Science.gov

Sample records for 3 6 12

  1. FUN3D Manual: 12.6

    NASA Technical Reports Server (NTRS)

    Biedron, Robert T.; Derlaga, Joseph M.; Gnoffo, Peter A.; Hammond, Dana P.; Jones, William T.; Kleb, William L.; Lee-Rausch, Elizabeth M.; Nielsen, Eric J.; Park, Michael A.; Rumsey, Christopher L.; Thomas, James L.; Wood, William A.

    2015-01-01

    This manual describes the installation and execution of FUN3D version 12.6, including optional dependent packages. FUN3D is a suite of computational fluid dynamics simulation and design tools that uses mixed-element unstructured grids in a large number of formats, including structured multiblock and overset grid systems. A discretely-exact adjoint solver enables efficient gradient-based design and grid adaptation to reduce estimated discretization error. FUN3D is available with and without a reacting, real-gas capability. This generic gas option is available only for those persons that qualify for its beta release status.

  2. 12 CFR 3.6 - Minimum capital ratios.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Minimum capital ratios. 3.6 Section 3.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Minimum Capital Ratios § 3.6 Minimum capital ratios. (a) Risk-based capital ratio....

  3. 12 CFR 3.6 - Minimum capital ratios.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Minimum capital ratios. 3.6 Section 3.6 Banks... maintain Tier 1 capital in an amount equal to at least 3.0 percent of adjusted total assets. (c) Additional... banks meeting the conditions set forth in this paragraph (c), the minimum Tier 1 leverage ratio is...

  4. 12 CFR 3.6 - Minimum capital ratios.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Minimum capital ratios. 3.6 Section 3.6 Banks... maintain Tier 1 capital in an amount equal to at least 3.0 percent of adjusted total assets. (c) Additional... banks meeting the conditions set forth in this paragraph (c), the minimum Tier 1 leverage ratio is...

  5. 12 CFR 3.6 - Minimum capital ratios.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Minimum capital ratios. 3.6 Section 3.6 Banks... national banks must have and maintain the minimum risk-based capital ratio as set forth in appendix A (and, for certain banks, in appendix B). (b) Total assets leverage ratio. All national banks must have...

  6. White upconversion emission in Li+/Yb3+/Tm3+/Er3+-doped Gd6MoO12 phosphors

    NASA Astrophysics Data System (ADS)

    Sun, Jiayue; Xue, Bing; Du, Haiyan

    2013-07-01

    The Yb3+/Er3+/Tm3+-doped Gd6MoO12 phosphors and Li+/Yb3+/Er3+/Tm3+-doped Gd6MoO12 phosphors were synthesized by the high-temperature solid-state method. Under 980 nm laser diode excitation, the Gd6MoO12:Li+/Yb3+/Er3+/Tm3+ phosphors show the white upconversion (UC) emission at the pump power of 200 mW/cm2, which is composed of the blue (1G4→3H6 of Tm3+), green (2H11/2, 4S3/2→4I15/2 of Er3+), and red (4F9/2→4I15/2 of Er3+) UC emissions. The calculated CIE color coordinates of Gd6MoO12:Tm3+/Er3+/Yb3+ phosphors changed from blue area to white area after the Li+ ion doping. Then, the effect of Li+ ions mixing on the emission was analysed. The relative UC mechanisms and properties were also investigated and proposed based on their spectral. The additional mixed Li+ ions enhanced the red and green upconversion emission largely in this phosphor and then formed the white UC emission, which indicated that the Li+ is a promising dopant for tuning white light luminescence in some case.

  7. High resolution infrared spectrum and global analysis of ν5, ν12, and ν12 + ν6 - ν6 in CH 3SiH 3

    NASA Astrophysics Data System (ADS)

    Borvayeh, L.; Ozier, I.; Bauder, A.; Moazzen-Ahmadi, N.

    2009-06-01

    The vibration-torsion-rotation spectrum of CH 3SiH 3 has been measured from 470 to 725 cm -1 at near-Doppler resolution. The full-width at half - maximum of the lines observed near 600 cm -1 was 0.0011 cm -1. The spectra were obtained using a Bruker IFS 125 HR Fourier transform spectrometer with the broadband source radiation being supplied from the synchrotron emission of the storage ring at the Canadian Light Source. Three vibrational bands were investigated: the lowest lying perpendicular fundamental ν12 centred near 524 cm -1, the lowest lying parallel fundamental ν5 near 703 cm -1, and the torsional hot band ν12 + ν6 - ν6 near 534 cm -1. For ν12 and ν5, the resolution and sensitivity are much improved over those in earlier studies, with many of the torsional multiplets now being resolved even in the cases where the upper levels are unperturbed. The primary motivation for the present work was the hot band, here reported for the first time, where the dependence of the silyl rock in ν12 on the torsional motion is much more pronounced. In addition, for the vibrational ground state ( gs), two "forbidden" high torsional overtones v6 = 3 ← 0 and 5 ← 0 have been observed that become allowed through resonant mixing of the upper states with ν12 and ν5, respectively. In each case, two ( K, σ) series have been measured where the mixing is largest. Here σ = 0, 1, -1 labels the torsional sub-levels. Using the Fourier transform waveguide spectrometer at E. T. H., the three σ-components of the ( J = 1 ← 0) transition in ν12 + ν6 were observed, and a series of direct l-doubling transitions in ν12 + ν6 were measured for σ = 0. In a global fit, all the new data have been analysed along with the frequencies for other transitions obtained in earlier investigations. The analysis takes into account the relevant interactions among the torsional stacks of levels in the gs, ν12, and ν5. These include the previously known ( gs, ν12) Coriolis-like and ( gs, ν5

  8. 17 CFR 240.3a12-6 - Definition of “common trust fund” as used in section 3(a)(12) of the Act.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... § 240.3a12-6 Definition of “common trust fund” as used in section 3(a)(12) of the Act. The term common trust fund as used in section 3(a)(12) of the Act (15 U.S.C. 78c(a)(12)) shall include a common trust..., That: (a) The common trust fund is operated in compliance with the same state and federal...

  9. Lattice Effective Field Theory Calculations for A=3, 4, 6, 12 Nuclei

    SciTech Connect

    Epelbaum, Evgeny; Krebs, Hermann; Lee, Dean; Meissner, Ulf-G.

    2010-04-09

    We present lattice results for the ground state energies of tritium, helium-3, helium-4, lithium-6, and carbon-12 nuclei. Our analysis includes isospin breaking, Coulomb effects, and interactions up to next-to-next-to-leading order in chiral effective field theory.

  10. Nqrs Data for C24H48I12O42S12Tl12 [C12H24O6·12(CH2IO3STl)] (Subst. No. 1591)

    NASA Astrophysics Data System (ADS)

    Chihara, H.; Nakamura, N.

    This document is part of Subvolume B 'Substances Containing C10H16 … Zn' of Volume 48 'Nuclear Quadrupole Resonance Spectroscopy Data' of Landolt-Börnstein - Group III 'Condensed Matter'. It contains an extract of Section '3.2 Data tables' of the Chapter '3 Nuclear quadrupole resonance data' providing the NQRS data for C24H48I12O42S12Tl12 [C12H24O6·12(CH2IO3STl)] (Subst. No. 1591)

  11. Structure and magnetism of S = 1/2 kagome antiferromagnets NiCu3(OH)6Cl2 and CoCu3(OH)6Cl2.

    PubMed

    Li, Yue-sheng; Zhang, Qing-ming

    2013-01-16

    We have successfully synthesized S = 1/2 kagome antiferromagnets MCu(3)(OH)(6)Cl(2) (M = Ni and Co) by a hydrothermal method with a rotating pressure vessel. Structural characterization shows that both compounds have similar crystal structure to ZnCu(3)(OH)(6)Cl(2) with R3m symmetry. As with ZnCu(3)(OH)(6)Cl(2), the compounds show no obvious hysteresis at 2 K. A spin-glass transition is found in both NiCu(3)(OH)(6)Cl(2) and CoCu(3)(OH)(6)Cl(2) at low temperatures (6.0 and 3.5 K respectively) by AC susceptibility measurements. This indicates no long-range magnetic order and a strong spin frustration. The substitution of Zn(2+) by magnetic ions Ni(2+) or Co(2+) effectively enhances the interlayer exchange coupling and changes the ground state of the kagome spin system.

  12. Volumetric Properties of the Mixture (+,-)-Methyl-1,3-dioxolan-2-one C4H6O3 + C6H12O3 2,4,6-Trimethyl-1,3,5-trioxane (VMSD1511, LB4523_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture (+,-)-Methyl-1,3-dioxolan-2-one C4H6O3 + C6H12O3 2,4,6-Trimethyl-1,3,5-trioxane (VMSD1511, LB4523_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  13. Volumetric Properties of the Mixture Dimethyl carbonate C3H6O3 + C6H12O3 2,4,6-Trimethyl-1,3,5-trioxane (VMSD1511, LB4517_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Dimethyl carbonate C3H6O3 + C6H12O3 2,4,6-Trimethyl-1,3,5-trioxane (VMSD1511, LB4517_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  14. New measurements of the 12. 6 millisecond pulsar in Cygnus X-3

    SciTech Connect

    Brazier, K.T.S.; Carraminana, A.; Chadwick, P.M.; Dipper, N.A.; Lincoln, E.W. )

    1990-02-01

    Evidence for a 12.59 ms pulsar in Cygnus X-3 is presented on the basis of TeV gamma-ray observations. Evidence for pulsed emission at a phase in the 4.8 hr cycle and with a pulsar period and secular period derivative are compatible with earlier measurements (Chadwick et al., 1985). The conservative overall Rayleigh probability of uniformity of phase for this new result is 1.7 x 10 to the -6th. Data from observations of Cygnus X-3 from 1981 to 1985 are analyzed using a new X-ray ephemeris of the 4.8 hr X-ray cycle. This suggests that Cygnus X-3 is producing sporadic very high energy gamma rays at a fixed time in the 4.8 hr X-ray cycle. 28 refs.

  15. Microwave spectrum and structure of 3,6-dihydro-1,2-dioxin

    NASA Astrophysics Data System (ADS)

    Tanimoto, Mitsutoshi; Kondo, Toshihiko

    1994-07-01

    The microwave spectrum of 3,6-dihydro-1,2-dioxin, a cyclic peroxide derived from buta-1,3-diene, was measured in the frequency range 10-26 GHz. Rotational and centrifugal distortion constants were determined from a least-squares fit to the observed b-type rotational transition frequencies. The molecular structure is inferred on the basis of the rotational constants. The molecule is found to have a skewed boat form as found in cyclohexene. The NMR spectrum of the molecule was observed at temperatures down to -100°C and analyzed in terms of interchanging conformations. The activation energy and entropy of the puckering motion were derived.

  16. 12 CFR 12.6 - Fees.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... SECURITIES TRANSACTIONS § 12.6 Fees. A national bank may charge a reasonable fee for providing notification pursuant to § 12.5(b), (c), and (e). A national bank may not charge a fee for providing notification... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Fees. 12.6 Section 12.6 Banks and...

  17. 12 CFR 12.6 - Fees.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... SECURITIES TRANSACTIONS § 12.6 Fees. A national bank may charge a reasonable fee for providing notification pursuant to § 12.5(b), (c), and (e). A national bank may not charge a fee for providing notification... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Fees. 12.6 Section 12.6 Banks and...

  18. Software Design Document Vehicle Simulation CSCI (5). Volume 3, Sections 2.5.4 - 2.6.18.12.1

    DTIC Science & Technology

    1991-06-01

    vec sub Section 2.6.2.65 vec mag3 /simnet/common/include/global/sim macros.h zero qet-new velocities Section 2.5.12.29.3 f mat copy Section 2.6.2.12.1...Section 2.1.2.2.3.1.1 vehicle place Section 2.5.19.1.2 v_mag Macro defined in /simnet/releasesrclibsrc/include/dyn state.h mag3 Macro defined in

  19. Hydrothermal synthesis of Yb3+, Tm3+ co-doped Gd6MoO12 and its upconversion properties

    NASA Astrophysics Data System (ADS)

    Di, Qiu-Mei; Sun, Yu-Mei; Xu, Qi-Guang; Han, Liu; Xue, Bing; Sun, Jia-Yue

    2015-06-01

    Yb3+, Tm3+ co-doped Gd6MoO12 phosphors with different morphologies are prepared by the hydrothermal method. The dendrites present different morphologies (including hexagonal prisms, spindles, and spheres) after changing the pH value and edetate disodium (EDTA) usage. It is found that each of the two factors plays a crucial role in forming different morphologies. The up-conversion (UC) luminescence is studied. Under 980-nm semiconductor laser excitation, relatively strong blue emission and weak red emission are observed. Finally, the effect of pumping power on the UC luminescence properties and the level diagram mechanism of Gd6MoO12:Yb3+/Tm3+ phosphor are also discussed. Project supported by the National Natural Science Foundation of China (Grant No. 20976002), the Beijing Natural Science Foundation, China (Grant No. 2122012), the Key Projects for Science and Technology of Beijing Education Commission, China (Grant No. KZ201310011013), and the Education and Research Fund of Guangdong Province, China (Grant No. 2011B090400100).

  20. Europium gallium garnet (Eu3Ga5O12) and Eu3GaO6: Synthesis and material properties

    NASA Astrophysics Data System (ADS)

    Sawada, Kenji; Nakamura, Toshihiro; Adachi, Sadao

    2016-10-01

    Eu-Ga-O ternary compounds were synthesized from a mixture of cubic (c-) Eu2O3 and monoclinic Ga2O3 (β-Ga2O3) raw powders using the solid-state reaction method by calcination at Tc = 1200 °C. The structural and optical properties of the Eu-Ga-O ternary compounds were investigated using X-ray diffraction analysis, photoluminescence (PL) analysis, PL excitation (PLE) spectroscopy, and Raman scattering measurements. Stoichiometric compounds such as cubic Eu3Ga5O12 (EGG) and orthorhombic Eu3GaO6 were synthesized using molar ratios of x = 0.375 and 0.75 [x≡Eu2O3/(Eu2O3 + Ga2O3)], respectively, together with the end-point binary compounds β-Ga2O3 (x = 0) and monoclinic (m-) Eu2O3 (x = 1.0). The structural change from "cubic" to "monoclinic" in Eu2O3 is due to the structural phase transition occurring at Tc ≥ 1050 °C. In principle, the perovskite-type EuGaO3 and monoclinic Eu4Ga2O9 can also be synthesized at x = 0.5 and 0.667, respectively; however, such stoichiometric compounds could not be synthesized in this study. The PL and PLE properties of EGG and Eu3GaO6 were studied in detail. The temperature dependence of the PL spectra was observed through measurements carried out between T = 20 and 300 K and explained using a newly developed model. Raman scattering measurements were also performed on the Eu-Ga-O ternary systems over the entire composition range from x = 0 (β-Ga2O3) to 1.0 (m-Eu2O3).

  1. Synthesis of polyamide oligomers based on 14-amino-3,6,9, 12-tetraoxatetradecanoic acid.

    PubMed

    Dhawan, R; Kadijk, M G; Joikinen, T J; Feng, M; Ansell, S M

    2000-01-01

    A series of oligomers of polyamides based on 14-amino-3,6,9, 12-tetraoxatetradecanoic acid monomers (ATTAn) was synthesized. These materials were designed as monodisperse analogues of poly(ethylene glycol) for use in biomedical applications where reproducible behavior is important. Synthesis of the monomer was evaluated using two routes. For small-scale preparations, tetraethylene glycol (TEG) was monoprotected with dihydropyran, converted to an alkoxide, and alkylated with ethyl bromoacetate. On larger scales, TEG was alkylated directly by treatment with sodium, followed by ethyl bromoacetate. The amine function was introduced by mesylation followed by treatment with sodium azide. Reduction of the azide to amino groups was performed over Pd/C using either hydrogen or formic acid as proton sources. Assembly of the oligomers was accomplished using standard DCC/NHS chemistry and an iterative dimerization sequence after appropriate deprotection of a pair of monomers. The amino group was protected by retaining the azido group as a latent amine. A series of ATTAn oligomers was prepared (n = 1-8). A lipid conjugate of the octamer, ATTA8-DSPE, was synthesized.

  2. Cubic Yb3+-activated Y6MoO12 micro-powder - optical material operating in NIR region

    NASA Astrophysics Data System (ADS)

    Bieza, M.; Guzik, M.; Tomaszewicz, E.; Guyot, Y.; Boulon, G.

    2017-01-01

    We present Yb3+-doped Y6MoO12 solid solutions as a very promising NIR emitting phosphor with some hope to obtain them in the nearest future in the form of transparent ceramics due to their cubic structure. The samples are crystallizing in the cubic system with the space group Fm-3m. To perform a full structural and spectroscopic analysis on the well crystallized samples they were obtained in the uniform micro-crystal forms. The ternary Y6MoO12 and Yb3+-doped Y6MoO12 solid solutions containing a large concentration range of activator (0.1, 1, 3, 5, 10, 20 mol%) have been prepared by a high-temperature solid-state reaction method using the Yb2O3/Y2O3/MoO3 mixtures annealed in the air in the temperature range of 550-1550 °C for 6 h. As-obtained samples were systematically characterized by the X-ray powder diffraction (XRD), scanning electron microscopy (SEM), UV-Vis-NIR reflectance. Furthermore, to check the thermal stability of these molybdates the thermogravimetric analysis have been performed. Finally, the luminescent properties of Yb3+ ions activated Y6MoO12 microcrystals were investigated by using the high resolution absorption and emission techniques including the site selective spectroscopy at room and low temperatures. Basing on the absorption and emission spectra the Yb3+ electronic energy levels diagram has been proposed for the main site. The concentration quenching mechanism of Yb3+ ion in this host lattice was also discussed. Obtained results have demonstrated that Yb3+-doped Y6MoO12 microcrystals exhibited good luminescent properties and possess many advantages compared to other compounds based on molybdates and might have potential applications in the laser technology.

  3. [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.

  4. Epoxyeicosatrienoic acids induce growth inhibition and calpain/caspase-12 dependent apoptosis in PDGF cultured 3T6 fibroblast.

    PubMed

    Nieves, Diana; Moreno, Juan J

    2007-11-01

    Previous studies have demonstrated that arachidonic acid (AA) metabolites released by the cyclooxygenase pathway is involved in serum-induced 3T6 fibroblast cycle progression and proliferation. However, these results also suggest that other AA cascade pathways might be involved. Recently, we also described the role of hydroxyeicosatetraenoic acids, which are produced by cytochrome P450 monooxygenases (CYP), in 3T6 fibroblast growth. AA can be also metabolized by the epoxygenase activity of CYP-producing epoxyeicosatrienoic acids (EETs). Finally, the cytosolic epoxide hydrolases catalyze the hydration of the EETs, transforming them into dihydroxyeicosatetraenoic acids (DHETEs). In this work, we have studied the role of the EETs/DHETEs on 3T6 fibroblasts growth. Our results show that PDGF stimulates 3T6 fibroblast proliferation and [3H]thymidine incorporation, while the addition of 5,6-EET, 8,9-EET, 11,12-EET or 14,15-EET (0.1-1 microM) inhibit these processes. Furthermore, 5,6-DHETE and 11,12-DHETE (0.1-1 microM) also inhibit cell proliferation and DNA synthesis. Interestingly, this growth inhibition was correlated with an induction of apoptosis. Thus, we observed that in the presence of PDGF, EETs or DHETEs (0.1-1 microM) induce phosphatidylserine externalization (as measured by annexin V-binding) and DNA fragmentation (as quantified using a TUNEL assay). Our results show that calpain, as well as caspase-12 and caspase-3, are involved in these events. Therefore, EETs and DHETEs have anti-proliferative and pro-apoptotic effects on PDGF-stimulated 3T6 fibroblasts.

  5. Synthesis of novel 3-(alkylcarbamoyl)-2-aryl-1,2-dihydro-6,7-(methylenedioxy)-3H-quinazolin-4-ones as anticonvulsant agents.

    PubMed

    Micale, Nicola; Postorino, Giovanna; Grasso, Silvana; Zappalà, Maria; Zuccalà, Giuseppe; Ferreri, Guido; De Sarro, Giovambattista

    2006-03-01

    A series of 3-(alkylcarbamoyl)-2-aryl-1,2-dihydro-6,7-(methylenedioxy)-3H-quinazolin-4-ones, compounds 3-6, were synthesized, and screened as anticonvulsant agents in DBA/2 mice against sound-induced seizure (Table). The new compounds were found to display anticonvulsant properties inferior to those of the known dehydro congeners 1 and 2. The binding affinities of 1-6 at the AMPA and NMDA receptors were also evaluated.

  6. 625 kb microduplication at Xp22.12 including RPS6KA3 in a child with mild intellectual disability.

    PubMed

    Bertini, Veronica; Cambi, Francesca; Bruno, Rossella; Toschi, Benedetta; Forli, Francesca; Berrettini, Stefano; Simi, Paolo; Valetto, Angelo

    2015-12-01

    Here, we report on a patient with a 625 kb duplication in Xp22.12, detected by array comparative genomic hybridization (CGH). The duplicated region contains only one gene, RPS6KA3, that results in partial duplication. The same duplication was present in his mother and his maternal uncle. This partial duplication inhibits the RPS6KA3 expression, mimicking the effect of loss-of-function mutations associated with Coffin-Lowry syndrome (CLS). The phenotype of the patient here presented is not fully evocative of this syndrome because he does not present some of the facial, digital and skeletal abnormalities that are considered the main diagnostic features of CLS. This case is one of the few examples where RPS6KA3 mutations are associated with a non-specific X-linked mental retardation.

  7. Stereoselective synthesis of (all-Z)-hentriaconta-3,6,9,12,15,19,22,25,28-nonaene.

    PubMed

    Filippova, Liudmila; Aarum, Ida; Ringdal, Martine; Dahl, Martin Kirkhus; Hansen, Trond Vidar; Stenstrøm, Yngve

    2015-04-28

    Several microorganisms produce small quantities of polyunsaturated hydrocarbons and such natural products are of interest. Starting from the ethyl ester of eicosapentaenoic acid, the total synthesis of the natural product (all-Z)-hentriaconta-3,6,9,12,15,19,22,25,28-nonaene has been achieved in eight steps and 15% overall yield. The synthesis is based on a stereoselective Wittig reaction and confirms the all-Z-configuration of the nine double bonds in this highly unsaturated natural product.

  8. Synthesis, NMR analysis and X-ray crystal structure of 3-(2-naphthoyl)-6,12-diphenyl-3,9-diazatetraasterane

    NASA Astrophysics Data System (ADS)

    Tan, Hong-bo; Song, Xiu-qing; Yan, Hong; Xin, Hong-xing

    2017-02-01

    Novel 3-(2-naphthoyl)-6,12-diphenyl-3,9-diazatetraasterane (3, Tetraethyl 3-(2-naphthoyl)-6,12-diphenyl-3,9-diazapentacyclo [6.4.0.02,7.04,11.05,10]dodecane-1,5,7,11-tetracarboxylate) was prepared by naphthoylation of 3,9-diazatetraasterane (2). The target compound was isolated and unambiguously confirmed by NMR spectra, high-resolution mass spectrometry, and single-crystal X-ray diffraction analysis. In order to discuss the spatial effects on the NMR of 3 by the naphthoyl group, spectra analysis (1D-NMR and 2D-NMR) of 2 and 3 was conducted in details by the shifts and assignments of signals. Single-crystal X-ray diffraction assists to explain the molecular asymmetry of 3 and elucidates the effects of naphthoyl group on the geometry of the central cage of 3,9-diazatetraasterane.

  9. Solvent effects on infrared spectra of progesterone in CHCl 3/ cyclo-C 6H 12 binary solvent systems

    NASA Astrophysics Data System (ADS)

    Liu, Qing; Wang, Xiao-yan; Zhang, Hui

    2007-01-01

    The infrared spectroscopy studies of the C 3 and C 20 carbonyl stretching vibrations ( υ(C dbnd O)) of progesterone in CHCl 3/ cyclo-C 6H 12 binary solvent systems were undertaken to investigate the solute-solvent interactions. With the mole fraction of CHC1 3 in the binary solvent mixtures increase, three types of C 3 and C 20 carbonyl stretching vibration band of progesterone are observed, respectively. The assignments of υ(C dbnd O) of progesterone are discussed in detail. In the CHCl 3-rich binary solvent systems or pure CHCl 3 solvent, two kinds of solute-solvent hydrogen bonding interactions coexist for C 20 C dbnd O. Comparisons are drawn for the solvent sensitivities of υ(C dbnd O) for acetophenone and 5α-androstan-3,17-dione, respectively.

  10. Synthesis of N-unsubstituted and N-methyl derivatives of 4-aryl-2,6-dimethyl-1,2-dihydropyridine-3,5-dicarbonitriles

    SciTech Connect

    Zandersons, A.Z.; Lusis, V.K.; Mutsenietse, D.Kh.; Dubur, G.Ya.

    1987-07-01

    In the reduction of 2,6-dimethyl-4-arylpyridine-3,5-dicarbonitriles or their N-oxides by sodium borohydride, a mixture of 1,2- and 1,4-dihydropyridine-3,5-dicarbonitriles is formed. 1,2,6-Trimethyl-4-aryl-1,2-dihydropyridine-3,5-dicarbonitriles were obtained by reducing the corresponding pyridinium perchlorates or by alkylating 4-acryl-2,6-dimethyl-1,2-dihydropyridine-3,5-dicarbonitrile derivatives by methyl iodide.

  11. Volumetric Properties of the Mixture Butyl ethanoate C6H12O2 + C6H14O2 3-Oxaheptan-1-ol (VMSD1412, LB4315_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Butyl ethanoate C6H12O2 + C6H14O2 3-Oxaheptan-1-ol (VMSD1412, LB4315_V)' providing data by calculation of isentropic compressibility from low-pressure density and thermodynamic speed of sound data at variable mole fraction and constant temperature, in the single-phase region(s).

  12. Volumetric Properties of the Mixture Butyl ethanoate C6H12O2 + C6H14O2 3-Oxaheptan-1-ol (VMSD1511, LB4138_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Butyl ethanoate C6H12O2 + C6H14O2 3-Oxaheptan-1-ol (VMSD1511, LB4138_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  13. Characterization of a New Organic-Cation Cyclotetraphosphate: (1,4-HOC 6H 4NH 3) 4P 4O 12· 6H 2O

    NASA Astrophysics Data System (ADS)

    Soumhi, E. H.; Saadoune, I.; Driss, A.; Jouini, T.

    1999-05-01

    The tetra(para-phenolammonium)cyclotetraphosphate hexahydrate, (1,4-HOC6H4NH3)4P4O12· 6H2O (M=864.51 g mol-1), is monoclinicP21/cwith the unit cell parametersa=9.836(2) Å,b=8.591(1) Å,c:22.769(5) Å,β=95.41(2)°. The structure of this compound can be described as a succession of inorganic and organic sheets parallel to the (001) plane. The existence of the OH and NH3groups in positionparato the organic cation leads to the cohesion of the inorganic sheets, forming a three-dimensional network.The IR spectrum of (1,4-HOC6H4NH3)4P4O12· 6H2O is reported and discussed according to the theoretical group analysis. The IR data confirm the atomic arrangement within the structure. The coupled TG-DTA thermal study shows the successive departure of four and two water molecules, confirming the hydrated character of this cyclophosphate.

  14. Precision lifetime measurements of Cs 6p 2P1/2 and 6p 2P3/2 levels by single-photon counting

    NASA Astrophysics Data System (ADS)

    Young, L.; Hill, W. T., III; Sibener, S. J.; Price, Stephen D.; Tanner, C. E.; Wieman, C. E.; Leone, Stephen R.

    1994-09-01

    Time-correlated single-photon counting is used to measure the lifetimes of the 6p 2P1/2 and 6p 2P3/2 levels in atomic Cs with accuracies ~=0.2-0.3 %. A high-repetition-rate, femtosecond, self-mode-locked Ti:sapphire laser is used to excite Cs produced in a well-collimated atomic beam. The time interval between the excitation pulse and the arrival of a fluorescence photon is measured repetitively until the desired statistics are obtained. The lifetime results are 34.75(7) and 30.41(10) ns for the 6p 2P1/2 and 6p 2P3/2 levels, respectively. These lifetimes fall between those extracted from ab initio many-body perturbation-theory calculations by Blundell, Johnson, and Sapirstein [Phys. Rev. A 43, 3407 (1991)] and V. A. Dzuba et al. [Phys. Lett. A 142, 373 (1989)] and are in all cases within 0.9% of the calculated values. The measurement errors are dominated by systematic effects, and methods to alleviate these and to approach an accuracy of 0.1% are discussed. The technique is a viable alternative to the fast-beam laser approach for measuring lifetimes with extreme accuracy.

  15. New example of spontaneous resolution among aryl glycerol ethers: 3-(2,6-dichlorophenoxy)propane-1,2-diol

    NASA Astrophysics Data System (ADS)

    Bredikhina, Zemfira A.; Kurenkov, Alexey V.; Zakharychev, Dmitry V.; Krivolapov, Dmitry B.; Bredikhin, Alexander A.

    2016-08-01

    Using a set of simple tests, based on the properties of ideal conglomerate phase diagrams, it has been suggested to the conglomerate-formative nature of 3-(2,6-dichlorophenoxy)-propane-1,2-diol 1. Additional arguments have been drawn during the study of a single crystal X-ray diffraction study of the compound. The crystal packing details have been evaluated and discussed. Racemic 1 have been resolved into individual (S)- and (R)-components by a preferential crystallization procedure.

  16. Synthesis of Substituted 2,3,5,6-tetraarylbenzo(1,2-b:5,4-b')difurans

    NASA Technical Reports Server (NTRS)

    Abdul-Aziz, Mahmoud; Auping, Judith V.; Meador, Michael A.

    1995-01-01

    A series of substituted 2,3,5,6-tetraarylbenzo(l,2-b:5,4-b')difurans 1 was synthesized. This synthesis is based upon the photocyclization of 2,5-dibenzoylresorcinol dibenzyl ethers to the corresponding tetrahydrobenzo(1,2-b:5,4-b')difurans. Treatment of the photoproducts with methanesulfonyl chloride in pyridine afforded 1 in overall yields ranging from 30-72%. A number of these compounds have high fluorescence quantum yields (of phi(sub f) = 0.76-0.90), and their fluorescence spectra exhibit large solvatochromic shifts. These compounds may be suitable for use as fluorescent probes.

  17. Multiferroic properties of CoFe2O4/Bi3.4La0.6Ti3O12 bilayer structure at room temperature

    NASA Astrophysics Data System (ADS)

    Charris-Hernández, A.; Melgarejo, R.; Barrionuevo, D.; Kumar, A.; Tomar, M. S.

    2013-07-01

    Bi3.4La0.6Ti3O12/CoFe2O4 bilayer films were synthesized by chemical solution method and deposited by spin coating on Pt (Pt/TiO2/SiO2/Si) substrate. X-ray diffraction of the bilayer system revealed the composite-like structure. The leakage current is less than 10-7 A at electric field below100 kV/cm, and it shows the ohmic behavior. Dielectric constant decreases with increasing frequency and reaches to 140 at 10-6 Hz. Bi3.4La0.6Ti3O12/CoFe2O4 system shows the co-existence of ferroelectric polarization (Pr) = 51 μC/cm2 and magnetization (Mr) = 206 emu/cm3 at room temperature. Observed ferromagnetic and ferroelectric responses in bilayer system may be useful for bi-functional devices.

  18. Magnetic properties of the S =1/2 honeycomb lattice antiferromagnet 2 -Cl -3 ,6 -F2-V

    NASA Astrophysics Data System (ADS)

    Okabe, Toshiki; Yamaguchi, Hironori; Kittaka, Shunichiro; Sakakibara, Toshiro; Ono, Toshio; Hosokoshi, Yuko

    2017-02-01

    We successfully synthesized single crystals of the verdazyl radical 2 -Cl -3 ,6 -F2-V [=3-(2-chloro-3,6-difluorophenyl)-1,5-diphenylverdazyl], which is a rare model compound with an S =1/2 Heisenberg antiferromagnetic (HAF) honeycomb lattice. Ab initio molecular orbital calculations indicate two dominant AF interactions, forming a slightly distorted honeycomb lattice. We explain the magnetic susceptibility and the magnetization curve up to the saturation field based on the expected spin model using the quantum Monte Carlo method. In the low-temperature regions, we found a phase transition to an AF ordered state at about 0.77 K for the zero field and obtained the magnetic field-temperature phase diagram from the magnetic susceptibility and the specific heat for various magnetic fields. Through the analysis considering the effect of lattice distortion on magnetic behavior, we confirm that the lattice distortion of the present model is small enough that it does not affect the intrinsic behavior of the uniform S =1/2 HAF honeycomb lattice.

  19. Noncollinear magnetic order in the S=(1)/(2) magnet Sr3ZnRhO6

    NASA Astrophysics Data System (ADS)

    Hillier, A. D.; Adroja, D. T.; Kockelmann, W.; Chapon, L. C.; Rayaprol, S.; Manuel, P.; Michor, H.; Sampathkumaran, E. V.

    2011-01-01

    The compound Sr3ZnRhO6 with S=1/2 belongs to a family of pseudo-one-dimensional (1D) spin-chain systems with general formula A3A'BO6. The nature of the ground state of Sr3ZnRhO6 is investigated using microscopic techniques such as muon spin relaxation (μSR) and powder neutron diffraction in addition to bulk characterization using magnetization, ac-susceptibility, and heat capacity. Our μSR study clearly reveals the presence of three frequencies, below 16 K, whose temperature dependence follow a mean-field order parameter indicating long-range magnetic ordering of the Rh4+ moment. Powder neutron diffraction reveals the presence of four weak magnetic Bragg peaks below 16 K, indexed by the propagation vector k=(0,(1)/(2),1) in the hexagonal setting of the space group R3̲c. Analysis of the magnetic diffraction pattern constrained to symmetry-adapted magnetic modes reveals a noncollinear magnetic structure with an ordered magnetic moment of Rh4+=0.7(1) μB. This is the first compound in this spin chain family which exhibits noncollinear magnetic order with the moment tilting away from the c axis, highlighting the important role of interchain and intrachain interactions.

  20. Antioxidant properties and PC12 cell protective effects of a novel curcumin analogue (2E,6E)-2,6-bis(3,5- dimethoxybenzylidene)cyclohexanone (MCH).

    PubMed

    Ao, Gui-Zhen; Chu, Xiao-Jing; Ji, Yuan-Yuan; Wang, Jian-Wen

    2014-03-05

    The antioxidative properties of a novel curcumin analogue (2E,6E)-2,6-bis(3,5-dimethoxybenzylidene)cyclohexanone (MCH) were assessed by several in vitro models, including superoxide anion, hydroxyl radical and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging and PC12 cell protection from H2O2 damage. MCH displayed superior O2•- quenching abilities compared to curcumin and vitamin C. In vitro stability of MCH was also improved compared with curcumin. Exposure of PC12 cells to 150 µM H2O2 caused a decrease of antioxidant enzyme activities, glutathione (GSH) loss, an increase in malondialdehyde (MDA) level, and leakage of lactate dehydrogenase (LDH), cell apoptosis and reduction in cell viability. Pretreatment of the cells with MCH at 0.63-5.00 µM before H2O2 exposure significantly attenuated those changes in a dose-dependent manner. MCH enhanced cellular expression of transcription factor NF-E2-related factor 2 (Nrf2) at the transcriptional level. Moreover, MCH could mitigate intracellular accumulation of reactive oxygen species (ROS), the loss of mitochondrial membrane potential (MMP), and the increase of cleaved caspase-3 activity induced by H2O2. These results show that MCH protects PC12 cells from H2O2 injury by modulating endogenous antioxidant enzymes, scavenging ROS, activating the Nrf2 cytoprotective pathway and prevention of apoptosis.

  1. Hierarchical cobalt-formate framework series with (4{sup 12}⋅6{sup 3})(4{sup 9}⋅6{sup 6}){sub n} (n = 1–3) topologies exhibiting slow dielectric relaxation and weak ferromagnetism

    SciTech Connect

    Shang, Ran; Chen, Sa; Hu, Ke-Li; Jiang, Ze-Chun; Wang, Bing-Wu; Wang, Zhe-Ming E-mail: gaosong@pku.edu.cn; Gao, Song E-mail: gaosong@pku.edu.cn; Kurmoo, Mohamedally

    2014-12-01

    The employment of linear di-, tri-, and tetra-ammoniums has generated a hierarchy in the binodal (4{sup 12}⋅6{sup 3})(4{sup 9}⋅6{sup 6}){sub n} topologies with n = 1, 2, and 3, respectively, for the cobalt formate frameworks with increasing length of the cavities to match the ammoniums. This indicates the length-directing effect of the polyammoniums. The dynamic movements of polyammoniums between favored sites or orientations within the cavities lead to slow dielectric relaxations. All materials are spin-canted antiferromagnets in low temperatures and show reduced spontaneous magnetizations from di- and tri-, to tetra-ammoniums, because of the increased number of unique Co ions or the antiferromagnetically coupled sublattices.

  2. [4+2] Cycloaddition of 2-substituted 1,2-dihydropyridines with nitrosobenzene: asymmetric synthesis of trans-2-substituted 3-amino-1,2,3,6-tetrahydropyridines.

