energy-saving potential. We have recently synthesized two novel carbazole-based donor-acceptor compounds and analyzed their optical properties to determine their suitability for use as blue emitters in OLEDs. These compounds show remarkable photo-stability and high quantum yields in the blue region of the spectrum. In addition, they have highly solvatochromic emission. In non-polar solvents, bright, blue-shifted (λmax ≈ 398 nm), and highly structured emission is seen. With increasing solvent dielectric constant, the emission becomes weaker, red-shifted (λmax ≈ 507 nm), and broad. We aim to determine the underlying cause of these changes. Electronic structure calculations indicate the presence of multiple excited states with comparable oscillator strength. These states are of interest because there are several with charge-transfer (CT) character, and others centered on the donor moiety. We theorize that CT states play a role in the observed changes in emission lineshape and may promote charge mobility for electrofluorescence in OLEDs. In the future, we plan to use Stark spectroscopy to analyze the polarity of excited states and transient absorption spectroscopy to observe the dynamics in the excited state.

  19. Dielectric and conductivity characteristics of CuCl2 doped poly(N-vinyl carbazole) and its hybrid nanocomposite with Fe3O4.

    PubMed

    Haldar, Ipsita; Biswas, Mukul; Nayak, Arabinda

    2014-08-01

    Copper(II) chloride (CuCl2) doped poly(N-vinyl carbazole) (PNVC)-ferric oxide (Fe3O4) hybrid composites have been prepared and characterized by Fourier transform infrared spectroscopic studies, UV-Vis spectroscopy, high resolution transmission electron microscopy (HRTEM) and X-ray diffraction analyses and evaluated in regard to dielectric response and ac/dc conductivity characteristics. HRTEM images for CuCl2-(PNVC-Fe3O4) composite indicate the co-existence of both the CuCl2 and Fe3O4 nanoparticles in the composite and characteristic lattice fringes are clearly observed which endorse the formation of thin layer interfaces between Fe3O4 and CuCl2 nanoparticles. The dielectric constants of the CuCl2 doped PNVC and PNVC-Fe3O4 composites increase substantially relative to the corresponding values of the polymer and the polymer composite respectively. Likewise, the conductivities (ac and dc) are also improved substantially after doping with CuCl2. The dependence of these functional properties on the extent of metal salt loading has been evaluated and a quantitative estimation of the contribution of the grain boundary and resistance parameters has been attempted in terms of Maxwell-Wagner two-layered model. PMID:25936001

  20. Carbazole Dye-Sensitized Solar Cells Studied from Femtoseconds to Seconds-Effect of Additives in Cobalt- and Iodide-Based Electrolytes.

    PubMed

    Sobuś, Jan; Kubicki, Jacek; Burdziński, Gotard; Ziółek, Marcin

    2015-09-21

    Comprehensive studies of all charge-separation processes in efficient carbazole dye-sensitized solar cells are correlated with their photovoltaic parameters. An important role of partial, fast electron recombination from the semiconductor nanoparticles to the oxidized dye is revealed; this takes place on the picosecond and sub-nanosecond timescales. The charge-transfer dynamics in cobalt tris(bipyridyl) based electrolytes and iodide-based electrolyte is observed to depend on potential-determining additives in a similar way. Upon addition of 0.5 M 4-tert-butylpiridine to both types of electrolytes, the stability of the cells is greatly improved; the cell photovoltage increases by 150-200 mV, the electron injection rate decreases about five times (from 5 to 1 ps(-1) ), and fast recombination slows down about two to three times. Dye regeneration proceeds at a rate of about 1 μs(-1) in all electrolytes. Electron recombination from titania to cobalt electrolytes is much faster than that to iodide ones.

  1. A shock-tube determination of the CN ground state dissociation energy and electronic transition moments for the CN violet and red band systems

    NASA Technical Reports Server (NTRS)

    Arnold, J. O.; Nicholls, R. W.

    1973-01-01

    The CN ground state dissociation energy and the sum of squares of the electronic transition moments of the CN violet bands have been simultaneously determined from spectral emission measurements behind incident shock waves. The unshocked test gases were composed of various CO2-CO-N2-Ar mixtures, and the temperatures behind the incident shocks ranged from 3500 to 8000 K. The variation of the electronic transition moment with internuclear separation was found to be small for both the CN violet and red band systems.

  2. Ultra-violet radiation is responsible for the differences in global epidemiology of chickenpox and the evolution of varicella-zoster virus as man migrated out of Africa

    PubMed Central

    2011-01-01

    Background Of the eight human herpes viruses, varicella-zoster virus, which causes chickenpox and zoster, has a unique epidemiology. Primary infection is much less common in children in the tropics compared with temperate areas. This results in increased adult susceptibility causing outbreaks, for example in health-care workers migrating from tropical to temperate countries. The recent demonstration that there are different genotypes of varicella-zoster virus and their geographic segregation into tropical and temperate areas suggests a distinct, yet previously unconsidered climatic factor may be responsible for both the clinical and molecular epidemiological features of this virus infection. Presentation of the hypothesis Unlike other human herpes viruses, varicella-zoster virus does not require intimate contact for infection to occur indicating that transmission may be interrupted by a geographically restricted climatic factor. The factor with the largest difference between tropical and temperate zones is ultra-violet radiation. This could reduce the infectiousness of chickenpox cases by inactivating virus in vesicles, before or after rupture. This would explain decreased transmissibility in the tropics and why the peak chickenpox incidence in temperate zones occurs during winter and spring, when ultra-violet radiation is at its lowest. The evolution of geographically restricted genotypes is also explained by ultra-violet radiation driving natural selection of different virus genotypes with varying degrees of resistance to inactivation, tropical genotypes being the most resistant. Consequently, temperate viruses should be more sensitive to its effects. This is supported by the observation that temperate genotypes are found in the tropics only in specific circumstances, namely where ultra-violet radiation has either been excluded or significantly reduced in intensity. Testing the Hypothesis The hypothesis is testable by exposing different virus genotypes to ultra-violet

  3. Determination of residues of three triphenylmethane dyes and their metabolites (malachite green, leuco malachite green, crystal violet, leuco crystal violet, and brilliant green) in aquaculture products by LC/MS/MS: first action 2012.25.

    PubMed

    Hurtaud-Pessel, Dominique; Couëdor, Pierrick; Verdon, Eric; Dowell, Dawn

    2013-01-01

    During the AOAC Annual Meeting held from September 30 to October 3, 2012 in Las Vegas, NV, the Expert Review Panel (ERP) on Veterinary Drug Residues reviewed data for the method for determination of residues of three triphenylmethane dyes and their metabolites (malachite green, leuco malachite green, crystal violet, leuco crystal violet, and brilliant green) in aquaculture products by LC/MS/MS, previously published in the Journal of Chromatography A 1218, 1632-1645 (2006). The method data were reviewed and compared to the standard method performance requirements (SMPRs) found in SMPR 2009.001, published in AOAC's Official Methods of Analysis, 19th Ed. (2012). The ERP determined that the data were acceptable, and the method was approved AOAC Official First Action. The method uses acetonitrile to isolate the analyte from the matrix. Then determination is conducted by LCIMS/MS with positive electrospray ionization. Accuracy ranged from 100.1 to 109.8% for samples fortified at levels of 0.5, 0.75, 1.0, and 2.0 microg/kg. Precision ranged from 2.0 to 10.3% RSD for the intraday samples and 1.9 to 10.6% for the interday samples analyzed over 3 days. The described method is designed to accurately operate in the analytical range from 0.5 to 2 microg/kg, where the minimum required performance limit for laboratories has been fixed in the European Union at 2.0 microg/kg for these banned substances and their metabolites. Upper levels of concentrations (1-100 microg/kg) can be analyzed depending on the different optional calibrations used.