    PubMed

    Lemire, Alexandre; Beaudoin, Daniel; Grenon, Michel; Charette, André B

    2005-03-18

    [reaction: see text] A new methodology for the stereoselective synthesis of trans-2-substituted 3-amino-1,2,3,6-tetrahydropyridines is reported. The preparation of these 3-aminopiperidines is achieved by cycloaddition of nitrosobenzene with 2-substituted 1,2-dihydropyridines followed by chemoselective reduction of the cycloadducts. Enantioenriched 1,2-dihydropyridine derivatives are easily prepared from pyridine and a chiral amide following a previous report from our laboratories. Moreover, the in situ hydrogenation of these cycloadducts over palladium in a solution of hydrogen chloride in methanol led to tetrahydropyrroloimidazoles.

  3. Potential bile acid metabolites. 19. The epimeric 3 alpha,6,7 beta-trihydroxy- and 3 alpha,6,7 beta,12 alpha-tetrahydroxy-5 alpha-cholanoic acids.

    PubMed

    Iida, T; Nishida, S; Chang, F C; Niwa, T; Goto, J; Nambara, T

    1993-04-01

    Syntheses by a new procedure of the known 3 alpha,6 alpha,7 beta- and 3 alpha,6 beta,7 beta-trihydroxy-5 alpha-cholanoic acids, and of the once-reported analog 3 alpha,6 alpha,7 beta,12 alpha-, as well as the new 3 alpha,6 beta,7 beta,12 alpha-tetrahydroxy-5 alpha-cholanoic acids, are described. Key intermediates of the syntheses are the 6-oxo-7 beta-ols of the respective 5 alpha-cholanoic acids (and their methyl esters) prepared by allomerization at C-5 of appropriate 6-bromo-7-oxo derivatives of the corresponding 5 beta-acids. Successful reduction of the 6,7-ketols to the desired products depended on the proper choice of reagents, either Zn(BH4)2 or Li/NH3/MeOH.

  4. Volumetric Properties of the Mixture Diethyl carbonate C5H10O3 + C6H12O3 2,4,6-Trimethyl-1,3,5-trioxane (VMSD1511, LB4522_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Diethyl carbonate C5H10O3 + C6H12O3 2,4,6-Trimethyl-1,3,5-trioxane (VMSD1511, LB4522_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  5. Excitation-transfer collisions in cesium vapor: CS(5d (5/2)) + CS(6s (1/2)) yields CS(5d (3/2)) + CS(6s (1/2))

    SciTech Connect

    Keramati, B.; Masters, M.; Huennekens, J.

    1988-11-01

    The excitation-transfer collision Cs(5D5/2) + Cs(6S) yields CS(5D3/2) + Cs(6S) was studied. The upper 5D5/2 state was excited by a c-w dye laser tuned to the one photon, quadrupole-allowed 6S yields 5D5/2 transition. Since the direct 5D yields 6P fluorescence could not be detected with our apparatus we monitored instead the cascade 6P yields 6S fluorescence. The ratio of 6P 1/2 to 6P3/2 fluorescence contains information on the collisional mixing that takes place in the 5D levels but also includes a significant contribution from mixing in the 6P levels. This latter contribution could effectively be subtracted out using the results of a second experiment in which a tunable cw diode laser was used to pump the 6P3/2 state, and the same fluorescence ratio monitored. The 5D mixing cross section obtained, 70 A, is significantly larger than previous indirect determinations.

  6. Excitation-transfer collisions in cesium vapor: Cs(5D/sub 5/2/)+Cs(6S/sub 1/2/). -->. Cs (5D/sub 3/2/)+ Cs(6S/sub 1/2/)

    SciTech Connect

    Keramati, B.; Masters, M.; Huennekens, J.

    1988-11-01

    We report an experimental investigation of the excitation-transfer collision Cs(5D/sub 5/2/)+Cs(6S)..-->..CS ((5D/sub 3/2/)+Cs(6S). The upper 5D/sub 5/2/ state was excited by a cw dye laser tuned to the one-photon, quadrupole-allowed 6S..-->..5D/sub 5/2/ transition. Since the direct 5D..-->..6P fluorescence could not be detected with our apparatus, we monitored instead the cascade 6P..-->..6S fluorescence. The ratio of 6P/sub 1/2/ to 6P/sub 3/2/ fluorescence contains information on the collisional mixing that takes place in the 5D levels but also includes a significant contribution from mixing in the 6P levels. This latter contribution could effectively be subtracted out using the results of a second experiment in which a tunable cw diode laser was used to pump the 6P/sub 3/2/ state, and the same fluorescence ratio monitored. The 5D mixing cross section we obtain, 70 A/sup 2/, is significantly larger than previous indirect determinations.

  7. Pyrrolo[3',2':6,7]cyclohepta[1,2-b]pyridines with potent photo-antiproliferative activity.

    PubMed

    Spanò, Virginia; Giallombardo, Daniele; Cilibrasi, Vincenzo; Parrino, Barbara; Carbone, Anna; Montalbano, Alessandra; Frasson, Ilaria; Salvador, Alessia; Richter, Sara N; Doria, Filippo; Freccero, Mauro; Cascioferro, Stella; Diana, Patrizia; Cirrincione, Girolamo; Barraja, Paola

    2017-03-10

    Pyrrolo[3',2':6,7]cyclohepta[1,2-b]pyridines were synthesized as a new class of tricyclic system in which the pyridine ring is annelated to a cycloheptapyrrole scaffold, with the aim of obtaining new photosensitizing agents with improved antiproliferative activity and lower undesired toxic effects. A versatile synthetic pathway was approached, which allowed the isolation of derivatives of the title ring system with a good substitution pattern on the pyrrole moiety. Photobiological studies revealed that the majority of the new compounds showed a potent cytotoxic effect upon photoactivation with light of the proper wavelength, especially when decorated with a 2-ethoxycabonyl group and a N-benzyl substituted moiety, with EC50 values reaching the submicromolar level. The mechanism of action was evaluated.

  8. 12 CFR 262.6 - Forms.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... § 262.6 Forms. Necessary forms to be used in connection with applications and other matters are available at the Federal Reserve Banks. A list of all such forms, which is reviewed and revised periodically... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Forms. 262.6 Section 262.6 Banks and...

  9. 12 CFR 3.12 - Procedures.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Establishment of Minimum Capital Ratios for an Individual Bank § 3.12 Procedures. (a) Notice. When the OCC determines that minimum capital ratios above those set forth in § 3.6 or other legal authority are...

  10. 12 CFR 3.12 - Procedures.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Establishment of Minimum Capital Ratios for an Individual Bank § 3.12 Procedures. (a) Notice. When the OCC determines that minimum capital ratios above those set forth in § 3.6 or other legal authority are...

  11. Chemical bond properties and charge transfer bands of O(2-)-Eu(3+), O(2-)-Mo(6+) and O(2-)-W(6+) in Eu(3+)-doped garnet hosts Ln3M5O12 and ABO4 molybdate and tungstate phosphors.

    PubMed

    Liu, Xiaoguang; Li, Ling; Noh, Hyeon Mi; Moon, Byung Kee; Choi, Byung Chun; Jeong, Jung Hyun

    2014-06-21

    Charge transfer (CT) energy from the ligand to the central ions is an important factor in luminescence properties for rare earth doped inorganic phosphors. The dielectric theory of complex crystals was used to calculate chemical bond properties. Combining the photoluminescence and the dielectric theory of complex crystals, the CT bands of O(2-)-Eu(3+), O(2-)-Mo(6+) and O(2-)-W(6+) for Eu(3+)-doped inorganic phosphors have been investigated experimentally and theoretically. Taking Eu(3+)-doped Ln3M5O12 (Ln = Y, Lu and M = Al, Ga), Gd3Ga5O12, MMoO4 (M = Ca, Sr, Ba) and MWO4 (M = Ca, Sr, Ba) as typical phosphors, we investigated the effects of the cation size on the CT bands and chemical bond properties including the bond length (d), the covalency (fc), the bond polarizability (αb) and the environmental factor (he) of O(2-)-Eu(3+), O(2-)-Mo(6+) and O(2-)-W(6+), respectively. For systematic isostructural Ln3M5O12 (Ln = Y, Lu and M = Al, Ga) phosphors, with the increasing M ion radius, the bond length of Ln-O decreases, but fc and αb increase, which is the main reason that the environmental factor increased. For the isostructural MMoO4:Eu, with the increasing M ion radius, the Mo-O bond length increases, but fc and αb decrease, and thus he decreases. However, in the compound system MWO4:Eu (M = Ca, Ba) with the increasing M ion radius, the O-W bond length increases, but fc and αb increase, and thus he increases and the O-W CT energy decreases. Their O(2-)-Eu(3+), O(2-)-Mo(6+) and O(2-)-W(6+) CT bands as well as their full width at half maximum (FWHM) were directly influenced by he. And with the increasing he, CT bands of O-Eu or O-Mo or O-W decrease and their FWHM increases. These results indicate a promising approach for changing the material properties, searching for new Eu(3+) doped molybdate, tungstate or other oxide phosphors and analyzing the experimental result.

  12. Mineralogical studies of the nitrate deposits of Chile: VII. Two new saline minerals with the composition K6(Na,K)4Na6Mg10 (XO4) 12(IO3)12.12H2O: fuenzalidaite (X = S) and carlosruizite (X = Se)

    USGS Publications Warehouse

    Konnert, J.A.; Evans, H.T.; McGee, J.J.; Ericksen, G.E.

    1994-01-01

    Two new isostructural saline minerals from the nitrate deposits of northern Chile have the composition K6(Na,K)4Na6Mg10(XO4)12(IO3)12.12H2O: fuenzalidaite (X = S) and carlosruizite (X = Se,S,Cr). -from Authors

  13. A toxological study of 3,6-BIS(3,5-Dimethyl-1-1-Pyrazolyl)1,2-Dihydro-1,2,4,5-Tetrazine

    SciTech Connect

    London, J.E.

    1993-03-01

    The acute oral LD{sub 30/50} values for 3,6-BIS(3,5-Dimethyl-1-Pyrazolyl)-1,2-Dihydro-1,2,4,5-Tetrazine BIS(DMP)DHT are greater than 5g/kg. According to classical guidelines, the material would be considered only slightly toxic or practically nontoxic in both rats and mice. The sensitization study in the guinea pig did not show BIS(DMP)SHT to have potential sensitizing effects. Skin application studies on the rabbit demonstrated the material was cutaneously nonirritating. This material was also nonirritating in the rabbit eye application studies.

  14. A toxological study of 3,6-BIS(3,5-Dimethyl-1-1-Pyrazolyl)1,2-Dihydro-1,2,4,5-Tetrazine

    SciTech Connect

    London, J.E.

    1993-03-01

    The acute oral LD[sub 30/50] values for 3,6-BIS(3,5-Dimethyl-1-Pyrazolyl)-1,2-Dihydro-1,2,4,5-Tetrazine BIS(DMP)DHT are greater than 5g/kg. According to classical guidelines, the material would be considered only slightly toxic or practically nontoxic in both rats and mice. The sensitization study in the guinea pig did not show BIS(DMP)SHT to have potential sensitizing effects. Skin application studies on the rabbit demonstrated the material was cutaneously nonirritating. This material was also nonirritating in the rabbit eye application studies.

  15. 12 CFR 12.3 - Recordkeeping.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Recordkeeping. 12.3 Section 12.3 Banks and... REQUIREMENTS FOR SECURITIES TRANSACTIONS § 12.3 Recordkeeping. (a) General rule. A national bank effecting...) Notifications. A copy of the written notification required by §§ 12.4 and 12.5. (b) Manner of maintenance....

  16. 12 CFR 12.3 - Recordkeeping.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Recordkeeping. 12.3 Section 12.3 Banks and... REQUIREMENTS FOR SECURITIES TRANSACTIONS § 12.3 Recordkeeping. (a) General rule. A national bank effecting...) Notifications. A copy of the written notification required by §§ 12.4 and 12.5. (b) Manner of maintenance....

  17. Phase I trial of a humanized, Fc receptor nonbinding anti-CD3 antibody, hu12F6mu in patients receiving renal allografts

    PubMed Central

    Du, Li; Tan, Min; Hou, Sheng; Qian, Weizhu; Li, Bohua; Zhang, Dapeng; Dai, Jianxin; Wang, Hao; Zhang, Xu

    2010-01-01

    Hu12F6mu is an Fc-mutated, humanized anti-CD3 antibody developed in our lab. The aim of this study was to assess single dose escalation pharmacokinetics (PK) and safety profile of hu12F6mu and to measure the effects of the antibody on levels of circulating T cells over time. Twenty-seven patients receiving renal allografts were randomized to receive hu12F6mu intravenously at a single-dose of 2.5, 5 or 10 mg. The concentration-time data obtained by a validated ELISA method were subjected to non-compartmental PK analysis by DAS 2.1 software. Subgroups of CD2+, CD3+, CD4+ and CD8+ lymphocytes were monitored periodically by flow cytometry. Our results showed that hu12F6mu exhibited linear PK over the dose range of 2.5–10 mg. A significant decline in the proportion of T cells was observed immediately after the infusion, followed by a progressive increase occurring over the ensuing days of therapy. A significant negative correlation was observed between serum concentration of hu12F6mu and CD3+ cell proportion. Intravenous infusion of hu12F6mu was well-tolerated in patients receiving renal allografts. These results suggest that hu12F6mu may have potential as a therapeutic agent, although further studies are needed. PMID:20519962

  18. Synthesis of biologically active 1'-(2-oxo-2H-benzopyran-6-yl)- 5'-hydroxy-2'-methylindole-3'-amido-2"-phenyl-thiazolidene-4"-ones.

    PubMed

    Mulwad, Vinata V; Parmar, Hitesh T; Mir, Abid A

    2011-01-01

    6-Aminocoumarins on refluxing with ethyl acetoacetate in 1,2-dichloroethane gave two products: 3'-(2-oxo-2H-benzopyran-6-yl-amino)-but-2'-enoic acid ethyl ester 2a-c and N-(-2-oxo-2H-benzopyran-6-yl)-3'-oxo-butyramide 3a-c. Compounds 2a-c on treatment with 1,4-benzoquinone in N2-atmosphere yielded 1'-( 2-oxo-2H-benzopyran-6-yl)-5'-hydroxy-2'-methyl-3'-carbethoxyindoles 4a-c, which on further treatment with hydrazine hydrate gave 1'-(2-oxo-2H-benzopyran-6-yl)-5'-hydroxy-2'-methylindole-3'-acid hydrazides 5a-c. These acid hydrazides were treated with benzaldehyde to give 1'-(2-oxo-2H-benzopyran-6-yl)-5'-hydroxy-2'-methylindole-3'-benzylidene hydrazides 6a-c, which on further treatment with mercaptoacetic acid in 1,4-dioxane yielded 1'-(2-oxo-2H-benzopyran-6-yl)-5'-hydroxy-2'-methylindole-3'-amido-2"-phenylthiazolidene-4"-ones 7a-c. The structures of the compounds have been established on the basis of spectral and analytical data. All compounds have been screened for their antimicrobial activity and have been found to exhibit significant antibacterial and antifungal activities.

  19. Preparation in Acidic and Alkaline Conditions and Characterization of α-Bi2Mo3O12 and γ-Bi2MoO6 Powders

    NASA Astrophysics Data System (ADS)

    Chen, Tao; Wang, Mao-Hua; Ma, Xiao-Yu

    2016-08-01

    α-Bi2Mo3O12 and γ-Bi2MoO6 powders have been successfully fabricated via a sol-gel method starting from bismuth nitrate and ammonium molybdate. The as-synthesized samples were characterized by x-ray powder diffraction analysis, thermogravimetry and differential thermogravimetry, scanning electron microscopy, and ultraviolet-visible (UV-Vis) absorption spectroscopy. The results indicated the formation of α-Bi2Mo3O12 and γ-Bi2MoO6 powders in acidic (pH 5) and alkaline (pH 9) conditions, respectively. α-Bi2Mo3O12 exhibited irregular shape, while γ-Bi2MoO6 showed approximately flake-like morphology. The bandgap of pure α-Bi2Mo3O12 and γ-Bi2MoO6 was estimated to be about 2.83 eV and 2.85 eV, respectively, according to UV-Vis studies. The slight shift of the absorption edge towards longer wavelength for α-Bi2Mo3O12 indicated a decrease of the optical bandgap. Photocatalytic experiments showed that γ-Bi2MoO6 exhibited higher photodegradation activity of methylene blue compared with α-Bi2Mo3O12.

  20. Concise synthesis and anti-HIV activity of pyrimido[1,2-c][1,3]benzothiazin-6-imines and related tricyclic heterocycles.

    PubMed

    Mizuhara, Tsukasa; Oishi, Shinya; Ohno, Hiroaki; Shimura, Kazuya; Matsuoka, Masao; Fujii, Nobutaka

    2012-09-07

    3,4-Dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine (PD 404182) is a virucidal heterocyclic compound active against various viruses, including HCV, HIV, and simian immunodeficiency virus. Using facile synthetic approaches that we developed for the synthesis of pyrimido[1,2-c][1,3]benzothiazin-6-imines and related tricyclic derivatives, the parallel structural optimizations of the central 1,3-thiazin-2-imine core, the benzene part, and the cyclic amidine part of PD 404182 were investigated. Replacement of the 6-6-6 pyrimido[1,2-c][1,3]benzothiazin-6-imine framework with 5-6-6 or 6-6-5 derivatives led to a significant loss of anti-HIV activity, and introduction of a hydrophobic group at the 9- or 10-positions improved the potency. In addition, we demonstrated that the PD 404182 derivative exerts anti-HIV effects at an early stage of viral infection.

  1. 40 CFR 721.7280 - 1,3-Propanediamine, N,N′-1,2-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl...-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl-4..., reaction products with N-butyl-2,2,6,6-tetramethyl-4-piperidinamine (PMN P-89-632) is subject to...

  2. 40 CFR 721.7280 - 1,3-Propanediamine, N,N′-1,2-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl...-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl-4..., reaction products with N-butyl-2,2,6,6-tetramethyl-4-piperidinamine (PMN P-89-632) is subject to...

  3. 40 CFR 721.7280 - 1,3-Propanediamine, N,N′-1,2-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl...-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl-4..., reaction products with N-butyl-2,2,6,6-tetramethyl-4-piperidinamine (PMN P-89-632) is subject to...

  4. 40 CFR 721.7280 - 1,3-Propanediamine, N,N′-1,2-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl...-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl-4..., reaction products with N-butyl-2,2,6,6-tetramethyl-4-piperidinamine (PMN P-89-632) is subject to...

  5. 40 CFR 721.7280 - 1,3-Propanediamine, N,N′-1,2-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-ethanediylbis-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl...-, polymer with 2,4,6-trichloro-1,3,5-triazine, reaction products with N-butyl-2,2,6,6-tetramethyl-4..., reaction products with N-butyl-2,2,6,6-tetramethyl-4-piperidinamine (PMN P-89-632) is subject to...

  6. Dating groundwater with trifluoromethyl sulfurpentafluoride (SF 5CF3), sulfur hexafluoride (SF6), CF 3Cl (CFC-13), and CF2Cl2 (CFC-12)

    USGS Publications Warehouse

    Busenberg, E.; Plummer, L.N.

    2008-01-01

    [1] A new groundwater dating procedure using the transient atmospheric signal of the environmental tracers SF5CF3, CFC-13, SF6, and CFC-12 was developed. The analytical procedure determines concentrations of the four tracers in air and water samples. SF 5CF3 and CFC-13 can be used to date groundwaters in some environments where the CFCs and SF6 have previously failed because these new tracers have increasing atmospheric input functions, no known terrigenic source, and are believed to be stable under reducing conditions. SF5CF3 has a dating range from 1970 to modern; the mixing ratio (mole fraction) in North American air has increased from the detection limit of 0.005 parts per trillion (ppt) to the 2006 mole fraction of about 0.16 ppt. No evidence was found for degradation of SF5CF3 in laboratory anaerobic systems. The solubility of SF5CF3 was measured in water from 1 to 35??C. Groundwater samples that contained large amounts of terrigenic SF6 did not contain terrigenic SF 5CF3. CFC-13 is a trace atmospheric gas with a dating range in groundwater of about 1965 to modem. CFC-13 has been used primarily in very low-temperature refrigeration; thus groundwater environments are less likely to be contaminated with nonatmospheric sources as compared to other widely used CFCs. Because of the low solubility of SF5CF3 and CFC-13 in water, an excess air correction must be applied to the apparent ages. The new dating procedure was tested in water samples from wells and springs from Maryland, Virginia, and West Virginia.

  7. Crystal structure and physicochemical characterization of 3β-hydroxyolea-12-en-28-oic acid-3,5,6-trimethylpyrazin-2-methyl ester

    NASA Astrophysics Data System (ADS)

    Fu, Jing; Dong, Xiaoxv; Yin, Xinbing; Cao, Sali; Yang, Chunjing; He, Huyiligeqi; Ni, Jian

    2017-02-01

    3β-hydroxyolea-12-en-28-oic acid-3,5,6-trimethylpyrazin-2-methyl ester (T-OA) is a newly discovered potential antitumor compound. However, the poor solubility of T-OA leads to poor dissolution and limited clinical application. So as to enhance the dissolution and bioavailability of T-OA, an investigation of the polymorphism of T-OA was successfully undertaken. A new solvate and an amorphous form of T-OA were discovered through a comprehensive polymorph screening experiments. Their structures were elucidated by single-crystal structure analysis and extensively characterized by PXRD, DSC and SEM. The powder dissolution rates were compared with those of the previously known polymorph. Thermodynamic stability and phase transformation are also discussed in detail.

  8. Measurements of electron attachment lineshapes and cross sections at ultralow electron energies for c-C6F10, c-C6F12, C8F16 and 1,1,2-C2Cl3F3

    NASA Technical Reports Server (NTRS)

    Alajajian, S. H.; Chutjian, A.

    1986-01-01

    Electron attachment cross sections are reported in the electron energy range 0-160 meV and at energy resolutions of 4.5-7.5 meV (FWHM) for the molecules c-C6F10 (perfluorocyclohexene), c-C6F12 (perfluoro-1,2-dimethylcyclobutane), C8F16 (perfluoro-1,3-dimethylcyclohexane) and 1,1,2-C2Cl3F3 (1,1,2-trichlorotrifluoroethane). Use is made of the Kr photoionization technique, and measured attachment lineshapes are converted to cross sections by normalization through attachment rate constants. Comparisons are made with attachment cross sections derived from swarm-measured rate constants. Similar to previous results in eight other molecules, the present four molecules exhibit resolution-limited onsets at a threshold consistent with an s-wave attachment behavior and with a neutral-negative-ion curve crossing at zero energy.

  9. Modified kagome physics in the natural spin-1/2 kagome lattice systems: kapellasite Cu3Zn(OH)6Cl2 and haydeeite Cu3Mg(OH)6Cl2.

    PubMed

    Janson, O; Richter, J; Rosner, H

    2008-09-05

    The recently discovered natural minerals Cu3Zn(OH)6Cl2 and Cu3Mg(OH)6Cl2 are spin 1/2 systems with an ideal kagome geometry. Based on electronic structure calculations, we develop a realistic model which includes couplings across the kagome hexagons beyond the original kagome model that are intrinsic in real kagome materials. Exact diagonalization studies for the derived model reveal a strong impact of these couplings on the magnetic ground state. Our predictions could be compared to and supplied with neutron scattering, thermodynamic data, and NMR data.

  10. 12 CFR 3.12 - Procedures.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Procedures. 3.12 Section 3.12 Banks and Banking... Establishment of Minimum Capital Ratios for an Individual Bank § 3.12 Procedures. (a) Notice. When the OCC... minimum capital ratios or the deadline for their achievement. (c) Decision. After the close of the...

  11. 12 CFR 3.12 - Procedures.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Procedures. 3.12 Section 3.12 Banks and Banking... Establishment of Minimum Capital Ratios for an Individual Bank § 3.12 Procedures. (a) Notice. When the OCC... minimum capital ratios or the deadline for their achievement. (c) Decision. After the close of the...

  12. Li6La3SnMO12 (M = Sb, Nb, Ta), a Family of Lithium Garnets with High Li-Ion Conductivity

    SciTech Connect

    Bridges, Craig A; Goodenough, J. B.; Gupta, Dr Asha; Nakanishi, Masahiro; Paranthaman, Mariappan Parans; Sokolov, Alexei P; Bi, Zhonghe; Li, Yutao; Han, Jiantao; Dong, Youzhong; Wang, Long; Xu, Maowen

    2012-01-01

    In order to investigate the influence of covalent bonding within the garnet framework on the conductivity of Li+ in the interstitial space, the Li+ conductivities in the family of Sn-based compounds Li6La3 SnMO12 (M = Sb, Nb, Ta) have been obtained and are compared with those of Li6La3ZrMO12. Refinement of the neutron diffraction pattern of Li6La3 SnNbO12shows that the interstitial tetrahedral sites (24d ) are about half-occupied and most of the Li in the interstitial bridging octahedral sites are displaced from the center position (48g ). The Sb-based compound has the largest lattice parameter while the Ta-based compound has the highest Li+-ion conductivity of 0.42 10 4 Scm 1.

  13. Subchronic toxicity study of 3-monochloropropane-1,2-diol administered by drinking water to B6C3F1 mice.

    PubMed

    Cho, Wan-Seob; Han, Beom Seok; Lee, Hakyung; Kim, Cheulkyu; Nam, Ki Taek; Park, Kidae; Choi, Mina; Kim, Sung Jun; Kim, Seung Hee; Jeong, Jayoung; Jang, Dong Deuk

    2008-05-01

    3-Monochloropropane-1,2-diol (3-MCPD) is a food processing contaminant in a wide range of foods and ingredients and is a suspected cause of cancer. In this study, the 13-week toxicity of 3-MCPD was examined in B6C3F1 mice (10/sex/group) administered 3-MCPD doses of 0, 5, 25, 100, 200 and 400 ppm dissolved in their drinking water over a 13-week period. All the mice survived to the end of study. The mean body weight gains in the males and females given 400 ppm were significantly lower than those of the controls. The relative kidney weights of the males and females given 200 and 400 ppm were significantly higher than those of the controls without any corresponding histopathological changes. The sperm motility was lower in the 400 ppm group than the control, and there was a significant increase in the incidence of germinal epithelium degeneration in the 200 and 400 ppm groups. A delayed total estrus cycle length was observed in the 400 ppm group without any histopathological changes. Based on these results, the target organ was determined to be kidney, testis, and ovary. The no-observed-adverse-effect level (NOAEL) was found to be 100 ppm (18.05 mg/kg/day for males and 15.02 mg/kg/day for females).

  14. Lithium ion diffusion measurements on a garnet-type solid conductor Li6.6La3Zr1.6Ta0.4O12 by using a pulsed-gradient spin-echo NMR method.

    PubMed

    Hayamizu, Kikuko; Matsuda, Yasuaki; Matsui, Masaki; Imanishi, Nobuyuki

    2015-09-01

    The garnet-type solid conductor Li7-xLa3Zr2-xTaxO12 is known to have high ionic conductivity. We synthesized a series of compositions of this conductor and found that cubic Li6.6La3Zr1.6Ta0.4O12 (LLZO-Ta) has a high ionic conductivity of 3.7×10(-4)Scm(-1) at room temperature. The (7)Li NMR spectrum of LLZO-Ta was composed of narrow and broad components, and the linewidth of the narrow component varied from 0.69kHz (300K) to 0.32kHz (400K). We carried out lithium ion diffusion measurements using pulsed-field spin-echo (PGSE) NMR spectroscopy and found that echo signals were observed at T≥313K with reasonable sensitivity. The lithium diffusion behavior was measured by varying the observation time and pulsed-field gradient (PFG) strength between 313 and 384K. We found that lithium diffusion depended significantly on the observation time and strength of the PFG, which is quite different from lithium ion diffusion in liquids. It was shown that lithium ion migration in the solid conductor was distributed widely in both time and space.

  15. Lanthanide complexes of chiral 3 + 3 macrocycles derived from (1R,2R)-1,2-diaminocyclohexane and 2,6-diformyl-4-methylphenol.

    PubMed

    Paluch, Marta; Lisowski, Jerzy; Lis, Tadeusz

    2006-01-14

    The enantiopure amine macrocycle H(3)L, as well as the parent macrocyclic Schiff base H(3)L1, the 3 + 3 condensation product of (1R,2R)-1,2-diaminocyclohexane and 2,6-diformyl-4-methylphenol, are able to form mononuclear complexes with lanthanide(III) ions. The lanthanide(III) complexes of H(3)L have been studied in solution using NMR spectroscopy and electrospray mass spectrometry. The NMR spectra indicate the presence of complexes of low C(1) and C(2) symmetry. The (1)H and (13)C NMR signals of the Lu(III) complex obtained from H(3)L have been assigned on the basis of COSY, TOCSY, NOESY, ROESY and HMQC spectra. The NMR data reveal unsymmetrical binding of lanthanide(III) ion and the presence of a dynamic process corresponding to rotation of Lu(III) within the macrocycle. The [Ln(H(4)L)(NO(3))(2)](NO(3))(2)(Ln = Sm(III), Eu(III), Dy(III), Yb(III) and Lu(III)) complexes of the cationic ligand H(4)L(+) have been isolated in pure form. The X-ray analysis of the [Eu(H(4)L)(NO(3))(2)](NO(3))(2) complex confirms the coordination mode of the macrocycle determined on the basis of NMR results. In this complex the europium(III) ion is bound to three phenolate oxygen atoms and two amine nitrogen atoms of the monoprotonated macrocycle H(4)L(+), as well as to two axial bidendate nitrate anions. In the presence of a base, mononuclear La(III), Ce(III) and Pr(III) complexes of the deprotonated form of the ligand L(3-) can be obtained. When 2 equivalents of Pr(III) are used in this synthesis Na(3)[Pr(2)L(NO(3))(2)(OH)(2)](2)NO(3).5H(2)O is obtained. The NMR, ES MS and an X-ray crystal model of this complex show coordination of two Pr(III) ions by the macrocycle L. The X-ray crystal structure of the free macrocycle H(3)L1 has also been determined. In contrast to macrocyclic amine H(3)L, the Schiff base H(3)L1 adopts a cone-type conformation resembling calixarenes.

  16. Organopromoted direct synthesis of 6-iodo-3-methylthioimidazo[1,2-a]pyridines via convergent integration of three self-sorting domino sequences.

    PubMed

    Liu, Shan; Xi, Hailing; Zhang, Jingjing; Wu, Xia; Gao, Qinghe; Wu, Anxin

    2015-09-07

    An NH2CN-promoted convergent integration of three self-sorting domino sequences is described for the construction of 6-iodo-3-methylthioimidazo[1,2-a]pyridines from aryl methyl ketones and 2-aminopyridines. This strategy allows the construction of an imidazo[1,2-a]pyridine ring along with methylthiolation at C-3 and iodination at C-6. Preliminary mechanistic studies indicate that this process terminates at the iodination stage without Kornblum oxidation in the presence of I2 and DMSO.

  17. Symmetry reduction due to gallium substitution in the garnet Li6.43(2)Ga0.52(3)La2.67(4)Zr2O12

    PubMed Central

    Robben, Lars; Merzlyakova, Elena; Heitjans, Paul; Gesing, Thorsten M.

    2016-01-01

    Single-crystal structure refinements on lithium lanthanum zirconate (LLZO; Li7La3Zr2O12) substituted with gallium were successfully carried out in the cubic symmetry space group I 3d. Gallium was found on two lithium sites as well as on the lanthanum position. Due to the structural distortion of the resulting Li6.43(2)Ga0.52(3)La2.67(4)Zr2O12 (Ga–LLZO) single crystals, a reduction of the LLZO cubic garnet symmetry from Ia d to I 3d was necessary, which could hardly be analysed from X-ray powder diffraction data. PMID:27006788

  18. 45 CFR 12a.6 - Suitability criteria.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 45 Public Welfare 1 2012-10-01 2012-10-01 false Suitability criteria. 12a.6 Section 12a.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION USE OF FEDERAL REAL PROPERTY TO ASSIST THE HOMELESS § 12a.6 Suitability criteria. (a) All properties, buildings and land will...

  19. 45 CFR 12a.6 - Suitability criteria.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 45 Public Welfare 1 2011-10-01 2011-10-01 false Suitability criteria. 12a.6 Section 12a.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION USE OF FEDERAL REAL PROPERTY TO ASSIST THE HOMELESS § 12a.6 Suitability criteria. (a) All properties, buildings and land will...

  20. 45 CFR 12a.6 - Suitability criteria.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 45 Public Welfare 1 2014-10-01 2014-10-01 false Suitability criteria. 12a.6 Section 12a.6 Public Welfare Department of Health and Human Services GENERAL ADMINISTRATION USE OF FEDERAL REAL PROPERTY TO ASSIST THE HOMELESS § 12a.6 Suitability criteria. (a) All properties, buildings and land will...

  1. 45 CFR 12a.6 - Suitability criteria.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 45 Public Welfare 1 2013-10-01 2013-10-01 false Suitability criteria. 12a.6 Section 12a.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION USE OF FEDERAL REAL PROPERTY TO ASSIST THE HOMELESS § 12a.6 Suitability criteria. (a) All properties, buildings and land will...

  2. 45 CFR 12a.6 - Suitability criteria.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Suitability criteria. 12a.6 Section 12a.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION USE OF FEDERAL REAL PROPERTY TO ASSIST THE HOMELESS § 12a.6 Suitability criteria. (a) All properties, buildings and land will...

  3. 40 CFR 721.5400 - 3,6,9,12,15,18,21-Hepta-oxa-tetra-triaoctanoic acid, sodium salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 3,6,9,12,15,18,21-Hepta-oxa-tetra-triaoctanoic acid, sodium salt. 721.5400 Section 721.5400 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical...

  4. Single crystal growth and characterization of the reduced barium sodium siliconiobate, Ba3Na0.32Nb6O12(Si2O7)2

    NASA Astrophysics Data System (ADS)

    Cortese, Anthony J.; Wilkins, Branford; Smith, Mark D.; Morrison, Gregory; zur Loye, Hans-Conrad

    2015-10-01

    Single crystals of Ba3Na0.32Nb6O12(Si2O7)2 were grown for the first time. The use of an alkali/alkaline earth eutectic flux facilitated the crystal growth. Ba3Na0.32Nb6O12(Si2O7)2, a mixed valent Nb(V)/Nb(IV) compound, crystallizes in the noncentrosymmetric hexagonal space group P-62m with a = 8.9998(10) Å and c = 7.8119(17) Å. The temperature dependence of the magnetic susceptibility was measured and found to be paramagnetic across the entire 2-300 K temperature range measured. Although noncentrosymmetric, Ba3Na0.32Nb6O12(Si2O7)2 was not found to be second harmonic generation active. Ba3Na0.32Nb6O12(Si2O7)2 was further characterized by IR and UV/Vis spectroscopies.

  5. Efficient traceless solid-phase synthesis of 3,4-dihydropyrazino[1,2-b]indazoles and their 6-oxides.

    PubMed

    Pudelová, Nadezda; Krchnák, Viktor

    2009-01-01

    A highly efficient novel traceless solid-phase synthesis of 3,4-dihydropyrazino[1,2-b]indazoles and their 6-oxides was developed by using commercially available building blocks, diamines, 2-nitrobenzenesulfonyl chlorides, and bromoketones/bromoacetates. Mild reaction conditions, diversely substituted building blocks, and high purity of crude products enabled effective combinatorial syntheses of libraries.

  6. Nqrs Data for C3H10INO6 [C3H7NO2·HIO3·(1/2)(H2O)] (Subst. No. 0642)

    NASA Astrophysics Data System (ADS)

    Chihara, H.; Nakamura, N.

    This document is part of Subvolume A `Substances Containing Ag … C10H15' of Volume 48 `Nuclear Quadrupole Resonance Spectroscopy Data' of Landolt-Börnstein - Group III `Condensed Matter'. It contains an extract of Section `3.2 Data tables' of the Chapter `3 Nuclear quadrupole resonance data' providing the NQRS data for C3H10INO6 [C3H7NO2·HIO3·(1/2)(H2O)] (Subst. No. 0642)

  7. Synthesis of polysubstituted 1,2-dihydroquinolines and indoles via cascade reactions of arylamines and propargylic alcohols catalyzed by FeCl3·6H2O.

    PubMed

    Shao, Min; Wu, Yunjun; Feng, Zhijun; Gu, Xiaoxia; Wang, Shaoyin

    2016-02-28

    An efficient, environmentally friendly and high-yielding route from inexpensive starting materials to 1,2-dihydroquinolines has been developed. This procedure proceeded via a cascade Friedel-Crafts-type reaction and 6-endo-trig hydroamination under the catalysis of FeCl3·6H2O, involving the formation of two new σ (C-C and C-N) bonds in a single operation for the construction of a 1,2-dihydroquinoline skeleton in good to excellent yields.

  8. 12 CFR 12.3 - Recordkeeping.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Recordkeeping. 12.3 Section 12.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY RECORDKEEPING AND CONFIRMATION... an adequate basis for the audit of the information. Record maintenance may include the use...

  9. Thermally stable compositions including 2,4,8,10-tetranitro-5H-pyrido[3',2':4,5][1,2,3]triazolo[1,2-a]benzotriazo- l-6-ium, inner salt

    DOEpatents

    Hiskey, Michael A.; Huynh, My Hang

    2010-01-26

    An explosive formulation including 2,4,8,10-tetranitro-5H-pyrido[3',2':4,5][1,2,3]triazolo[1,2-a]benzotriazo- l-6-ium, inner salt and a high temperature binder is disclosed together with a process of preparing 2,4,8,10-tetranitro-5H-pyrido[3',2':4,5][1,2,3]triazolo[1,2-a]benzotriazo- l-6-ium, inner salt.

  10. Upper bounds on ɛ'/ ɛ parameters B 6 (1/2) and B 8 (3/2) from large N QCD and other news

    NASA Astrophysics Data System (ADS)

    Buras, Andrzej J.; Gérard, Jean-Marc

    2015-12-01

    We demonstrate that in the large N approach developed by the authors in collaboration with Bardeen, the parameters B 6 (1/2) and B 8 (3/2) parametrizing the K → ππ matrix elements < Q 6>0 and < Q 8>2 of the dominant QCD and electroweak operators receive both negative O(1/N) corrections such that B 6 (1/2) ≤ B 8 (3/2) < 1 in agreement with the recent lattice results of the RBC-UKQCD collaboration. We also point out that the pattern of the size of the hadronic matrix elements of all QCD and electroweak penguin operators Q i contributing to the K → ππ amplitudes A 0 and A 2, obtained by this lattice collaboration, provides further support to our large N approach. In particular, the lattice result for the matrix element < Q 8>0 implies for the corresponding parameter B 8 (1/2) = 1.0 ± 0.2 to be compared with large N value B 8 (1/2) = 1.1 ± 0.1. We discuss briefly the implications of these findings for the ratio ɛ' /ɛ. In fact, with the precise value for B 8 (3/2) from RBC-UKQCD collaboration, our upper bound on B 6 (1/2) implies ɛ' /ɛ in the SM roughly by a factor of two below its experimental value (16 .6± 2 .3) × 10-4. We also briefly comment on the parameter {widehat{B}}_K and the Δ I = 1 /2 rule.

  11. ±J Ising model on mixed Archimedean lattices: (33,42), (32,4,3,4), (3,122), (4,6,12)

    NASA Astrophysics Data System (ADS)

    Lebrecht, W.; Valdés, J. F.

    2013-10-01

    This paper addresses the problem of finding analytical expressions describing the ground state properties of mixed Archimedean lattices over which a generalized Edwards-Anderson model (±J Ising model) is defined. A local frustration analysis is performed based on representative cells for (33,42), (32,4,3,4), (3,122) and (4,6,12) lattices, following the notation proposed by Grünbaum and Shephard. The concentration of ferromagnetic (F) bonds x is used as the independent variable in the analysis (1-x is the concentration for antiferromagnetic (A) bonds), where x spans the range [0.00,1.00]. The presence of A bonds brings frustration, whose clear manifestation is when bonds around the minimum possible circuit of bonds (plaquette) cannot be simultaneously satisfied. The distribution of curved (frustrated) plaquettes within the representative cell is determinant for the evaluation of the parameters of interest such as average frustration segment, energy per bond, and fractional content of unfrustrated bonds. Two methods are developed to cope with this analysis: one based on the direct probability of a plaquette being curved; the other one is based on the consideration of the different ways bonds contribute to the particular plaquette configuration. Exact numerical simulations on a large number of randomly generated samples associated to (33,42) and (32,4,3,4) lattices allow to validate the previously described theoretical analysis. It is found that the first method presents slight advantages over the second one. However, both methods give an excellent description for most of the range for x. The small deviations at specific intervals of x for each lattice are relevant to the self-imposed limitations of both methods due to practical reasons. A particular discussion for the point x=0.50 for each one of the four lattices also sheds light on the general trends of the properties described here.

  12. 6a-Nitro-6-phenyl-6,6a,6b,7,8,9,10,12a-octa­hydro­spiro­[chromeno[3,4-a]indol­izine-12,3′-indolin]-2′-one

    PubMed Central

    Devi, Seenivasan Karthiga; Srinivasan, Thothadri; Rao, Jonnalagadda Naga Siva; Raghunathan, Raghavachary; Velmurugan, Devadasan

    2013-01-01

    In the title compound, C28H25N3O4, the central pyrrolidine ring adopts adopts an envelope conformation with the N atom as the flap and the piperidine ring adopts a chair conformation. The pendant pyrrolidine ring is almost planar (r.m.s. deviation = 0.008 Å). An intra­molecular C—H⋯O inter­action closes an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R 2 2(8) loops. PMID:23795144

  13. A 4-week study of four 3-monochloropropane-1,2-diol diesters on lipid metabolism in C57BL/6J mice.

    PubMed

    Lu, Jing; Wang, Zhenning; Ren, Mengrou; Feng, Guangxin; Ye, Beining; Wang, Yi; Fang, Baochen; Deng, Xuming; Guan, Shuang

    2015-09-01

    3-Monochloropropane-1,2-diol (3-MCPD) esters have been detected in many foods, which have become a new safety issue worldwide. In the study, we investigated the effect of four 3-MCPD diesters (palmitate diester: CDP; stearate diester: CDS; oleate diester: CDO; linoleate diester: CDL) on lipid metabolism in C57BL/6J mice. The results showed that CDP, CDS, CDO and CDL significantly increased the serum TC, LDL-C levels and liver TG, TC levels at dose of 16.5μmol/kg/day. These results indicated that 3-MCPD diesters could potentially cause hyperlipidemia in C57BL/6J mice. Moreover, oil red O staining confirmed fat accumulation in liver induced by 3-MCPD diesters. Our work will provide more information for safety evaluation of 3-MCPD diesters. However, whether free 3-MCPD or free fatty acids or combined action compensates for the hyperlipidemia effects should be elucidated in the future.

  14. Determination of Hepatotoxicity and Its Underlying Metabolic Basis of 1,2-Dichloropropane in Male Syrian Hamsters and B6C3F1 Mice.

    PubMed

    Gi, Min; Fujioka, Masaki; Yamano, Shotaro; Shimomura, Eri; Ishii, Naomi; Kakehashi, Anna; Takeshita, Masanori; Wanibuchi, Hideki

    2015-05-01

    1,2-Dichloropropane (1,2-DCP) has recently been reclassified from not classifiable as to its carcinogenicity to humans (Group 3) to carcinogenic to humans (Group 1) by the International Agency for Research on Cancer. This was based on the findings of epidemiological studies in Japan that occupational exposure to paint stripers containing 1,2-DCP was associated with increased cholangiocarcinomas. It is known that 1,2-DCP is negative for cholangiocarcinogenicity in rats and mice. However, its toxicity and carcinogenicity has not been examined in hamsters and little is known about the regulation of its metabolism in hamsters. The purpose of this study was to determine the hepatobiliary toxicity of 1,2-DCP in hamsters and to characterize and compare the altered patterns of hepatic xenometabolic enzymes in hamsters and mice. Male Syrian hamsters and male B6C3F1 mice were treated with various doses of 1,2-DCP for 4 h or 3 days or 4 weeks. These experiments demonstrated that a high dose of 1,2-DCP induced centrilobular hepatocellular necrosis in hamsters. CYP2E1 is possibly the key enzyme responsible for bioactivation and the consequent hepatocytotoxicity of 1,2-DCP, and GSH conjugation catalyzed by GST-T1 may exert a cytoprotective role in hamsters and mice. Notably, the expression pattern of GST-T1 in bile duct epithelial cells differed between hamsters and mice: GST-T1 was expressed in bile duct epithelial cells of mice but not hamsters. This indicates that responses to 1,2-DCP in the bile duct of hamsters might differ from that of mice, and suggests that long-term studies are necessary to clarify the chalangiocarcinogenicity of 1,2-DCP in hamsters, though no biliary toxicity was observed in the present short-term experiments.

  15. Bis(dimethyl-ammonium) 3,3'-dicarb-oxy-5,5'-(5,7,12,14-tetra-oxo-6,13-diaza-tetra-cyclo-[6.6.2.0(4,16).0(11,15)]hexa-deca-1,3,8,10,15-penta-ene-6,13-di-yl)dibenzoate dihydrate.

    PubMed

    Xu, Lan-Ping; Qin, Lan; Han, Lei

    2012-07-01

    The title compound, 2C(2)H(8)N(+)·C(30)H(12)N(2)O(12) (2-)·2H(2)O, comprises dimethyl-ammonium cations, 3,3'-dicarb-oxy-5,5'-(5,7,12,14-tetra-oxo-6,13-diaza-tetra-cyclo-[6.6.2.0(4,16).0(11,15)]hexa-deca-1,3,8,10,15-penta-ene-6,13-di-yl)dibenzoate dianions and water mol-ecules. The dianion is situated on a crystallographic inversion centre. Two very strong symmetry-restricted O⋯H⋯O hydrogen bonds are present which are situated about the crystallographic inversion centres. In one of these hydrogen bonds, the H atom is situated at its centre, while in the other one the H atom is disordered about its centre. Both H atoms are involved in the chain-like C(2) (2)(16) motif, and not in a more common motif R(2) (2)(8) that is composed of a pair of hydrogen carboxyl-ates with the H atoms situated about the centre between the pair of O atoms. In the crystal, inter-action of these hydrogen bonds results in formation of anionic layers of dianions parallel to (-111). The water mol-ecules donate their H atoms to one of two of the carboxyl-ate O atoms, forming strong hydrogen bonds. The dimethyl-ammonium donates a bifurcated hydrogen bond to an oxo group of the dianion, forming weak hydrogen bonds. All the hydrogen bonds form a three-dimensional hydrogen-bonded network.

  16. High-Temperature Thermoelectric Properties of the Solid–Solution Zintl Phase Eu11Cd6Sb12–xAsx (x < 3)

    SciTech Connect

    Kazem, Nasrin; Xie, Weiwei; Ohno, Saneyuki; Zevalkink, Alexandra; Miller, Gordon J; Snyder, G Jeffrey; Kauzlarich, Susan M

    2014-02-11

    Zintl phases are compounds that have shown promise for thermoelectric applications. The title solid–solution Zintl compounds were prepared from the elements as single crystals using a tin flux for compositions x = 0, 1, 2, and 3. Eu11Cd6Sb12–xAsx (x < 3) crystallize isostructurally in the centrosymmetric monoclinic space group C2/m (no. 12, Z = 2) as the Sr11Cd6Sb12 structure type (Pearson symbol mC58). Efforts to make the As compositions for x exceeding ~3 resulted in structures other than the Sr11Cd6Sb12 structure type. Single-crystal X-ray diffraction indicates that As does not randomly substitute for Sb in the structure but is site specific for each composition. The amount of As determined by structural refinement was verified by electron microprobe analysis. Electronic structures and energies calculated for various model structures of Eu11Cd6Sb10As2 (x = 2) indicated that the preferred As substitution pattern involves a mixture of three of the six pnicogen sites in the asymmetric unit. In addition, As substitution at the Pn4 site opens an energy gap at the Fermi level, whereas substitution at the other five pnicogen sites remains semimetallic with a pseudo gap. Thermoelectric properties of these compounds were measured on hot-pressed, fully densified pellets. Samples show exceptionally low lattice thermal conductivities from room temperature to 775 K: 0.78–0.49 W/mK for x = 0; 0.72–0.53 W/mK for x = 1; and 0.70–0.56 W/mK for x = 2. Eu11Cd6Sb12 shows a high p-type Seebeck coefficient (from +118 to 153 μ V/K) but also high electrical resistivity (6.8 to 12.8 mΩ·cm). The value of zT reaches 0.23 at 774 K. The properties of Eu11Cd6Sb12–xAsx are interpreted in discussion with the As site substitution.

  17. Enhanced infrared-to-visible up-conversion emission and temperature sensitivity in (Er3+,Yb3+, and W6+) tri-doped Bi4Ti3O12 ferroelectric oxide

    NASA Astrophysics Data System (ADS)

    Bokolia, Renuka; Mondal, Manisha; Rai, V. K.; Sreenivas, K.

    2017-02-01

    Strong up conversion (UC) luminescence at 527, 550, and 662 nm is compared under an excitation of 980 nm in single doped (Er3+), co-doped (Er3+/Yb3+), and (Er3+/Yb3+/W6+) tri-doped bismuth titanate (Bi4Ti3O12). For the co-doped system, the frequency (UC) emission intensity due to Er3+ ions is enhanced significantly in the green bands due to the efficient energy transfer from Yb3+ to Er3+ ions. Further increase in the emission intensity is seen with non-luminescent W6+ ions in the tri-doped system due to the modification in the local crystal field around the Er3+ ions, and is evidenced through a gradual change in the crystal structure of the host lattice with increasing W6+ content. The observed changes in the fluorescence lifetime and the associated energy transfer mechanisms are discussed. A progressive reduction of the lifetime of the 4S3/2 levels of Er3+ ions from 72 to 58.7 μs with the introduction of Yb3+ and W6+ dopant increases the transition probability and enhances the UC emission intensity. The efficiency of the energy transfer process ( η ) in the co-doped and tri-doped systems is found to be 9.4% and 18.6%, respectively, in comparison to the single doped system. Temperature sensing based on the fluorescence intensity ratio (FR) technique shows high sensitivity (0.0123 K-1) in the high temperature range (293 to 523 K) for an optimum content of Er3+, Yb3+, and W6+ with x = 0.03, y = 0.18, and z = 0.06 at. % in the tri-doped Bi4-x-yErxYbyTi3-zWzO12 ferroelectric composition, and is found useful for potential applications in optical thermometry.

  18. The Impact of Screening, Brief Intervention and Referral for Treatment in Emergency Department Patients’ Alcohol Use: A 3-, 6- and 12-month Follow-up

    PubMed Central

    2010-01-01

    Aims: This study aims to determine the impact of Screening, Brief Intervention and Referral for Treatment (SBIRT) in reducing alcohol consumption in emergency department (ED) patients at 3, 6, and 12 months following exposure to the intervention. Methods: Patients drinking above the low-risk limits (at-risk to dependence), as defined by National Institute of Alcohol Abuse and Alcoholism (NIAAA), were recruited from 14 sites nationwide from April to August 2004. A quasi-experimental comparison group design included sequential recruitment of intervention and control patients at each site. Control patients received a written handout. The Intervention group received the handout and participated in a brief negotiated interview with direct referral for treatment if indicated. Follow-up surveys were conducted at 3, 6, and 12 months by telephone using an Interactive Voice Response (IVR) system. Results: Of the 1132 eligible patients consented and enrolled (581 control, 551 intervention), 699 (63%), 575 (52%) and 433 (38%) completed follow-up surveys via IVR at 3, 6, and 12 months, respectively. Regression analysis adjusting for the clustered sampling design and using multiple imputation procedures to account for subject attrition revealed that those receiving SBIRT reported roughly three drinks less per week than controls (B = −3.00, SE = 1.06, P < 0.05) and the level of maximum drinks per occasion was approximately three-fourths of a drink less than controls (B = -0.76, SE = 0.29, P < 0.05) at 3 months. At 6 and 12 months post-intervention, these effects had weakened considerably and were no longer statistically or substantively significant. Conclusion: SBIRT delivered by ED providers appears to have short-term effectiveness in reducing at-risk drinking, but multi-contact interventions or booster programs may be necessary to maintain long-term reductions in risky drinking. PMID:20876217

  19. Structure-activity relationship study of pyrimido[1,2-c][1,3]benzothiazin-6-imine derivatives for potent anti-HIV agents.

    PubMed

    Mizuhara, Tsukasa; Oishi, Shinya; Ohno, Hiroaki; Shimura, Kazuya; Matsuoka, Masao; Fujii, Nobutaka

    2012-11-01

    3,4-Dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine (PD 404182) is an antiretroviral agent with submicromolar inhibitory activity against human immunodeficiency virus-1 (HIV-1) and HIV-2 infection. In the current study, the structure-activity relationships of accessory groups at the 3- and 9-positions of pyrimido[1,2-c][1,3]benzothiazin-6-imine were investigated for the development of more potent anti-HIV agents. Several different derivatives containing a 9-aryl group were designed and synthesized using Suzuki-Miyaura cross-coupling and Ullmann coupling reactions. Modification of the m-methoxyphenyl or benzo[d][1,3]dioxol-5-yl group resulted in improved anti-HIV activity. In addition, the 2,4-diazaspiro[5.5]undec-2-ene-fused benzo[e][1,3]thiazine derivatives were designed and tested for their anti-HIV activities. The most potent 9-(benzo[d][1,3]dioxol-5-yl) derivative was two-threefold more effective against several strains of HIV-1 and HIV-2 than the parent compound, PD 404182.

  20. 12 CFR 3.12-3.19 - [Reserved

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false 3.12-3.19 Section 3.12-3.19 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY CAPITAL ADEQUACY STANDARDS Capital Ratio Requirements and Buffers §§ 3.12-3.19...

  1. A Historical Evaluation of the U12t Tunnel, Nevada Test Site, Nye County, Nevada, Volume 3 of 6

    SciTech Connect

    Harold Drollinger; Robert C. Jones; and Thomas F. Bullard; Desert Research Institute, Laurence J. Ashbaugh, Southern Nevada Courier Service and Wayne R. Griffin, Stoller-Navarro Joint Venture

    2009-02-01

    This report presents a historical evaluation of the U12t Tunnel on the Nevada Test Site in southern Nevada. The work was conducted by the Desert Research Institute at the request of the U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office and the U.S. Department of Defense, Defense Threat Reduction Agency (DTRA). The U12t Tunnel is one of a series of tunnels used for underground nuclear weapons effects tests on the east side of Rainier and Aqueduct Mesas. Six nuclear weapons effects tests, Mint Leaf, Diamond Sculls, Husky Pup, Midas Myth/Milagro, Mighty Oak, and Mission Ghost, and one high explosive test, SPLAT, were conducted within the U12t Tunnel from 1970 to 1987. All six of the nuclear weapons effects tests and the high explosive test were sponsored by DTRA. Two conventional weapons experiments, Dipole Knight and Divine Eagle, were conducted in the tunnel portal area in 1997 and 1998. These experiments were sponsored by the Defense Special Weapons Agency. The U12t Tunnel complex is composed of the Portal and Mesa Areas and includes an underground tunnel with a main access drift and nine primary drifts, a substantial tailings pile fronting the tunnel portal, a series of discharge ponds downslope of the tailings pile, and two instrumentation trailer parks and 16 drill holes on top of Aqueduct Mesa. A total of 89 cultural features were recorded: 54 at the portal and 35 on the mesa. In the Portal Area, cultural features are mostly concrete pads and building foundations; other features include the portal, rail lines, the camel back, ventilation and cooling system components, communication equipment, and electrical equipment. On the mesa are drill holes, a few concrete pads, a loading ramp, and electrical equipment.

  2. Rabbit Achilles tendon full transection model - wound healing, adhesion formation and biomechanics at 3, 6 and 12 weeks post-surgery.

    PubMed

    Meier Bürgisser, Gabriella; Calcagni, Maurizio; Bachmann, Elias; Fessel, Gion; Snedeker, Jess G; Giovanoli, Pietro; Buschmann, Johanna

    2016-09-15

    After tendon rupture repair, two main problems may occur: re-rupture and adhesion formation. Suitable non-murine animal models are needed to study the healing tendon in terms of biomechanical properties and extent of adhesion formation. In this study 24 New Zealand White rabbits received a full transection of the Achilles tendon 2 cm above the calcaneus, sutured with a 4-strand Becker suture. Post-surgical analysis was performed at 3, 6 and 12 weeks. In the 6-week group, animals received a cast either in a 180 deg stretched position during 6 weeks (adhesion provoking immobilization), or were re-casted with a 150 deg position after 3 weeks (adhesion inhibiting immobilization), while in the other groups (3 and 12 weeks) a 180 deg position cast was applied for 3 weeks. Adhesion extent was analyzed by histology and ultrasound. Histopathological scoring was performed according to a method by Stoll et al. (2011), and the main biomechanical properties were assessed. Histopathological scores increased as a function of time, but did not reach values of healthy tendons after 12 weeks (only around 15 out of 20 points). Adhesion provoking immobilization led to an adhesion extent of 82.7±9.7%, while adhesion inhibiting immobilization led to 31.9±9.8% after 6 weeks. Biomechanical properties increased over time, however, they did not reach full strength nor elastic modulus at 12 weeks post-operation. Furthermore, the rabbit Achilles tendon model can be modulated in terms of adhesion formation to the surrounding tissue. It clearly shows the different healing stages in terms of histopathology and offers a suitable model regarding biomechanics because it exhibits similar biomechanics as the human flexor tendons of the hand.

  3. Rabbit Achilles tendon full transection model – wound healing, adhesion formation and biomechanics at 3, 6 and 12 weeks post-surgery

    PubMed Central

    Meier Bürgisser, Gabriella; Calcagni, Maurizio; Bachmann, Elias; Fessel, Gion; Snedeker, Jess G.; Giovanoli, Pietro

    2016-01-01

    ABSTRACT After tendon rupture repair, two main problems may occur: re-rupture and adhesion formation. Suitable non-murine animal models are needed to study the healing tendon in terms of biomechanical properties and extent of adhesion formation. In this study 24 New Zealand White rabbits received a full transection of the Achilles tendon 2 cm above the calcaneus, sutured with a 4-strand Becker suture. Post-surgical analysis was performed at 3, 6 and 12 weeks. In the 6-week group, animals received a cast either in a 180 deg stretched position during 6 weeks (adhesion provoking immobilization), or were re-casted with a 150 deg position after 3 weeks (adhesion inhibiting immobilization), while in the other groups (3 and 12 weeks) a 180 deg position cast was applied for 3 weeks. Adhesion extent was analyzed by histology and ultrasound. Histopathological scoring was performed according to a method by Stoll et al. (2011), and the main biomechanical properties were assessed. Histopathological scores increased as a function of time, but did not reach values of healthy tendons after 12 weeks (only around 15 out of 20 points). Adhesion provoking immobilization led to an adhesion extent of 82.7±9.7%, while adhesion inhibiting immobilization led to 31.9±9.8% after 6 weeks. Biomechanical properties increased over time, however, they did not reach full strength nor elastic modulus at 12 weeks post-operation. Furthermore, the rabbit Achilles tendon model can be modulated in terms of adhesion formation to the surrounding tissue. It clearly shows the different healing stages in terms of histopathology and offers a suitable model regarding biomechanics because it exhibits similar biomechanics as the human flexor tendons of the hand. PMID:27635037

  4. Differential Regulation of ERK1/2 and mTORC1 Through T1R1/T1R3 in MIN6 Cells.

    PubMed

    Wauson, Eric M; Guerra, Marcy L; Dyachok, Julia; McGlynn, Kathleen; Giles, Jennifer; Ross, Elliott M; Cobb, Melanie H

    2015-08-01

    The MAPKs ERK1/2 respond to nutrients and other insulin secretagogues in pancreatic β-cells and mediate nutrient-dependent insulin gene transcription. Nutrients also stimulate the mechanistic target of rapamycin complex 1 (mTORC1) to regulate protein synthesis. We showed previously that activation of both ERK1/2 and mTORC1 in the MIN6 pancreatic β-cell-derived line by extracellular amino acids (AAs) is at least in part mediated by the heterodimeric T1R1/T1R3, a G protein-coupled receptor. We show here that AAs differentially activate these two signaling pathways in MIN6 cells. Pretreatment with pertussis toxin did not prevent the activation of either ERK1/2 or mTORC1 by AAs, indicating that G(I) is not central to either pathway. Although glucagon-like peptide 1, an agonist for a G(s-)coupled receptor, activated ERK1/2 well and mTORC1 to a small extent, AAs had no effect on cytosolic cAMP accumulation. Ca(2+) entry is required for ERK1/2 activation by AAs but is dispensable for AA activation of mTORC1. Pretreatment with UBO-QIC, a selective G(q) inhibitor, reduced the activation of ERK1/2 but had little effect on the activation of mTORC1 by AAs, suggesting a differential requirement for G(q). Inhibition of G(12/13) by the overexpression of the regulator of G protein signaling domain of p115 ρ-guanine nucleotide exchange factor had no effect on mTORC1 activation by AAs, suggesting that these G proteins are also not involved. We conclude that AAs regulate ERK1/2 and mTORC1 through distinct signaling pathways.

  5. Differential Regulation of ERK1/2 and mTORC1 Through T1R1/T1R3 in MIN6 Cells

    PubMed Central

    Wauson, Eric M.; Guerra, Marcy L.; Dyachok, Julia; McGlynn, Kathleen; Giles, Jennifer; Ross, Elliott M.

    2015-01-01

    The MAPKs ERK1/2 respond to nutrients and other insulin secretagogues in pancreatic β-cells and mediate nutrient-dependent insulin gene transcription. Nutrients also stimulate the mechanistic target of rapamycin complex 1 (mTORC1) to regulate protein synthesis. We showed previously that activation of both ERK1/2 and mTORC1 in the MIN6 pancreatic β-cell-derived line by extracellular amino acids (AAs) is at least in part mediated by the heterodimeric T1R1/T1R3, a G protein-coupled receptor. We show here that AAs differentially activate these two signaling pathways in MIN6 cells. Pretreatment with pertussis toxin did not prevent the activation of either ERK1/2 or mTORC1 by AAs, indicating that Gi is not central to either pathway. Although glucagon-like peptide 1, an agonist for a Gs-coupled receptor, activated ERK1/2 well and mTORC1 to a small extent, AAs had no effect on cytosolic cAMP accumulation. Ca2+ entry is required for ERK1/2 activation by AAs but is dispensable for AA activation of mTORC1. Pretreatment with UBO-QIC, a selective Gq inhibitor, reduced the activation of ERK1/2 but had little effect on the activation of mTORC1 by AAs, suggesting a differential requirement for Gq. Inhibition of G12/13 by the overexpression of the regulator of G protein signaling domain of p115 ρ-guanine nucleotide exchange factor had no effect on mTORC1 activation by AAs, suggesting that these G proteins are also not involved. We conclude that AAs regulate ERK1/2 and mTORC1 through distinct signaling pathways. PMID:26168033

  6. TRPC6 channel-mediated neurite outgrowth in PC12 cells and hippocampal neurons involves activation of RAS/MEK/ERK, PI3K, and CAMKIV signaling.

    PubMed

    Heiser, Jeanine H; Schuwald, Anita M; Sillani, Giacomo; Ye, Lian; Müller, Walter E; Leuner, Kristina

    2013-11-01

    The non-selective cationic transient receptor canonical 6 (TRPC6) channels are involved in synaptic plasticity changes ranging from dendritic growth, spine morphology changes and increase in excitatory synapses. We previously showed that the TRPC6 activator hyperforin, the active antidepressant component of St. John's wort, induces neuritic outgrowth and spine morphology changes in PC12 cells and hippocampal CA1 neurons. However, the signaling cascade that transmits the hyperforin-induced transient rise in intracellular calcium into neuritic outgrowth is not yet fully understood. Several signaling pathways are involved in calcium transient-mediated changes in synaptic plasticity, ranging from calmodulin-mediated Ras-induced signaling cascades comprising the mitogen-activated protein kinase, PI3K signal transduction pathways as well as Ca(2+) /calmodulin-dependent protein kinase II (CAMKII) and CAMKIV. We show that several mechanisms are involved in TRPC6-mediated synaptic plasticity changes in PC12 cells and primary hippocampal neurons. Influx of calcium via TRPC6 channels activates different pathways including Ras/mitogen-activated protein kinase/extracellular signal-regulated kinases, phosphatidylinositide 3-kinase/protein kinase B, and CAMKIV in both cell types, leading to cAMP-response element binding protein phosphorylation. These findings are interesting not only in terms of the downstream targets of TRPC6 channels but also because of their potential to facilitate further understanding of St. John's wort extract-mediated antidepressant activity. Alterations in synaptic plasticity are considered to play an important role in the pathogenesis of depression. Beside several other proteins, TRPC6 channels regulate synaptic plasticity. This study demonstrates that different pathways including Ras/MEK/ERK, PI3K/Akt, and CAMKIV are involved in the improvement of synaptic plasticity by the TRPC6 activator hyperforin, the antidepressant active constituent of St. John

  7. 12 CFR 561.6 - Audit period.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 6 2012-01-01 2012-01-01 false Audit period. 561.6 Section 561.6 Banks and... SAVINGS ASSOCIATIONS § 561.6 Audit period. The audit period of a savings association means the twelve month period (or other period in the case of a change in audit period) covered by the annual...

  8. 12 CFR 583.6 - Company.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 6 2013-01-01 2012-01-01 true Company. 583.6 Section 583.6 Banks and Banking... AND LOAN HOLDING COMPANIES § 583.6 Company. The term company means any corporation, partnership, trust, joint-stock company, or similar organization, but does not include: (a) The Federal Deposit...

  9. 12 CFR 583.6 - Company.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 6 2014-01-01 2012-01-01 true Company. 583.6 Section 583.6 Banks and Banking... AND LOAN HOLDING COMPANIES § 583.6 Company. The term company means any corporation, partnership, trust, joint-stock company, or similar organization, but does not include: (a) The Federal Deposit...

  10. 12 CFR 583.6 - Company.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 6 2012-01-01 2012-01-01 false Company. 583.6 Section 583.6 Banks and Banking... AND LOAN HOLDING COMPANIES § 583.6 Company. The term company means any corporation, partnership, trust, joint-stock company, or similar organization, but does not include: (a) The Federal Deposit...

  11. 12 CFR 703.6 - Credit analysis.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Credit analysis. 703.6 Section 703.6 Banks and... ACTIVITIES § 703.6 Credit analysis. A Federal credit union must conduct and document a credit analysis on an... Federal Deposit Insurance Corporation. A Federal credit union must update this analysis at least...

  12. 12 CFR 703.6 - Credit analysis.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 6 2011-01-01 2011-01-01 false Credit analysis. 703.6 Section 703.6 Banks and... ACTIVITIES § 703.6 Credit analysis. A Federal credit union must conduct and document a credit analysis on an... Federal Deposit Insurance Corporation. A Federal credit union must update this analysis at least...

  13. Enantioselective effect of 12(S)-hydroxyeicosatetraenoic acid on 3T6 fibroblast growth through ERK 1/2 and p38 MAPK pathways and cyclin D1 activation.

    PubMed

    Nieves, Diana; Moreno, Juan J

    2008-09-01

    Hydroxyeicosatetraenoic acids (HETEs) have numerous physiological effects, including modulation of cell proliferation and differentiation. However, little is known about the selective effects of HETE enantiomers on cell proliferation and cell signalling pathways involved in the regulation of cell growth. Furthermore, information on epithelial and endothelial cells growth is controversial. Recently, we demonstrated that 5-, 12-, and 15-HETE are involved in the control of 3T6 fibroblast growth though serine/treonine Akt/PKB (Akt) pathway. Here we examined the participation of both enantiomers (S and R) of HETEs in the control of 3T6 fibroblast growth. Our results show that HETEs (5-, 12-, and 15-HETE) are enantioselective on protein and DNA synthesis and 3T6 fibroblast growth. Furthermore, we observed that 12(S)-HETE induces the enhancement of cAMP and intracellular calcium concentration, whereas 12(R)-HETE was uneffective. Our findings also demonstrated that 12(S)-HETE exerts these effects through enantiospecific interactions with a cellular element, probably a plasma membrane receptor coupling to a pertussis toxin-sensitive protein G. Moreover, these elements may be involved in the activation of mitogen-activated protein kinase pathways which induce the enhancement of cyclin D(1) levels.

  14. 12 CFR 203.6 - Enforcement.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... section 305(b) of the Act (12 U.S.C. 2804(b). (b) Bona fide errors. (1) An error in compiling or recording... 12 Banks and Banking 2 2012-01-01 2012-01-01 false Enforcement. 203.6 Section 203.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM HOME MORTGAGE...

  15. Effect of lairage time ( 0h, 3 h, 6 h or 12 h) on glycogen content and meat quality parameters in suckling lambs.

    PubMed

    Díaz, M T; Vieira, C; Pérez, C; Lauzurica, S; de Chávarri, E González; Sánchez, M; De la Fuente, J

    2014-02-01

    The effect of slaughter at arrival (L0) or after 3 (L3), 6 (L6), 12 (L12) h of lairage on carcass and meat quality of suckling lambs has been studied. Lairage time had a slight effect on carcass quality traits, but most of the meat quality parameters at 24h post mortem were affected. Weight losses increased and glycogen content of liver and longissimus muscle decreased as lairage time increased. Longissimus muscle from L3 lambs had the highest pH, shear force and toughness and the lowest b* and C* values, at 24h post mortem. L3 and L6 had the higher proportion of expelled juice, or low water holding capacity (WHC), at 24h post mortem. Texture parameters and WHC were similar among groups after 5 days of storage. Despite the fact that the effects of lairage time on meat quality disappears after storage, from the point of view of weight losses the slaughter of suckling lambs at arrival is recommended.

  16. Iodination of carbohydrate-derived 1,2-oxazines to enantiopure 5-iodo-3,6-dihydro-2H-1,2-oxazines and subsequent palladium-catalyzed cross-coupling reactions

    PubMed Central

    Medvecký, Michal; Linder, Igor; Schefzig, Luise

    2016-01-01

    Iodination of carbohydrate-derived 3,6-dihydro-2H-1,2-oxazines of type 3 using iodine and pyridine in DMF furnished 5-iodo-substituted 1,2-oxazine derivatives 4 with high efficacy. The alkenyl iodide moiety of 1,2-oxazine derivatives syn-4 and anti-4 was subsequently exploited for the introduction of new functionalities at the C-5 position by applying palladium-catalyzed carbon–carbon bond-forming reactions such as Sonogashira, Heck, or Suzuki coupling reactions as well as a cyanation reaction. These cross-coupling reactions led to a series of 5-alkynyl-, 5-alkenyl-, 5-aryl- and 5-cyano-substituted 1,2-oxazine derivatives being of considerable interest for further synthetic elaborations. This was exemplarily demonstrated by the hydrogenation of syn-21 and anti-24 and by a click reaction of a 5-alkynyl-substituted precursor. PMID:28144363

  17. 1,3-Bis(prop-2-yn-1-yl)-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione

    PubMed Central

    Afrakssou, Zahra; Haoudi, Amal; Capet, Frédéric; Mazzah, Ahmed; Rolando, Christian; El Ammari, Lahcen

    2013-01-01

    In the title compound, C21H12N2O3, the fused-ring system is roughly planar, the largest deviation from the mean plane being 0.084 (2) Å. The two prop-2-yn-1-yl groups are almost perpendicular to the fused ring plane, making C—C—N—C torsion angles of −103.4 (2) and −105.3 (2)°, and point in opposite directions with respect to the plane. In the crystal, mol­ecules are linked by weak C—H⋯O hydrogen bonds, forming a three-dimensional network. PMID:23795107

  18. Cs7Sm11[TeO3]12Cl16 and Rb7Nd11[TeO3]12Br16, the new tellurite halides of the tetragonal Rb6LiNd11[SeO3]12Cl16 structure type

    NASA Astrophysics Data System (ADS)

    Charkin, Dmitri O.; Black, Cameron; Downie, Lewis J.; Sklovsky, Dmitry E.; Berdonosov, Peter S.; Olenev, Andrei V.; Zhou, Wuzong; Lightfoot, Philip; Dolgikh, Valery A.

    2015-12-01

    Two new rare-earth - alkali - tellurium oxide halides were synthesized by a salt flux technique and characterized by single-crystal X-ray diffraction. The structures of the new compounds Cs7Sm11[TeO3]12Cl16 (I) and Rb7Nd11[TeO3]12Br16 (II) (both tetragonal, space group I4/mcm) correspond to the sequence of [MLn11(TeO3)12] and [M6X16] layers and bear very strong similarities to those of known selenite analogs. We discuss the trends in similarities and differences in compositions and structural details between the Se and Te compounds; more members of the family are predicted.

  19. Lasing in a Tm:Ho:Yb{sub 3}Al{sub 5}O{sub 12} crystal pumped into the {sup 3}H{sub 6} – {sup 3}F{sub 4} transition

    SciTech Connect

    Zavartsev, Yu D; Zagumennyi, A I; Kalachev, Yu L; Kutovoi, S A; Mikhailov, V A; Shcherbakov, I A

    2016-03-31

    A growth technology has been developed, and a Tm:Ho:Yb{sub 3}Al{sub 5}O{sub 12} laser crystal of high optical quality has been grown by Czochralski method. Its spectral and luminescent characteristics are studied. Lasing at a wavelength of 2100 nm is obtained under pumping into the absorption line on the {sup 3}H{sub 6} – {sup 3}F{sub 4} transition of the Tm{sup 3+} ion at a wavelength of 1678 nm. The slope and total (optical) efficiencies of the laser at an output power of up to 320 mW reach 41% and 30%, respectively. (lasers)

  20. 11-Methyl-12a-phenyl-9a,12a-dihydrophenanthro[9',10:5,6][1,4]dioxino[2,3-d]thiazole.

    PubMed

    Usman, Anwar; Razak, Ibrahim Abdul; Fun, Hoong Kun; Chantrapromma, Suchada; Zhang, Yan; Xu, Jian Hua

    2002-09-01

    In the title compound, C(24)H(17)NO(2)S, the dioxine and thiazoline rings are distorted from planarity towards a half-chair and an envelope conformation, respectively. The configurations of the dioxine ring, the thiazoline ring and the attached phenyl ring are conditioned by the sp(3) state of the two bridgehead C atoms. The phenanthrene system is nearly coplanar with the dioxine ring, while the attached phenyl ring is orthogonal to the thiazoline ring.

  1. Aktashite Cu6Hg3As4S12 from the Aktash deposit, Altai, Russia: Refinement and crystal chemical analysis of the structure

    NASA Astrophysics Data System (ADS)

    Vasil'Ev, V. I.; Pervukhina, N. V.; Borisov, S. V.; Magarill, S. A.; Naumov, D. Yu.; Kurat'eva, N. V.