  4. Discovery of a Neuroprotective Chemical, (S)-N-(3-(3,6-Dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-6-methoxypyridin-2-amine [(−)-P7C3-S243], with Improved Druglike Properties

    PubMed Central

    2015-01-01

    (−)-P7C3-S243 is a neuroprotective aminopropyl carbazole with improved druglike properties compared with previously reported compounds in the P7C3 class. It protects developing neurons in a mouse model of hippocampal neurogenesis and protects mature neurons within the substantia nigra in a mouse model of Parkinson’s disease. A short, enantioselective synthesis provides the neuroprotective agent in optically pure form. It is nontoxic, orally bioavailable, metabolically stable, and able to cross the blood–brain barrier. As such, it represents a valuable lead compound for the development of drugs to treat neurodegenerative diseases and traumatic brain injury. PMID:24697290

  5. Focused ion beam and field-emission microscopy of metallic filaments in memory devices based on thin films of an ambipolar organic compound consisting of oxadiazole, carbazole, and fluorene units

    USGS Publications Warehouse

    Pearson, Christopher; Bowen, Leon; Lee, Myung Won; Fisher, Alison L.; Linton, Katherine E.; Bryce, Martin R.; Petty, Michael C.

    2013-01-01

    We report on the mechanism of operation of organic thin film resistive memory architectures based on an ambipolar compound consisting of oxadiazole, carbazole, and fluorene units. Cross-sections of the devices have been imaged by electron microscopy both before and after applying a voltage. The micrographs reveal the growth of filaments, with diameters of 50 nm–100 nm, on the metal cathode. We suggest that these are formed by the drift of aluminium ions from the anode and are responsible for the observed switching and negative differential resistance phenomena in the memory devices.

  6. 5′,11′-Dihydro­dispiro­[cyclo­hexane-1,6′-indolo[3,2-b]carbazole-12′,1′′-cyclo­hexa­ne

    PubMed Central

    Guzei, Ilia A.; Spencer, Lara C.; Codner, Eric; Boehm, Joshua M.

    2012-01-01

    The title compound, C28H30N2, is a symmetrical 2:2 product from the condensation of indole and cyclo­hexa­none. It is the only reported 5,11-dihydro­indolo[3,2-b]carbazole compound in which the spiro atoms are quaternary C atoms. Crystals were grown by vapor diffusion in a three-zone electric furnace. The mol­ecule resides on a crystallographic inversion center. The cyclo­hexyl rings are in a slightly distorted chair conformation, whereas the indole units and the spiro-carbons are coplanar within 0.014 Å. PMID:22259386

  7. Clinical usefulness of intradermal fluorescein and patent blue violet dyes for sentinel lymph node identification in dogs.

    PubMed

    Wells, S; Bennett, A; Walsh, P; Owens, S; Peauroi, J

    2006-06-01

    The first lymph node receiving drainage from a specific anatomic region is referred to as the sentinel lymph node (SLN). This study sought to evaluate the intradermal use of two dyes, patent blue violet (PBV) and fluorescein (FL), for SLN mapping in the dog. Multiple intradermal injections were performed in five healthy dogs using two dyes, PBV in 0.9% NaCl and FL in solutions of 0.9% NaCl and 6% hetastarch. Skin flaps were raised and followed to the first area of discrete stain uptake. Areas of uptake were identified as lymph nodes grossly and by cytology. Identification of a SLN for each area of intradermal injection was accomplished for 98% of the injection sites. Intradermal injections of both PBV and FL dyes produce readily visible staining of lymphatic vessels and SLNs in healthy dogs and are sufficient to allow ready identification of these structures during postmortem dissection.

  8. Modification of the photocatalytic activity of TiO2 by β-Cyclodextrin in decoloration of ethyl violet dye

    PubMed Central

    Velusamy, Ponnusamy; Pitchaimuthu, Sakthivel; Rajalakshmi, Subramanian; Kannan, Nagarathinam

    2012-01-01

    The photocatalytic decoloration of an organic dye, ethyl violet (EV), has been studied in the presence of TiO2 and the addition of β-Cyclodextrin (β-CD) with TiO2 (TiO2-β-CD) under UV-A light irradiation. The different operating parameters like initial concentration of dye, illumination time, pH and amount of catalyst used have also been investigated. The photocatalytic decoloration efficiency is more in the TiO2-β-CD/UV-A light system than TiO2/UV-A light system. The mineralization of EV has been confirmed by Chemical Oxygen Demand (COD) measurements. The complexation patterns have been confirmed with UV–Visible and FT-IR spectral data and the interaction between TiO2 and β-CD have been characterized by powder XRD analysis and UV–Visible diffuse reflectance spectroscopy. PMID:25685468

  9. Non-Contact and Non-Destructive Characterization of Shallow Implanted Silicon PN Junctions using Ultra-Violet Raman Spectroscopy

    NASA Astrophysics Data System (ADS)

    Fukumoto, Masashi; Hasuike, Noriyuki; Harima, Hiroshi; Yoshimoto, Masahiro; Yoo, Woo Sik

    2011-01-01

    Ultra-shallow boron implanted (B+ 1 keV 1×1015 cm-2) n-type Si wafers were prepared and characterized by four point probe, SIMS and 363.8 nm excited ultra-violet (UV) Raman spectroscopy before and after rapid thermal annealing (RTA). The penetration depth of 363.8 nm laser radiation in a backscattering Raman configuration, is approximately 5 nm. As junction depth increases from high temperature RTA, sheet resistance decreases. Raman peaks shift in the lower wavenumber direction and its full-width-at-half-maximum (FWHM) broadens. There is clear correlation between junction depth and Raman spectra data. UV Raman spectroscopy can be used as a very powerful non-contact, non-destructive, in-line characterization and monitoring technique for ultra-shallow junctions (USJs).

  10. Effect of Ultra Violet Radiation on Surface Properties: Comparison of RTV 655 and Silica--Based Aerogels

    NASA Astrophysics Data System (ADS)

    Sinden-Redding, Mackenzie; Sabri, Firouzeh

    2009-11-01

    The broad spectrum of ultra violet (UV) radiation causes material property changes such as chalkiness, brittleness, color change, and ultimately complete mechanical failure. UV radiation is also known to modify the surface charge state of insulators. These effects are intensified for materials used in space exploration due to the lack of an atmosphere. In this work, we compare the radiation response and the material properties of RTV 655 (existing calibration targets material on Phoenix Mars Lander) and silica-based aerogels. The extreme light-weight and ability to color-code aerogels makes this material a candidate for the next generation of calibration targets. The radiation response of both materials will be studied using Kelvin Probe, UV-VIS spectrophotometry, and ESR techniques.

  11. Adsorption and subsequent partial photodegradation of methyl violet 2B on Cu/Al layered double hydroxides

    NASA Astrophysics Data System (ADS)

    Guzmán-Vargas, Ariel; Lima, Enrique; Uriostegui-Ortega, Gisselle A.; Oliver-Tolentino, Miguel A.; Rodríguez, Esaú E.

    2016-02-01

    Uncalcined Cu/Al LDH was studied as adsorbent and photocatalyst in the adsorption and subsequent photodegradation of methyl violet 2B dye (MV2B). Physicochemical characterization was carried out by XRD, FTIR, UV-vis, including photoactive properties, DSC/TGA and SEM. Kinetic and thermodynamic models showed great affinity and sorption capacity, the maximum adsorption capacity was 361.0 mg g-1 obtained by Langmuir model, in addition, the results showed that the dye was adsorbed on the LDH surface. Photocatalytic activity was evaluated in the MV2B dye photodegradation process, and it was confirmed by the presence rad OH radicals monitored by EPR spin trapping technique, additionally, COD and TOC parameters were measured, 13C NMR showed differences for the adsorbed and photodegraded samples.

  12. Crystal violet as an i-motif structure probe for reversible and label-free pH-driven electrochemical switch.

    PubMed

    Zhang, Xi Yuan; Luo, Hong Qun; Li, Nian Bing

    2014-06-15

    A simple pH-induced electrochemical switch based on an i-motif structure is developed by using crystal violet as a selective electrochemical probe for the i-motif structure. Thiol-modified cytosine-rich single-strand oligonucleotide (C-rich ssDNA) can be self-assembled on the gold electrode surface via gold-sulfur interaction. Crystal violet is employed as an electrochemical probe for the i-motif structure because of its capability of binding with the i-motif structure through an end-stacking mode. In acidic aqueous solution, crystal violet may approach the electrode surface owing to the formation of the i-motif structure, resulting in an obvious signal, so-called "ON" state. Whereas in neutral or basic aqueous solution, the i-motif structure unfolds to dissociative single strand, which causes crystal violet to leave from the electrode surface, and a weak signal is obtained, so-called "OFF" state. In addition, in the range of pH 4.6-7.3, the increase in current has a good linear relationship (R=0.989) with pH value in the testing solutions. This pH-driven electrochemical switch has the advantages of simplicity, sensitivity, high selectivity, and good reversibility. Furthermore, it provides a possible platform for pH measurement.

  13. The Importance of the 5-Alkyl Substituent for the Violet Smell of Ionones: Synthesis of Racemic 5-Demethyl-α-ionone.

    PubMed

    Chierici, Serena; Bugoni, Serena; Porta, Alessio; Zanoni, Giuseppe; Vidari, Giovanni

    2015-06-01

    The synthesis and the odor tonalities of racemic 5-demethyl-α-ionone are described. This synthetic ionone derivative did not show the typical floral-woody violet smell of α-ionone, definitely proving the importance of a suitably sized and spatially oriented alkyl substituent at C(5) for stimulating olfactory receptors of ionones.

  14. Scanning electron microscopic observations of Basic Violet-1 induced changes in the gill morphology of Labeo rohita.

    PubMed

    Kaur, Kirandeep; Kaur, Satinder; Kaur, Arvinder

    2016-08-01

    Scanning electron microscopic observations were made for the changes in the surface ultra morphology of gill of Labeo rohita as indicators of the stress of lethal (0.1, 0.2, 0.4, 0.6, and 0.8 mg/L dye) and sublethal (0.0225, 0.045, and 0.09 mg/L dye) doses of Basic Violet-1 (CI: 42535, Trade name- Methyl Violet-2B). Present study was taken up as insufficient data exist regarding safety of this dye. The dye was observed to be cytotoxic in nature during the short term (96 h) exposure to lethal doses and tumorogenic as well as cytotoxic during the long term (150 day) exposure to sublethal doses. The dye caused reduction or complete loss of microridges, proliferation of chloride cells, and degeneration of gill lamellae and rakers. The toxic effects became more pronounced with duration as 0.0225 mg/L dye caused remarkable distortion of the normal structure of gills after 150 days of exposure. Such changes may have become the underlying cause for 45-50 % mortality of fish exposed to even sublethal doses of dye as the gills of fish perform a range of vital functions. In the present study, changes in ultra morphology were observed on the 50th day whereas mortality was noticed between 100 and 150 days of subchronic exposure. Therefore, time to time monitoring of ultra morphology of gill will provide us early indicators for the stress of very low levels of pollutants which may later cause mortality of the fish.

  15. Inferring species networks from gene trees in high-polyploid North American and Hawaiian violets (Viola, Violaceae).

    PubMed

    Marcussen, Thomas; Jakobsen, Kjetill S; Danihelka, Jirí; Ballard, Harvey E; Blaxland, Kim; Brysting, Anne K; Oxelman, Bengt

    2012-01-01

    The phylogenies of allopolyploids take the shape of networks and cannot be adequately represented as bifurcating trees. Especially for high polyploids (i.e., organisms with more than six sets of nuclear chromosomes), the signatures of gene homoeolog loss, deep coalescence, and polyploidy may become confounded, with the result that gene trees may be congruent with more than one species network. Herein, we obtained the most parsimonious species network by objective comparison of competing scenarios involving polyploidization and homoeolog loss in a high-polyploid lineage of violets (Viola, Violaceae) mostly or entirely restricted to North America, Central America, or Hawaii. We amplified homoeologs of the low-copy nuclear gene, glucose-6-phosphate isomerase (GPI), by single-molecule polymerase chain reaction (PCR) and the chloroplast trnL-F region by conventional PCR for 51 species and subspecies. Topological incongruence among GPI homoeolog subclades, owing to deep coalescence and two instances of putative loss (or lack of detection) of homoeologs, were reconciled by applying the maximum tree topology for each subclade. The most parsimonious species network and the fossil-based calibration of the homoeolog tree favored monophyly of the high polyploids, which has resulted from allodecaploidization 9-14 Ma, involving sympatric ancestors from the extant Viola sections Chamaemelanium (diploid), Plagiostigma (paleotetraploid), and Viola (paleotetraploid). Although two of the high-polyploid lineages (Boreali-Americanae, Pedatae) remained decaploid, recurrent polyploidization with tetraploids of section Plagiostigma within the last 5 Ma has resulted in two 14-ploid lineages (Mexicanae, Nosphinium) and one 18-ploid lineage (Langsdorffianae). This implies a more complex phylogenetic and biogeographic origin of the Hawaiian violets (Nosphinium) than that previously inferred from rDNA data and illustrates the necessity of considering polyploidy in phylogenetic and

  16. Inferring Species Networks from Gene Trees in High-Polyploid North American and Hawaiian Violets (Viola, Violaceae)

    PubMed Central

    Marcussen, Thomas; Jakobsen, Kjetill S.; Danihelka, Jiří; Ballard, Harvey E.; Blaxland, Kim; Brysting, Anne K.; Oxelman, Bengt

    2012-01-01

    The phylogenies of allopolyploids take the shape of networks and cannot be adequately represented as bifurcating trees. Especially for high polyploids (i.e., organisms with more than six sets of nuclear chromosomes), the signatures of gene homoeolog loss, deep coalescence, and polyploidy may become confounded, with the result that gene trees may be congruent with more than one species network. Herein, we obtained the most parsimonious species network by objective comparison of competing scenarios involving polyploidization and homoeolog loss in a high-polyploid lineage of violets (Viola, Violaceae) mostly or entirely restricted to North America, Central America, or Hawaii. We amplified homoeologs of the low-copy nuclear gene, glucose-6-phosphate isomerase (GPI), by single-molecule polymerase chain reaction (PCR) and the chloroplast trnL-F region by conventional PCR for 51 species and subspecies. Topological incongruence among GPI homoeolog subclades, owing to deep coalescence and two instances of putative loss (or lack of detection) of homoeologs, were reconciled by applying the maximum tree topology for each subclade. The most parsimonious species network and the fossil-based calibration of the homoeolog tree favored monophyly of the high polyploids, which has resulted from allodecaploidization 9–14 Ma, involving sympatric ancestors from the extant Viola sections Chamaemelanium (diploid), Plagiostigma (paleotetraploid), and Viola (paleotetraploid). Although two of the high-polyploid lineages (Boreali-Americanae, Pedatae) remained decaploid, recurrent polyploidization with tetraploids of section Plagiostigma within the last 5 Ma has resulted in two 14-ploid lineages (Mexicanae, Nosphinium) and one 18-ploid lineage (Langsdorffianae). This implies a more complex phylogenetic and biogeographic origin of the Hawaiian violets (Nosphinium) than that previously inferred from rDNA data and illustrates the necessity of considering polyploidy in phylogenetic and

  17. Induction of long interspersed nucleotide element-1 (L1) retrotransposition by 6-formylindolo[3,2-b]carbazole (FICZ), a tryptophan photoproduct.