    2010-12-01

    The composition and structure of aktashite from the Aktash deposit, Gorny Altai, Russia, have been studied by electron microprobe and X-ray structural analysis. On the basis of close compositions and crystal structures, the identity of aktashite from the Gal-Khaya and Aktash deposits has been demonstrated. Crystals of aktashite are of trigonal symmetry; the unit-cell dimensions are: a = 13.7500(4), c = 9.3600(3) Å, V = 532.54(8) Å3, space group R3, Z = 3 for the composition of Cu6Hg3As4S12, R = 0.043. The structure of aktashite as a framework of vertex-shared HgS4- and CuS4- tetrahedrons of the same orientation is intimately related to the sphalerite-type structure. The earlier identified uncommon cluster group [As4] has been verified and its parameters have been refined. It is shown that the structure may be represented as construction blocks (As4S12)12- packed according to the law of the distorted cubic I-cell.

  2. 12 CFR 1102.6 - Waiver extension.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 9 2012-01-01 2012-01-01 false Waiver extension. 1102.6 Section 1102.6 Banks and Banking FEDERAL FINANCIAL INSTITUTIONS EXAMINATION COUNCIL APPRAISER REGULATION Temporary Waiver Requests § 1102.6 Waiver extension. The ASC may initiate an extension of temporary waiver relief and...

  3. 12 CFR 161.6 - Audit period.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Audit period. 161.6 Section 161.6 Banks and... SAVINGS ASSOCIATIONS § 161.6 Audit period. The audit period of a savings association means the twelve month period (or other period in the case of a change in audit period) covered by the annual...

  4. 12 CFR 1.6 - Convertible securities.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false Convertible securities. 1.6 Section 1.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY INVESTMENT SECURITIES § 1.6 Convertible securities. A national bank may not purchase securities convertible into stock at the option...

  5. 12 CFR 1.6 - Convertible securities.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Convertible securities. 1.6 Section 1.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY INVESTMENT SECURITIES § 1.6 Convertible securities. A national bank may not purchase securities convertible into stock at the option...

  6. 12 CFR 1.6 - Convertible securities.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Convertible securities. 1.6 Section 1.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY INVESTMENT SECURITIES § 1.6 Convertible securities. A national bank may not purchase securities convertible into stock at the option...

  7. 12 CFR 262.6 - Forms.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... PROCEDURE § 262.6 Forms. Necessary forms to be used in connection with applications and other matters are available at the Federal Reserve Banks. A list of all such forms, which is reviewed and revised periodically... 12 Banks and Banking 4 2013-01-01 2013-01-01 false Forms. 262.6 Section 262.6 Banks and...

  8. 12 CFR 212.6 - General exemption.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 2 2011-01-01 2011-01-01 false General exemption. 212.6 Section 212.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.6 General exemption. (a) Exemption. The Board may, by agency order, exempt...

  9. 12 CFR 212.6 - General exemption.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 2 2013-01-01 2013-01-01 false General exemption. 212.6 Section 212.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.6 General exemption. (a) Exemption. The Board may, by agency order, exempt...

  10. 12 CFR 212.6 - General exemption.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 2 2012-01-01 2012-01-01 false General exemption. 212.6 Section 212.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.6 General exemption. (a) Exemption. The Board may, by agency order, exempt...

  11. 12 CFR 212.6 - General exemption.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 2 2014-01-01 2014-01-01 false General exemption. 212.6 Section 212.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.6 General exemption. (a) Exemption. The Board may, by agency order, exempt...

  12. 12 CFR 583.6 - Company.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 5 2011-01-01 2011-01-01 false Company. 583.6 Section 583.6 Banks and Banking... AND LOAN HOLDING COMPANIES § 583.6 Company. The term company means any corporation, partnership, trust, joint-stock company, or similar organization, but does not include: (a) The Federal Deposit...

  13. 12 CFR 583.6 - Company.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Company. 583.6 Section 583.6 Banks and Banking... AND LOAN HOLDING COMPANIES § 583.6 Company. The term company means any corporation, partnership, trust, joint-stock company, or similar organization, but does not include: (a) The Federal Deposit...

  14. 12 CFR 703.6 - Credit analysis.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 7 2012-01-01 2012-01-01 false Credit analysis. 703.6 Section 703.6 Banks and... ACTIVITIES § 703.6 Credit analysis. A Federal credit union must conduct and document a credit analysis on an... Federal Deposit Insurance Corporation. A Federal credit union must update this analysis at least...

  15. 12 CFR 703.6 - Credit analysis.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 7 2013-01-01 2013-01-01 false Credit analysis. 703.6 Section 703.6 Banks and... ACTIVITIES § 703.6 Credit analysis. A Federal credit union must conduct and document a credit analysis on an... Federal Deposit Insurance Corporation. A Federal credit union must update this analysis at least...

  16. 12 CFR 703.6 - Credit analysis.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 7 2014-01-01 2014-01-01 false Credit analysis. 703.6 Section 703.6 Banks and... ACTIVITIES § 703.6 Credit analysis. A Federal credit union must conduct and document a credit analysis on an... Federal Deposit Insurance Corporation. A Federal credit union must update this analysis at least...

  17. 12 CFR 214.6 - Amendments.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Amendments. 214.6 Section 214.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM RELATIONS WITH FOREIGN BANKS AND BANKERS (REGULATION N) Regulations § 214.6 Amendments. The Board of Governors of the...

  18. 12 CFR 561.6 - Audit period.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Audit period. 561.6 Section 561.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY DEFINITIONS FOR REGULATIONS AFFECTING ALL SAVINGS ASSOCIATIONS § 561.6 Audit period. The audit period of a savings association means the...

  19. Crossed beam reactions of the phenyl (C6H5; X(2)A1) and phenyl-d5 radical (C6D5; X(2)A1) with 1,2-butadiene (H2CCCHCH3; X(1)A').

    PubMed

    Yang, Tao; Parker, Dorian S N; Dangi, Beni B; Kaiser, Ralf I; Kislov, Vadim V; Mebel, Alexander M

    2014-06-26

    We explored the reactions on the phenyl (C6H5; X(2)A1) and phenyl-d5 (C6D5; X(2)A1) radical with 1,2-butadiene (C4H6; X(1)A') at a collision energy of about 52 ± 3 kJ mol(-1) in a crossed molecular beam apparatus. The reaction of phenyl with 1,2-butadiene is initiated by adding the phenyl radical with its radical center to the π electron density at the C1/C3 carbon atom of 1,2-butadiene. Later, the initial collision complexes isomerize via phenyl group migration from the C1/C3 carbon atoms to the C2 carbon atom of the allene moiety of 1,2-butadiene. The resulting intermediate undergoes unimolecular decomposition through hydrogen atom emission from the methyl group of the 1,2-butadiene moiety via a rather loose exit transition state leading to 2-phenyl-1,3-butadiene in an overall exoergic reaction (ΔRG = -72 ± 10 kJ mol(-1)). This finding reveals the strong collision-energy dependence of this system when the data are compared with those of the phenyl radical with 1,2-butadiene previously recorded at collision energies up to 160 kJ mol(-1), with the previous study exhibiting the thermodynamically less stable 1-phenyl-3-methylallene (ΔRG = -33 ± 10 kJ mol(-1)) and 1-phenyl-2-butyne (ΔRG = -24 ± 10 kJ mol(-1)) to be the dominant products.

  20. Refining the spin Hamiltonian in the spin-1/2 kagome lattice antiferromagnet ZnCu3(OH)6Cl2 using single crystals.

    PubMed

    Han, Tianheng; Chu, Shaoyan; Lee, Young S

    2012-04-13

    We report thermodynamic measurements of the S=1/2 kagome lattice antiferromagnet ZnCu3(OH)6Cl2, a promising candidate system with a spin-liquid ground state. Using single crystal samples, the magnetic susceptibility both perpendicular and parallel to the kagome plane has been measured. A small, temperature-dependent anisotropy has been observed, where χ(z)/χ(p)>1 at high temperatures and χ(z)/χ(p)<1 at low temperatures. Fits of the high-temperature data to a Curie-Weiss model also reveal an anisotropy. By comparing with theoretical calculations, the presence of a small easy-axis exchange anisotropy can be deduced as the primary perturbation to the dominant Heisenberg nearest neighbor interaction. These results have great bearing on the interpretation of theoretical calculations based on the kagome Heisenberg antiferromagnet model to the experiments on ZnCu3(OH)6Cl2.

  1. High level accumulation of gamma linolenic acid (C18:3Δ6.9,12 cis) in transgenic safflower (Carthamus tinctorius) seeds.

    PubMed

    Nykiforuk, Cory L; Shewmaker, Christine; Harry, Indra; Yurchenko, Olga P; Zhang, Mei; Reed, Catherine; Oinam, Gunamani S; Zaplachinski, Steve; Fidantsef, Ana; Boothe, Joseph G; Moloney, Maurice M

    2012-04-01

    Gamma linolenic acid (GLA; C18:3Δ6,9,12 cis), also known as γ-Linolenic acid, is an important essential fatty acid precursor for the synthesis of very long chain polyunsaturated fatty acids and important pathways involved in human health. GLA is synthesized from linoleic acid (LA; C18:2Δ9,12 cis) by endoplasmic reticulum associated Δ6-desaturase activity. Currently sources of GLA are limited to a small number of plant species with poor agronomic properties, and therefore an economical and abundant commercial source of GLA in an existing crop is highly desirable. To this end, the seed oil of a high LA cultivated species of safflower (Carthamus tinctorius) was modified by transformation with Δ6-desaturase from Saprolegnia diclina resulting in levels exceeding 70% (v/v) of GLA. Levels around 50% (v/v) of GLA in seed oil was achieved when Δ12-/Δ6-desaturases from Mortierella alpina was over-expressed in safflower cultivars with either a high LA or high oleic (OA; C18:1Δ9 cis) background. The differences in the overall levels of GLA suggest the accumulation of the novel fatty acid was not limited by a lack of incorporation into the triacylgylcerol backbone (>66% GLA achieved), or correlated with gene dosage (GLA levels independent of gene copy number), but rather reflected the differences in Δ6-desaturase activity from the two sources. To date, these represent the highest accumulation levels of a newly introduced fatty acid in a transgenic crop. Events from these studies have been propagated and recently received FDA approval for commercialization as Sonova™400.

  2. 40 CFR 721.9790 - Benzenesulfonic acid, 2,2′-(1,2-ethenediyl)bis[5-[[4-[bis(2-hydroxypropyl) amino]- 6-[(3...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6-......

  3. 40 CFR 721.9790 - Benzenesulfonic acid, 2,2′-(1,2-ethenediyl)bis[5-[[4-[bis(2-hydroxypropyl) amino]- 6-[(3...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6-......

  4. 40 CFR 721.9790 - Benzenesulfonic acid, 2,2′-(1,2-ethenediyl)bis[5-[[4-[bis(2-hydroxypropyl) amino]- 6-[(3...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6-......

  5. 40 CFR 721.9790 - Benzenesulfonic acid, 2,2′-(1,2-ethenediyl)bis[5-[[4-[bis(2-hydroxypropyl) amino]- 6-[(3...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6-......

  6. 40 CFR 721.9790 - Benzenesulfonic acid, 2,2′-(1,2-ethenediyl)bis[5-[[4-[bis(2-hydroxypropyl) amino]- 6-[(3...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl...); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6-......

  7. Organocatalytic Asymmetric Michael/Friedel-Crafts Cascade Reaction of 3-Pyrrolyl-oxindoles and α,β-Unsaturated Aldehydes for the Construction of Chiral Spiro[5,6-dihydropyrido[1,2-a]pyrrole-3,3'-oxindoles].

    PubMed

    You, Yong; Cui, Bao-Dong; Zhou, Ming-Qiang; Zuo, Jian; Zhao, Jian-Qiang; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng

    2015-06-05

    An efficient and unprecedented organocatalytic asymmetric reaction of 3-pyrrolyl-oxindoles with α,β-unsaturated aldehydes to generate spirocyclic oxindole compounds was developed. The reactions were catalyzed by diphenylprolinol silyl ether and 2-fluorobenzoic acid via an asymmetric Michael/Friedel-Crafts cascade process, followed by dehydration with p-toluenesulfonic acid to afford a wide variety of structurally diverse spiro[5,6-dihydropyrido[1,2-a]pyrrole-3,3'-oxindole] derivatives in high yields (up to 93%) and with high to excellent diastereo- and enantioselectivities (up to >99:1 dr and 97% ee).

  8. Crystal structure of 2-(4-meth­oxy­phen­yl)-6-nitro­imidazo[1,2-a]pyridine-3-carbaldehyde

    PubMed Central

    Koudad, Mohamed; Elaatiaoui, Abdelmalik; Benchat, Noureddine; Saadi, Mohamed; El Ammari, Lahcen

    2015-01-01

    In the title compound, C15H11N3O4, the imidazo[1,2-a] pyridine ring system is almost planar [r.m.s. deviation = 0.028 (2) Å]. Its mean plane makes dihedral angles of 33.92 (7) and 34.56 (6)° with the meth­oxy­phenyl ring and the nitro group, respectively. The cohesion of the crystal structure is ensured by C—H⋯N and C—H⋯O hydrogen bonds, forming layers almost parallel to the ac plane. PMID:26870561

  9. Crystal structure of 2-(4-meth-oxy-phen-yl)-6-nitro-imidazo[1,2-a]pyridine-3-carbaldehyde.

    PubMed

    Koudad, Mohamed; Elaatiaoui, Abdelmalik; Benchat, Noureddine; Saadi, Mohamed; El Ammari, Lahcen

    2015-12-01

    In the title compound, C15H11N3O4, the imidazo[1,2-a] pyridine ring system is almost planar [r.m.s. deviation = 0.028 (2) Å]. Its mean plane makes dihedral angles of 33.92 (7) and 34.56 (6)° with the meth-oxy-phenyl ring and the nitro group, respectively. The cohesion of the crystal structure is ensured by C-H⋯N and C-H⋯O hydrogen bonds, forming layers almost parallel to the ac plane.

  10. Volumetric Properties of the Mixture 2-Methoxyethanol C3H8O2 + C6H12O2 Butyl ethanoate (VMSD1412, LB4311_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture 2-Methoxyethanol C3H8O2 + C6H12O2 Butyl ethanoate (VMSD1412, LB4311_V)' providing data by calculation of isentropic compressibility from low-pressure density and thermodynamic speed of sound data at variable mole fraction and constant temperature, in the single-phase region(s).

  11. Volumetric Properties of the Mixture Methyl ethanoate C3H6O2 + C5H12O Pentan-1-ol (VMSD1511, LB4030_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Methyl ethanoate C3H6O2 + C5H12O Pentan-1-ol (VMSD1511, LB4030_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  12. Volumetric Properties of the Mixture 2-Methoxyethanol C3H8O2 + C6H12O2 Butyl ethanoate (VMSD1511, LB4134_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture 2-Methoxyethanol C3H8O2 + C6H12O2 Butyl ethanoate (VMSD1511, LB4134_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  13. Volumetric Properties of the Mixture 1,3-Dioxane C4H8O2 + C6H12 Cyclohexane (VMSD1511, LB5121_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture 1,3-Dioxane C4H8O2 + C6H12 Cyclohexane (VMSD1511, LB5121_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  14. Distribution of Al{sub 12}Fe{sub 3}Si and (FeAl{sub 6})Si in a HIPed Al-10.71 wt. % Si casting

    SciTech Connect

    Chama, C.C.

    1996-10-01

    An investigation on microstructural development in a hot isostatically pressed (HIPed) Al-10.71 wt. % Si casting is described. The as-cast material contained 0.006 total volume fraction of Al{sub 12}Fe{sub 3}Si and (FeAl{sub 6})Si particles but HIPing at 550 C and 68.95 MPa produced a moderate increase in this fraction, to a maximum value of 0.061 when HIPed for 120 min. Dislocations appeared to be the dominant nucleation sites for the particles in both the as-cast and the HIPed materials.

  15. Volumetric Properties of the Mixture Cyclohexanone C6H10O + C9H12 1,3,5-Trimethylbenzene (VMSD1511, LB4832_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume A 'Binary Liquid Systems of Nonelectrolytes I' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Cyclohexanone C6H10O + C9H12 1,3,5-Trimethylbenzene (VMSD1511, LB4832_V)' providing data from direct measurement of low-pressure thermodynamic speed of sound at variable mole fraction and constant temperature, in the single-phase region(s).

  16. Volumetric Properties of the Mixture Cyclohexanone C6H10O + C9H12 1,3,5-Trimethylbenzene (VMSD1212, LB4827_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume A 'Binary Liquid Systems of Nonelectrolytes I' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Cyclohexanone C6H10O + C9H12 1,3,5-Trimethylbenzene (VMSD1212, LB4827_V)' providing data by calculation of molar excess volume from low-pressure density measurements at variable mole fraction and constant temperature.

  17. Volumetric Properties of the Mixture Cyclohexanone C6H10O + C9H12 1,3,5-Trimethylbenzene (VMSD1111, LB4822_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume A 'Binary Liquid Systems of Nonelectrolytes I' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Cyclohexanone C6H10O + C9H12 1,3,5-Trimethylbenzene (VMSD1111, LB4822_V)' providing data from direct low-pressure measurement of mass density at variable mole fraction and constant temperature, in the single-phase region(s).

  18. Acute Dermal Toxicity Potential of (E)-1,2,3,4-Tetrahydro-6-Methyl-1-(2-Methyl-1-Oxo-2-Butenyl) Quinoline (CHR 5) in Rabbits.

    DTIC Science & Technology

    1983-06-01

    typical of bacterial infection and the liver lesions were compatible with those caused by Eimeria stiedae , a protozoan parasite that frequently infects...quinoline (CHR 5) IN RABBITS LAWRENCE MULLEN, BS, SP4 MARTHA A. HANES, DVM, CPT VC and PAUL MELLICK, DVM, PhD, LTC VC TOXICOLOGY GROUP, DIVISION OF...I = ඛ 08 22 058 4. Acute Dermal Toxicity Potential of (E)-1,2,3,4-Tetrahydro-6-Methyl- 1-(2-Methyl-l-Oxo-2-Butenyl) Quinoline (CHR5) in Rabbits

  19. Heat of Mixing and Solution of Cyclohexa-1,3-diene C6H8 + C12H22 Bicyclohexyl (HMSD1111, LB4033_H)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Heat of Mixing and Solution of Cyclohexa-1,3-diene C6H8 + C12H22 Bicyclohexyl (HMSD1111, LB4033_H)' providing data from direct low-pressure calorimetric measurement of molar excess enthalpy at variable mole fraction and constant temperature.

  20. Heat of Mixing and Solution of Cyclohexa-1,3-diene C6H8 + C12H16 Cyclohexylbenzene (HMSD1111, LB4039_H)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Heat of Mixing and Solution of Cyclohexa-1,3-diene C6H8 + C12H16 Cyclohexylbenzene (HMSD1111, LB4039_H)' providing data from direct low-pressure calorimetric measurement of molar excess enthalpy at variable mole fraction and constant temperature.

  1. Volumetric Properties of the Mixture Cyclohexa-1,3-diene C6H8 + C12H16 Cyclohexylbenzene (VMSD1211, LB3967_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Cyclohexa-1,3-diene C6H8 + C12H16 Cyclohexylbenzene (VMSD1211, LB3967_V)' providing data from direct low-pressure dilatometric measurement of molar excess volume at variable mole fraction and constant temperature.

  2. Volumetric Properties of the Mixture Cyclohexa-1,3-diene C6H8 + C12H22 Bicyclohexyl (VMSD1211, LB3961_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Cyclohexa-1,3-diene C6H8 + C12H22 Bicyclohexyl (VMSD1211, LB3961_V)' providing data from direct low-pressure dilatometric measurement of molar excess volume at variable mole fraction and constant temperature.

  3. Transfer between the cesium 6 {sup 2}P{sub 1/2} and 6 {sup 2}P{sub 3/2} levels induced by collisions with H{sub 2}, HD, D{sub 2}, CH{sub 4}, C{sub 2}H{sub 6}, CF{sub 4}, and C{sub 2}F{sub 6}

    SciTech Connect

    Pitz, Greg A.; Fox, Charles D.; Perram, Glen P.

    2011-09-15

    The cross sections of spin-orbit energy exchange between the cesium 6 {sup 2}P{sub 1/2}{r_reversible}6 {sup 2}P{sub 3/2} states induced by collisions with N{sub 2}, H{sub 2}, HD, D{sub 2}, CH{sub 4}, C{sub 2}H{sub 6}, CF{sub 4}, and C{sub 2}F{sub 6} were obtained for pressures less than 100 Torr at room temperature by means of steady-state laser-induced fluorescence techniques. The spin-orbit energy exchange rate with N{sub 2}, H{sub 2}, HD, D{sub 2}, CH{sub 4}, C{sub 2}H{sub 6}, CF{sub 4}, and C{sub 2}F{sub 6}, have been measured as {sigma}{sub 21}(6 {sup 2}P{sub 3/2}{yields}6 {sup 2}P{sub 1/2})= 16.3, 34.1, 30.0, 22.7, 21.4, 65.6, 64.8, and 137 A{sup 2} and {sigma}{sub 12}(6 {sup 2}P{sub 1/2}{yields}6 {sup 2}P{sub 3/2})= 1.8, 4.4, 4.1, 3.0, 2.9, 13.3, 9.7, and 16.3 A{sup 2}, respectively. Correlations of the spin-orbit transfer probabilities with rotational-energy defect and vibrational-energy defect have been shown.

  4. Determination of the intersublattice exchange interactions in GdCo12-xFexB6 (x = 0-3) intermetallic compounds by high field magnetization measurements

    NASA Astrophysics Data System (ADS)

    Diop, L. V. B.; Isnard, O.; Skourski, Y.; Ballon, G.

    2013-05-01

    High field magnetization measurements up to 60 T on free powder samples from GdCo12-xFexB6 (x = 0-3) compounds are reported. The data were used to evaluate the microscopic exchange interaction integral, JGd-3d, between Gd and 3d (Co,Fe) spins. The systems are ferrimagnets; they order magnetically between TC = 95 K for x = 3 and TC = 165 K for x = 0. The low temperature magnetization curves as well as the temperature dependence of intrinsic magnetic parameters are determined by magnetic measurements in pulsed magnetic field. The average magnetic moment ⟨μCo+Fe⟩ per mean transition metal atom (Co + Fe) is small and increases with increasing Fe concentration from 0.44 μΒ for x = 0 to 0.51 μΒ for x = 3 at T = 4 K. From high field magnetization curves, a value of JGd-3d/kB = -4.65 K is derived for x = 0, whereas mean field approximation yields a much larger 3d-3d exchange integral of JCo-Co/kB = 105 K. The obtained results reveal an increase of -JGd-3d/kB with Fe concentration. For x = 0.5, the intersublattice coefficient nGd-3d is found to keep an almost constant value of 5.87 ± 0.13 T*f.u.*μB-1 whatever the temperature in the 2 to 60 K range.

  5. Diethyl 2,6,11-trioxo-2,3-dihydro-1H-anthra[1,2-d]imidazole-1,3-diacetate

    PubMed Central

    Afrakssou, Zahra; Haoudi, Amal; Capet, Frédéric; Rolando, Christian; El Ammari, Lahcen

    2011-01-01

    The title compound, C23H20N2O7, consists of three fused six-membered rings (A, B and C) and one five-membered ring (D), linked to two ethyl acetate groups. The four fused rings are slightly folded around the O=C⋯C=O direction of the anthraquinone system, with a dihedral angle of 3.07 (8)° between the fused five- and six-membered rings (C and D) and the terminal ring (A). The planes through the atoms forming each acetate group are nearly perpendicular to the mean plane of the anthra[1,2-d]imidazole system, as indicated by the dihedral angles between them of 79.94 (9) and 85.90 (9)°. The crystal packing displays non-classical C—H⋯O hydrogen bonds. PMID:22091102

  6. 12 CFR 517.6 - Certification.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Certification. 517.6 Section 517.6 Banks and... Certification. In order to qualify as an Outreach Program participant, each business or contractor must either... Program Advocate a completed and signed ABELS Registration/Certification Form, as prescribed by the...

  7. 12 CFR 203.6 - Enforcement.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Enforcement. 203.6 Section 203.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM HOME MORTGAGE DISCLOSURE... imposition of civil money penalties, where applicable. Compliance is enforced by the agencies listed...

  8. 12 CFR 203.6 - Enforcement.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 2 2011-01-01 2011-01-01 false Enforcement. 203.6 Section 203.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM HOME MORTGAGE DISCLOSURE... imposition of civil money penalties, where applicable. Compliance is enforced by the agencies listed...

  9. 12 CFR 1780.6 - Public hearings.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Public hearings. 1780.6 Section 1780.6 Banks... hearings. (a) General rule. All hearings shall be open to the public, unless the Director, in his discretion, determines that holding an open hearing would be contrary to the public interest. The...

  10. 12 CFR 32.6 - Nonconforming loans.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Nonconforming loans. 32.6 Section 32.6 Banks... Nonconforming loans. (a) A loan, within a bank's legal lending limit when made, will not be deemed a violation but will be treated as nonconforming if the loan is no longer in conformity with the bank's...

  11. 12 CFR 359.6 - Filing instructions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 4 2011-01-01 2011-01-01 false Filing instructions. 359.6 Section 359.6 Banks and Banking FEDERAL DEPOSIT INSURANCE CORPORATION REGULATIONS AND STATEMENTS OF GENERAL POLICY GOLDEN... nondiscriminatory severance plan payments pursuant to § 359.1(f)(2)(v) and golden parachute payments permitted...

  12. 12 CFR 359.6 - Filing instructions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Filing instructions. 359.6 Section 359.6 Banks and Banking FEDERAL DEPOSIT INSURANCE CORPORATION REGULATIONS AND STATEMENTS OF GENERAL POLICY GOLDEN... nondiscriminatory severance plan payments pursuant to § 359.1(f)(2)(v) and golden parachute payments permitted...

  13. Quasi-two-dimensional S =1/2 magnetism of Cu[ C6H2 (COO)4][ C2H5NH3 ] 2

    NASA Astrophysics Data System (ADS)

    Nath, R.; Padmanabhan, M.; Baby, S.; Thirumurugan, A.; Ehlers, D.; Hemmida, M.; Krug von Nidda, H.-A.; Tsirlin, A. A.

    2015-02-01

    We report structural and magnetic properties of the spin-1/2 quantum antiferromagnet Cu[ C6H2(COO) 4 ][ C2H5NH3 ] 2 by means of single-crystal x-ray diffraction, magnetization, heat capacity, and electron-spin-resonance (ESR) measurements on polycrystalline samples, as well as band-structure calculations. The triclinic crystal structure of this compound features CuO4 plaquette units connected into a two-dimensional framework through anions of the pyromellitic acid [ C6H2(COO) 4 ]4 -. The ethylamine cations [ C2H5NH3]+ are located between the layers and act as spacers. Magnetic susceptibility and heat capacity measurements establish a quasi-two-dimensional, weakly anisotropic, and nonfrustrated spin-1/2 square lattice with the ratio of the couplings Ja/Jc≃0.7 along the a and c directions, respectively. No clear signatures of the long-range magnetic order are seen in thermodynamic measurements down to 1.8 K. However, the gradual broadening of the ESR line suggests that magnetic ordering occurs at lower temperatures. Leading magnetic couplings are mediated by the organic anion of the pyromellitic acid and exhibit a nontrivial dependence on the Cu-Cu distance, with the stronger coupling between those Cu atoms that are farther apart.

  14. Precision lifetime measurements of Cs 6p 2P1/2 and 6p 2P3/2 levels by single-photon counting

    NASA Astrophysics Data System (ADS)

    Young, L.; Hill, W. T.; Sibener, S. J.; Price, Stephen D.; Tanner, C. E.; Wieman, C. E.; Leone, Stephen R.

    Time-correlated single-photon counting is used to measure the lifetimes of the 6p 2P1/2 and 6p 2P3/2 levels in atomic Cs with accuracies ≈ 0.2-0.3 %. A high-repetition-rate, femtosecond, self-mode-locked Ti:sapphire laser is used to excite Cs produced in a well-collimated atomic beam. The time interval between the excitation pulse and the arrival of a fluorescence photon is measured repetitively until the desired statistics are obtained. The lifetime results are 34.75(7) and 30.41(10) ns for the 6p 2P1/2 and 6p2P3/2 levels, respectively. These lifetimes fall between those extracted from ab initio many-body perturbation-theory calculations by Blundell, Johnson, and Sapirstein [Phys. Rev. A 43, 3407 (1991)] and V. A. Dzuba et al. [Phys. Lett. A 142, 373 (1989)] and are in all cases within 0.9% of the calculated values. The measurement errors are dominated by systematic effects, and methods to alleviate these and to approach an accuracy of 0.1% are discussed. The technique is a viable alternative to the fast-beam laser approach for measuring lifetimes with extreme accuracy.

  15. 7 CFR 12.6 - Administration.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12... converted wetland by a landlord's tenant or sharecropper is required under the terms and conditions of the... wetland was commenced before December 23, 1985, for the purposes of § 12.5(b)(3); (vii) Whether...

  16. 7 CFR 12.6 - Administration.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12... converted wetland by a landlord's tenant or sharecropper is required under the terms and conditions of the... wetland was commenced before December 23, 1985, for the purposes of § 12.5(b)(3); (vii) Whether...

  17. 7 CFR 12.6 - Administration.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12... converted wetland by a landlord's tenant or sharecropper is required under the terms and conditions of the... wetland was commenced before December 23, 1985, for the purposes of § 12.5(b)(3); (vii) Whether...

  18. 7 CFR 12.6 - Administration.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12... converted wetland by a landlord's tenant or sharecropper is required under the terms and conditions of the... wetland was commenced before December 23, 1985, for the purposes of § 12.5(b)(3); (vii) Whether...

  19. 7 CFR 12.6 - Administration.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12... converted wetland by a landlord's tenant or sharecropper is required under the terms and conditions of the... wetland was commenced before December 23, 1985, for the purposes of § 12.5(b)(3); (vii) Whether...

  20. 12 CFR 265.6 - Functions delegated to General Counsel.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... incomplete under that Act or Regulation Y (12 CFR part 225) or contains material information that is... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Functions delegated to General Counsel. 265.6... Rules of Procedure (12 CFR part 262), in connection with any application or notice filed with the...

  1. Effects of donor-acceptor groups on the structural and electronic properties of 4-(methoxymethyl)-6-methyl-5-nitro-2-oxo-1,2-dihydropyridine-3-carbonitrile

    NASA Astrophysics Data System (ADS)

    Gümüş, Hacer Pir; Tamer, Ömer; Avcı, Davut; Atalay, Yusuf

    2014-11-01

    Quantum chemical calculations on the geometric parameters, harmonic vibrational wavenumbers and 1H and 13C nuclear magnetic resonance (NMR) chemical shifts values of 4-(methoxymethyl)-6-methyl-5-nitro-2-oxo-1,2-dihydropyridine-3-carbonitrile [C9H9N3O4] molecule in ground state were performed using the ab initio HF and density functional theory (DFT/B3LYP) methods with 6-311++G(d,p) basis set. The results of optimized molecular structure were presented and compared with X-ray diffraction results. The theoretical vibrational frequencies and 1H and 13C NMR chemical shifts values were compared with experimental values of the investigated molecule. The observed and calculated values were found to be in good agreement. Since the title compound contains different electron-donor and -acceptor groups as well as lone pair electrons, and multiple bonds, the effects of these groups on the structural and electronic properties are found out. In addition, conformational, natural bond orbital (NBO), nonlinear optical (NLO) analysis, frontier molecular orbital energies, molecular surfaces, Mulliken charges and atomic polar tensor based charges were investigated using HF and DFT methods.

  2. Synthesis, Structure Analysis, and Characterization of a New Thiostannate, (C(12)H(25)NH(3))(4)[Sn(2)S(6)].2H(2)O.

    PubMed

    Li, Jianquan; Marler, Bernd; Kessler, Henri; Soulard, Michel; Kallus, Stefan

    1997-10-08

    A new thiostannate, (C(12)H(25)NH(3))(4)[Sn(2)S(6)].2H(2)O, was synthesized from SnCl(4), Na(2)S, and dodecylamine (DDA) in the ethanol-water two-solvent system at room temperature. First a suspension was obtained. With increasing crystallization time, single crystals up to several millimeters in size were found at the bottom of the vessel. The compound was characterized by single-crystal X-ray diffraction, solid state (119)Sn CPMAS NMR and (13)C CPMAS NMR, IR absorption spectroscopy, and thermal analysis. The crystal data are a = 7.533(2) Å, b = 10.162(2) Å, c = 21.688(4) Å, alpha = 101.22(3) degrees, beta = 90.76(3) degrees, gamma = 101.82(3) degrees, triclinic, space group = P&onemacr;, and Z = 1. The structure consists of one [Sn(2)S(6)](4)(-) anion, four n-dodecylammonium cations, and two water molecules per unit cell. The [Sn(2)S(6)](4)(-) dimers are formed by two edge-sharing [SnS(4)] tetrahedra. The hydrocarbon chains of the cations are straight with the chain direction running parallel to [001]. The chains are in van der Waals contact to each other with the nitrogen atoms pointing in opposite directions for neighboring chains. The positions of all hydrogen atoms were determined; in particular three positions were found which may suggest that the nitrogen atoms are protonated to form cationic groups. The nonorganic constituents of the structure, i.e., anions, water molecules, and ammonium groups, interact to form an infinite layer-like unit parallel to (001).

  3. Theoretical investigations of a high density cage compound 10-(1-nitro-1, 2, 3, 4-tetraazol-5-yl)) methyl-2, 4, 6, 8, 12-hexanitrohexaazaisowurtzitane.

    PubMed

    Zhang, Jian-ying; Du, Hong-chen; Wang, Fang; Gong, Xue-dong; Huang, Yin-sheng

    2012-01-01

    A new polynitro cage compound with the framework of HNIW and a tetrazole unit, i.e., 10-(1-nitro-1, 2, 3, 4-tetraazol-5-yl)) methyl-2, 4, 6, 8, 12-hexanitrohexaazaisowurtzitane (NTz-HNIW) has been proposed and studied by density functional theory (DFT) and molecular mechanics methods. Properties such as IR spectrum, heat of formation, thermodynamic properties, and crystal structure were predicted. The compound belongs to the Pbca space group, with the lattice parameters a = 15.07 Å, b = 12.56 Å, c = 18.34 Å, Z = 8, and ρ = 1.990 g·cm(-3). The stability of the compound was evaluated by the bond dissociation energies and results showed that the first step of pyrolysis is the rupture of the N-NO(2) bond in the side chain. The detonation properties were estimated by the Kamlet-Jacobs equations based on the calculated crystal density and heat of formation, and the results were 9.240 km·s(-1) for detonation velocity and 40.136 GPa for detonation pressure. The designed compound has high thermal stability and good detonation properties and is probably a promising high energy density compound (HEDC).

  4. Synthesis and antiproliferative mechanism of action of pyrrolo[3',2':6,7] cyclohepta[1,2-d]pyrimidin-2-amines as singlet oxygen photosensitizers.

    PubMed

    Spanò, Virginia; Frasson, Ilaria; Giallombardo, Daniele; Doria, Filippo; Parrino, Barbara; Carbone, Anna; Montalbano, Alessandra; Nadai, Matteo; Diana, Patrizia; Cirrincione, Girolamo; Freccero, Mauro; Richter, Sara N; Barraja, Paola

    2016-11-10

    A new series of pyrrolo[3',2':6,7]cyclohepta[1,2-d]pyrimidin-2-amines, was conveniently prepared using a versatile and high yielding multistep sequence. A good number of derivatives was obtained and the cellular photocytotoxicity was evaluated in vitro against three different human tumor cell lines with EC50 (0.08-4.96 μM) values reaching the nanomolar level. Selected compounds were investigated by laser flash photolysis. The most photocytotoxic derivative, exhibiting a fairly long-lived triplet state (τ ∼ 7 μs) and absorbance in the UV-Vis, was tested in the photo-oxidations of 9,10-anthracenedipropionic acid (ADPA) by singlet oxygen. The photosentizing properties are responsible for the compounds' ability to photoinduce massive cell death with involvement of mitochondria.

  5. AC conductivity and dielectric relaxation of tris(N,N-dimethylanilinium) hexabromidostannate(IV) bromide: (C8H12N)3SnBr6.Br

    NASA Astrophysics Data System (ADS)

    Chouaib, H.; Kamoun, S.

    2015-10-01

    The X-ray powder analysis, thermogravimetric analysis, differential scanning calorimetry analysis and complex impedance spectroscopic data have been carried out on (C8H12N)3SnBr6.Br compound. The results show that this compound exhibits a phase transition at (T=365±2 K) which has been characterized by differential scanning calorimetry (DSC), AC conductivity and dielectric measurements. The AC conductivity, the modulus analysis, the dielectric constants and the polarizability have been studied using impedance in the temperature range from 334 K to 383 K and in the frequency range between 20 Hz and 2 MHz. The temperature dependence of DC conductivity follows the Arrhenius law. Moreover, the frequency dependence of conductivity follows Jonscher's dynamical law with the relation: σ(ω , T) =σDC + B(T)ω s(T) . Relaxation peaks can be observed in the complex modulus analysis and after a transformation of the complex permittivity ε* to the complex polarizability α*.