    PubMed

    Okudaira, Noriyuki; Iijima, Kenta; Koyama, Takayoshi; Minemoto, Yuzuru; Kano, Shigeyuki; Mimori, Akio; Ishizaka, Yukihito

    2010-10-26

    Long interspersed nucleotide element-1 (L1) is a retroelement comprising about 17% of the human genome, of which 80-100 copies are competent as mobile elements (retrotransposition: L1-RTP). Although the genetic structures modified during L1-RTP have been clarified, little is known about the cellular signaling cascades involved. Herein we found that 6-formylindolo[3,2-b]carbazole (FICZ), a tryptophan photoproduct postulated as a candidate physiological ligand of the aryl hydrocarbon receptor (AhR), induces L1-RTP. Notably, RNA-interference experiments combined with back-transfection of siRNA-resistant cDNAs revealed that the induction of L1-RTP by FICZ is dependent on AhR nuclear translocator-1 (ARNT1), a binding partner of AhR, and the activation of cAMP-responsive element-binding protein. However, our extensive analyses suggested that AhR is not required for L1-RTP. FICZ stimulated the interaction of the L1-encoded open reading frame-1 (ORF1) and ARNT1, and recruited ORF1 to chromatin in a manner dependent on the activation of mitogen-activated protein kinase. Along with our additional observations that the cellular cascades for FICZ-induced L1-RTP were different from those of L1-RTP triggered by DNA damage, we propose that the presence of the cellular machinery of ARNT1 mediates L1-RTP. A possible role of ARNT1-mediated L1-RTP in the adaptation of living organisms to environmental changes is discussed.

  18. Delineation of G-Quadruplex Alkylation Sites Mediated by 3,6-Bis(1-methyl-4-vinylpyridinium iodide)carbazole-Aniline Mustard Conjugates.

    PubMed

    Chen, Chien-Han; Hu, Tsung-Hao; Huang, Tzu-Chiao; Chen, Ying-Lan; Chen, Yet-Ran; Cheng, Chien-Chung; Chen, Chao-Tsen

    2015-11-23

    A new G-quadruplex (G-4)-directing alkylating agent BMVC-C3M was designed and synthesized to integrate 3,6-bis(1-methyl-4-vinylpyridinium iodide)carbazole (BMVC) with aniline mustard. Various telomeric G-4 structures (hybrid-2 type and antiparallel) and an oncogene promoter, c-MYC (parallel), were constructed to react with BMVC-C3M, yielding 35 % alkylation yield toward G-4 DNA over other DNA categories (<6 %) and high specificity under competition conditions. Analysis of the intact alkylation adducts by electrospray ionization mass spectroscopy (ESI-MS) revealed the stepwise DNA alkylation mechanism of aniline mustard for the first time. Furthermore, the monoalkylation sites and intrastrand cross-linking sites were determined and found to be dependent on G-4 topology based on the results of footprinting analysis in combination with mass spectroscopic techniques and in silico modeling. The results indicated that BMVC-C3M preferentially alkylated at A15 (H26), G12 (H24), and G2 (c-MYC), respectively, as monoalkylated adducts and formed A15-C3M-A21 (H26), G12-C3M-G4 (H24), and G2-C3M-G4/G17 (c-MYC), respectively, as cross-linked dialkylated adducts. Collectively, the stability and site-selective cross-linking capacity of BMVC-C3M provides a credible tool for the structural and functional characterization of G-4 DNAs in biological systems. PMID:26769627

  19. Delineation of G-Quadruplex Alkylation Sites Mediated by 3,6-Bis(1-methyl-4-vinylpyridinium iodide)carbazole-Aniline Mustard Conjugates.

    PubMed

    Chen, Chien-Han; Hu, Tsung-Hao; Huang, Tzu-Chiao; Chen, Ying-Lan; Chen, Yet-Ran; Cheng, Chien-Chung; Chen, Chao-Tsen

    2015-11-23

    A new G-quadruplex (G-4)-directing alkylating agent BMVC-C3M was designed and synthesized to integrate 3,6-bis(1-methyl-4-vinylpyridinium iodide)carbazole (BMVC) with aniline mustard. Various telomeric G-4 structures (hybrid-2 type and antiparallel) and an oncogene promoter, c-MYC (parallel), were constructed to react with BMVC-C3M, yielding 35 % alkylation yield toward G-4 DNA over other DNA categories (<6 %) and high specificity under competition conditions. Analysis of the intact alkylation adducts by electrospray ionization mass spectroscopy (ESI-MS) revealed the stepwise DNA alkylation mechanism of aniline mustard for the first time. Furthermore, the monoalkylation sites and intrastrand cross-linking sites were determined and found to be dependent on G-4 topology based on the results of footprinting analysis in combination with mass spectroscopic techniques and in silico modeling. The results indicated that BMVC-C3M preferentially alkylated at A15 (H26), G12 (H24), and G2 (c-MYC), respectively, as monoalkylated adducts and formed A15-C3M-A21 (H26), G12-C3M-G4 (H24), and G2-C3M-G4/G17 (c-MYC), respectively, as cross-linked dialkylated adducts. Collectively, the stability and site-selective cross-linking capacity of BMVC-C3M provides a credible tool for the structural and functional characterization of G-4 DNAs in biological systems.

  20. Successful Treatment of Severe Tungiasis in Pigs Using a Topical Aerosol Containing Chlorfenvinphos, Dichlorphos and Gentian Violet

    PubMed Central

    Mutebi, Francis; von Samson-Himmelstjerna, Georg; Feldmeier, Hermann; Waiswa, Charles; Bukeka Muhindo, Jeanne; Krücken, Jürgen

    2016-01-01

    Background In endemic communities, zoonotic tungiasis, a severe skin disease caused by penetrating female sand fleas, is a public health hazard causing significant human and animal morbidity. No validated drugs are currently available for treatment of animal tungiasis. Due to the reservoir in domestic animals, integrated management of human and animal tungiasis is required to avert its negative effects. Methods and principal findings A topical aerosol containing chlorfenvinphos 4.8%, dichlorphos 0.75% and gentian violet 0.145% licensed to treat tick infestations, myiasis and wound sepsis in animals in the study area, was tested for its potential tungicidal effects in a randomized controlled field trial against pig tungiasis in rural Uganda. Animals with at least one embedded flea were randomized in a treatment (n = 29) and a control (n = 26) group. One week after treatment, 58.6% of the treated pigs did not show any viable flea lesion whereas all control pigs had at least one viable lesion. After treatment the number of viable lesions (treated median = 0, overall range = 0–18 vs. control median = 11.5, range = 1–180) and the severity score for estimating acute pathology in pig tungiasis (treated median = 1, range = 0–3.5 vs. control median = 7, range = 0–25) were significantly lower in treated than in control pigs (p < 0.001). In the treatment group the median number of viable flea lesions decreased from 8.5 to 0 (p < 0.001). Similarly, the median acute severity score dropped from 6 to 1 (p < 0.001). Every pig in the treatment group showed a decrease in the number of viable fleas and tungiasis-associated acute morbidity while medians for both increased in the control group. Conclusions The study demonstrates that a topical treatment based on chlorfenvinphos, dichlorphos and gentian violet is highly effective against pig tungiasis. Due to its simplicity, the new approach can be used for the treatment of individual animals as well as in mass campaigns. PMID

  1. The role of human cytochrome P4503A4 in biotransformation of tissue-specific derivatives of 7H-dibenzo[c,g]carbazole

    SciTech Connect

    Mesarosova, Monika; Valovicova, Zuzana; Srancikova, Annamaria; Krajcovicova, Zdenka; Milcova, Alena; Sokolova, Romana; Schmuczerova, Jana; Topinka, Jan; Gabelova, Alena

    2011-09-15

    The environmental pollutant 7H-dibenzo[c,g]carbazole (DBC) and its derivative, 5,9-dimethylDBC (DiMeDBC), produced significant and dose-dependent levels of micronuclei followed by a substantial increase in the frequency of apoptotic cells in the V79MZh3A4 cell line stably expressing the human cytochrome P450 (hCYP) 3A4. In contrast, neither micronuclei nor apoptosis were found in cells exposed to the sarcomagenic carcinogen, N-methylDBC (N-MeDBC). A slight but significant level of gene mutations and DNA adducts detected in V79MZh3A4 cells treated with N-MeDBC, only at the highest concentration (30 {mu}M), revealed that this sarcomagenic carcinogen was also metabolized by hCYP3A4. Surprisingly, DBC increased the frequency of 6-thioguanine resistant (6-TG{sup r}) mutations only at the highest concentration (30 {mu}M), while DiMeDBC failed to increase the frequency of these mutations. The resistance to 6-thioguanine is caused by the mutations in the hypoxanthine-guanine phosphoribosyltransferase (Hprt) gene. The molecular analysis of the coding region of Hprt gene showed a deletion of the entire exon 8 in DiMeDBC-induced 6-TG{sup r} mutants, while no changes in the nucleotide sequences were identified in 6-TG{sup r} mutants produced by DBC and N-MeDBC. Based on our results, we suggest that hCYP3A4 is involved in the metabolism of DBC and its tissue-specific derivatives. While hCYP3A4 probably plays an important role in biotransformation of the liver carcinogens, DBC and DiMeDBC, it might only have a marginal function in N-MeDBC metabolism. - Highlights: > DBC activation via CYP3A4 resulted in micronuclei, DNA adduct formation and mutations in V79MZh3A4 cells. > The CYP3A4-mediated DiMeDBC activation caused micronuclei followed by apoptosis in V79MZh3A4 cells. > The genotoxic effects produced by N-MeDBC in V79MZh3A4 cells were negligible. > The hCYP3A4 may play an important role in DBC and DiMeDBC metabolism. > The CYP3A4 might only have a marginal function in N

  2. Post-column reaction for simultaneous analysis of chromatic and leuco forms of malachite green and crystal violet by high-performance liquid chromatography with photometric detection

    USGS Publications Warehouse

    Allen, J.L.; Meinertz, J.R.

    1991-01-01

    The chromatic and leuco forms of malachite green and crystal violet were readily separated and detected by a sensitive and selective high-performance liquid chromatographic procedure. The chromatic and leuco forms of the dyes were separated within 11 min on a C18 column with a mobile phase of 0.05 M sodium acetate and 0.05 M acetic acid in water (19%) and methanol (81%). A reaction chamber, containing 10% PbO2 in Celite 545, was placed between the column and the spectrophotometric detector to oxidize the leuco forms of the dyes to their chromatic forms. Chromatic and leuco malachite green were quantified by their absorbance at 618 nm; and chromatic and leuco Crystal Violet by their absorbance at 588 nm. Detection limits for chromatic and leuco forms of both dyes ranged from 0.12 to 0.28 ng. A linear range of 1 to 100 ng was established for both forms of the dyes.

  3. Application of ionic liquid-based microwave-assisted extraction of malachite green and crystal violet from water samples.

    PubMed

    Gao, Zhanqi; Liu, Tingfeng; Yan, Xiaoju; Sun, Cheng; He, Huan; Yang, Shaogui

    2013-03-01

    A simple, environment friendly and efficient technique, ionic liquid-based microwave-assisted extraction was first used to determine malachite green and crystal violet (CV) from water samples coupled to HPLC. The key parameters influencing extraction efficiency were investigated, such as the type of ionic liquids, the volume of ionic liquid, extraction time, and so on. Under the optimum conditions, good reproducibility of the extraction performance was obtained (RSD, 1.0% for malachite green (MG) and 5.9% for CV, n = 5). Good linearity (0.10-25 μg L(-1)) was observed with correlation coefficients between 0.9991 and 0.9964. The detection limits of MG and CV were 0.080 and 0.030 μg L(-1), respectively. The proposed method had been successfully applied to determine MG and CV in real water samples with recoveries ranging from 95.4 to 102.8%. Compared with the previous technologies, the proposed method required less extraction time (2 min), and provided lower detection limits and higher enrichment factors. Moreover, there were no volatile and hazardous organic solvents released. Based on these simple, environment friendly, rapid, and highly efficient results, the proposed approach provides a new and promising alternative for simultaneously extracting trace amounts of MG and CV from water.

  4. Unusual spectral shifts on fast violet-B and benzanilide: Effect of solvents, pH and β-cyclodextin

    NASA Astrophysics Data System (ADS)

    Antony Muthu Prabhu, A.; Sankaranarayanan, R. K.; Siva, S.; Rajendiran, N.

    2009-10-01

    The absorption and fluorescence spectra of fast violet-B (FVB) and benzanilide (BA) have been analysed in different solvents, pH and β-cyclodextrin. The inclusion complex of FVB with β-CD is investigated by UV-visible, fluorimetry, AM 1, FTIR and SEM. The absorption maximum of FVB (anilino substitution) is red shifted than that of BA, but the benzoyl substitution hardly changed the ground state structure of BA. Compared to BA, the emission maxima of FVB largely blue shifted in cyclohexane and aprotic solvents, but red shifted in protic solvents and the longer wavelength maxima in FVB is due to the intramolecular charge transfer (TICT). In BA, the normal emission originates from a locally excited state and the longer wavelength band due to intramolecular proton transfer in non-polar/aprotic solvents and in protic solvents it is due to TICT state. β-CD studies reveal that, FVB forms 1:2 complex from 1:1 complex and BA forms 1:2 complex with β-CD.

  5. Batch and continuous (fixed-bed column) biosorption of crystal violet by Artocarpus heterophyllus (jackfruit) leaf powder.