  6. Twenty-six-week oral carcinogenicity study of 3-monochloropropane-1,2-diol in CB6F1-rasH2 transgenic mice.

    PubMed

    Lee, Byoung-Seok; Park, Sang-Jin; Kim, Yong-Bum; Han, Ji-Seok; Jeong, Eun Ju; Son, Hwa-Young; Moon, Kyoung-Sik

    2017-01-01

    The carcinogenic potential of 3-monochloro-1,2-propanediol (3-MCPD) was evaluated in a short-term carcinogenicity testing study using CB6F1 rasH2-Tg (rasH2-Tg) mice. 3-MCPD is found in many foods and food ingredients as a result of storage or processing and is regarded as a carcinogen since it is known to induce Leydig cell and kidney tumors in rats. Male and female rasH2-Tg mice were administered 3-MCPD once daily by oral gavage at doses of 0, 10, 20, and 40 mg/kg body weight (bw) per day for 26 weeks. As a positive control, N-methyl-N-nitrosourea (MNU) was administered as a single intraperitoneal injection (75 mg/kg). In 3-MCPD-treated mice, there was no increase in the incidence of neoplastic lesions compared to the incidence in vehicle control mice. However, 3-MCPD treatment resulted in an increased incidence of tubular basophilia in the kidneys and germ cell degeneration in the testes, with degenerative germ cell debris in the epididymides of males at 20 and 40 mg/kg bw per day. In 3-MCPD-treated females, vacuolation of the brain and spinal cord was observed at 40 mg/kg bw per day; however, only one incidence of vacuolation was observed in males. Forestomach and cutaneous papilloma and/or carcinoma and lymphoma were observed in most rasH2 mice receiving MNU treatment. We concluded that 3-MCPD did not show carcinogenic potential in the present study using rasH2-Tg mice. The findings of this study suggest that the carcinogenic potential of 3-MCPD is species specific.

  7. Davinciite, Na12K3Ca6Fe{3/2+}Zr3(Si26O73OH)Cl2, a New K,Na-Ordered mineral of the eudialyte group from the Khibiny Alkaline Pluton, Kola Peninsula, Russia

    NASA Astrophysics Data System (ADS)

    Khomyakov, A. P.; Nechelyustov, G. N.; Rastsvetaeva, R. K.; Rozenberg, K. A.

    2013-12-01

    This paper presents a description of a new zirconosilicate of the eudialyte group, which was named davinciite in honor of Leonardo da Vinci (1452-1519), a famous Italian scientist, painter, sculptor and architect. The new mineral has been found in hyperagpaitic pegmatite at the Rasvumchorr Mountain, Khibiny Pluton, Kola Peninsula, as relict inclusions, up to 1-2 mm in size in a rastsvetaevite matrix. It is associated with nepheline, sodalite, potassium feldspar, delhayelite, aegirine, shcherbakovite, villiaumite, nitrite, nacaphite, rasvumite, and djerfisherite. Davinciite is dark lavender and transparent, with a vitreous luster and white streak. The new mineral is brittle, with conchoidal fracture; the Mohs' hardness is 5. No indications of cleavage or parting were observed. The measured density is 2.82(2) g/cm3 (volumetric method); the calculated density is 2.848 g/cm3. Davinciite is optically uniaxial, positive; ω = 1.603(2), ɛ = 1.605(2). It is nonpleochroic and nonfluorescent in UV light. The new mineral slowly breaks down and gelates in 50% HCl and HNO3. It is trigonal, space group R3m. The unit-cell dimensions are a = 14.2956(2), c = 30.0228(5) Å, V=5313.6(2) Å3. The strongest reflections in the X-ray powder diffraction pattern [ d, Å ( I, %) ( hkl)] are as follows: 2.981(100)(315), 2.860(96)(404), 4.309(66)(205), 3.207(63)(208), 6.415(54)(104), 3.162(43)(217). The chemical composition (electron microprobe, H2O calculated from X-ray diffraction data) is as follows, wt %: 12.69 Na2O, 3.53 K2O, 11.02 CaO, 0.98 SrO, 0.15 BaO, 5.33 FeO, 0.37 MnO, 0.07 Al2O3, 51.20 SiO2, 0.39 TiO2, 11.33 ZrO2, 0.21HfO2, 0.09 Nb2O5, 1.89 Cl, 0.93H2O, -O = Cl2 0.43; total is 99.75. The empirical formula calculated on the basis of Si + Al + Zr + Hf + Ti + Nb = 29 ( Z = 3) is (Na1l.75Sr0.29Ba0.03)Σ12.07(K2.28Na0.72)Σ3Ca5.99(Fe2.26Mn0.16)Σ2.42(Zr2.80Ti0.15Hf0.03Nb0.02) Σ3(Si1.96Al0.04)Σ2[Si3O9]2 [Si9O27]2[(OH)1.42O0.58]Σ2[Cl1.62(H2O)0.38]Σ2 · 0.48H2O. The simplified

  8. 12 CFR 26.6 - General exemption.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... serves low-and moderate-income areas; (2) Is controlled or managed by persons who are members of a...; or (4) Is deemed to be in “troubled condition” as defined in 12 CFR 5.51(c)(6). (c) Duration....

  9. New single-molecule magnet based on Mn12 oxocarboxylate clusters with mixed carboxylate ligands, [Mn12O12(CN-o-C6H4CO2)12(CH3CO2)4(H2O)4]·8CH2Cl2: Synthesis, crystal and electronic structure, magnetic properties.

    PubMed

    Kushch, L A; Sasnovskaya, V D; Dmitriev, A I; Yagubskii, E B; Koplak, O V; Zorina, L V; Boukhvalov, D W

    2012-11-28

    A new high symmetry Mn(12) oxocarboxylate cluster [Mn(12)O(12)(CN-o-C(6)H(4)CO(2))(12)(CH(3)CO(2))(4)(H(2)O)(4)]·8CH(2)Cl(2) (1) with mixed carboxylate ligands is reported. It was synthesized by the standard carboxylate substitution method. 1 crystallizes in the tetragonal space group I4(1)/a. Complex 1 contains a [Mn(12)O(12)] core with eight CN-o-C(6)H(4)CO(2) ligands in the axial positions, four CH(3)CO(2) and four CN-o-C(6)H(4)CO(2) in equatorial positions. Four H(2)O molecules are bonded to four Mn atoms in an alternating up, down, up, down arrangement indicating a 1 : 1 : 1 : 1 isomer. The Mn(12) molecules in 1 are self-assembled by complementary hydrogen C-H···N bonds formed with participation of the axial o-cyanobenzoate ligands of the adjacent Mn(12) clusters. The lattice solvent molecules (CH(2)Cl(2)) are weakly interacted with Mn(12) units that results in solvent loss immediately after removal of the crystals from the mother liquor. The electronic structure and the intramolecular exchange parameters have been calculated. Mn 3d bands of 1 are rather broad, and the center of gravity of the bands shifts down from the Fermi level. The overlap between Mn 3d bands and 2p ones of the oxygen atoms from the carboxylate bridges is higher than in the parent Mn(12)-acetate cluster. These changes in the electronic structure provide a significant difference in the exchange interactions in comparison to Mn(12)-acetate. The magnetic properties have been studied on a dried (solvent-free) polycrystalline sample of 1. The dc magnetic susceptibility measurements in the 2-300 K temperature range support a high-spin ground state (S = 10). A bifurcation of temperature dependencies of magnetization taken under zero field cooled and field cooled conditions observed below 4.5 K is due to slow magnetization relaxation. Magnetization versus applied dc field exhibited a stepwise hysteresis loop at 2 K. The ac magnetic susceptibility data revealed the frequency dependent out

  10. Docosahexaenoic Acid Status in Pregnancy Determines the Maternal Docosahexaenoic Acid Status 3-, 6- and 12 Months Postpartum. Results from a Longitudinal Observational Study

    PubMed Central

    Markhus, Maria Wik; Rasinger, Josef Daniel; Malde, Marian Kjellevold; Frøyland, Livar; Skotheim, Siv; Braarud, Hanne Cecilie; Stormark, Kjell Morten; Graff, Ingvild Eide

    2015-01-01

    Background Essential fatty acid status as well as docosahexaenoic acid (DHA, 22:6n-3) declines during pregnancy and lactation. As a result, the DHA status may not be optimal for child development and may increase the risk for maternal postpartum depression. The objective of this study was to assess changes in the maternal fatty acid status from pregnancy to 12 months postpartum, and to study the impact of seafood consumption on the individual fatty acid status. Methods Blood samples and seafood consumption habits (gestation week 28, and three-, six- and 12 months postpartum) were collected in a longitudinal observational study of pregnant and postpartum women (n = 118). Multilevel linear modeling was used to assess both changes over time in the fatty acid status of red blood cells (RBC), and in the seafood consumption. Results Six fatty acids varied the most (>80%) across the four time points analyzed, including the derivative of the essential α-linoleic acid (ALA, 18:3n-3), DHA; the essential linoleic acid (LA, 18:2 n-6); and the LA derivative, arachidonic acid (AA, 20:4n-6). Over all, a large variation in individuals’ DHA- and AA status was observed; however, over the 15-month study period only small inter-individual differences in the longitudinal trajectory of DHA- and AA abundance in the RBC were detected. The median intake of seafood was lower than recommended. Regardless, the total weekly frequency of seafood and eicosapentaenoic acid (EPA, 20:5n-3)/DHA-supplement intake predicted the maternal level of DHA (μg/g RBC). Conclusion The period of depletion of the maternal DHA status during pregnancy and lactation, seem to turn to repletion from about six months postpartum towards one year after childbirth, irrespective of RBC concentration of DHA during pregnancy. Seafood and EPA/DHA-supplement intake predicted the DHA levels over time. Trial Registration www.helseforskning.etikkom.no 2009/570/REC, project number: 083.09 PMID:26331947

  11. The Amidohydrolases IAR3 and ILL6 Contribute to Jasmonoyl-Isoleucine Hormone Turnover and Generate 12-Hydroxyjasmonic Acid Upon Wounding in Arabidopsis Leaves*

    PubMed Central

    Widemann, Emilie; Miesch, Laurence; Lugan, Raphaël; Holder, Emilie; Heinrich, Clément; Aubert, Yann; Miesch, Michel; Pinot, Franck; Heitz, Thierry

    2013-01-01

    Jasmonates (JAs) are a class of signaling compounds that mediate complex developmental and adaptative responses in plants. JAs derive from jasmonic acid (JA) through various enzymatic modifications, including conjugation to amino acids or oxidation, yielding an array of derivatives. The main hormonal signal, jasmonoyl-l-isoleucine (JA-Ile), has been found recently to undergo catabolic inactivation by cytochrome P450-mediated oxidation. We characterize here two amidohydrolases, IAR3 and ILL6, that define a second pathway for JA-Ile turnover during the wound response in Arabidopsis leaves. Biochemical and genetic evidence indicates that these two enzymes cleave the JA-Ile signal, but act also on the 12OH-JA-Ile conjugate. We also show that unexpectedly, the abundant accumulation of tuberonic acid (12OH-JA) after wounding originates partly through a sequential pathway involving (i) conjugation of JA to Ile, (ii) oxidation of the JA-Ile conjugate, and (iii) cleavage under the action of the amidohydrolases. The coordinated actions of oxidative and hydrolytic branches in the jasmonate pathway highlight novel mechanisms of JA-Ile hormone turnover and redefine the dynamic metabolic grid of jasmonate conversion in the wound response. PMID:24052260

  12. Structural Basis for Substrate Specificity in Phosphate Binding (beta/alpha)8-Barrels: D-Allulose 6-Phosphate 3-Epimerase from Escherichia coli K-12

    SciTech Connect

    Chan,K.; Fedorov, A.; Almo, S.; Gerlt, J.

    2008-01-01

    Enzymes that share the ({beta}/{alpha})8-barrel fold catalyze a diverse range of reactions. Many utilize phosphorylated substrates and share a conserved C-terminal ({beta}/a)2-quarter barrel subdomain that provides a binding motif for the dianionic phosphate group. We recently reported functional and structural studies of d-ribulose 5-phosphate 3-epimerase (RPE) from Streptococcus pyogenes that catalyzes the equilibration of the pentulose 5-phosphates d-ribulose 5-phosphate and d-xylulose 5-phosphate in the pentose phosphate pathway [J. Akana, A. A. Fedorov, E. Fedorov, W. R. P. Novack, P. C. Babbitt, S. C. Almo, and J. A. Gerlt (2006) Biochemistry 45, 2493-2503]. We now report functional and structural studies of d-allulose 6-phosphate 3-epimerase (ALSE) from Escherichia coli K-12 that catalyzes the equilibration of the hexulose 6-phosphates d-allulose 6-phosphate and d-fructose 6-phosphate in a catabolic pathway for d-allose. ALSE and RPE prefer their physiological substrates but are promiscuous for each other's substrate. The active sites (RPE complexed with d-xylitol 5-phosphate and ALSE complexed with d-glucitol 6-phosphate) are superimposable (as expected from their 39% sequence identity), with the exception of the phosphate binding motif. The loop following the eighth {beta}-strand in ALSE is one residue longer than the homologous loop in RPE, so the binding site for the hexulose 6-phosphate substrate/product in ALSE is elongated relative to that for the pentulose 5-phosphate substrate/product in RPE. We constructed three single-residue deletion mutants of the loop in ALSE, ?T196, ?S197 and ?G198, to investigate the structural bases for the differing substrate specificities; for each, the promiscuity is altered so that d-ribulose 5-phosphate is the preferred substrate. The changes in kcat/Km are dominated by changes in kcat, suggesting that substrate discrimination results from differential transition state stabilization. In both ALSE and RPE, the phosphate

  13. Coordination chemistry of verdazyl radicals: group 12 metal (Zn, Cd, Hg) complexes of 1,4,5,6-tetrahydro-2,4-dimethyl-6-(2 pyridiyl)-1,2,4,5-tetrazin -3(2H)-one (pvdH3) and 1,5-dimethyl-3-(2 pyridil)-6-oxoverdazyl (pvd).

    PubMed

    Brook, D J; Fornell, S; Stevens, J E; Noll, B; Koch, T H; Eisfeld, W

    2000-02-07

    Ferricyanide oxidation of 1,4,5,6-tetrahydro-2,4-dimethyl-6-(2'-pyridyl)-1,2,4,5-tetrazin-3(2H)-one (pvdH3) produces the stable chelating free radical 1,5-dimethyl-3-(2'-pyridyl)-6-oxoverdazyl (pvd) as an orange solid. Combination of group 12 metal halides with the ligand pvdH3 in acetonitrile results in precipitation of metal complexes. The mercuric chloride complex crystallizes in the monoclinic space group P2(1/c) with unit cell dimensions a = 8.5768(8) A, b = 19.1718(17) A, c = 8.5956(8) A, beta = 90.405 degrees, and V = 1413.4(2) A3. The mercuric ion is tricoordinate with a distorted trigonal planar geometry. Cadmium iodide and zinc chloride induce ring opening of the tetrazine resulting in pentacoordinate complexes of a hydrazone ligand. The cadmium iodide complex crystallizes in the triclinic space group P1 with cell dimensions a = 7.7184(8) A, b = 8.0240(9) A, c = 13.348(2) A, alpha = 97.876(4) degrees, beta = 95.594(6) degrees, gamma = 107.304(6) degrees, and V = 773.40(21) A3. Oxidation of all three metal complexes produces verdazyl radicals. Metal coordination is indicated by small changes in the EPR spectrum and by changes in the UV-visible spectrum, in particular the changes in the position of bands in the visible region. The metal halide-pvd complexes can also be synthesized by direct combination of metal halides with the free radical.

  14. Rate coefficients for the reaction of O(1D) with the atmospherically long-lived greenhouse gases NF3, SF3CF3, CHF3, C2F6, c-C3F8, n-C5F12, and n-C6F14

    NASA Astrophysics Data System (ADS)

    Baasandorj, M.; Hall, B. D.; Burkholder, J. B.

    2012-09-01

    The contribution of atmospherically persistent (long-lived) greenhouse gases to the radiative forcing of Earth has increased over the past several decades. The impact of highly fluorinated saturated compounds, in particular perfluorinated compounds, on climate change is a concern because of their long atmospheric lifetimes, which are primarily determined by stratospheric loss processes, as well as their strong absorption in the infrared "window" region. A potentially key stratospheric loss process for these compounds is their gas-phase reaction with electronically excited oxygen atoms, O(1D). Therefore, accurate reaction rate coefficient data is desired for input to climate change models. In this work, rate coefficients, k, were measured for the reaction of O(1D) with several key long-lived greenhouse gases, namely NF3, SF5CF3, CHF3 (HFC-23), C2F6, c-C4F8, n-C5F12, and n-C6F14. Room temperature rate coefficients for the total reaction, kTot, corresponding to loss of O(1D), and reactive channel, kR, corresponding to the loss of the reactant compound, were measured for NF3 and SF5CF3 using competitive reaction and relative rate methods, respectively. kR was measured for the CHF3 reaction and improved upper-limits were determined for the perfluorinated compounds included in this study. For NF3, kTot was determined to be (2.55 ± 0.38) × 10-11 cm3 molecule-1 s-1 and kR, which was measured using CF3Cl, N2O, CF2ClCF2Cl (CFC-114), and CF3CFCl2 (CFC-114a) as reference compounds, was determined to be (2.21 ± 0.33) × 10-11 cm3 molecule-1 s-1 corresponding to a reactive branching ratio of 0.87 ± 0.13. For SF5CF3, kTot = (3.24 ± 0.50) × 10-13 cm3 molecule-1 s-1 and kR < 5.8 × 10-14 cm3 molecule-1 s-1 were measured, where kR is a factor of three lower than the current recommendation of kTot for use in atmospheric modeling. For CHF3, kR was determined to be (2.35 ± 0.35) × 10-12 cm3 molecule-1 s-1, which corresponds to a reactive channel yield of 0.26 ± 0.04, and

  15. 12. Historic American Buildings Survey, Stanley Jones, Photographer July 6, ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    12. Historic American Buildings Survey, Stanley Jones, Photographer July 6, 1936, copied from portrait, PORTRAIT OF WILLIAM HENRY 3RD, OWNER OF HENRY GUN FACTORY. - Henry Gun Factory, Belfast, Northampton County, PA

  16. 12 CFR 230.6 - Periodic statement disclosures.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Periodic statement disclosures. 230.6 Section 230.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM TRUTH IN SAVINGS (REGULATION DD) § 230.6 Periodic statement disclosures. (a) General rule. If...

  17. 12 CFR 220.6 - Good faith account.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 3 2013-01-01 2013-01-01 false Good faith account. 220.6 Section 220.6 Banks... (CONTINUED) CREDIT BY BROKERS AND DEALERS (REGULATION T) § 220.6 Good faith account. In a good faith account...: (a) Securities entitled to good faith margin—(1) Permissible transactions. A creditor may effect...

  18. 12 CFR 220.6 - Good faith account.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Good faith account. 220.6 Section 220.6 Banks... BY BROKERS AND DEALERS (REGULATION T) § 220.6 Good faith account. In a good faith account, a creditor...) Securities entitled to good faith margin—(1) Permissible transactions. A creditor may effect and...

  19. 12 CFR 220.6 - Good faith account.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 3 2014-01-01 2014-01-01 false Good faith account. 220.6 Section 220.6 Banks... (CONTINUED) CREDIT BY BROKERS AND DEALERS (REGULATION T) § 220.6 Good faith account. In a good faith account...: (a) Securities entitled to good faith margin—(1) Permissible transactions. A creditor may effect...

  20. 12 CFR 220.6 - Good faith account.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 3 2012-01-01 2012-01-01 false Good faith account. 220.6 Section 220.6 Banks... BY BROKERS AND DEALERS (REGULATION T) § 220.6 Good faith account. In a good faith account, a creditor...) Securities entitled to good faith margin—(1) Permissible transactions. A creditor may effect and...

  1. 12 CFR 230.6 - Periodic statement disclosures.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Periodic statement disclosures. 230.6 Section 230.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM TRUTH IN SAVINGS (REGULATION DD) § 230.6 Periodic statement disclosures. (a) General rule. If...

  2. Adipic acid-2,4-diamino-6-(4-meth-oxy-phen-yl)-1,3,5-triazine (1/2).

    PubMed

    Thanigaimani, Kaliyaperumal; Razak, Ibrahim Abdul; Arshad, Suhana; Jagatheesan, Rathinavel; Santhanaraj, Kulandaisamy Joseph

    2012-10-01

    The asymmetric unit of the title compound, 2C(10)H(11)N(5)O·C(6)H(10)O(4), consists of a 2,4-diamino-6-(4-meth-oxy-phen-yl)-1,3,5-triazine mol-ecule and one-half mol-ecule of adipic acid which lies about an inversion center. The triazine ring makes a dihedral angle of 12.89 (4)° with the adjacent benzene ring. In the crystal, the components are linked by N-H⋯O and O-H⋯N hydrogen bonds, thus generating a centrosymmetric 2 + 1 unit of triazine and adipic acid mol-ecules with R(2) (2)(8) motifs. The triazine mol-ecules are connected to each other by N-H⋯N hydrogen bonds, forming an R(2) (2)(8) motif and a supra-molecular ribbon along the c axis. The 2 + 1 units and the supra-molecular ribbons are further inter-linked by weak N-H⋯O, C-H⋯O and C-H⋯π inter-actions, resulting in a three-dimensional network.

  3. Pharmacokinetic analysis of trichloroethylene metabolism in male B6C3F1 mice: Formation and disposition of trichloroacetic acid, dichloroacetic acid, S-(1,2-dichlorovinyl)glutathione and S-(1,2-dichlorovinyl)-L-cysteine

    SciTech Connect

    Kim, Sungkyoon; Kim, David; Pollack, Gary M.; Collins, Leonard B.; Rusyn, Ivan

    2009-07-01

    Trichloroethylene (TCE) is a well-known carcinogen in rodents and concerns exist regarding its potential carcinogenicity in humans. Oxidative metabolites of TCE, such as dichloroacetic acid (DCA) and trichloroacetic acid (TCA), are thought to be hepatotoxic and carcinogenic in mice. The reactive products of glutathione conjugation, such as S-(1,2-dichlorovinyl)-L-cysteine (DCVC), and S-(1,2-dichlorovinyl) glutathione (DCVG), are associated with renal toxicity in rats. Recently, we developed a new analytical method for simultaneous assessment of these TCE metabolites in small-volume biological samples. Since important gaps remain in our understanding of the pharmacokinetics of TCE and its metabolites, we studied a time-course of DCA, TCA, DCVG and DCVG formation and elimination after a single oral dose of 2100 mg/kg TCE in male B6C3F1 mice. Based on systemic concentration-time data, we constructed multi-compartment models to explore the kinetic properties of the formation and disposition of TCE metabolites, as well as the source of DCA formation. We conclude that TCE-oxide is the most likely source of DCA. According to the best-fit model, bioavailability of oral TCE was {approx} 74%, and the half-life and clearance of each metabolite in the mouse were as follows: DCA: 0.6 h, 0.081 ml/h; TCA: 12 h, 3.80 ml/h; DCVG: 1.4 h, 16.8 ml/h; DCVC: 1.2 h, 176 ml/h. In B6C3F1 mice, oxidative metabolites are formed in much greater quantities ({approx} 3600 fold difference) than glutathione-conjugative metabolites. In addition, DCA is produced to a very limited extent relative to TCA, while most of DCVG is converted into DCVC. These pharmacokinetic studies provide insight into the kinetic properties of four key biomarkers of TCE toxicity in the mouse, representing novel information that can be used in risk assessment.

  4. Infrared band intensities and global warming potentials of CF4, C2F6, C3F8, C4F10, C5F12, and C6F14

    NASA Astrophysics Data System (ADS)

    Roehl, C. M.; Boglu, D.; Brühl, C.; Moortgat, G. K.

    1995-04-01

    IR band intensities have been measured for the species: CF4, C2F6, C3F8, C4F10, C5F12, and C6F14 via Fourier transform spectroscopy and compared to previous literature values if available. Relative radiative forcing calculations have been performed using these data in order to determine the global warming potential of the particular species. The relative forcing (compared to CFC11, per volume) increases with molecular weight in the above series from 0.47 to 2.1, the GWP for a time horizon of 100 yrs from 1.1 to 4.7. This corresponds to a GWP on CO2 basis per mass of about 5000.

  5. Crystal structure of dimethyl 3,4,5,6-tetra-phenyl-cyclo-hexa-3,5-diene-1,2-di-carboxyl-ate.

    PubMed

    Greenberg, Fred H; Nazarenko, Alexander Y

    2016-07-01

    In the title compound, C34H28O4, the cyclo-hexa-diene ring has a screw-boat conformation with a torsion angle between the double bonds being on average ca 15° [15.2 (3) and -15.3 (3) in the two independent mol-ecules]. All four phenyl rings in both mol-ecules are arranged in a propeller-like conformation. The two mol-ecules exhibit S,R- and R,S- chirality, respectively, and are connected via C-H⋯O inter-molecular inter-actions. In turn, these weakly bound dimers form the mol-ecular crystal.

  6. Near-UV and blue wavelength excitable Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} high efficiency red phosphors

    SciTech Connect

    Khanna, A.; Dutta, P.S.

    2015-05-15

    Red phosphors with narrow emission around 615 nm (with FWHM~5–10 nm) having chemical compositions of A{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} (A=Mg, Sr) have been found to exhibit the highest luminescence amongst the molybdate–tungstate family when excited by sources in the 380–420 nm wavelength range. Thus they are most suitable for enhancing color rendering index and lowering color temperature in phosphor converted white LEDs (pc-WLEDs) with near-UV/blue LED excitation sources. The excitation band edge in the near UV/blue wavelength in the reported phosphor has been attributed to the coordination environment of the transition metal ion (Mo{sup 6+}, W{sup 6+}) and host crystal structure. Furthermore the quantum efficiency of the phosphors has been enhanced by adjusting activator concentration, suitable compositional alloying using substitutional alkaline earth metal cations and charge compensation mechanisms. - Graphical abstract: The charge transfer excitation of orthorhombic Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} is significantly higher than tetragonal CaMoO{sub 4}: Eu{sup 3+} phosphors making Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} prime candidates for fabrication of warm white phosphor-converted LEDs. - Highlights: • LED excitable Mg{sub 0.6}Ca{sub 2.16}Mo{sub 0.2}W{sub 0.8}O{sub 6}: Eu{sub 0.12}{sup 3+}/Na{sub 0.12}{sup +} phosphors were synthesized. • These phosphors are 10 times more intense than CaMoO{sub 4}: Eu{sup 3+} red phosphors. • Their intensity and efficiency were enhanced by materials optimization techniques. • Such techniques include compositional alloying, charge compensation, etc.

  7. 1,3-Bis[3-(1,3-dioxoisoindolin-2-yl)prop­yl]-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione

    PubMed Central

    Afrakssou, Zahra; Rodi, Youssef Kandri; Capet, Frédéric; Essassi, El Mokhtar; Ng, Seik Weng

    2011-01-01

    The title compound, C37H26N4O7, is a 1H-anthra[2,1-d]imidazole-2,6,11(3H)-trione derivative having isoindolindionylpropyl substitutents attached to the imidazole N atoms. The anthraquinone fragment is buckled, the dihedral angle between the two benzene rings being 1.6 (1)°. The two isoindoline rings of the substituents of the imidazole ring are positioned on opposite sides of the five-membered ring; these are nearly mutually perpendicular [dihedral angle between isoindoline rings = 88.3 (1)°]. PMID:22091154

  8. 11-Methyl-12a-phenyl-9a,12a-dihydrophenanthro[9',10':5,6][1,4]dioxino[2,3-d]oxazole and 9a-(10-hydroxyphenanthren-9-yl)-11,12a-diphenyl-9a,12a-dihydrophenanthro[9',10':5,6][1,4]dioxino[2,3-d]oxazole.

    PubMed

    Usman, Anwar; Razak, Ibrahim Abdul; Fun, Hoong-Kun; Chantrapromma, Suchada; Zhang, Yan; Xu, Jian-Hua

    2002-08-01

    In the title compounds, C(24)H(17)NO(3), (I), and C(43)H(27)NO(5), (II), the dioxine ring is not planar and tends toward a boat conformation. The oxazoline ring adopts a twisted conformation in molecule (I) but is essentially planar in molecule (II). The configuration of the dioxine-oxazoline system is determined by the sp(3) state of the two shared atoms. The phenanthrene moiety is nearly coplanar with the dioxine ring, while the phenyl ring is perpendicular to the attached oxazole ring. The triclinic unit cell of (II) contains two crystallographically independent molecules related by a pseudo-inversion centre.

  9. Dynamic compression of dense oxide (Gd3Ga5O12) from 0.4 to 2.6 TPa: Universal Hugoniot of fluid metals

    DOE PAGES

    Ozaki, N.; Nellis, W. J.; Mashimo, T.; ...

    2016-05-19

    Materials at high pressures and temperatures are of great current interest for warm dense matter physics, planetary sciences, and inertial fusion energy research. Shock-compression equation-of-state data and optical reflectivities of the fluid dense oxide, Gd3Ga5O12 (GGG), were measured at extremely high pressures up to 2.6 TPa (26 Mbar) generated by high-power laser irradiation and magnetically-driven hypervelocity impacts. Above 0.75 TPa, the GGG Hugoniot data approach/reach a universal linear line of fluid metals, and the optical reflectivity most likely reaches a constant value indicating that GGG undergoes a crossover from fluid semiconductor to poor metal with minimum metallic conductivity (MMC). Thesemore » results suggest that most fluid compounds, e.g., strong planetary oxides, reach a common state on the universal Hugoniot of fluid metals (UHFM) with MMC at sufficiently extreme pressures and temperatures. Lastly, the systematic behaviors of warm dense fluid would be useful benchmarks for developing theoretical equation-of-state and transport models in the warm dense matter regime in determining computational predictions.« less

  10. Dating of young groundwater using four anthropogenic trace gases (SF6, SF5CF3, CFC-12 and Halon-1301): methodology and first results.

    PubMed

    Bartyzel, Jakub; Rozanski, Kazimierz

    2016-01-01

    A dedicated, GC-based analytical system is presented which allows detection of four anthropogenic trace gases (SF6, SF5CF3, CFC-12 and Halon-1301) in a single water sample, with detection limits and measurement uncertainties sufficiently low to employ them as quantitative indicators of groundwater age. The gases dissolved in water are extracted in the field using the method based on a dynamic head-space concept. In the laboratory, the investigated gases are cryogenically enriched, separated and measured using an electron capture detector. Reproducibility of the analyses is in the order of 2-5 %. The investigated tracers were measured in several production wells located in the recharge area of an intensively exploited aquifer in southern Poland. While the piston-flow ages of groundwater in the investigated wells revealed internal consistency, they appeared to be generally smaller than the ages derived from time series of tritium content in those wells, interpreted by lumped-parameter models. This difference stems mainly from significantly longer travel times of tritium through the unsaturated zone, when compared to the gaseous tracers being used. The results of this study highlight the benefits of using multiple tracing in quantifying timescales of groundwater flow in shallow aquifer systems.

  11. Dynamic compression of dense oxide (Gd3Ga5O12) from 0.4 to 2.6 TPa: Universal Hugoniot of fluid metals

    PubMed Central

    Ozaki, N.; Nellis, W. J.; Mashimo, T.; Ramzan, M.; Ahuja, R.; Kaewmaraya, T.; Kimura, T.; Knudson, M.; Miyanishi, K.; Sakawa, Y.; Sano, T.; Kodama, R.

    2016-01-01

    Materials at high pressures and temperatures are of great current interest for warm dense matter physics, planetary sciences, and inertial fusion energy research. Shock-compression equation-of-state data and optical reflectivities of the fluid dense oxide, Gd3Ga5O12 (GGG), were measured at extremely high pressures up to 2.6 TPa (26 Mbar) generated by high-power laser irradiation and magnetically-driven hypervelocity impacts. Above 0.75 TPa, the GGG Hugoniot data approach/reach a universal linear line of fluid metals, and the optical reflectivity most likely reaches a constant value indicating that GGG undergoes a crossover from fluid semiconductor to poor metal with minimum metallic conductivity (MMC). These results suggest that most fluid compounds, e.g., strong planetary oxides, reach a common state on the universal Hugoniot of fluid metals (UHFM) with MMC at sufficiently extreme pressures and temperatures. The systematic behaviors of warm dense fluid would be useful benchmarks for developing theoretical equation-of-state and transport models in the warm dense matter regime in determining computational predictions. PMID:27193942

  12. 12 CFR 3.3 - Transitional rules.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Transitional rules. 3.3 Section 3.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Authority and Definitions § 3.3 Transitional rules. Intangible assets, other than...

  13. 12 CFR 3.3 - Transitional rules.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Transitional rules. 3.3 Section 3.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Authority and Definitions § 3.3 Transitional rules. Intangible assets, other than...

  14. Unusual Magnetic State with Dual Magnetic Excitations in the Single Crystal of S = 1/2 Kagome Lattice Antiferromagnet CaCu3(OH)6Cl2 • 0.6H2O

    NASA Astrophysics Data System (ADS)

    Yoshida, Hiroyuki; Noguchi, Naoya; Matsushita, Yoshitaka; Ishii, Yuto; Ihara, Yoshihiko; Oda, Migaku; Okabe, Hirotaka; Yamashita, Satoshi; Nakazawa, Yasuhiro; Takata, Atsushi; Kida, Takanori; Narumi, Yasuo; Hagiwara, Masayuki

    2017-03-01

    We have succeeded in preparing single crystals of CaCu3(OH)6Cl2 • 0.6H2O, a candidate for the S = 1/2 Kagome lattice antiferromagnet. Magnetic properties of the compound are dominated by the nearest neighbor antiferromagnetic interaction J1, and the next nearest neighbor ferromagnetic J2 and an antiferromagnetic Jd across a hexagon, which is different from related compounds Kapellasite and Haydeeite with ferromagnetic J1. Magnetic susceptibility exhibits a sudden increase below 13 K and a cusp anomaly at T* = 7.2 K in the ab-plane, whereas only a moderate enhancement is observed below T* along the c-axis. A tiny peak detected in heat capacity at T* indicates the occurrence of a magnetic phase transition. The low temperature magnetic heat capacity was reproduced by assuming a two-dimensional spin-wave component and a temperature-linear term. The spin-wave contribution suggests a magnon excitation in a short-range ordered region, whereas the relatively large T-linear term 5.9 mJ/(Cu-mol·K2) at H = 0 T of this insulating compound suggests the existence of an unusual quasi-particle excitation below T*. They apparently reveal the unconventionality of the ground state of this S = 1/2 Kagome lattice antiferromagnet.

  15. 1,3-Dibenzyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione

    PubMed Central

    Afrakssou, Zahra; Kandri Rodi, Youssef; Capet, Frédéric; Essassi, El Mokhtar; El Ammari, Lahcen

    2011-01-01

    The mol­ecule of the title compound, C29H20N2O3, contains four fused rings, three are six-membered rings and one is the five-membered imidazole ring. The fused-ring system is linked to two benzyl groups. The four fused rings are folded around the O=C⋯C=O direction of the anthraquinone, with a dihedral angle of 16.36 (8)° between the two terminal rings (A and D). The imidazole ring (D) is almost perpendicular to the two benzyl groups (E and F) with dihedral angles of 86.69 (17) and 83.15 (13)°, respectively. In the crystal, adjacent mol­ecules are linked by inter­molecular C—H⋯O hydrogen bonding. PMID:21754544

  16. Crystal structure of (2,11-di-aza-[3.3](2,6)pyridino-phane-κ (4) N,N',N'',N''')(1,6,7,12-tetra-aza-perylene-κ (2) N (1),N (12))ruthenium(II) bis-(hexa-fluorido-phosphate) aceto-nitrile 1.422-solvate.

    PubMed

    Brietzke, Thomas; Rottke, Falko Otto; Kelling, Alexandra; Schilde, Uwe; Holdt, Hans-Jürgen

    2014-10-01

    In the title compound, [Ru(C14H16N4)(C16H8N4)](PF6)2·1.422CH3CN, discrete dimers of complex cations, [Ru(L-N4H2)tape](2+) are formed {L-N4H2 = 2,11-di-aza-[3.3](2,6)pyridino-phane; tape = 1,6,7,12-tetra-aza-perylene}, held together by π-π stacking inter-actions via the tape ligand moieties with a centroid-centroid distance of 3.49 (2) Å, assisted by hydrogen bonds between the non-coordinating tape ligand α,α'-di-imine unit and the amine proton of a 2,11-di-aza-[3.3](2,6)-pyridino-phane ligand of the opposite complex cation. The combination of these inter-actions leads to an unusual nearly face-to-face π-π stacking mode. Additional weak C-H⋯N, C-H⋯F, N-H⋯F and P-F⋯π-ring (tape, py) (with F⋯centroid distances of 2.925-3.984 Å) inter-actions are found, leading to a three-dimensional architecture. The Ru(II) atom is coordinated in a distorted octa-hedral geometry, particularly manifested by the Namine-Ru-Namine angle of 153.79 (10)°. The counter-charge is provided by two hexa-fluorido-phosphate anions and the asymmetric unit is completed by aceto-nitrile solvent mol-ecules of crystallization. Disorder was observed for both the hexa-fluorido-phosphate anions as well as the aceto-nitrile solvate mol-ecules, with occupancies for the major moieties of 0.801 (6) for one of the PF6 anions, and a shared occupancy of 0.9215 (17) for the second PF6 anion and a partially occupied aceto-nitrile mol-ecule. A second CH3CN mol-ecule is fully occupied, but 1:1 disordered across a crystallographic inversion center.

  17. 12 CFR 225.6 - Penalties for violations.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Penalties for violations. 225.6 Section 225.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General Provisions §...

  18. 12 CFR 225.6 - Penalties for violations.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 3 2013-01-01 2013-01-01 false Penalties for violations. 225.6 Section 225.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General...

  19. 12 CFR 225.6 - Penalties for violations.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Penalties for violations. 225.6 Section 225.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General Provisions §...

  20. 12 CFR 225.6 - Penalties for violations.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 3 2014-01-01 2014-01-01 false Penalties for violations. 225.6 Section 225.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General...