    PubMed

    Saha, Papita Das; Chakraborty, Sagnik; Chowdhury, Shamik

    2012-04-01

    In this study, batch and fixed-bed column experiments were performed to investigate the biosorption potential of Artocarpus heterophyllus (jackfruit) leaf powder (JLP) to remove crystal violet (CV) from aqueous solutions. Batch biosorption studies were carried out as a function of solution pH, contact time, initial dye concentration and temperature. The biosorption equilibrium data showed excellent fit to the Langmuir isotherm model with maximum monolayer biosorption capacity of 43.39 mg g(-1) at pH 7.0, initial dye concentration=50 mg L(-1), temperature=293 K and contact time=120 min. According to Dubinin-Radushkevich (D-R) isotherm model, biosorption of CV by JLP was chemisorption. The biosorption kinetics followed the pseudo-second-order kinetic model. Thermodynamic analysis revealed that biosorption of CV from aqueous solution by JLP was a spontaneous and exothermic process. In order to ascertain the practical applicability of the biosorbent, fixed-bed column studies were also performed. The breakthrough time increased with increasing bed height and decreased with increasing flow rate. The Thomas model as well as the BDST model showed good agreement with the experimental results at all the process parameters studied. It can be concluded that JLP is a promising biosorbent for removal of CV from aqueous solutions.

  6. Tinea Capitis: Mixed or Consecutive Infection with White and Violet Strains of Trichophyton violaceum: A Diagnostic or Therapeutic Challenge

    PubMed Central

    Goyal, Roma

    2015-01-01

    Tinea capitis is a common dermatophyte infection affecting scalp and hair of pre-pubertal children. With introduction of Griseofulvin in 1958, there has been considerable improvement in the treatment of tinea capitis. A seven-year-old male child was brought to the dermatology clinic. He presented with diffuse white scaly patches of alopecia on scalp of one-year duration. The child was sent to the microbiology section of the National Health laboratory, Botswana for the collection of the samples. The samples consisted of scalp scrapings and few plucked hairs from the suspicious areas, which were collected by swab and scalpel blade methods. Potassium hydroxide (10% KOH) mounts were prepared for scales and hair samples. Scales were positive for fungal elements and endothrix type of perforation was seen in hair. Cultures on Sabouraud’s dextrose agar (SDA) and Derm agar were incubated at 25°C, which yielded white variant of Trichophyton violaceum after two weeks of incubation. T. vioaceum (white variant) grew in all the plates. After six weeks of treatment with griseofulvin, the repeat culture grew only T. violaceum (violet strain). The child showed a definite clinical improvement. PMID:26814801

  7. Highly selective etching of SnO2 absorber in binary mask structure for extreme ultra-violet lithography.

    PubMed

    Lee, Soo Jin; Jung, Chang Yong; Park, Sung Jin; Hwangbo, Chang Kweun; Seo, Hwan Seok; Kim, Sung Soo; Lee, Nae-Eung

    2012-04-01

    Among the core EUVL (extreme ultra-violet lithography) technologies for nanoscale patterning below the 30 nm node for Si chip manufacturing, new materials and fabrication processes for high-performance EUVL masks are of considerable importance due to the use of new reflective optics. In this work, the selective etching of SnO2 (tin oxide) as a new absorber material, with high EUV absorbance due to its large extinction coefficient, for the binary mask structure of SnO2 (absorber layer)/Ru (capping/etch stop layer)/Mo-Si multilayer (reflective layer)/Si (substrate), was investigated. Because infinitely high selectivity of the SnO2 layer to the Ru ESL is required due to the ultrathin nature of the Ru layer, various etch parameters were assessed in the inductively coupled Cl2/Ar plasmas in order to find the process window required for infinitely high etch selectivity of the SnO2 layer. The results showed that the gas flow ratio and V(dc) value play an important role in determining the process window for the infinitely high etch selectivity of SnO2 to Ru ESL. The high EUV-absorbance SnO2 layer, patternable by a dry process, allows a smaller absorber thickness, which can mitigate the geometric shadowing effects observed for high-performance binary EUVL masks.

  8. Fish erythrocytes as biomarkers for the toxicity of sublethal doses of an azo dye, Basic Violet-1 (CI: 42535).

    PubMed

    Kaur, Kirandeep; Kaur, Arvinder

    2015-02-01

    The aim of the present study was to investigate poikilocytosis in Labeo rohita (an important food fish) as an early indicator of stress due to an azo dye, Basic Violet-1 (CI: 42535). This dye was observed to be very toxic to test fish (96 h LC50 as0.45 mg/L dye). Fish were given short-term (96 h) and subchronic (150 days) exposures to the dye, and poikilocytosis was recorded under light and scanning electron microscopy (SEM). Light microscopy helped in identification of micronuclei along with irregularities, notches, blebs, lobes, crenation, clumps, chains, spherocytes, vacuolation, and necrosis in erythrocytes. However, SEM indicated shrinkage, oozing of cytoplasm, and several new abnormal shapes including marginal foldings, discocytes, keratocytes, dacrocytes, degmacytes, acanthocytes, echinocytes, protuberances, stomatocytes, drepanocytes, holes in the membrane, stippling/spicules, crescent-shaped cells, triangular cells, and pentagonal cells. Earlier studies speculated changes in the membrane to be responsible for clumping and chaining of erythrocytes, whereas the present SEM study clearly indicates that oozing out of cytoplasm is also responsible for the formation of chains and clumps. This study also shows that erythrocytes exhibit pathological symptoms before the appearance of other external symptoms such as abnormal behavior or mortality of fish. There was a dose- and duration-dependent increase; therefore, poikilocytosis, especially echinocytes, spherocytes, and clumps, can act as a biomarker for the stress caused by azo dyes.

  9. Ultra-violet Sensing Characteristic and Field Emission Properties of Vertically Aligned Aluminum Doped Zinc Oxide Nanorod Arrays

    SciTech Connect

    Mamat, M. H.; Malek, M. F.; Musa, M. Z.; Khusaimi, Z.; Rusop, M.

    2011-05-25

    Ultra-violet (UV) sensing behavior and field emission characteristic have been investigated on vertically aligned aluminum (Al) doped zinc oxide (ZnO) nanorod arrays prepared using sol-gel immersion method. Uniform and high coverage density of ZnO nanorod arrays have been successfully deposited on seeded-catalyst coated substrates. The synthesized nanorods have diameter sizes between 50 nm to 150 nm. The XRD spectra show Al doped ZnO nanorod array has high crystallinity properties with the dominancy of crystal growth along (002) plane or c-axis. UV photoresponse measurement indicates that Al doped ZnO nanorod array sensitively detects UV light as shown by conductance increment after UV illumination exposure. The nanorod array shows good field emission properties with low turn on field and threshold field at 2.1 V/{mu}m and 5.6 V/{mu}m, respectively. The result suggested that Al doped ZnO nanorod arrays prepared by low-cost sol-gel immersion method show promising result towards fabrication of multi applications especially in UV photoconductive sensor and field emission displays.

  10. Bandgap-tailored NiO nanospheres: an efficient photocatalyst for the degradation of crystal violet dye solution

    NASA Astrophysics Data System (ADS)

    Vahini, Raja; Kumar, Puvaneswaran Senthil; Karuthapandian, Swaminathan

    2016-08-01

    Bandgap-tailored NiO nanospheres were successfully synthesized by facile precipitation method for the first time and characterized by XRD, EDX, SEM, TEM, FTIR, UV and PL. Interestingly, the modification of the band gap was observed using UV-Vis (DRS) spectroscopy, and the observed band gap is 3.31 eV. The morphology of the materials was analysed by SEM and TEM which show the sphere like structures of NiO with the particle size of ~20 nm. The efficiency of the materials was examined by the degradation of crystal violet dye under UV light illumination. The complete degradation was achieved within 60 min, and the mechanism of the degradation were also been proposed. In addition, the degradation of rhodamine B (RhB) and methylene blue dye solution was also carried out to extend the practical applications of NiO nanospheres. The involvement of reactive oxidative species (ROS) was found out by trapping experiment, and the ROS is superoxide radical anion.

  11. Potential suppressive effects of gentian violet on human breast cancer MDA-MB-231 cells in vitro: Comparison with gemcitabine

    PubMed Central

    Yamaguchi, Masayoshi; Murata, Tomiyasu

    2016-01-01

    Gentian violet (GV), a cationic triphenylmethane dye, is used as an antifungal and antibacterial agent. Recently, attention has been focused on GV as a potential chemotherapeutic and antiangiogenic agent. The present study was undertaken to determine the suppressive effects of GV on human breast cancer MDA-MB-231 cells in vitro. The proliferation of MDA-MB-231 cells was suppressed by culture with GV (1–200 nM). The suppressive effects of GV on cell proliferation were not potentiated in the presence of various inhibitors that induce cell cycle arrest in vitro. This finding suggested that GV inhibits G1 and G2/M phase cell cycle arrest in MDA-MB-231 cells. The suppressive effects of GV on proliferation are mediated through the inhibition of various signaling pathways or nuclear transcription in vitro. Moreover, the suppressive effects of GV on cell proliferation were compared with that of gemcitabine, a strong antitumor agent that induces nuclear DNA damage. Notably, the culture with gemcitabine >50 nM suppressed cell proliferation, while the effects of GV were observed at >1 nM. The suppressive effects of gemcitabine on cell proliferation were not potentiated by GV. Overall, the present study demonstrated that GV exhibits a potential suppressive effect on the proliferation of human breast cancer MDA-MB-231 cells in vitro. PMID:27446479

  12. Effect of heat shock on the chilling sensitivity of trichomes and petioles of African violet (Saintpaulia ionantha).

    PubMed

    Saltveit, Mikal E.; Hepler, Peter K.

    2004-05-01

    Chilling at 6 degrees C caused an immediate cessation of protoplasmic streaming in trichomes from African violets (Saintpaulia ionantha), and a slower aggregation of chloroplasts in the cells. Streaming slowly recovered upon warming to 20 degrees C, reaching fairly stable rates after 4, 15, 25 and 35 min for tissue chilled for 2 min and for 2, 14 and 24 h, respectively. The rate of ion leakage from excised petioles into an isotonic 0.2 M mannitol solution increased after 12 h of chilling and reached a maximum after 3 days of chilling. A heat shock at 45 degrees C for 6 min reduced chilling-induced rates of ion leakage from excised 1-cm petiole segments by over 50%, namely to levels near that from non-chilled control tissue. Heat-shock treatments themselves had no effect on the rate of ion leakage from non-chilled petiole segments. Protoplasmic streaming was stopped by 1 min of heat shock at 45 degrees C, but slowly recovered to normal levels after about 30 min Chloroplasts aggregation was prevented by a 1 or 2 min 45 degrees C heat-shock treatment administered 1.5 h before chilling, but heat-shock treatments up to 6 min only slightly delayed the reduction in protoplasmic streaming caused by chilling. Tradescantia virginiana did not exhibit symptoms associated with chilling injury in sensitive species (i.e. cessation of protoplasmic streaming in stamen hairs and increased ion leakage from leaf tissue). PMID:15086815

  13. Plant regeneration and floral bud formation from intact floral parts of African violet (Saintpaulia ionantha H. Wendl.) cultured in vitro.

    PubMed

    Daud, N; Taha, R M

    2008-04-01

    Intact immature flower buds of African violet (Saintpaulia ionantha H. Wendl.) were used as explant sources for in vitro studies. The effect of exogenous hormones, NAA and BAP on the indirect organogenesis of this species was observed. Callus was formed on the cut end (base) of pedicels of floral buds where they were in contact with the medium. When maintained on the same medium, callus was differentiated into adventitious shoots after 10 weeks in culture. MS media supplemented with 2.0 mg L(-1) NAA and 1.0 mg L(-1) BAP gave the highest number of sterile or vegetative floral buds from the surface of callus of the explants, but these buds failed to develop further. The floral buds were expanded as abnormal flowers. The floral structures were smaller in size compared to intact flowers. Petals (corolla) were white to purple in colour but did not form any reproductive organs, i.e., stamens or pistils. All sterile or vegetative floral buds and abnormal flowers survived for 3 months in culture but failed to reach anthesis. PMID:18810979

  14. Experimental design approach applied to the elimination of crystal violet in water by electrocoagulation with Fe or Al electrodes.

    PubMed

    Durango-Usuga, Paula; Guzmán-Duque, Fernando; Mosteo, Rosa; Vazquez, Mario V; Peñuela, Gustavo; Torres-Palma, Ricardo A

    2010-07-15

    An experimental design methodology was applied to evaluate the decolourization of crystal violet (CV) dye by electrocoagulation using iron or aluminium electrodes. The effects and interactions of four parameters, initial pH (3-9), current density (6-28 A m(-2)), substrate concentration (50-200 mg L(-1)) and supporting electrolyte concentration (284-1420 mg L(-1) of Na(2)SO(4)), were optimized and evaluated. Although the results using iron anodes were better than for aluminium, the effects and interactions of the studied parameters were quite similar. With a confidence level of 95%, initial pH and supporting electrolyte concentration showed limited effects on the removal rate of CV, whereas current density, pollutant concentration and the interaction of both were significant. Reduced models taking into account significant variables and interactions between variables have shown good correlations with the experimental results. Under optimal conditions, almost complete removal of CV and chemical oxygen demand were obtained after electrocoagulation for 5 and 30 min, using iron and aluminium electrodes, respectively. These results indicate that electrocoagulation with iron anodes is a rapid, economical and effective alternative to the complete removal of CV in waters. Evolutions of pH and residual iron or aluminium concentrations in solution are also discussed. PMID:20303653

  15. Electrochemical degradation of crystal violet with BDD electrodes: effect of electrochemical parameters and identification of organic by-products.

    PubMed

    Palma-Goyes, Ricardo E; Guzmán-Duque, Fernando L; Peñuela, Gustavo; González, Ignacio; Nava, Jose L; Torres-Palma, Ricardo A

    2010-09-01

    This paper explores the applicability of electrochemical oxidation on a triphenylmethane dye compound model, hexamethylpararosaniline chloride (or crystal violet, CV), using BDD anodes. The effect of the important electrochemical parameters: current density (2.5-15 m A cm(-2)), dye concentration (33-600 mg L(-1)), sodium sulphate concentration (7.1-50.0 g L(-1)) and initial pH (3-11) on the efficiency of the electrochemical process was evaluated. The results indicated that while the current density was lower than the limiting current density, no side products (hydrogen peroxide, peroxodisulphate, ozone and chlorinated oxidizing compounds) were generated and the degradation, through OH radical attack, occurred with high efficiency. Analysis of intermediates using GC-MS investigation identified several products: N-methylaniline, N,N-dimethylaniline, 4-methyl-N,N-dimethylaniline, 4-methyl-N-methylaniline, 4-dimethylaminophenol, 4-dimethylaminobenzoic acid, 4-(N,N-dimethylamino)-4'-(N',N'-dimethylamino) diphenylmethane, 4-(4-dimethylaminophenyl)-N,N-dimethylaniline, 4-(N,N-dimethylamino)-4'-(N',N'-dimethylamino) benzophenone. The presence of these aromatic structures showed that the main CV degradation pathway is related to the reaction of CV with the OH radical. Under optimal conditions, practically 100% of the initial substrate and COD were eliminated in approximately 35 min of electrolysis; indicating that the early CV by-products were completely degraded by the electrochemical system. PMID:20709357

  16. Vacuum ultra-violet damage and damage mitigation for plasma processing of highly porous organosilicate glass dielectrics

    NASA Astrophysics Data System (ADS)

    de Marneffe, J.-F.; Zhang, L.; Heyne, M.; Lukaszewicz, M.; Porter, S. B.; Vajda, F.; Rutigliani, V.; el Otell, Z.; Krishtab, M.; Goodyear, A.; Cooke, M.; Verdonck, P.; Baklanov, M. R.