  1. 12 CFR 225.6 - Penalties for violations.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 3 2012-01-01 2012-01-01 false Penalties for violations. 225.6 Section 225.6 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General Provisions §...

  2. Generation and intermolecular trapping of 1,2-diaza-4-silacyclopentane-3,5-diyls in the denitrogenation of 2,3,5,6-tetraaza-7-silabicyclo[2.2.1]hept-2-ene: an experimental and computational study.

    PubMed

    Nakamura, Takeshi; Takegami, Akinobu; Abe, Manabu

    2010-03-19

    In our previous computational study, we found that silicon and nitrogen atoms have a notable effect on the reactivity of 1,2-diaza-4-silacyclopentane-3,5-diyls. Thus, the singlet state of the diradical was calculated to be much more stable than the corresponding ring-closing product, i.e., 2,3-diaza-5-silabicyclo[2.1.0]pentane, and the triplet state of the diradical. In the present study, derivatives of the diradical were generated experimentally in the denitrogenation of precursor azoalkanes, i.e., 2,3,5,6-tetraaza-7-silabicyclo[2.2.1]hept-2-enes, which can be prepared by cycloaddition of a diazasilole with 4-phenyl-1,2,4-triazole-3,5-dione (PTAD) or 4-methyl-1,2,4-triazole-3,5-dione (MTAD). The diradicals were trapped intermolecularly to afford polycyclic compounds. The computational studies (UB3LYP/6-31G*) of the denitrogenation of a model azoalkane suggested that stepwise denitrogenation with an activation energy of ca. 22 kcal/mol is the thermodynamically favored pathway for generation of the singlet diradical 1,2-diaza-4-silacyclopentane-3,5-diyl derivative via a 1,4-diazenyldiradical intermediate. The low activation energy of the denitrogenation reaction was consistent with the experimental observation that the azoalkane was labile under the preparation conditions used in this study.

  3. CYP2C19 but not CYP2B6, CYP3A4, CYP3A5, ABCB1, PON1 or P2Y12 genetic polymorphism impacts antiplatelet response after clopidogrel in Koreans.

    PubMed

    Zhang, Hong-Zhe; Kim, Moo Hyun; Guo, Long-Zhe; Serebruany, Victor

    2017-01-01

    Clopidogrel response variability (CRV) is well documented, and may affect clinical outcomes. Impact of genetic polymorphisms is important for assessing and predicting CRV. The extensive evidence indicates the importance of CYP2C19 variants in reducing efficacy of clopidogrel. This study defined the impact of numerous genetic polymorphisms on CRV before and after percutaneous coronary interventions (PCI) exclusively in a Korean cohort assuming less genetic variability noise. One hundred and thirty-six patients of Korean origin undergoing PCI were included. Platelet reactivity was measured by VerifyNow assay before and after PCI. Genetic polymorphism of seven single nucleotides of CYP2B6, CYP2C19, CYP3A4, CYP3A5, ABCB1, PON1, and P2Y12 were evaluated and matched with platelet reactivity. Carriers of at least one CYP2C19*2 or *3 allele uniformly exhibited higher platelet reactivity compared to 0-carrier pre-PCI (odds ratio 3.1, 95% confidence interval 1.4-6.9, P < 0.01) and post-PCI (odds ratio 3.4, 95% confidence interval 1.7-6.8, P < 0.001). The carriers of other gene allele variants lack uniformed impact on CRV. The Korean carriers of CYP2C19*2 or *3 allele are linked to CRV, whereas CYP2B6, CYP3A4, CYP3A5, ABCB1, PON1, and P2Y12 failed to predict CRV. The exact clinical utility of these findings is uncertain, and requires a large randomized national trial for proof of concept.

  4. Dating of young groundwater using tritium and gaseous tracers (SF6, SF5CF3, CFC-12, H-1301): case study from southern Poland

    NASA Astrophysics Data System (ADS)

    Rozanski, Kazimierz; Bartyzel, Jakub; Dulinski, Marek; Kuc, Tadeusz; Sliwka, Ireneusz; Mochalski, Pawel; Kania, Jaroslaw; Witczak, Stanislaw

    2013-04-01

    was employed. Apart of well-established tracers such as SF6 and CFC-12, also other trace gases present in the atmosphere (SF5CF3 and H-1301) were tested as age indicators of young groundwater. Time series of tracer concentrations in the sampled boreholes were interpreted with the aid of lumped-parameter models. In parallel, the arrival times of tracers to the selected wells were calculated with the aid of 3D flow and transport model available for the studied groundwater system and compared with the RTD functions obtained from lumped-parameter modeling. Acknowledgements. Partial financial support of this work through GENESIS project (http:/www.thegenesisproject.eu) funded by the European Commission 7FP contract 226536 and through the funds from the Polish Ministry of Science and High Education (projects Nr. N N525 362637 and 11.11.220.01) is kindly acknowledged.

  5. Very high frequency electron paramagnetic resonance of 2,2,6,6-tetramethyl-1-piperidinyloxy in 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine liposomes: partitioning and molecular dynamics.

    PubMed Central

    Smirnov, A I; Smirnova, T I; Morse, P D

    1995-01-01

    Partitioning and molecular dynamics of 2,2,6,6,-tetramethylpiperedine-1-oxyl (TEMPO) nitroxide radicals in large unilamellar liposomes (LUV) composed from 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine were investigated by using very high frequency electron paramagnetic resonance (EPR) spectroscopy. Experiments carried out at a microwave frequency of 94.3 GHz completely resolved the TEMPO EPR spectrum in the aqueous and hydrocarbon phases. An accurate computer simulation method combined with Levenberg-Marquardt optimization was used to analyze the TEMPO EPR spectra in both phases. Spectral parameters extracted from the simulations gave the actual partitioning of the TEMPO probe between the LUV hydrocarbon and aqueous phases and allowed analysis of picosecond rotational dynamics of the probe in the LUV hydrocarbon phase. In very high frequency EPR experiments, phase transitions in the LUV-TEMPO system were observed as sharp changes in both partitioning and rotational correlation times of the TEMPO probe. The phase transition temperatures (40.5 +/- 0.2 and 32.7 +/- 0.5 degrees C) are in agreement with previously reported differential scanning microcalorimetry data. Spectral line widths were analyzed by using existing theoretical expressions for motionally narrowed nitroxide spectra. It was found that the motion of the small, nearly spherical, TEMPO probe can be well described by anisotropic Brownian diffusion in isotropic media and is not restricted by the much larger hydrocarbon chains existing in ripple structure (P beta') or fluid bilayer structure (L alpha) phases. PMID:7647239

  6. Infrared (1.2-1.6 microm) luminescence in Cr4+:Yb3Al5O12 single crystal with 940 nm diode pumping.

    PubMed

    Xu, Xiaodong; Zhao, Zhiwei; Song, Pingxin; Zhou, Guoqing; Xu, Jun; Deng, Peizhen; Bourdet, Gilbert; Chanteloup, Jean Christophe; Zou, Ji-Ping; Fulop, Annabelle

    2005-09-01

    Infrared (1.2-1.6 microm) luminescence in a ytterbium aluminium garnet (YbAG) crystal, doped with Cr (0.05at.%) ions, was investigated under CW laser diode pumping (lambda=940 nm). The Cr4+ emission band was observed with its peak at 1.34 microm and measured to be about 1.3 times with respect to Yb3+ IR luminescence (lambda=1.03 microm). We demonstrate that for the excitation wavelength of 940 nm Yb3+ ions act as sensitizers of the 3B2(3T2)-3B1(3A2) emission of Cr4+ ions. This crystal is promising as a high-efficient system for tunable laser (1.2-1.6 microm) output.

  7. 12 CFR 3.3 - Transitional rules.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Transitional rules. 3.3 Section 3.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF... December 31, 1992, only those intangible assets that meet the criteria contained in section 2(c)(2)...

  8. 12 CFR 3.3 - Transitional rules.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Transitional rules. 3.3 Section 3.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF... December 31, 1992, only those intangible assets that meet the criteria contained in section 2(c)(2)...

  9. 49 CFR 172.411 - EXPLOSIVE 1.1, 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... MATERIALS REGULATIONS HAZARDOUS MATERIALS TABLE, SPECIAL PROVISIONS, HAZARDOUS MATERIALS COMMUNICATIONS..., 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label. (a) Except for size and color... addition to complying with § 172.407, the background color on the EXPLOSIVE 1.1, EXPLOSIVE 1.2...

  10. 49 CFR 172.411 - EXPLOSIVE 1.1, 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... MATERIALS REGULATIONS HAZARDOUS MATERIALS TABLE, SPECIAL PROVISIONS, HAZARDOUS MATERIALS COMMUNICATIONS..., 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label. (a) Except for size and color... addition to complying with § 172.407, the background color on the EXPLOSIVE 1.1, EXPLOSIVE 1.2...

  11. 49 CFR 172.411 - EXPLOSIVE 1.1, 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... MATERIALS REGULATIONS HAZARDOUS MATERIALS TABLE, SPECIAL PROVISIONS, HAZARDOUS MATERIALS COMMUNICATIONS..., 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label. (a) Except for size and color... addition to complying with § 172.407, the background color on the EXPLOSIVE 1.1, EXPLOSIVE 1.2...

  12. 49 CFR 172.411 - EXPLOSIVE 1.1, 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... MATERIALS REGULATIONS HAZARDOUS MATERIALS TABLE, SPECIAL PROVISIONS, HAZARDOUS MATERIALS COMMUNICATIONS..., 1.2, 1.3, 1.4, 1.5 and 1.6 labels, and EXPLOSIVE Subsidiary label. (a) Except for size and color... addition to complying with § 172.407, the background color on the EXPLOSIVE 1.1, EXPLOSIVE 1.2...

  13. Effect of Al2O3 on the sintering of garnet-type Li6.5La3Zr1.5Ta0.5O12

    SciTech Connect

    Wang, Yuxing; Yan, Pengfei; Xiao, Jie; Lu, Xiaochuan; Zhang, Ji-Guang; Sprenkle, Vincent L.

    2016-10-01

    It is widely recognized that Al plays a dual role in the fabrication of garnet-type solid electrolytes, i.e., as a dopant that stabilizes the cubic structure and a sintering aid that facilitates the densification. However, the sintering effect of Al2O3 has not been well understood so far because Al is typically “unintentionally” introduced into the sample from the crucible during the fabrication process. In this study, we have investigated the sintering effect of Al on the phase composition, microstructure, and ionic conductivity of Li6.5La3Zr1.5Ta0.5O12 by using an Al-free crucible and intentionally adding various amounts of γ-Al2O3. It was found that the densification of Li6.5La3Zr1.5Ta0.5O12 occurred via liquid-phase sintering, with evidence of morphology change among different compositions. Among all of the compositions, samples with 0.05 mol of Al per unit formula of garnet oxide (i.e., 0.3 wt% Al2O3) exhibited the optimal microstructure and the highest total ionic conductivity of 5 10-4 S cm-1 at room temperature.

  14. Volumetric Properties of the Mixture Cyclohexa-1,3-diene C6H8 + C10H12 1,2,3,4-Tetrahydronaphthalene (VMSD1211, LB3964_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Cyclohexa-1,3-diene C6H8 + C10H12 1,2,3,4-Tetrahydronaphthalene (VMSD1211, LB3964_V)' providing data from direct low-pressure dilatometric measurement of molar excess volume at variable mole fraction and constant temperature.

  15. Heat of Mixing and Solution of Cyclohexa-1,3-diene C6H8 + C10H12 1,2,3,4-Tetrahydronaphthalene (HMSD1111, LB4036_H)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume B 'Binary Liquid Systems of Nonelectrolytes II' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Heat of Mixing and Solution of Cyclohexa-1,3-diene C6H8 + C10H12 1,2,3,4-Tetrahydronaphthalene (HMSD1111, LB4036_H)' providing data from direct low-pressure calorimetric measurement of molar excess enthalpy at variable mole fraction and constant temperature.

  16. Outcome and clinical changes in patients 3, 6, 12 months after a severe or major hand injury - can sense of coherence be an indicator for rehabilitation focus?

    PubMed Central

    2010-01-01

    Background Our objective was to explore outcome and clinical changes in hand function, satisfaction in daily occupations, sleep disturbances, health and quality of life in consecutive patients after a severe or major hand injury. Our objective was also to investigate possible differences between groups according to severity of injury, presence of peripheral nerve injury and the patients' sense of coherence. Methods A postal questionnaire, including demographic data, disabilities of the arm, shoulder and hand (DASH), QoL (SF-36), EuroQol (EQ-5D VAS), hand function (VAS), satisfaction in daily occupation (SDO), was sent out 3, 6 and 12 months after injury to 45 consecutive patients with a severe or major hand injury. Sense of coherence (SOC) was evaluated at 6 months. For the descriptive study, non-parametric tests were used since almost all results were measured with ordinal scales, the study sample was small, and most variables not normally distributed. Results Almost all self-assessed aspects of hand function, satisfaction in daily occupations, health (DASH), and physical QoL (SF-36) improved statistically for the whole group over time. Large clinical improvement was seen for physical QoL and health, while a low or no improvement was observed for mental QoL, and cold sensitivity. Few differences were found between participants with a severe or major of hand injury or with or without a major nerve injury. No significant differences in demographic data were observed between participants with high or low SOC, but participants with low SOC showed significantly lower satisfaction in daily occupations, higher DASH scores, lower mental QoL, more sleep disturbances, and bodily pain. Correlation was found between SOC, and QoL, health and satisfaction in daily occupations. Conclusions SOC had a significant influence on patients with a severe or major traumatic hand injury. Patients with lower SOC would probably benefit from extra support and help to master their daily life

  17. 12 CFR 703.3 - Investment policies.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Investment policies. 703.3 Section 703.3 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS INVESTMENT AND DEPOSIT ACTIVITIES § 703.3 Investment policies. A Federal credit union's board of directors must...

  18. 12 CFR 568.3 - Security program.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 6 2014-01-01 2012-01-01 true Security program. 568.3 Section 568.3 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY SECURITY PROCEDURES § 568.3 Security program. (a) Contents of security program. The security program shall: (1) Establish procedures...

  19. 12 CFR 725.3 - Regular membership.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 6 2011-01-01 2011-01-01 false Regular membership. 725.3 Section 725.3 Banks... UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.3 Regular membership. (a) A natural person credit... stock subscription;1 and 1 A credit union which submits its application for membership prior to...

  20. 12 CFR 725.3 - Regular membership.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Regular membership. 725.3 Section 725.3 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS NATIONAL CREDIT UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.3 Regular membership. (a) A natural person...

  1. DFT studies on a high-energy density cage compound 1, 3, 5, 7, 9, 11-hexo(N(CH3)NO2)-2, 4, 6, 8, 10, 12-hexaazatetracyclo[5, 5, 0, 0, 0] dodecane

    NASA Astrophysics Data System (ADS)

    Li, Xiao-Hong; Yong, Yong-Liang; Zhang, Xian-Zhou

    2014-04-01

    The infrared and Raman spectra, heat of formation (HOF) and thermodynamic properties were investigated by B3LYP/6-31G** method for a new designed polynitro cage compound 1,3,5,7,9,11-hexo(N(CH3)NO2)-2,4,6,8,10,12-hexaazatetracyclo[5,5,0,0,0]dodecane. The detonation velocity (D) and pressure (P) were predicted by the Kamlet-Jacobs equations based on the theoretical density and condensed HOF. The bond dissociation energies and bond orders for the weakest bonds were analysed to investigate the thermal stability of the title compound. The computational result shows that the detonation velocity and pressure of the title compound are superior to those of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), but inferior to those of 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane (HMX) and hexanitrohexaazaisowurtzitane (HNIW). And the analysis of thermal stability shows that the first step of pyrolysis is the rupture of the N7-NO2 bond. The crystal structure obtained by molecular mechanics belongs to the P21 space group, with the lattice parameters Z = 2, a = 11.8246 Å, b = 10.4632 Å, c = 15.9713 Å, ρ = 1.98 g cm-3.

  2. Crystal structure of (2R*,3aR*)-2-phenyl­sulfonyl-2,3,3a,4,5,6-hexa­hydro­pyrrolo­[1,2-b]isoxazole

    PubMed Central

    Hernández, Yaiza; Marcos, Isidro; Garrido, Narciso M.; Sanz, Francisca; Diez, David

    2017-01-01

    The title compound, C12H15NO3S, was prepared by 1,3-dipolar cyclo­addition of 3,4-di­hydro-2H-pyrrole 1-oxide and phenyl vinyl sulfone. In the mol­ecule, both fused five-membered rings display a twisted conformation. In the crystal, C—H⋯O hydrogen bonds link neighbouring mol­ecules, forming chains running parallel to the b axis. PMID:28083143

  3. Crystal structure of (2R*,3aR*)-2-phenyl-sulfonyl-2,3,3a,4,5,6-hexa-hydro-pyrrolo-[1,2-b]isoxazole.

    PubMed

    Hernández, Yaiza; Marcos, Isidro; Garrido, Narciso M; Sanz, Francisca; Diez, David

    2017-01-01

    The title compound, C12H15NO3S, was prepared by 1,3-dipolar cyclo-addition of 3,4-di-hydro-2H-pyrrole 1-oxide and phenyl vinyl sulfone. In the mol-ecule, both fused five-membered rings display a twisted conformation. In the crystal, C-H⋯O hydrogen bonds link neighbouring mol-ecules, forming chains running parallel to the b axis.

  4. Synthesis and biological evaluation of novel 5-alkyl-2-arylthio-6-((3,4-dihydroquinolin-1(2H)-yl)methyl)pyrimidin-4(3H)-ones as potent non-nucleoside HIV-1 reverse transcriptase inhibitors.

    PubMed

    Zhang, Jing; Zhan, Peng; Wu, Jingde; Li, Zhenyu; Jiang, Yan; Ge, Weiying; Pannecouque, Christophe; De Clercq, Erik; Liu, Xinyong

    2011-07-15

    A series of novel S-DABO analogues of 5-alkyl-2-arylthio-6-((3,4-dihydroquinolin-1(2H)-yl)methyl)pyrimidin-4(3H)-ones were synthesized and evaluated as inhibitors of human immunodeficiency virus type-1 (HIV-1). Among them, the most potent HIV-1 inhibitors were compounds 6c1,6c6, and 6b1 (EC(50)=0.24 ± 0.05, 0.38 ± 0.13, 0.39 ± 0.05 μM, respectively), which possess improved or similar HIV-1 inhibitory activity compared with nevirapine (NVP) (EC(50)=0.21 μM) and delavirdine (DLV) (EC(50)=0.32 μM). None of these compounds were active against HIV-2 replication. Furthermore, enzyme inhibitory assays were performed with selected derivatives against HIV-1 wtRT, confirming that the main target of these compounds is the HIV-1 RT and these new S-DABOs are acting as NNRTIs. The preliminary structure-activity relationship (SAR) of these new congeners is discussed briefly and rationalized by docking studies.

  5. Material properties and structural characterization of M3Si6O12N2:Eu2+ (M = Ba, Sr)--a comprehensive study on a promising green phosphor for pc-LEDs.

    PubMed

    Braun, Cordula; Seibald, Markus; Börger, Saskia L; Oeckler, Oliver; Boyko, Teak D; Moewes, Alexander; Miehe, Gerhard; Tücks, Andreas; Schnick, Wolfgang

    2010-08-16

    The efficient green phosphor Ba(3)Si(6)O(12)N(2):Eu(2+) and its solid-solution series Ba(3-x)Sr(x)Si(6)O(12)N(2) (with x approximately = 0.4 and 1) were synthesized in a radio-frequency furnace under nitrogen atmosphere at temperatures up to 1425 degrees C. The crystal structure (Ba(3)Si(6)O(12)N(2), space group P3 (no. 147), a = 7.5218(1), c = 6.4684(1) A, wR2 = 0.048, Z = 1) has been solved and refined on the basis of both single-crystal and powder X-ray diffraction data. Ba(3)Si(6)O(12)N(2):Eu(2+) is a layer-like oxonitridosilicate and consists of vertex-sharing SiO(3)N-tetrahedra forming 6er- and 4er-rings as fundamental building units (FBU). The nitrogen atoms are connected to three silicon atoms (N3), while the oxygen atoms are either terminally bound (O1) or bridge two silicon atoms (O2) (numbers in superscripted square brackets after atoms indicate the coordination number of the atom in question). Two crystallographically independent Ba(2+) sites are situated between the silicate layers. Luminescence investigations have shown that Ba(3)Si(6)O(12)N(2):Eu(2+) exhibits excellent luminescence properties (emission maximum at approximately 527 nm, full width at half maximum (FWHM) of approximately 65 nm, low thermal quenching), which provides potential for industrial application in phosphor-converted light-emitting diodes (pc-LEDs). In-situ high-pressure and high-temperature investigations with synchrotron X-ray diffraction indicate decomposition of Ba(3)Si(6)O(12)N(2) under these conditions. The band gap of Ba(3)Si(6)O(12)N(2):Eu(2+) was measured to be 7.05+/-0.25 eV by means of X-ray emission spectroscopy (XES) and X-ray absorption near edge spectroscopy (XANES). This agrees well with calculated band gap of 6.93 eV using the mBJ-GGA potential. Bonding to the Ba atoms is highly ionic with only the 4p(3/2) orbitals participating in covalent bonds. The valence band consists primarily of N and O p states and the conduction band contains primarily Ba d and f states

  6. 12 CFR 703.3 - Investment policies.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 6 2011-01-01 2011-01-01 false Investment policies. 703.3 Section 703.3 Banks... extent of that authority. Those with authority must be qualified by education or experience to assess the... requirement of this part; and (k) How the Federal credit union will conduct investment trading activities,...

  7. Oxalate-based soluble 2D magnets: the series [K(18-crown-6)]3[M(II)3(H2O)4{M(III)(ox)3}3] (M(III) = Cr, Fe; M(II) = Mn, Fe, Ni, Co, Cu; ox = C2O4(2-); 18-crown-6 = C12H24O6).

    PubMed

    Coronado, Eugenio; Galán-Mascarós, José R; Martí-Gastaldo, Carlos; Waerenborgh, João C; Gaczyński, Piotr

    2008-08-04

    The synthesis and magnetic properties of the oxalate-based molecular soluble magnets with general formula [K(18-crown-6)] 3[M (II) 3(H 2O) 4{M (III)(ox) 3} 3] (M (III) = Cr, Fe; M (II) = Mn, Fe, Ni, Co, Cu; ox = C 2O 4 (2-)) are here described. All the reported compounds are isostructural and built up by 2D bimetallic networks formed by alternating M (III) and M (II) ions connected through oxalate anions. Whereas the Cr (III)M (II) derivatives behave as ferromagnets with critical temperatures up to 8 K, the Fe (III)M (II) present ferri- or weak ferromagnetic ordering up to 26 K.

  8. Tanshinone IIA increases protein expression levels of PERK, ATF6, IRE1α, CHOP, caspase‑3 and caspase‑12 in pancreatic cancer BxPC‑3 cell‑derived xenograft tumors.

    PubMed

    Chiu, Tsung-Lang; Su, Chin Cheng

    2017-03-22

    Tanshinone (Tan)-IIA is a derivative of phenanthrenequinone and the main active ingredient isolated from Salviae miltiorrhizae radix (Danshen). Previous studies have demonstrated that Tan‑IIA increased the protein expressions levels of protein kinase RNA‑like endoplasmic reticulum kinase (PERK), activating transcription factor (ATF) 6, caspase‑12 and CCAAT‑enhancer‑binding protein homologous protein (CHOP), to induce endoplasmic reticulum (ER) stress and apoptosis in human pancreatic cancer BxPC‑3 cells. However, to the best of our knowledge, the effects of Tan‑IIA on pancreatic cancer cells have not been investigated in vivo. Further studies are required to elucidate the therapeutic potential of Tan‑IIA in inducing ER stress in cancer cells in vivo. The present study aimed to investigate the effects of Tan‑IIA on the expression of ER stress‑related proteins in BxPC‑3‑derived xenograft tumors. A total of 30 male severe combined immunodeficiency mice (age, 4 weeks) were implanted with BxPC‑3 cells (2x106/0.2 ml) and subsequently treated with various doses of Tan‑IIA (0, 30 and 90 mg/kg) for 4 weeks. After mice were sacrificed on day 33, the xenograft tumors were dissected and total protein was extracted for western blot analysis. The results of the present study demonstrated that Tan‑IIA inhibited the growth of BxPC‑3‑derived xenograft tumors. In addition, Tan‑IIA increased the protein expression levels of PERK, ATF6, caspase‑12, inositol‑requiring enzyme (IRE) 1α, eukaryotic initiation factor (eIF) 2α, phosphorylated (p)‑c‑Jun N‑terminal kinase (JNK), CHOP and caspase‑3 in a dose‑dependent manner. These results indicated that Tan‑IIA induced ER stress via increasing the protein expression levels of PERK, ATF6, caspase‑12, IRE1α, eIF2α, p‑JNK, CHOP and caspase‑3 in BxPC‑3 cells in vivo. Therefore, it may be hypothesized that Tan‑IIA has potential for the development of novel therapeutic

  9. Dermal Sensitization Potential of Insect Repellents: Methyl N,N’-Dihexylethylenediaminemonocarbamate (CHR4), (E)-1,2,3,4-Tetrahydro-6-Methyl-1-(2-Methyl-1-Oxo-2-Butenyl) Quinoline (CHR5), and 1,2,3,4-Tetrahydro-6-Methyl-1-(3-Methyl-1-Oxo-2-Butenyl) Quinoline (CHR6).

    DTIC Science & Technology

    1984-05-20

    Chemical name: Methyl-N,N’-Dihexylethylenediamine- monocarbamate (CHR4) Chemical Abstract Service Registry No.: None Structural formula: CH3 (C11 2 )sNH...Quinoline (CRj5) Chemical Abstract Service Registry No.: None Structural formula: CH I C=O CH 3 ’CH 3 Empirical formula: C H NO- 3. Chemical Name...l,2,3,4-Tetralhydro-6-Me thyl-l-(3-Methiyi- l-Oxo-2-Sutenyl) Quinoline (CdiR6) Chemical Abstract Service Registry No.: None Ieia

  10. Preparation of Two New Diasteromeric Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and (R)- or (S)-1-(1-Naphthyl)ethylamine and Chiral Tethering Group Effect on the Chiral Recognition.

    PubMed

    Agneeswari, Rajalingam; Sung, Ji Yeong; Jo, Eun Sol; Jeon, Hee Young; Tamilavan, Vellaiappillai; Hyun, Myung Ho

    2016-08-12

    Two new diastereomeric chiral stationary phases (CSPs) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral tethering group and a Π-basic chiral unit such as (R)-1-(1-naphthyl)ethylamine (CSP 1) or (S)-1-(1-naphthyl)ethylamine (CSP 2) were prepared. The two CSPs were applied to the enantiomeric separation of N-(3,5-dinitrobenzoyl)-1-phenylalkylamines and N-(3,5-dinitrobenzoyl)-α-amino acid derivatives using 20% isopropyl alcohol in hexane as a normal mobile phase. To elucidate the effect of the two chiral units on the chiral recognition, the chiral recognition abilities of the two CSPs were compared with each other and with that of a CSP (CSP 3) based on (R)-1-(1-naphthyl)ethylamine. From the chromatographic chiral recognition results, (R)-1-(1-naphthyl)ethylamine and (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid constituting CSP 1 were concluded to show a cooperative ("matched") effect on the chiral recognition while (S)-1-(1-naphthyl)ethylamine and (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid constituting CSP 2 were concluded to show an uncooperative ("mismatched") effect on the chiral recognition. From these results, it was concluded that (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid can be successfully used as a chiral tethering group for the preparation of new CSPs.

  11. Temporal Differential Gene Expression in Explanted Human Retinal Pigment Epithelial Cells at 0.5, 1.0, 3.0, 6.0, 12 and 24 Hours Post-Exposure to 1064 nm, 3.6 ns Pulsed Laser Light

    DTIC Science & Technology

    2005-05-01

    USAFA TR 2005-05 Temporal Differential Gene Expression in Explanted Human Retinal Pigment Epithelial Cells at 0.5, 1.0, 3.0, 6.0, 12 and 24 Hours...AIR FORCE ACADEMY COLORADO 80840 20050630 417 USAFA TR 2005-05 This article, "Temporal Differential Gene Expression in Explanted Human Retinal ...Differential Gene Expression in Explanted Human Retinal Pigment USAFA F05611-02-P-0471 Epithelial Cells at 0.5, 1.0, 3.0, 6.0, 12 and 24-Hours Post-Exposure

  12. Cs(3)Sm(7)Se(12).

    PubMed

    Schneck, Christof; Elbe, Andreas; Schurz, Christian M; Schleid, Thomas

    2012-01-01

    The title compound, tricaesium hepta-samarium(III) dodeca-selenide, is setting a new starting point for realization of the channel structure of the Cs(3)M(7)Se(12) series, now with M = Sm, Gd-Er. This Cs(3)Y(7)Se(12)-type arrangement is structurally based on the Z-type sesquiselenides M(2)Se(3) adopting the Sc(2)S(3) structure. Thus, the structural set-up of Cs(3)Sm(7)Se(12) consists of edge- and vertex-connected [SmSe(6)](9-) octa-hedra [d(Ø)(Sm(3+) - Se(2-)) = 2.931 Å], forming a rock-salt-related network [Sm(7)Se(12)](3-) with channels along [001] that are apt to take up monovalent cations (here Cs(+)) with coordination numbers of 7 + 1 for one and of 6 for the second cation. The latter cation has a trigonal-prismatic coordination and shows half-occupancy, resulting in an impossible short distance [2.394 (4) Å] between symmetrically coupled Cs(+) cations of the same kind. While one Sm atom occupies Wyckoff position 2b with site symmetry ..2/m, all other 11 crystallographically different atoms (namely 2 × Cs, 3 × Sm and 6 × Se) are located at Wyckoff positions 4g with site symmetry ..m.

  13. 50 CFR 12.6 - Bonded release.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ..., payment of the value as determined under § 12.12) in place of any property seized under the Endangered Species Act, 16 U.S.C. 1531 et seq.; Marine Mammal Protection Act, 16 U.S.C. 1361 et seq.; Lacey Act, 18 U.S.C. 43; Lacey Act Amendments of 1981, 16 U.S.C. 3371 et seq.; Airborne Hunting Act, 16 U.S.C....

  14. 50 CFR 12.6 - Bonded release.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ..., payment of the value as determined under § 12.12) in place of any property seized under the Endangered Species Act, 16 U.S.C. 1531 et seq.; Marine Mammal Protection Act, 16 U.S.C. 1361 et seq.; Lacey Act, 18 U.S.C. 43; Lacey Act Amendments of 1981, 16 U.S.C. 3371 et seq.; Airborne Hunting Act, 16 U.S.C....

  15. 50 CFR 12.6 - Bonded release.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ..., payment of the value as determined under § 12.12) in place of any property seized under the Endangered Species Act, 16 U.S.C. 1531 et seq.; Marine Mammal Protection Act, 16 U.S.C. 1361 et seq.; Lacey Act, 18 U.S.C. 43; Lacey Act Amendments of 1981, 16 U.S.C. 3371 et seq.; Airborne Hunting Act, 16 U.S.C....

  16. 50 CFR 12.6 - Bonded release.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ..., payment of the value as determined under § 12.12) in place of any property seized under the Endangered Species Act, 16 U.S.C. 1531 et seq.; Marine Mammal Protection Act, 16 U.S.C. 1361 et seq.; Lacey Act, 18 U.S.C. 43; Lacey Act Amendments of 1981, 16 U.S.C. 3371 et seq.; Airborne Hunting Act, 16 U.S.C....

  17. 50 CFR 12.6 - Bonded release.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ..., payment of the value as determined under § 12.12) in place of any property seized under the Endangered Species Act, 16 U.S.C. 1531 et seq.; Marine Mammal Protection Act, 16 U.S.C. 1361 et seq.; Lacey Act, 18 U.S.C. 43; Lacey Act Amendments of 1981, 16 U.S.C. 3371 et seq.; Airborne Hunting Act, 16 U.S.C....

  18. 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropil­idene-5-C-nitro­methyl-a-d-glucofuran­ose

    PubMed Central

    Pampín, Begoña; Valencia, Laura; Estévez, Juan C.; Estévez, Ramón J.

    2009-01-01

    The title compound, C24H27NO9, is one of the epimers of the Henry reaction of 3-O-benzyl-6-O-benzoyl-2-O-isopropyl­idene-a-d-glucofuran-5-one with nitro­methane. The conformation of the five membered rings is as expected from the precursor compound and the mol­ecule is folded with a dihedral angle of 51.4 (2)° between the aromatic rings. One O—H⋯O hydrogen bond and some intra­molecular and inter­molecular C—H⋯O inter­actions are observed in the structure. PMID:21581936

  19. (E)-1-[2-Hy-droxy-4,6-bis-(meth-oxy-meth-oxy)phen-yl]-3-phenyl-prop-2-en-1-one.

    PubMed

    Niu, Chao; Liu, Y Q; He, Y W; Aisa, H A

    2013-05-01

    The title compound, C19H20O6, consists of a tetra-substituted benzene ring with one substituent being an α,β-unsaturated cinnamoyl group, which forms an extended conjugated system in the mol-ecule. In addition, two meth-oxy-meth-oxy and one hy-droxy group are bonded to the central benzene ring. The dihedral angle between eh rings is 10.22 (10)°. An intra-molecular hydrogen bond is observed between the hy-droxy group and the carbonyl O atom. One of the meth-oxy-meth-oxy substituents is conformationally disordered over two sets of sites with site-occupation factors of 0.831 (3) and 0.169 (3).

  20. Influence of Au nanoparticles on the photoluminescent and electrical properties of Bi{sub 3.6}Eu{sub 0.4}Ti{sub 3}O{sub 12} ferroelectric thin films

    SciTech Connect

    Su, Li; Qin, Ni E-mail: stsbdh@mail.sysu.edu.cn; Xie, Wei; Fu, Jianhui; Bao, Dinghua E-mail: stsbdh@mail.sysu.edu.cn

    2014-07-21

    Au-doped Bi{sub 3.6}Eu{sub 0.4}Ti{sub 3}O{sub 12} (BET) thin films were prepared on fused silica and Pt/Ti/SiO{sub 2}/Si substrates by a chemical solution deposition method. The existence of Au nanoparticles (NPs) has been confirmed by X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscope analysis. Enhanced photoluminescence (PL) of Eu{sup 3+} ions was obtained in a wide range of Au doping level. Role of the Au NPs in the PL enhancement was investigated by means of optical absorption, excitation, and emission spectra, as well as decay lifetime measurements. The results indicated that the intra-4f transition of Eu{sup 3+} ions can be intensively activated by the coupling of the charge transfer band of BET with the {sup 5}D{sub 0} state of Eu{sup 3+} ions. The influence of Au NPs on the PL properties of Eu{sup 3+} ions in the present thin films was attributed to the band bending at Au/BET interface and the localized surface plasma resonance absorption of Au NPs in the visible light region. The dielectric and ferroelectric properties of Au-doped BET thin films were investigated as well.

  1. 45 CFR 12.6 - Notice of available property.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Notice of available property. 12.6 Section 12.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION DISPOSAL AND UTILIZATION OF SURPLUS REAL PROPERTY FOR PUBLIC HEALTH PURPOSES § 12.6 Notice of available property. Reasonable publicity will be given to the availability...

  2. First-principles determination of Heisenberg Hamiltonian parameters for the spin-(1)/(2) kagome antiferromagnet ZnCu3(OH)6Cl2

    NASA Astrophysics Data System (ADS)

    Jeschke, Harald O.; Salvat-Pujol, Francesc; Valentí, Roser

    2013-08-01

    Herbertsmithite [ZnCu3(OH)6Cl2] is often discussed as the best realization of the highly frustrated antiferromagnetic kagome lattice known so far. We employ density functional theory (DFT) calculations to determine eight exchange coupling constants of the underlying Heisenberg Hamiltonian. We find the nearest-neighbor coupling J1 to exceed all other couplings by far. However, next-nearest-neighbor kagome layer couplings of 0.019J1 and interlayer couplings of up to -0.035J1 slightly modify the perfect antiferromagnetic kagome Hamiltonian. Interestingly, the largest interlayer coupling is ferromagnetic, even without Cu impurities in the Zn layer. In addition, we validate our DFT approach by applying it to kapellasite, a polymorph of herbertsmithite, which is known experimentally to exhibit competing exchange interactions.

  3. 12 CFR 337.6 - Brokered deposits.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... AND UNSOUND BANKING PRACTICES § 337.6 Brokered deposits. (a) Definitions. For the purposes of this... a pension plan or other employee benefit plan provided that person is performing managerial... such acceptance, renewal or rollover does not constitute an unsafe or unsound practice with respect...

  4. Enhanced hydrogen adsorption on Li-coated B12C6N6.

    PubMed

    Jin, Xueling; Qi, Pengtang; Yang, Huihui; Zhang, Yan; Li, Jinyun; Chen, Hongshan

    2016-10-28

    The hydrogen storage property of Li-coated B12C6N6 is investigated by density functional theory calculations. B12C6N6 is an electron deficient fullerene. Li atoms can be strongly bound to this cage by donating their valance electrons to the virtual 2p orbitals of carbon in the cluster. The binding energy (-2.90 eV) is much larger than the cohesive energy (1.63 eV) of bulk Li, and it prevents the Li atoms from aggregation. The coated Li atoms have large positive charges and the adsorbed hydrogen molecules can be moderately polarized by the Li(+) ions. The computation shows that each Li atom coated on B12C6N6 can hold 2-3 H2 molecules with adsorption energies in the range of 0.21-0.24 eV/H2. The B12C6N6Li8 can adsorb 16 H2 and achieve a gravimetric hydrogen density of 8.63 wt. %. The present results indicate that alkali-metal atoms coated on electron deficient fullerenes can serve as hydrogen storage materials that can operate at ambient temperatures with high recycling storage capacity.

  5. Enhanced hydrogen adsorption on Li-coated B12C6N6

    NASA Astrophysics Data System (ADS)

    Jin, Xueling; Qi, Pengtang; Yang, Huihui; Zhang, Yan; Li, Jinyun; Chen, Hongshan

    2016-10-01

    The hydrogen storage property of Li-coated B12C6N6 is investigated by density functional theory calculations. B12C6N6 is an electron deficient fullerene. Li atoms can be strongly bound to this cage by donating their valance electrons to the virtual 2p orbitals of carbon in the cluster. The binding energy (-2.90 eV) is much larger than the cohesive energy (1.63 eV) of bulk Li, and it prevents the Li atoms from aggregation. The coated Li atoms have large positive charges and the adsorbed hydrogen molecules can be moderately polarized by the Li+ ions. The computation shows that each Li atom coated on B12C6N6 can hold 2-3 H2 molecules with adsorption energies in the range of 0.21-0.24 eV/H2. The B12C6N6Li8 can adsorb 16 H2 and achieve a gravimetric hydrogen density of 8.63 wt. %. The present results indicate that alkali-metal atoms coated on electron deficient fullerenes can serve as hydrogen storage materials that can operate at ambient temperatures with high recycling storage capacity.

  6. A 28-day oral gavage toxicity study of 3-monochloropropane-1,2-diol (3-MCPD) in CB6F1-non-Tg rasH2 mice.

    PubMed

    Lee, Byoung-Seok; Park, Sang-Jin; Kim, Yong-Bum; Han, Ji-Seok; Jeong, Eun-Ju; Moon, Kyoung-Sik; Son, Hwa-Young

    2015-12-01

    3-Monochloro-1,2-propanediol (3-MCPD) is a well-known contaminant of foods containing hydrolyzed vegetable protein. However, limited toxicity data are available for the risk assessment of 3-MCPD and its carcinogenic potential is controversial. To evaluate the potential toxicity and determine the dose levels for a 26-week carcinogenicity test using Tg rasH2 mice, 3-MCPD was administered once daily by oral gavage at doses of 0, 25, 50, and 100 mg/kg body weight (b.w.)/day for 28 days to male and female CB6F1-non-Tg rasH2 mice (N = 5 males and females per dose). The standard toxicological evaluations were conducted during the in-life and post-mortem phase. In the 100 mg/kg b.w./day group, 3 males and 1 female died during the study and showed clinical signs such as thin appearance and subdued behavior accompanied by significant decreases in mean b.w. Microscopy revealed tubular basophilia in the kidneys, exfoliated degenerative germ cells in the lumen of the seminiferous tubule of the testes, vacuolation in the brain, axonal degeneration of the sciatic nerve, and cardiomyopathy in the 100, ≥25, ≥50, 100, and 100 mg/kg b.w./day groups, respectively. In conclusion, 3-MCPD's target organs were the kidneys, testes, brain, sciatic nerve, and heart. The "no-observed-adverse-effect level" (NOAEL) of 3-MCPD was ≤25 and 25 mg/kg b.w./day in males and females, respectively.

  7. Combined molecular docking, molecular dynamics simulation and quantitative structure-activity relationship study of pyrimido[1,2-c][1,3]benzothiazin-6-imine derivatives as potent anti-HIV drugs

    NASA Astrophysics Data System (ADS)

    Deng, Fangfang; Xie, Meihong; Zhang, Xiaoyun; Li, Peizhen; Tian, Yueli; Zhai, Honglin; Li, Yang

    2014-06-01

    3,4-Dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine is an antiretroviral agent, which can act against human immunodeficiency virus (HIV) infection, but the mechanism of action of pyrimido[1,2-c][1,3]benzothiazin-6-imine derivatives remained ambiguous. In this study, multiple linear regression (MLR) was applied to establish a quite reliable model with the squared correlation coefficient (R2) of 0.8079. We also used chemical information descriptors based on the simplified molecular input line entry system (SMILES) to get a better model with R2 of 0.9086 for the training set, and R2 of 0.8031 for the test set. Molecular docking was utilized to provide more useful information between pyrimido[1,2-c][1,3]benzothiazin-6-imine derivatives and HIV-1 protease, such as active site, binding mode and important residues. Molecular dynamics simulation was employed to further validate the docking results. This work may lead to a better understanding of the mechanism of action and aid to design novel and more potent anti-HIV drugs.

  8. Progress toward measuring the 6S1/2 <--> 5D3/2 magnetic-dipole transition moment in Ba+

    NASA Astrophysics Data System (ADS)

    Williams, Spencer; Jayakumar, Anupriya; Hoffman, Matthew; Blinov, Boris; Fortson, Norval

    2015-05-01

    We report the latest results from our effort to measure the magnetic-dipole transition moment (M1) between the 6S1 / 2 and 5D3 / 2 manifolds in Ba+. We describe a new technique for calibrating view-port birefringence and how we will use it to enhance the M1 signal. To access the transition moment we use a variation of a previously proposed technique that allows us to isolate the magnetic-dipole coupling from the much larger electric-quadrupole coupling in the transition rates between particular Zeeman sub-levels. Knowledge of M1 is crucial for a parity-nonconservation experiment in the ion where M1 will be a leading source of systematic errors. No measurement of this M1 has been made in Ba+, however, there are three calculations that predict it to be 80 ×10-5μB, 22 ×10-5μB, and 17 ×10-5μB. A precise measurement may help resolve this theoretical discrepancy which originates from their different estimations of many-body effects. Supported by NSF Grant No. 09-06494F.

  9. 12 CFR 37.6 - Disclosures.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... solicitation, subject to the requirements of § 37.7(c). (5) Special rule for electronic transactions. The... requirements of the Electronic Signatures in Global and National Commerce Act, 15 U.S.C. 7001 et seq. (d) Form... disclosures in writing at that time. (3) Special rule for transactions by telephone. If the contract...

  10. 12 CFR 6.2 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... definition of tangible equity. The OCC reserves the right to require a bank to compute and maintain its... requires, the terms used in this subpart have the same meanings as set forth in section 38 and section 3 of... person. (d) Leverage ratio means the ratio of Tier 1 capital to adjusted total assets, as calculated...

  11. High-Temperature Thermoelectric Properties of the Solid-Solution Zintl Phase Eu11Cd6Sb12-xAsx (x < 3)

    SciTech Connect

    Kazem, Nasrin; Xie, Weiwei; Ohno, Saneyuki; Zevalkink, Alexandra; Miller, Gordon J.; Snyder, G. Jeffrey; Kauzlarich, Susan M.

    2014-02-20

    Zintl phases are compounds that have shown promise for thermoelectric applications. The title solid–solution Zintl compounds were prepared from the elements as single crystals using a tin flux for compositions x = 0, 1, 2, and 3. Eu11Cd6Sb12–xAsx (x < 3) crystallize isostructurally in the centrosymmetric monoclinic space group C2/m (no. 12, Z = 2) as the Sr11Cd6Sb12 structure type (Pearson symbol mC58). Efforts to make the As compositions for x exceeding ~3 resulted in structures other than the Sr11Cd6Sb12 structure type. Single-crystal X-ray diffraction indicates that As does not randomly substitute for Sb in the structure but is site specific for each composition. The amount of As determined by structural refinement was verified by electron microprobe analysis. Electronic structures and energies calculated for various model structures of Eu11Cd6Sb10As2 (x = 2) indicated that the preferred As substitution pattern involves a mixture of three of the six pnicogen sites in the asymmetric unit. In addition, As substitution at the Pn4 site opens an energy gap at the Fermi level, whereas substitution at the other five pnicogen sites remains semimetallic with a pseudo gap. Thermoelectric properties of these compounds were measured on hot-pressed, fully densified pellets. Samples show exceptionally low lattice thermal conductivities from room temperature to 775 K: 0.78–0.49 W/mK for x = 0; 0.72–0.53 W/mK for x = 1; and 0.70–0.56 W/mK for x = 2. Eu11Cd6Sb12 shows a high p-type Seebeck coefficient (from +118 to 153 μ V/K) but also high electrical resistivity (6.8 to 12.8 mΩ·cm). The value of zT reaches 0.23 at 774 K. The properties of Eu11Cd6Sb12–xAsx are interpreted in discussion with the As site substitution.

  12. Folding model calculations for 6He+12C elastic scattering

    NASA Astrophysics Data System (ADS)

    Awad, A. Ibraheem

    2016-03-01

    In the framework of the double folding model, we used the α+2n and di-triton configurations for the nuclear matter density of the 6He nucleus to generate the real part of the optical potential for the system 6He+12C. As an alternative, we also use the high energy approximation to generate the optical potential for the same system. The derived potentials are employed to analyze the elastic scattering differential cross section at energies of 38.3, 41.6 and 82.3 MeV/u. For the imaginary part of the potential we adopt the squared Woods-Saxon form. The obtained results are compared with the corresponding measured data as well as with available results in the literature. The calculated total reaction cross sections are investigated and compared with the optical limit Glauber model description.

  13. Acute Toxicities of the Saxitoxin Congeners Gonyautoxin 5, Gonyautoxin 6, Decarbamoyl Gonyautoxin 2&3, Decarbamoyl Neosaxitoxin, C-1&2 and C-3&4 to Mice by Various Routes of Administration

    PubMed Central

    Selwood, Andrew I.; Waugh, Craig; Harwood, David T.; Rhodes, Lesley L.; Reeve, John; Sim, Jim; Munday, Rex

    2017-01-01

    Paralytic shellfish poisoning results from consumption of seafood naturally contaminated by saxitoxin and its congeners, the paralytic shellfish toxins (PSTs). The levels of such toxins are regulated internationally, and maximum permitted concentrations in seafood have been established in many countries. A mouse bioassay is an approved method for estimating the levels of PSTs in seafood, but this is now being superseded in many countries by instrumental methods of analysis. Such analyses provide data on the levels of many PSTs in seafood, but for risk assessment, knowledge of the relative toxicities of the congeners is required. These are expressed as “Toxicity Equivalence Factors” (TEFs). At present, TEFs are largely based on relative specific activities following intraperitoneal injection in a mouse bioassay rather than on acute toxicity determinations. A more relevant parameter for comparison would be median lethal doses via oral administration, since this is the route through which humans are exposed to PSTs. In the present study, the median lethal doses of gonyautoxin 5, gonyautoxin 6, decarbamoyl neosaxitoxin and of equilibrium mixtures of decarbamoyl gonyautoxins 2&3, C1&2 and C3&4 by oral administration to mice have been determined and compared with toxicities via intraperitoneal injection. The results indicate that the TEFs of several of these substances require revision in order to more accurately reflect the risk these toxins present to human health. PMID:28230783

  14. Acute Toxicities of the Saxitoxin Congeners Gonyautoxin 5, Gonyautoxin 6, Decarbamoyl Gonyautoxin 2&3, Decarbamoyl Neosaxitoxin, C-1&2 and C-3&4 to Mice by Various Routes of Administration.

    PubMed

    Selwood, Andrew I; Waugh, Craig; Harwood, David T; Rhodes, Lesley L; Reeve, John; Sim, Jim; Munday, Rex

    2017-02-21

    Paralytic shellfish poisoning results from consumption of seafood naturally contaminated by saxitoxin and its congeners, the paralytic shellfish toxins (PSTs). The levels of such toxins are regulated internationally, and maximum permitted concentrations in seafood have been established in many countries. A mouse bioassay is an approved method for estimating the levels of PSTs in seafood, but this is now being superseded in many countries by instrumental methods of analysis. Such analyses provide data on the levels of many PSTs in seafood, but for risk assessment, knowledge of the relative toxicities of the congeners is required. These are expressed as "Toxicity Equivalence Factors" (TEFs). At present, TEFs are largely based on relative specific activities following intraperitoneal injection in a mouse bioassay rather than on acute toxicity determinations. A more relevant parameter for comparison would be median lethal doses via oral administration, since this is the route through which humans are exposed to PSTs. In the present study, the median lethal doses of gonyautoxin 5, gonyautoxin 6, decarbamoyl neosaxitoxin and of equilibrium mixtures of decarbamoyl gonyautoxins 2&3, C1&2 and C3&4 by oral administration to mice have been determined and compared with toxicities via intraperitoneal injection. The results indicate that the TEFs of several of these substances require revision in order to more accurately reflect the risk these toxins present to human health.

  15. 12 CFR 128.6 - Loan application register.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false Loan application register. 128.6 Section 128.6... § 128.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the OCC in accordance with 12 CFR part 203 must enter...

  16. 12 CFR 128.6 - Loan application register.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Loan application register. 128.6 Section 128.6... § 128.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the OCC in accordance with 12 CFR part 203 must enter...

  17. 12 CFR 128.6 - Loan application register.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Loan application register. 128.6 Section 128.6... § 128.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the OCC in accordance with 12 CFR part 203 must enter...

  18. Synthesis, NMR conformational analysis and pharmacological evaluation of 7,7a,13,14-tetrahydro-6H-cyclobuta[b]pyrimido[1,2-a:3,4-a']diindole analogues as melatonin receptor ligands.

    PubMed

    Attia, Mohamed I; Güclü, Deniz; Hertlein, Barbara; Julius, Justin; Witt-Enderby, Paula A; Zlotos, Darius P

    2007-07-07

    A structure for the self-condensation product of 2-(1H-indol-2-yl)ethyl tosylate 2a, previously proposed as 6,7,14,15-tetrahydro-15aH-azocino[1,2-a:6,5-b]diindole 3a, was revised based on the (13)C-2D-INADEQUATE experiment, and proved to be 7,7a,13,14-tetrahydro-6H-cyclobuta[b]pyrimido[1,2-a:3,4-a']diindole 4a. A mechanism for the unexpected formation of this novel hexacyclic heterocycle was proposed and its NMR solution structure was elucidated. Five derivatives of the title ring skeleton 12-16 designed as melatonin receptor ligands were synthesized and their affinities for the human MT(1) and MT(2) receptors were determined. Both butyramides 13 and 15, as well as the non-methoxy acetamide 12 exhibited micromolar binding affinities for both receptors being slightly MT(2) selective. The methoxy acetamide 14 showed the best pharmacological profile exhibiting a five times higher affinity for MT(1) (K(i) = 49 nM) than for MT(2) (K(i) = 246 nM) receptor.

  19. 6. VIEW OF THREE BEARS LAKE, SHOWING WASHED UP 12' ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    6. VIEW OF THREE BEARS LAKE, SHOWING WASHED UP 12' x 12' DAM SUPPORT TIMBERS, LOOKING NORTHEAST FROM SOUTH SIDE OF LAKE - Three Bears Lake & Dams, North of Marias Pass, East Glacier Park, Glacier County, MT

  20. Maternal Diet Supplementation with n-6/n-3 Essential Fatty Acids in a 1.2 : 1.0 Ratio Attenuates Metabolic Dysfunction in MSG-Induced Obese Mice

    PubMed Central

    Martin, Josiane Morais; Miranda, Rosiane Aparecida; Palma-Rigo, Kesia; Alves, Vander Silva; Fabricio, Gabriel Sergio; Pavanello, Audrei; Franco, Claudinéia Conationi da Silva; Ribeiro, Tatiane Aparecida; Visentainer, Jesuí Vergílio; Banafé, Elton Guntendeorfer; Martin, Clayton Antunes; Mathias, Paulo Cezar de Freitas

    2016-01-01

    Essential polyunsaturated fatty acids (PUFAs) prevent cardiometabolic diseases. We aimed to study whether a diet supplemented with a mixture of n-6/n-3 PUFAs, during perinatal life, attenuates outcomes of long-term metabolic dysfunction in prediabetic and obese mice. Seventy-day-old virgin female mice were mated. From the conception day, dams were fed a diet supplemented with sunflower oil and flaxseed powder (containing an n-6/n-3 PUFAs ratio of 1.2 : 1.0) throughout pregnancy and lactation, while control dams received a commercial diet. Newborn mice were treated with monosodium L-glutamate (MSG, 4 mg g−1 body weight per day) for the first 5 days of age. A batch of weaned pups was sacrificed to quantify the brain and pancreas total lipids; another batch were fed a commercial diet until 90 days of age, where glucose homeostasis and glucose-induced insulin secretion (GIIS) as well as retroperitoneal fat and Lee index were assessed. MSG-treated mice developed obesity, glucose intolerance, insulin resistance, pancreatic islet dysfunction, and higher fat stores. Maternal flaxseed diet-supplementation decreased n-6/n-3 PUFAs ratio in the brain and pancreas and blocked glucose intolerance, insulin resistance, GIIS impairment, and obesity development. The n-6/n-3 essential PUFAs in a ratio of 1.2 : 1.0 supplemented in maternal diet during pregnancy and lactation prevent metabolic dysfunction in MSG-obesity model. PMID:28050167

  1. Divalent metal incorporation in MIL-74, the super-sodalite aluminum phosphates MAl 6(PO 4) 12ṡ4 trenṡ17H 2O ( M=Mg, Mn, Co) and its gallium phosphate analogs M3'Ga 6(PO 4) 12ṡ4 trenṡ17H 2O ( M=Mg, Mn, Co, Fe, Zn)

    NASA Astrophysics Data System (ADS)

    Loiseau, Thierry; Beitone, Lionel; Taulelle, Francis; Férey, Gérard

    2006-03-01

    The mixed metal(II)-aluminum phosphates MAl 6(PO 4) 12ṡ4 trenṡ17H 2O ( M=Mg 2+, Mn 2+, Co 2+) and its gallium phosphate analogs M3'Ga 6(PO 4) 12ṡ4 trenṡ17H 2O ( M=Mg 2+, Mn 2+, Fe 2+, Co 2+, Zn 2+) have been hydrothermally synthesized with the tris(2-aminoethyl)amine ( tren) as a structure-directing agent (453 K, 36 hours, autogenous pressure). The solids were characterized by single-crystal X-ray diffraction. Their crystal structures are cubic, a≈16.8 Å and may be described in I -43m. The open-framework is built up from an enneameric unit ( T=Al or Ga / Mg, Mn, Fe, Co, Zn) containing five TO and four PO 4 tetrahedra (one of the P sbnd O bonding is terminal). A central TO tetrahedral unit shares all the corners with four phosphate groups. Two phosphate groups are connected to two other peripheral TO units. It results in the formation of a "pseudo" planar building block TP consisting of four square 4-rings. The connection of the TP units generates a three-dimensional framework, which defines a super-sodalite topology. The resulting cavities (diameter of 10 Å) are bound by 12-ring windows in which are located the tren species in interaction with the phosphate groups (mainly terminal P sbnd O bonding) through hydrogen bond. A (H 2O) 17 cluster is encapsulated in the super-sodalite cages. The Tsbnd O distances are discussed according to the ionic radii of the trivalent cations (Al, Ga) and the different divalent cations (Mg, Mn, Fe, Co, Zn).

  2. The responses of selected terrestrial plants to short (<12 days) and long term (2, 4 and 6 weeks) hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) exposure. Part I: Growth and developmental effects.

    PubMed

    Winfield, Linda E; Rodgers, John H; D'Surney, Stephen J

    2004-05-01

    Soils contaminated with explosive materials like hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is a concern nation-wide on military installations and sites where explosives are manufactured, stored, or disposed. Terrestrial plants are a vital group of receptor organism, yet limited published information is available on the potential impacts of RDX exposure in terrestrial plants. This research comprised the initial phases in the development of a short-term (<12 days) screening experiment for assessing the environmental impacts of RDX exposure in terrestrial plants. Fifteen plants (dicots and monocots) were exposed to three soils amended with 0-4000 microg g(-1) of RDX during the short-term screening experiments. Growth responses (maximum root and shoot lengths, percent emergence) and adverse developmental effects were the assessment endpoints. Sunflower was identified as the most RDX sensitive plant and selected for evaluation during the long-term (2, 4, and 6 weeks) experiments. Two life stages of sunflower (embryos and 2-week old seedlings) were exposed to Grenada soil amended with 0-100 microg g(-1) of RDX. The assessment endpoints during the long-term experiments included: biomass, maximum shoot and root length, root bio-volume, maximum stem diameter, number of leaves, and adverse developmental effects. Statistically significant differences were measured in several of the growth parameters following the short and long term exposure studies, however there were no consistent patterns. The consistent indicators of detrimental impacts from RDX exposure were the adverse developmental effects observed, regardless of life stage, soil type, or exposure duration. Typically, more adverse developmental effects were observed in dicots than monocots. The efficacy of the short-term screening experiments for estimating the impacts of long-term RDX exposure was validated.

  3. Tatarinovite Ca3Al(SO4)[B(OH)4](OH)6 · 12H2O, a new ettringite-group mineral from the Bazhenovskoe deposit, Middle Urals, Russia, and its crystal structure

    NASA Astrophysics Data System (ADS)

    Chukanov, N. V.; Kasatkin, A. V.; Zubkova, N. V.; Britvin, S. N.; Pautov, L. A.; Pekov, I. V.; Varlamov, D. A.; Bychkova, Ya. V.; Loskutov, A. B.; Novgorodova, E. A.

    2016-12-01

    A new mineral, tatarinovite, ideally Ca3Al(SO4)[B(OH)4](OH)6 · 12H2O, has been found in cavities of rhodingites at the Bazhenovskoe chrysotile asbestos deposit, Middle Urals, Russia. It occurs (1) colorless, with vitreous luster, bipyramidal crystals up to 1 mm across in cavities within massive diopside, in association with xonotlite, clinochlore, pectolite and calcite, and (2) as white granular aggregates up to 5 mm in size on grossular with pectolite, diopside, calcite, and xonotlite. The Mohs hardness is 3; perfect cleavage on (100) is observed. D meas = 1.79(1), D calc = 1.777 g/cm3. Tatarinovite is optically uniaxial (+), ω = 1.475(2), ɛ = 1.496(2). The IR spectrum contains characteristic bands of SO4 2-, CO3 2-, B(OH)4 -, B(OH)3, Al(OH)6 3-, Si(OH)6 2-, OH-, and H2O. The chemical composition of tatarinovite (wt %; ICP-AES; H2O was determined by the Alimarin method; CO2 was determined by selective sorption on askarite) is as follows: 27.40 CaO, 4.06 B2O3, 6.34 A12O3, 0.03 Fe2O3, 2.43 SiO2, 8.48 SO3, 4.2 CO2, 46.1 H2O, total is 99.04. The empirical formula (calculated on the basis of 3Ca apfu) is H31.41Ca3.00(Al0.76Si0.25)Σ1.01 · (B0.72S0.65C0.59)Σ1.96O24.55. Tatarinovite is hexagonal, space gr. P63, a = 11.1110(4) Å, c = 10.6294(6) Å, V = 1136.44(9) A3, Z = 2. Its crystal chemical formula is Ca3(Al0.70Si0.30) · {[SO4]0.34[B(OH)4]0.33[CO3]0.24}{[SO4]0.30[B(OH)4]0.34[CO3]0.30[B(OH)3]0.06}(OH5·73O0.27) · 12H2O. The strongest reflections of the powder X-ray diffraction pattern [ d, Å ( I, %) ( hkl)] are 9.63 (100) (100), 5.556 (30) (110), 4.654 (14) (102), 3.841 (21) (112), 3.441 (12) (211), 2.746 (10) (302), 2.538 (12) (213). Tatarinovite was named in memory of the Russian geologist and petrologist Pavel Mikhailovich Tatarinov (1895-1976), a well-known specialist in chrysotile asbestos deposits. Type specimens have been deposited at the Fersman Mineralogical Museum of the Russian Academy of Sciences, Moscow.

  4. Lipopolysaccharide inhibits transforming growth factor-beta1-stimulated Smad6 expression by inducing phosphorylation of the linker region of Smad3 through a TLR4-IRAK1-ERK1/2 pathway.

    PubMed

    Kim, Eun-Ye; Kim, Byung-Chul

    2011-03-09

    Smad6, one of the inhibitory Smads, plays an important role in transforming growth factor-beta1 (TGF-β1)-mediated negative regulation of pro-inflammatory signaling. In this study, we found that bacterial endotoxin lipopolysaccharide (LPS) inhibits TGF-β1-induced expression of Smad6 in RAW264.7 cells. This repression was accompanied by increased Smad3 linker phosphorylation at Thr-179 and Ser-208 and was dependent on ERK1/2 activity via the TLR4-IRAK1-linked signaling cascade. The expression of a mutant Smad3, that lacks the phosphorylation sites in the linker regions, significantly reversed the inhibitory effect of LPS on TGF-β1-induced Smad6 expression and its anti-inflammatory capacity. Collectively, our findings show how LPS pro-inflammatory signal antagonizes the anti-inflammatory activity of TGF-β1.

  5. In vitro and in vivo studies of 6,8-(diaryl)imidazo[1,2-a]pyrazin-3(7H)-ones as new antioxidants.

    PubMed

    De Wael, Frederic; Jeanjot, Paul; Moens, Cédric; Verbeuren, Tony; Cordi, Alex; Bouskela, Eliete; Rees, Jean-François; Marchand-Brynaert, Jacqueline

    2009-07-01

    A series of 5-aryl and 3,5-diaryl-2-amino-1,4-pyrazines and the derived imidazopyrazinones has been synthesized to study the chemical oxidative degradation of the bicyclic systems in vitro. Imidazopyrazinones mainly degraded following two independent pathways producing their precursors, namely aminopyrazines, and the corresponding amidopyrazines, respectively. Despite the fact that there is no influence of the substituent of the 3-aryl group on the ratio of the products aminopyrazine/amidopyrazine, diarylimidazopyrazinones and diarylaminopyrazines are good antioxidants in vivo. They protected against microvascular damages in ischemia/reperfusion with similar efficiencies.

  6. 12 CFR 707.6 - Periodic statement disclosures.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Periodic statement disclosures. 707.6 Section 707.6 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS TRUTH IN SAVINGS § 707.6 Periodic statement disclosures. (a) Rule when statement and crediting periods...

  7. 12 CFR 704.6 - Credit risk management.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Credit risk management. 704.6 Section 704.6... CREDIT UNIONS § 704.6 Credit risk management. (a) Policies. A corporate credit union must operate according to a credit risk management policy that is commensurate with the investment risks and...

  8. 12 CFR 528.6 - Loan application register.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 6 2013-01-01 2012-01-01 true Loan application register. 528.6 Section 528.6... REQUIREMENTS § 528.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the Office of Thrift Supervision in accordance...

  9. 12 CFR 528.6 - Loan application register.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 6 2012-01-01 2012-01-01 false Loan application register. 528.6 Section 528.6... REQUIREMENTS § 528.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the Office of Thrift Supervision in accordance...

  10. 12 CFR 528.6 - Loan application register.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 6 2014-01-01 2012-01-01 true Loan application register. 528.6 Section 528.6... REQUIREMENTS § 528.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the Office of Thrift Supervision in accordance...

  11. 12 CFR 705.6 - Community needs plan.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Community needs plan. 705.6 Section 705.6 Banks... DEVELOPMENT REVOLVING LOAN PROGRAM FOR CREDIT UNIONS § 705.6 Community needs plan. (a) The credit union's board of directors will prepare a Community Needs Plan and submit it with its loan application. The...

  12. 12 CFR 508.6 - Initiation of hearing.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 6 2013-01-01 2012-01-01 true Initiation of hearing. 508.6 Section 508.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY REMOVALS, SUSPENSIONS, AND PROHIBITIONS WHERE A CRIME IS CHARGED OR PROVEN § 508.6 Initiation of hearing. (a) Within 10 days of the...

  13. 12 CFR 508.6 - Initiation of hearing.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 6 2012-01-01 2012-01-01 false Initiation of hearing. 508.6 Section 508.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY REMOVALS, SUSPENSIONS, AND PROHIBITIONS WHERE A CRIME IS CHARGED OR PROVEN § 508.6 Initiation of hearing. (a) Within 10 days of the...

  14. 12 CFR 725.6 - Termination of membership.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 6 2011-01-01 2011-01-01 false Termination of membership. 725.6 Section 725.6... CREDIT UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.6 Termination of membership. (a) A member of... stock may withdraw from membership in the Facility six months after notifying the NCUA Board in...

  15. 12 CFR 725.6 - Termination of membership.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Termination of membership. 725.6 Section 725.6 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS NATIONAL CREDIT UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.6 Termination of membership. (a) A member...

  16. Synthesis, crystal structure and magnetic properties of new indium rhenium and scandium rhenium oxides, In 6ReO 12 and Sc 6ReO 12

    NASA Astrophysics Data System (ADS)

    Mikhailova, D.; Ehrenberg, H.; Fuess, H.

    2006-12-01

    The new complex indium rhenium and scandium rhenium oxides, In 6ReO 12 and Sc 6ReO 12, have been synthesized as single phases in sealed silica tubes and by high-pressure high-temperature syntheses, and their crystal structures have been determined by single crystal X-ray diffraction.The compounds crystallize in a rhombohedral structure related to the distorted fluorite structure like Ln 6ReO 12 for some rare earth elements, S. G.: R-3, Z=3, aH= 9.248(2) Å, cH=8.720(2) Å for Sc 6ReO 12 and aH=9.492(1) Å, cH=8.933(1) Å for In 6ReO 12. A maximum in magnetization is observed for Sc 6ReO 12 at T( Mmax)=1.89(2) K, whereas ferromagnetic ordering is found for In 6ReO 12 by a pronounced increase in the temperature dependence of magnetization at TC=7.5(5) K. The magnetic moment per rhenium ion in In 6ReO 12 and Sc 6ReO 12 is 0.84(1) and 0.65(1) μB, respectively, derived from the paramagnetic regions.

  17. Cs{sub 7}Sm{sub 11}[TeO{sub 3}]{sub 12}Cl{sub 16} and Rb{sub 7}Nd{sub 11}[TeO{sub 3}]{sub 12}Br{sub 16}, the new tellurite halides of the tetragonal Rb{sub 6}LiNd{sub 11}[SeO{sub 3}]{sub 12}Cl{sub 16} structure type

    SciTech Connect

    Charkin, Dmitri O.; Black, Cameron; Downie, Lewis J.; Sklovsky, Dmitry E.; Berdonosov, Peter S.; Olenev, Andrei V.; Zhou, Wuzong; Lightfoot, Philip; Dolgikh, Valery A.

    2015-12-15

    Two new rare-earth – alkali – tellurium oxide halides were synthesized by a salt flux technique and characterized by single-crystal X-ray diffraction. The structures of the new compounds Cs{sub 7}Sm{sub 11}[TeO{sub 3}]{sub 12}Cl{sub 16} (I) and Rb{sub 7}Nd{sub 11}[TeO{sub 3}]{sub 12}Br{sub 16} (II) (both tetragonal, space group I4/mcm) correspond to the sequence of [MLn{sub 11}(TeO{sub 3}){sub 12}] and [M{sub 6}X{sub 16}] layers and bear very strong similarities to those of known selenite analogs. We discuss the trends in similarities and differences in compositions and structural details between the Se and Te compounds; more members of the family are predicted. - Graphical abstract: Two new rare-earth – alkali – tellurium oxide halides were predicted and synthesized. - Highlights: • Two new rare-earth – alkali – tellurium oxide halides were synthesized. • They adopt slab structure of rare earth-tellurium-oxygen and CsCl-like slabs. • The Br-based CsCl-like slabs have been observed first in this layered family.

  18. 12 CFR 265.6 - Functions delegated to General Counsel.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... incomplete under that Act or Regulation Y (12 CFR part 225) or contains material information that is... 12 Banks and Banking 4 2013-01-01 2013-01-01 false Functions delegated to General Counsel. 265.6... Rules of Procedure (12 CFR part 262), in connection with any application or notice filed with the...

  19. 12 CFR 265.6 - Functions delegated to General Counsel.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... incomplete under that Act or Regulation Y (12 CFR part 225) or contains material information that is... 12 Banks and Banking 4 2014-01-01 2014-01-01 false Functions delegated to General Counsel. 265.6... Rules of Procedure (12 CFR part 262), in connection with any application or notice filed with the...

  20. 12 CFR 265.6 - Functions delegated to General Counsel.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... incomplete under that Act or Regulation Y (12 CFR part 225) or contains material information that is... 12 Banks and Banking 4 2012-01-01 2012-01-01 false Functions delegated to General Counsel. 265.6... Rules of Procedure (12 CFR part 262), in connection with any application or notice filed with the...

  1. Synthesis, evaluation and structure-activity relationships of 5-alkyl-2,3-dihydroimidazo[1,2-c] quinazoline, 2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-thiones and their oxo-analogues as new potential bronchodilators.

    PubMed

    Bahekar, R H; Rao, A R

    2001-01-01

    With an aim to obtain potent bronchodilators, two series of 5-alkyl-2,3-dihydroimidazo[1,2-c]quinazolines (Va-1), 2,3-dihydroimidazo[1,2-c]quinazolin-5-(6H)-thiones (VIIIa-d) and their oxo-analogues (IXa-d) have been designed. The compounds Va-1 were synthesized by two alternative routes. The former (Method A) based on the dehydrocyclization of 4-(1-hydroxyethyl)-aminoquinazoline (IV) and the latter (Method B) involves the usage of 2-aminobenzonitrile (VI) which on reaction with ethylenediamine leads to the formation of the key intermediate 2-(2-aminophenyl)-4,5-dihydro-1H-imidazoles (VII). Finally the intermediate VII on condensation with different acidanhydrides yielded the title compound V. In general method-A resulted the compound V in quantitatively higher yields. 2,3-Dihydroimidazo[1,2-c]quinazolin-5 (6H)-thiones (VIII) were obtained by condensing VII with carbon disulfide and a further oxidation of VIII gave their corresponding oxo-analogues (IX). The title compounds V, VIII and IX were evaluated for their bronchodilator activity using in vitro and in vivo (standard animal models) methods. All the test compounds exhibited bronchodilatory activity. The structure activity relationship studies indicated good correlation between the nature of the substituent and bronchodilatory activity. In the 5-alkyl substituted compounds V, a longer alkyl chain showed higher bronchodilatory activity. Compounds VIII and IX were found to be less potent and replacement of sulphur with oxygen showed no significant effect on the biological activity. The presence of halogens altered the biological activity in both the series. Among the compounds tested, 9-lodo-5-(n-propyl)-2,3-dihydroimidazo[1,2-c]quinazoline (VI) was found to be the most potent (percentage protection = 87.1%; relative activity = 1.1 compared to the standard aminophylline).

  2. Crystal structure of 13-phenyl-2,3,4,13-tetra-hydro-1H-indazolo[1,2-b]phthalazine-1,6,11-trione.

    PubMed

    Lamera, Esma; Benzerka, Saida; Bouraiou, Abdelmalek; Bouacida, Sofiane; Merazig, Hocine; Chibani, Aissa; Le Borgne, Marc; Bouaziz, Zouhair

    2015-12-01

    The title compound, C21H16N2O3, consists of an indazolone moiety, bearing a phenyl group, fused to a phthalazine ring system (r.m.s. deviation = 0.018 Å). The phenyl ring is almost normal to the mean plane of the five-membered ring of the indazolone moiety, making a dihedral angle of 89.64 (7)°. The six-membered ring of the indazolone moiety has an envelope conformation, with the central methyl-ene C atom as the flap. In the crystal, mol-ecules are linked via C-H⋯O hydrogen bonds, forming slabs parallel to the bc plane. The slabs are linked via C-H⋯π and π-π inter-actions [the shortest inter-centroid distance involving rings of pyrazolo-phthalazine moieties is 3.6430 (8) Å], forming a three-dimensional structure.

  3. 1-{2-Hy­droxy-6-[3-(pyrrol-1-yl)prop­oxy]phen­yl}ethanone

    PubMed Central

    Ourari, Ali; Aggoun, Djouhra; Bouacida, Sofiane

    2012-01-01

    In the title compound, C15H17NO3, the mean planes of the pyrrole and benzene rings form a dihedral angle of 81.92 (7)°. The mol­ecule contains an intra­molecular O—H⋯O hydrogen bond. In the crystal, weak C—H⋯π inter­actions link the mol­ecules into chains along [010]. PMID:22589947

  4. 12 CFR 1273.3 - Functions of the OF.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... section 21B(c)(6)(B) of the Bank Act (12 U.S.C. 1441b(c)(6)(B)). ... 12 Banks and Banking 9 2012-01-01 2012-01-01 false Functions of the OF. 1273.3 Section 1273.3... principal and interest due) consolidated obligations. (b) Preparation of combined financial reports. The...

  5. 12 CFR 1273.3 - Functions of the OF.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... section 21B(c)(6)(B) of the Bank Act (12 U.S.C. 1441b(c)(6)(B)). ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Functions of the OF. 1273.3 Section 1273.3... principal and interest due) consolidated obligations. (b) Preparation of combined financial reports. The...

  6. 12 CFR 1273.3 - Functions of the OF.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... section 21B(c)(6)(B) of the Bank Act (12 U.S.C. 1441b(c)(6)(B)). ... 12 Banks and Banking 9 2013-01-01 2013-01-01 false Functions of the OF. 1273.3 Section 1273.3... principal and interest due) consolidated obligations. (b) Preparation of combined financial reports. The...

  7. Unusual reactions of [{micro-(phthalazine-N2:N3)}Fe2(micro-CO)(CO)6] with organolithium reagents. A novel coordination mode of 1,2-diazane diiron carbonyl compounds.