    2015-10-01

    Porous organosilicate glass thin films, with k-value 2.0, were exposed to 147 nm vacuum ultra-violet (VUV) photons emitted in a Xenon capacitive coupled plasma discharge. Strong methyl bond depletion was observed, concomitant with a significant increase of the bulk dielectric constant. This indicates that, besides reactive radical diffusion, photons emitted during plasma processing do impede dielectric properties and therefore need to be tackled appropriately during patterning and integration. The detrimental effect of VUV irradiation can be partly suppressed by stuffing the low-k porous matrix with proper sacrificial polymers showing high VUV absorption together with good thermal and VUV stability. In addition, the choice of an appropriate hard-mask, showing high VUV absorption, can minimize VUV damage. Particular processing conditions allow to minimize the fluence of photons to the substrate and lead to negligible VUV damage. For patterned structures, in order to reduce VUV damage in the bulk and on feature sidewalls, the combination of both pore stuffing/material densification and absorbing hard-mask is recommended, and/or the use of low VUV-emitting plasma discharge.

  17. Effectiveness of photochemical and sonochemical processes in degradation of Basic Violet 16 (BV16) dye from aqueous solutions

    PubMed Central

    2012-01-01

    In this study, degradation of Basic Violet 16 (BV16) by ultraviolet radiation (UV), ultrasonic irradiation (US), UV/H2O2 and US/H2O2 processes was investigated in a laboratory-scale batch photoreactor equipped with a 55W immersed-type low-pressure mercury vapor lamp and a sonoreactor with high frequency (130kHz) plate type transducer at 100W of acoustic power. The effects of initial dye concentration, concentration of H2O2 and solution pH and presence of Na2SO4 was studied on the sonochemical and photochemical destruction of BV16 in aqueous phase. The results indicated that in the UV/H2O2 and US/H2O2 systems, a sufficient amount of H2O2 was necessary, but a very high H2O2 concentration would inhibit the reaction rate. The optimum H2O2 concentration was achieved in the range of 17 mmol/L at dye concentration of 30 mg/L. A degradation of 99% was obtained with UV/H2O2 within 8 minutes while decolorization efficiency by using UV (23%), US (<6%) and US/H2O2(<15%) processes were negligible for this kind of dye. Pseudo-first order kinetics with respect to dyestuffs concentrations was found to fit all the experimental data. PMID:23369268

  18. Vacuum ultra-violet damage and damage mitigation for plasma processing of highly porous organosilicate glass dielectrics

    SciTech Connect

    Marneffe, J.-F. de Lukaszewicz, M.; Porter, S. B.; Vajda, F.; Rutigliani, V.; Verdonck, P.; Baklanov, M. R.; Zhang, L.; Heyne, M.; El Otell, Z.; Krishtab, M.; Goodyear, A.; Cooke, M.

    2015-10-07

    Porous organosilicate glass thin films, with k-value 2.0, were exposed to 147 nm vacuum ultra-violet (VUV) photons emitted in a Xenon capacitive coupled plasma discharge. Strong methyl bond depletion was observed, concomitant with a significant increase of the bulk dielectric constant. This indicates that, besides reactive radical diffusion, photons emitted during plasma processing do impede dielectric properties and therefore need to be tackled appropriately during patterning and integration. The detrimental effect of VUV irradiation can be partly suppressed by stuffing the low-k porous matrix with proper sacrificial polymers showing high VUV absorption together with good thermal and VUV stability. In addition, the choice of an appropriate hard-mask, showing high VUV absorption, can minimize VUV damage. Particular processing conditions allow to minimize the fluence of photons to the substrate and lead to negligible VUV damage. For patterned structures, in order to reduce VUV damage in the bulk and on feature sidewalls, the combination of both pore stuffing/material densification and absorbing hard-mask is recommended, and/or the use of low VUV-emitting plasma discharge.

  19. Efficient degradation of crystal violet in magnetic CuFe2O4 aqueous solution coupled with microwave radiation.

    PubMed

    Chen, Hongzhe; Yang, Shaogui; Chang, Jiao; Yu, Kai; Li, Dongfang; Sun, Cheng; Li, Aimin

    2012-09-01

    Nanoscale copper ferrite was prepared by co-precipitation method, while citrate acid assisted method was used as reference. Microwave-induced degradation of crystal violet was performed with synthesized copper ferrite, and the behavior of copper ferrite in this process was studied by X-ray photoelectron spectroscopy, SEM/EDS and vector network analyzer. Microwave radiation could greatly enhance the activity of copper ferrite in organic oxidation. The variant of copper and iron on the surface and in the inner core of copper ferrite was studied here. Copper ferrite presents relatively low dielectric loss. Meanwhile, microwave radiation makes a faster degradation than conventional heating process, indicating an indispensable non-thermal effect of microwave with copper ferrite in the process. Microwave induced holes could be responsible for the efficient degradation. The effect of annealing on crystallization and degradation process was considered here, and the intermediates and products were studied by GC-MS and LC-MS to provide a comprehensively evaluation of degradation.

  20. Comparison of Fecal Coliform Agar and Violet Red Bile Lactose Agar for Fecal Coliform Enumeration in Foods

    PubMed Central

    Leclercq, A.; Wanegue, C.; Baylac, P.

    2002-01-01

    A 24-h direct plating method for fecal coliform enumeration with a resuscitation step (preincubation for 2 h at 37 ± 1°C and transfer to 44 ± 1°C for 22 h) using fecal coliform agar (FCA) was compared with the 24-h standardized violet red bile lactose agar (VRBL) method. FCA and VRBL have equivalent specificities and sensitivities, except for lactose-positive non-fecal coliforms such as Hafnia alvei, which could form typical colonies on FCA and VRBL. Recovery of cold-stressed Escherichia coli in mashed potatoes on FCA was about 1 log unit lower than that with VRBL. When the FCA method was compared with standard VRBL for enumeration of fecal coliforms, based on counting carried out on 170 different food samples, results were not significantly different (P > 0.05). Based on 203 typical identified colonies selected as found on VRBL and FCA, the latter medium appears to allow the enumeration of more true fecal coliforms and has higher performance in certain ways (specificity, sensitivity, and negative and positive predictive values) than VRBL. Most colonies clearly identified on both media were E. coli and H. alvei, a non-fecal coliform. Therefore, the replacement of fecal coliform enumeration by E. coli enumeration to estimate food sanitary quality should be recommended. PMID:11916678