    PubMed

    Xiao, Nu; Xu, Qiang; Sun, Jie; Chen, Jiabi

    2006-01-28

    [{Micro-(phthalazine-N2:N3)}Fe2(micro-CO)(CO)6](1) reacts with organolithium reagents, RLi (R = CH3, C6H5, p-CH3C6H4, p-CH3OC6H4, p-CF3C6H4, p-C6H5C6H4), followed by treatment with Me3SiCl to give the novel diiron carbonyl complexes with a saturated N-N six-membered diazane ring ligand, [{C6H4CH(R)NNCH2}Fe2(C=O)(CO)6](2, R = CH3; 3, R = C6H5; 4, R =p-CH3C6H4; 5, R =p-CH3OC6H4; 6, R =p-CF3C6H4; 7, R =p-C6H5C6H4). Compounds 4 and 5 were treated with [(NH4)2Ce(NO3)6] to afford the aryl-substituted phthalazine-coordinated diiron carbonyl compounds [(micro-{1-(p-CH3C6H4)-phthalazine-N2:N3})Fe2(micro-CO)(CO)6](8) and [(micro-{1-(p-CH3OC6H4)-phthalazine-N2:N3})Fe2(micro-CO)(CO)6](9), respectively. The structures of complexes 4 and 9 have been established by X-ray diffraction studies.

  8. Analysis of stereoelectronic properties, mechanism of action and pharmacophore of synthetic indolo[2,1-b]quinazoline-6,12-dione derivatives in relation to antileishmanial activity using quantum chemical, cyclic voltammetry and 3-D-QSAR CATALYST procedures.

    PubMed

    Bhattacharjee, Apurba K; Skanchy, David J; Jennings, Barton; Hudson, Thomas H; Brendle, James J; Werbovetz, Karl A

    2002-06-01

    Several indolo[2,1-b]quinazoline-6,12-dione (tryptanthrin) derivatives exhibited remarkable activity at concentrations below 100 ng/mL when tested against in vitro Leishmania donovani amastigotes. The in vitro toxicity studies indicate that the compounds are fairly well tolerated in both macrophage and neuronal lines. An analysis based on qualitative and quantitative structure-activity relationship studies between in vitro antileishmanial activity and molecular electronic structure of 27 analogues of indolo[2,1-b]quinazoline-6,12-dione is presented here by using a combination of semi-empirical AM1 quantum chemical, cyclic voltammetry and a pharmacophore generation (CATALYST) methods. A modest to good correlation is observed between activity and a few calculated molecular properties such as molecular density, octanol-water partition coefficient, molecular orbital energies, and redox potentials. Electron transfer seems to be a plausible path in the mechanism of action of the compounds. A pharmacophore generated by using the 3-D QSAR of CATALYST produced a fairly accurate predictive model of antileishmanial activity of the tryptanthrins. The validity of the pharmacophore model extends to structurally different class of compounds that could open new frontiers for study. The carbonyl group of the five- and six-membered rings in the indolo[2,1-b]quinazoline-6,12-dione skeleton and the electron transfer ability to the carbonyl atom appear to be crucial for activity.

  9. 7 CFR 12.3 - Applicability.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 7 Agriculture 1 2013-01-01 2013-01-01 false Applicability. 12.3 Section 12.3 Agriculture Office of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12.3..., 1990, for certain actions and determinations regarding wetlands and converted wetlands. Actions...

  10. 7 CFR 12.3 - Applicability.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 1 2010-01-01 2010-01-01 false Applicability. 12.3 Section 12.3 Agriculture Office of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12.3... actions and determinations regarding wetlands and converted wetlands. Actions taken and...

  11. 7 CFR 12.3 - Applicability.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 7 Agriculture 1 2012-01-01 2012-01-01 false Applicability. 12.3 Section 12.3 Agriculture Office of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12.3..., 1990, for certain actions and determinations regarding wetlands and converted wetlands. Actions...

  12. 7 CFR 12.3 - Applicability.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 1 2011-01-01 2011-01-01 false Applicability. 12.3 Section 12.3 Agriculture Office of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12.3... actions and determinations regarding wetlands and converted wetlands. Actions taken and...

  13. 7 CFR 12.3 - Applicability.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 7 Agriculture 1 2014-01-01 2014-01-01 false Applicability. 12.3 Section 12.3 Agriculture Office of the Secretary of Agriculture HIGHLY ERODIBLE LAND AND WETLAND CONSERVATION General Provisions § 12.3..., 1990, for certain actions and determinations regarding wetlands and converted wetlands. Actions...

  14. 50 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 50 Wildlife and Fisheries 1 2010-10-01 2010-10-01 false Definitions. 12.3 Section 12.3 Wildlife... FORFEITURE PROCEDURES General Provisions § 12.3 Definitions. (a) As used in this part: (1) Attorney General... price at which the seized property or similar property is freely offered for sale at the time and...

  15. Tris(2-ethylamino)amine ( tren) as template for the elaboration of fluorides: synthesis and crystal structures of [(C 2H 4NH 3) 3NH]·[Zr 3F 16(H 2O)], [(C 2H 4NH 3) 3N] 2·[ZrF 6]·[Zr 2F 12] and [(C 2H 4NH 3) 3N]·[TaF 7]·F

    NASA Astrophysics Data System (ADS)

    Goreshnik, E.; Leblanc, M.; Maisonneuve, V.

    2004-11-01

    Using tris(2-ethylamino)amine ( tren) as a template, three new fluorides are obtained by solvothermal synthesis: [(C 2H 4NH 3) 3NH]·[Zr 3F 16(H 2O)] ( I), [(C 2H 4NH 3) 3N] 2·[ZrF 6]·[Zr 2F 12] ( II) and [(C 2H 4NH 3) 3N]·[TaF 7]·F ( III). The structure determinations are performed by single crystal technique. The structure of I consists of infinite spiral-like [Zr 3F 16(H 2O)] 4- chains connected by tetraprotonated [ trenH 4] 4+ cations which possess a plane configuration. In II, isolated [ZrF 6] octahedra or [Zr 2F 12] dimers are linked to organic cations by a tridimensional hydrogen bond network. In III, [TaF 7] 2- monocapped trigonal prisms and "isolated" fluoride ions are connected by hydrogen bonds to template moieties. In II and III, every organic moiety is triprotonated [ trenH 3] 3+ with a "spider" configuration. In the tantalum phase, the hydrogen bond network leads to the formation of a layered structure.

  16. 12 CFR 908.6 - Civil money penalties.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Civil money penalties. 908.6 Section 908.6... Proceedings § 908.6 Civil money penalties. (a) Notice of assessment—(1) Grounds. The Finance Board may issue and serve a notice of assessment of a civil money penalty on any Bank or any executive officer...

  17. 12 CFR 908.6 - Civil money penalties.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Civil money penalties. 908.6 Section 908.6... Proceedings § 908.6 Civil money penalties. (a) Notice of assessment—(1) Grounds. The Finance Board may issue and serve a notice of assessment of a civil money penalty on any Bank or any executive officer...

  18. 12 CFR 995.6 - Budget and expenses.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 8 2013-01-01 2013-01-01 false Budget and expenses. 995.6 Section 995.6 Banks... § 995.6 Budget and expenses. (a) Directorate approval. The Financing Corporation shall submit annually to the Directorate for approval, a budget of proposed expenditures for the next calendar year...

  19. 12 CFR 995.6 - Budget and expenses.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Budget and expenses. 995.6 Section 995.6 Banks... § 995.6 Budget and expenses. (a) Directorate approval. The Financing Corporation shall submit annually to the Directorate for approval, a budget of proposed expenditures for the next calendar year...

  20. 12 CFR 995.6 - Budget and expenses.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 8 2012-01-01 2012-01-01 false Budget and expenses. 995.6 Section 995.6 Banks... § 995.6 Budget and expenses. (a) Directorate approval. The Financing Corporation shall submit annually to the Directorate for approval, a budget of proposed expenditures for the next calendar year...

  1. 12 CFR 108.6 - Initiation of hearing.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Initiation of hearing. 108.6 Section 108.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY REMOVALS, SUSPENSIONS, AND PROHIBITIONS WHERE A CRIME IS CHARGED OR PROVEN § 108.6 Initiation of hearing. (a) Within 10 days of the...

  2. 12 CFR 995.6 - Budget and expenses.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Budget and expenses. 995.6 Section 995.6 Banks... § 995.6 Budget and expenses. (a) Directorate approval. The Financing Corporation shall submit annually to the Directorate for approval, a budget of proposed expenditures for the next calendar year...

  3. 12 CFR 1030.6 - Periodic statement disclosures.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 9 2014-01-01 2014-01-01 false Periodic statement disclosures. 1030.6 Section 1030.6 Banks and Banking BUREAU OF CONSUMER FINANCIAL PROTECTION TRUTH IN SAVINGS (REGULATION DD) § 1030.6 Periodic statement disclosures. (a) General rule. If a depository institution mails or...

  4. 12 CFR 303.6 - Investigations and examinations.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Investigations and examinations. 303.6 Section 303.6 Banks and Banking FEDERAL DEPOSIT INSURANCE CORPORATION PROCEDURE AND RULES OF PRACTICE FILING PROCEDURES Rules of General Applicability § 303.6 Investigations and examinations. The FDIC may examine...

  5. 12 CFR 528.6 - Loan application register.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Loan application register. 528.6 Section 528.6... REQUIREMENTS § 528.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the Office of Thrift Supervision in accordance...

  6. 12 CFR 528.6 - Loan application register.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 5 2011-01-01 2011-01-01 false Loan application register. 528.6 Section 528.6... REQUIREMENTS § 528.6 Loan application register. Savings associations and other lenders required to file Home Mortgage Disclosure Act Loan Application Registers with the Office of Thrift Supervision in accordance...

  7. 12 CFR 108.6 - Initiation of hearing.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false Initiation of hearing. 108.6 Section 108.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY REMOVALS, SUSPENSIONS, AND PROHIBITIONS WHERE A CRIME IS CHARGED OR PROVEN § 108.6 Initiation of hearing. (a) Within 10 days of the...

  8. 12 CFR 508.6 - Initiation of hearing.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Initiation of hearing. 508.6 Section 508.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY REMOVALS, SUSPENSIONS, AND PROHIBITIONS WHERE A CRIME IS CHARGED OR PROVEN § 508.6 Initiation of hearing. (a) Within 10 days of the...

  9. 12 CFR 630.6 - Funding Corporation committees.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 6 2011-01-01 2011-01-01 false Funding Corporation committees. 630.6 Section 630.6 Banks and Banking FARM CREDIT ADMINISTRATION FARM CREDIT SYSTEM DISCLOSURE TO INVESTORS IN... oversee the Funding Corporation's preparation of the report to stockholders and investors; review...

  10. 12 CFR 46.6 - Stress test methodologies and practices.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Stress test methodologies and practices. 46.6 Section 46.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY ANNUAL STRESS TEST § 46.6 Stress test methodologies and practices. (a) Potential impact on capital. During each quarter...

  11. 12 CFR 46.6 - Stress test methodologies and practices.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false Stress test methodologies and practices. 46.6 Section 46.6 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY ANNUAL STRESS TEST § 46.6 Stress test methodologies and practices. (a) Potential impact on capital. During each quarter...

  12. 12 CFR 508.6 - Initiation of hearing.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 5 2011-01-01 2011-01-01 false Initiation of hearing. 508.6 Section 508.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY REMOVALS, SUSPENSIONS, AND PROHIBITIONS WHERE A CRIME IS CHARGED OR PROVEN § 508.6 Initiation of hearing. (a) Within 10 days of the...

  13. 12 CFR 725.6 - Termination of membership.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 7 2013-01-01 2013-01-01 false Termination of membership. 725.6 Section 725.6... CREDIT UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.6 Termination of membership. (a) A member of... stock may withdraw from membership in the Facility six months after notifying the NCUA Board in...

  14. 12 CFR 725.6 - Termination of membership.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 7 2012-01-01 2012-01-01 false Termination of membership. 725.6 Section 725.6... CREDIT UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.6 Termination of membership. (a) A member of... stock may withdraw from membership in the Facility six months after notifying the NCUA Board in...

  15. 12 CFR 704.6 - Credit risk management.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 7 2014-01-01 2014-01-01 false Credit risk management. 704.6 Section 704.6 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS CORPORATE CREDIT UNIONS § 704.6 Credit risk management. (a) Policies. A corporate credit union must...

  16. 12 CFR 1403.6 - Special procedures for medical records.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Special procedures for medical records. 1403.6 Section 1403.6 Banks and Banking FARM CREDIT SYSTEM INSURANCE CORPORATION PRIVACY ACT REGULATIONS § 1403.6 Special procedures for medical records. Medical records in the custody of the Farm Credit System...

  17. 12 CFR 980.6 - Finance Board consent.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Finance Board consent. 980.6 Section 980.6 Banks and Banking FEDERAL HOUSING FINANCE BOARD NEW FEDERAL HOME LOAN BANK ACTIVITIES NEW BUSINESS ACTIVITIES § 980.6 Finance Board consent. The Finance Board may at any time provide consent for a Bank...

  18. 12 CFR 931.6 - Transfer of capital stock.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Transfer of capital stock. 931.6 Section 931.6 Banks and Banking FEDERAL HOUSING FINANCE BOARD FEDERAL HOME LOAN BANK RISK MANAGEMENT AND CAPITAL STANDARDS FEDERAL HOME LOAN BANK CAPITAL STOCK § 931.6 Transfer of capital stock. A Bank in its capital...

  19. 12 CFR 956.6 - Use of hedging instruments.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Use of hedging instruments. 956.6 Section 956.6... ITEMS FEDERAL HOME LOAN BANK INVESTMENTS § 956.6 Use of hedging instruments. (a) Applicability of GAAP. Derivative instruments that do not qualify as hedging instruments pursuant to GAAP may be used only if a...

  20. 12 CFR 980.6 - Finance Board consent.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Finance Board consent. 980.6 Section 980.6 Banks and Banking FEDERAL HOUSING FINANCE BOARD NEW FEDERAL HOME LOAN BANK ACTIVITIES NEW BUSINESS ACTIVITIES § 980.6 Finance Board consent. The Finance Board may at any time provide consent for a Bank...

  1. Insight into the structures of [M(C(5)H(4)I)(CO)(3)] and [M(2)(C(12)H(8))(CO)(6)] (M = Mn and Re) containing strong I...O and pi(CO)-pi(CO) interactions.

    PubMed

    Romanov, Alexander S; Mulroy, Joseph M; Antipin, Mikhail Yu; Timofeeva, Tatiana V

    2009-11-01

    The compounds tricarbonyl(eta(5)-1-iodocyclopentadienyl)manganese(I), [Mn(C(5)H(4)I)(CO)(3)], (I), and tricarbonyl(eta(5)-1-iodocyclopentadienyl)rhenium(I), [Re(C(5)H(4)I)(CO)(3)], (III), are isostructural and isomorphous. The compounds [mu-1,2(eta(5))-acetylenedicyclopentadienyl]bis[tricarbonylmanganese(I)] or bis(cymantrenyl)acetylene, [Mn(2)(C(12)H(8))(CO)(6)], (II), and [mu-1,2(eta(5))-acetylenedicyclopentadienyl]bis[tricarbonylrhenium(I)], [Re(2)(C(12)H(8))(CO)(6)], (IV), are isostructural and isomorphous, and their molecules display inversion symmetry about the mid-point of the ligand C[triple-bond]C bond, with the (CO)(3)M(C(5)H(4)) (M = Mn and Re) moieties adopting a transoid conformation. The molecules in all four compounds form zigzag chains due to the formation of strong attractive I...O [in (I) and (III)] or pi(CO)-pi(CO) [in (I) and (IV)] interactions along the crystallographic b axis. The zigzag chains are bound to each other by weak intermolecular C-H...O hydrogen bonds for (I) and (III), while for (II) and (IV) the chains are bound to each other by a combination of weak C-H...O hydrogen bonds and pi(Csp(2))-pi(Csp(2)) stacking interactions between pairs of molecules. The pi(CO)-pi(CO) contacts in (II) and (IV) between carbonyl groups of neighboring molecules, forming pairwise interactions in a sheared antiparallel dimer motif, are encountered in only 35% of all carbonyl interactions for transition metal-carbonyl compounds.

  2. Determination of trace selenium by solid substrate-room temperature phosphorescence enhancing method based on potassium chlorate oxidizing phenyl hydrazine-1,2-dihydroxynaphthalene-3,6-disulfonic acid system

    NASA Astrophysics Data System (ADS)

    Liu, Jia-Ming; Cui, Xiao-Jie; Li, Lai-Ming; Fu, Geng-Min; Lin, Shao-Xian; Yang, Min-Lan; Xu, Mei-Ying; Wu, Zhi-Qun

    2007-04-01

    A new method for the determination of trace selenium based on solid substrate-room temperature phosphorimetry (SS-RTP) has been established. This method was based on the fact that in HCl-KCl buffer solution, potassium chlorate could oxidize phenyl hydrazine to form chloridize diazo-ion after being heated at 100 °C for 20 min, and then the diazo-ion reacted with 1,2-dihydroxynaphthalene-3,6-disulfonic acid to form red azo-compound which could emit strong room temperature phosphorescence (RTP) signal on filter paper. Selenium could catalyze potassium chlorate oxidizing the reaction between phenyl hydrazine and 1,2-dihydroxynaphthalene-3,6-disulfonic acid, which caused the sharp enhancement of SS-RTP. Under the optimum condition, the relationship between the phosphorescence emission intensity (Δ Ip) and the content of selenium obeyed Beer's law when the concentration of selenium is within the range of 1.60-320 fg spot -1 (or 0.0040-0.80 ng ml -1 with a sample volume of 0.4 μl). The regression equation of working curve can be expressed as Δ Ip = 13.12 + 0.4839 CSe(IV) (fg spot -1) ( n = 6), with correlation coefficient r = 0.9991 and a detection limit of 0.28 fg spot -1 (corresponding to a concentration range of 7.0 × 10 -13 g ml -1 Se(IV), n = 11). After 11-fold measurement, R.S.D. were 2.8 and 3.5% for the samples containing 0.0040 and 0.80 ng ml -1 of Se(IV), respectively. This accurate and sensitive method with good repeatability has been successfully applied to the determination of trace selenium in Chinese wolfberry and egg yolk with satisfactory results. The mechanism of the enhancement of phosphorescence was also discussed.

  3. Line Positions and Intensities for the ν12 Band of 13C12CH_6

    NASA Astrophysics Data System (ADS)

    Devi, V. Malathy; Benner, D. Chris; Sung, Keeyoon; Crawford, Timothy J.; Mantz, Arlan; Smith, Mary Ann H.

    2014-06-01

    High-resolution, high signal-to-noise spectra of mono-substituted 13C-ethane (13C12CH_6) in the 12.2 μm region were recorded with a Bruker IFS 125HR Fourier transform spectrometer. The spectra were obtained for four sample pressures at three different temperatures between 130 and 208 K using a 99% 13C-enriched ethane sample contained in a 20.38-cm long coolable absorption cell. A multispectrum nonlinear least squares fitting technique was used to fit the same intervals in the four spectra simultaneously to determine line positions and intensities. Similar to our previous analyses of 12C_2H_6 spectra in this same region, constraints were applied to accurately fit each pair of doublet components arising from torsional Coriolis interaction of the excited ν12 = 1 state with the nearby torsional ν_6 = 3 state. Line intensities corresponding to each spectrum temperature (130 K, 178 K and 208 K) are reported for 1660 ν12 absorption lines for which the assignments are known, and integrated intensities are estimated as the summation of the measured values. The measured line positions and intensities (re-scaled to 296 K) are compared with values in recent editions of spectroscopic databases. K. Sung, A. W. Mantz, L. R. Brown, et al., J. Mol. Spectrosc., 162 (2010) 124-134. D. C. Benner, C. P. Rinsland, V. Malathy Devi, M. A. H. Smith and D. Atkins, JQSRT, 53 (1995) 705-721. V. Malathy Devi, C. P. Rinsland, D. Chris Benner, et al., JQSRT, 111 (2010) 1234-1251 V. Malathy Devi, D. Chris Benner, C. P. Rinsland, et al., JQSRT, 111 (2010) 2481-2504. Research described in this paper was performed at Connecticut College, the College of William and Mary, NASA Langley Research Center and the Jet Propulsion Laboratory, California Institute of Technology, under contracts and cooperative agreements with the National Aeronautics and Space Administration.

  4. Isotope shifts of the 6d{sup 2} D{sub 3/2}-7 p{sup 2} P{sub 1/2} transition in trapped short-lived {sup 209-214}Ra{sup +}

    SciTech Connect

    Giri, G. S.; Versolato, O. O.; Berg, J. E. van den; Boell, O.; Dammalapati, U.; Hoek, D. J. van der; Jungmann, K.; Kruithof, W. L.; Mueller, S.; Nunez Portela, M.; Onderwater, C. J. G.; Santra, B.; Timmermans, R. G. E.; Wansbeek, L. W.; Willmann, L.; Wilschut, H. W.

    2011-08-15

    Laser spectroscopy of short-lived radium isotopes in a linear Paul trap has been performed. The isotope shifts of the 6d{sup 2} D{sub 3/2} -7 p{sup 2} P{sub 1/2} transition in {sup 209-214}Ra{sup +}, which are sensitive to the short-range part of the atomic wave functions, were measured. The results are essential experimental input for improving the precision of atomic structure calculations. This is indispensable for parity violation in Ra{sup +} aiming at the determination of the weak mixing angle.

  5. Discovery of a novel 2,3,11,11a-tetrahydro-1H-pyrazino[1,2-b]isoquinoline-1,4(6H)-dione series promoting neurogenesis of human neural progenitor cells.

    PubMed

    Lin, Hong; Fang, Haiyan; Wang, Jamie; Meng, Qinghua; Dai, Xuedong; Wu, Sharon; Luo, Jie; Pu, Dan; Chen, Libo; Minick, Douglas; Arai, Ken; Mandeville, Emiri T; Lo, Eng; Holder, Julie C; Chuang, Tsu Tshen; Zhao, Jing

    2015-09-01

    A novel neurogenic compound (1), discovered from a mouse neural progenitor cell (NPC) screen, showed profound neurogenic effect on human NPCs. Synthesis and SAR of this novel 2,3,11,11a-tetrahydro-1H-pyrazino[1,2-b]isoquinoline-1,4(6H)-dione series are described. Compound 20 is brain penetrable in rodents, and promotes neurogenesis in wild type mice, therefore it is a good tool molecule to study neurogenesis induction as a potential treatment for conditions associated with neurogenesis impairment diseases.

  6. Scaling and stress dependence of sub-coercive field dynamic hysteresis in 0.6Pb(Zr1/2Ti1/2)O3 0.4Pb(Zn1/3Nb2/3)O3 ceramic

    NASA Astrophysics Data System (ADS)

    Yimnirun, R.; Wongdamnern, N.; Triamnak, N.; Unruan, M.; Ngamjarurojana, A.; Ananta, S.; Laosiritaworn, Y.

    2008-10-01

    The scaling behavior of sub-coercive field dynamic ferroelectric hysteresis under the influence of stress was investigated in rhombohedral 0.6Pb(Zr0.5Ti0.5)O3-0.4Pb(Zn1/3Nb2/3)O3 (0.6PZT-0.4PZN) bulk ceramic. The scaling relation of hysteresis area \\langle A \\rangle against frequency f, field amplitude E0, and stress σ for the minor loops takes the form of \\langle {A-A_{\\sigma=0} } \\rangle \\propto f^{-0.36}E_0^{4.03} \\sigma^{0.19} , indicating the difference in the energy dissipation between the stressed and stress-free conditions. While the scaling obtained is very similar to that of soft and hard PZT ceramics, slightly faster responses to f and E0 indicate the ease of polarization orientation in this ceramic with a simpler domain structure compared to commercial PZT ceramics. However, the difference in mechanical properties of these materials could contribute to a variation in the response to stress. While the E0 exponent obtained in this study agreed well with that derived from the Monte Carlo simulation based on the Q-state planar Potts model, the difference in the f exponent obtained experimentally and theoretically was attributed to the depolarizing effects presented in the bulk ceramics.

  7. Calcioferrite with composition (Ca3.94Sr0.06)Mg1.01(Fe2.93Al1.07)(PO4)6(OH)4·12H2O

    PubMed Central

    Lafuente, Barbara; Downs, Robert T.; Yang, Hexiong; Jenkins, Robert A.

    2014-01-01

    Calcioferrite, ideally Ca4MgFe3+ 4(PO4)6(OH)4·12H2O (tetra­calcium magnesium tetrairon(III) hexakis-phosphate tetra­hydroxide dodeca­hydrate), is a member of the calcioferrite group of hydrated calcium phosphate minerals with the general formula Ca4 AB 4(PO4)6(OH)4·12H2O, where A = Mg, Fe2+, Mn2+ and B = Al, Fe3+. Calcioferrite and the other three known members of the group, montgomeryite (A = Mg, B = Al), kingsmountite (A = Fe2+, B = Al), and zodacite (A = Mn2+, B = Fe3+), usually occur as very small crystals, making their structure refinements by conventional single-crystal X-ray diffraction challenging. This study presents the first structure determination of calcioferrite with composition (Ca3.94Sr0.06)Mg1.01(Fe2.93Al1.07)(PO4)6(OH)4·12H2O based on single-crystal X-ray diffraction data collected from a natural sample from the Moculta quarry in Angaston, Australia. Calcioferrite is isostructural with montgomeryite, the only member of the group with a reported structure. The calcioferrite structure is characterized by (Fe/Al)O6 octa­hedra (site symmetries 2 and -1) sharing corners (OH) to form chains running parallel to [101]. These chains are linked together by PO4 tetra­hedra (site symmetries 2 and 1), forming [(Fe/Al)3(PO4)3(OH)2] layers stacking along [010], which are connected by (Ca/Sr)2+ cations (site symmetry 2) and Mg2+ cations (site symmetry 2; half-occupation). Hydrogen-bonding inter­actions involving the water mol­ecules (one of which is equally disordered over two positions) and OH function are also present between these layers. The relatively weaker bonds between the layers account for the cleavage of the mineral parallel to (010). PMID:24764934

  8. Crystal structure of 1,2-bis­(6-bromo-3,4-dihydro-2H-benz[e][1,3]oxazin-3-yl)ethane: a bromine-containing bis-benzoxazine

    PubMed Central

    Rivera, Augusto; Rojas, Jicli José’; Ríos-Motta, Jaime; Bolte, Michael

    2016-01-01

    The title benzoxazine molecule, C18H18Br2N2O2, was prepared by a Mannich-type reaction of 4-bromo­phenol with ethane-1,2-di­amine and formaldehyde. The title compound crystallizes in the monoclinic space group C2/c with a centre of inversion located at the mid-point of the C—C bond of the central CH2CH2 spacer. The oxazinic ring adopts a half-chair conformation. The structure is compared to those of other functionalized benzoxazines synthesized in our laboratory. In the crystal, weak C—H⋯Br and C—H⋯O hydrogen bonds stack the mol­ecules along the b-axis direction. PMID:27840727

  9. 12. Level 6 gringing pans, pump above dorr thickener. View ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    12. Level 6 gringing pans, pump above dorr thickener. View to west. - Kennecott Copper Corporation, Concentration Mill, On Copper River & Northwestern Railroad, Kennicott, Valdez-Cordova Census Area, AK

  10. Safety for Your Child: 6 to 12 Months

    MedlinePlus

    ... Share Safety for Your Child: 6 to 12 Months Page Content Article Body ​ Did you know that ... may climb before walking, or walk with support months before you expect. Your child will grasp at ...

  11. Medical Care and Your 6- to 12-Year-Old

    MedlinePlus

    ... compared with other kids the same age and gender. The doctor will take a medical and family ... Talking to Your Child About Puberty Understanding Puberty Communication and Your 6- to 12-Year-Old Contact ...

  12. Recovery 3 and 12 months after hysterectomy

    PubMed Central

    Theunissen, Maurice; Peters, Madelon L.; Schepers, Jan; Maas, Jacques W.M.; Tournois, Fleur; van Suijlekom, Hans A.; Gramke, Hans-Fritz; Marcus, Marco A.E.

    2016-01-01

    Abstract Chronic postsurgical pain (CPSP) is 1 important aspect of surgical recovery. To improve perioperative care and postoperative recovery knowledge on predictors of impaired recovery is essential. The aim of this study is to assess predictors and epidemiological data of CPSP, physical functioning (SF-36PF, 0–100), and global surgical recovery (global surgical recovery index, 0–100%) 3 and 12 months after hysterectomy for benign indication. A prospective multicenter cohort study was performed. Sociodemographic, somatic, and psychosocial data were assessed in the week before surgery, postoperatively up to day 4, and at 3- and 12-month follow-up. Generalized linear model (CPSP) and linear-mixed model analyses (SF-36PF and global surgical recovery index) were used. Baseline data of 468 patients were collected, 412 (88%) patients provided data for 3-month evaluation and 376 (80%) patients for 12-month evaluation. After 3 and 12 months, prevalence of CPSP (numeric rating scale ≥ 4, scale 0–10) was 10.2% and 9.0%, respectively, SF-36PF means (SD) were 83.5 (20.0) and 85.9 (20.2), global surgical recovery index 88.1% (15.6) and 93.3% (13.4). Neuropathic pain was reported by 20 (5.0%) patients at 3 months and 14 (3.9%) patients at 12 months. Preoperative pain, surgery-related worries, acute postsurgical pain on day 4, and surgery-related infection were significant predictors of CPSP. Baseline level, participating center, general psychological robustness, indication, acute postsurgical pain, and surgery-related infection were significant predictors of SF-36PF. Predictors of global surgical recovery were baseline expectations, surgery-related worries, American Society of Anesthesiologists classification, type of anesthesia, acute postsurgical pain, and surgery-related infection. Several predictors were identified for CPSP, physical functioning, and global surgical recovery. Some of the identified factors are modifiable and optimization of patients’ preoperative

  13. 12 CFR 1261.6 - Determination of member votes.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... the Bank Act (12 U.S.C. 1427(b)) that prohibit any member from casting any vote in excess of the... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Determination of member votes. 1261.6 Section... the members. (b) Number of votes. For each member directorship and each independent directorship...

  14. 12 CFR 1261.6 - Determination of member votes.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... the Bank Act (12 U.S.C. 1427(b)) that prohibit any member from casting any vote in excess of the... 12 Banks and Banking 9 2013-01-01 2013-01-01 false Determination of member votes. 1261.6 Section... the members. (b) Number of votes. For each member directorship and each independent directorship...

  15. 12 CFR 1261.6 - Determination of member votes.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... the Bank Act (12 U.S.C. 1427(b)) that prohibit any member from casting any vote in excess of the... 12 Banks and Banking 9 2012-01-01 2012-01-01 false Determination of member votes. 1261.6 Section... the members. (b) Number of votes. For each member directorship and each independent directorship...

  16. 9-Furfuryl-idene-2,3-dimethyl-6,7,8,9-tetrahydro-4H--thieno[2',3':4,5]pyrimidino[1,2-a]pyridin-4-one.

    PubMed

    Bozorov, Khurshed A; Elmuradov, Burkhon Zh; Okmanov, Rasul Ya; Tashkhodjaev, Bakhodir; Shakhidoyatov, Khusnutdin M

    2010-02-06

    The title compound, C(17)H(16)N(2)O(2)S, was obtained by condensation of 2,3-dimethyl-thieno[2',3':4,5]pyrimidino[1,2-a]pyridin-4-one with furfural in the presence of sodium hydroxide. One of the methyl-ene groups of the tetra-hydro-pyrido ring is disordered over two positions in a 0.87 (1):0.13 (1) ratio. The thieno[2,3-d]pyrimidin-4-one unit and the furan ring are both planar (r.m.s. deviation = 0.535 Å), and coplanar with each other, forming a dihedral angle of 5.4 (1)°. Four weak inter-molecular hydrogen bonds (C-H⋯O and C-H⋯N) are observed in the structure, which join mol-ecules into a network parallel to (101).

  17. Molecular structure, NMR, UV-Visible, vibrational spectroscopic and HOMO, LUMO analysis of (E)-1-(2, 6-bis (4-methoxyphenyl)-3, 3-dimethylpiperidine-4-ylidene)-2-(3-(3, 5-dimethyl-1H-pyrazol-1-yl) pyrazin-2-yl) hydrazine by DFT method

    NASA Astrophysics Data System (ADS)

    Alphonsa, A. Therasa; Loganathan, C.; Anand, S. Athavan Alias; Kabilan, S.

    2016-02-01

    We have synthesized (E)-1-(2, 6-bis (4-methoxyphenyl)-3, 3-dimethylpiperidine-4-ylidene)-2-(3-(3, 5-dimethyl-1H-pyrazol-1-yl) pyrazin-2-yl) hydrazine (PM6). It was characterized using FT-IR, FT-Raman, 1H NMR, 13C NMR techniques. To interpret the experimental data, ab initio computations of the vibrational frequencies were carried out using the Gaussian 09 program followed by the full optimizations done using Density Functional Theory (DFT) at B3LYP/6-311 G(d,p) level. The combined use of experiments and computations allowed a firm assignment of the majority of observed bands for the compound. The calculated stretching frequencies have been found to be in good agreement with the experimental frequencies. The electronic and charge transfer properties have been explained on the basis of highest occupied molecular orbitals (HOMOs), lowest unoccupied molecular orbitals (LUMOs) and density of states (DOS). The absorption spectra have been computed by using time dependent density functional theory (TD-DFT). 1H and 13C NMR spectra were recorded and 1H and 13C NMR chemical shifts of the molecule were calculated using the gauge independent atomic orbital (GIAO) method. From the optimized geometry of the molecule, molecular electrostatic potential (MEP) distribution, frontier molecular orbitals (FMOs) of the title compound have been calculated in the ground state theoretically. The theoretical results showed good agreement with the experimental values.

  18. Cluster Emission in 13C + 12C and 12C + 12C Reactions at ~ 6 Mev/nucleon

    NASA Astrophysics Data System (ADS)

    Rana, T. K.; Bhattacharya, C.; Kundu, S.; Banerjee, K.; Bhattacharya, S.; Mukherjee, G.; Ghosh, T. K.; Meena, J. K.; Dhara, P.; Biswas, M.; Pai, H.; Mahata, K.; Kumar, Suresh; Ramachandran, K.; Rout, P. C.; Pandit, S. K.; Nanal, V.; Pillay, R. G.

    Cluster state formation viz. the population of unbound 8Be and the Hoyle state of 12C produced in the reactions 12C(77 MeV) + 12C and 13C(75 MeV) + 12C have been studied using resonance particle spectroscopy. It was observed that there is a large difference in the cluster state formation in these two reactions and the yield of neutron rich isotopes of different fragments is more in the 13C + 12C compared to 12C + 12C reactions at 6 MeV/u.

  19. 12 CFR 403.6 - Systematic review for declassification.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Systematic review for declassification. 403.6..., AND SAFEGUARDING OF NATIONAL SECURITY INFORMATION § 403.6 Systematic review for declassification... permanent retention will be subject to systematic declassification review by the Archivist in...

  20. 12 CFR 403.6 - Systematic review for declassification.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 5 2012-01-01 2012-01-01 false Systematic review for declassification. 403.6..., AND SAFEGUARDING OF NATIONAL SECURITY INFORMATION § 403.6 Systematic review for declassification... permanent retention will be subject to systematic declassification review by the Archivist in...

  1. 12 CFR 403.6 - Systematic review for declassification.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 4 2011-01-01 2011-01-01 false Systematic review for declassification. 403.6..., AND SAFEGUARDING OF NATIONAL SECURITY INFORMATION § 403.6 Systematic review for declassification... permanent retention will be subject to systematic declassification review by the Archivist in...

  2. 12 CFR 403.6 - Systematic review for declassification.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Systematic review for declassification. 403.6..., AND SAFEGUARDING OF NATIONAL SECURITY INFORMATION § 403.6 Systematic review for declassification... permanent retention will be subject to systematic declassification review by the Archivist in...

  3. 12 CFR 403.6 - Systematic review for declassification.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 5 2014-01-01 2014-01-01 false Systematic review for declassification. 403.6..., AND SAFEGUARDING OF NATIONAL SECURITY INFORMATION § 403.6 Systematic review for declassification... permanent retention will be subject to systematic declassification review by the Archivist in...

  4. 12 CFR 917.6 - Internal control system.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Internal control system. 917.6 Section 917.6... internal control system that addresses: (i) The efficiency and effectiveness of Bank activities; (ii) The... activities necessary to maintain the internal control system required under paragraph (a)(1) of this...

  5. 12 CFR 917.6 - Internal control system.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Internal control system. 917.6 Section 917.6... internal control system that addresses: (i) The efficiency and effectiveness of Bank activities; (ii) The... activities necessary to maintain the internal control system required under paragraph (a)(1) of this...

  6. 12 CFR 208.6 - Establishment and maintenance of branches.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Establishment and maintenance of branches. 208.6 Section 208.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MEMBERSHIP OF STATE BANKING INSTITUTIONS IN THE FEDERAL RESERVE SYSTEM (REGULATION H)...

  7. 12 CFR 791.6 - Subject matter of a meeting.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 7 2013-01-01 2013-01-01 false Subject matter of a meeting. 791.6 Section 791... REGULATIONS; PUBLIC OBSERVATION OF NCUA BOARD MEETINGS Rules of NCUA Board Procedure § 791.6 Subject matter of... accompanied by an NCUA B-1 form and a Board Action Memorandum that states the specific issue(s) or...

  8. 12 CFR 1291.6 - Homeownership set-aside programs.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Homeownership set-aside programs. 1291.6... LOAN BANKS' AFFORDABLE HOUSING PROGRAM § 1291.6 Homeownership set-aside programs. (a) Establishment of program. A Bank may establish one or more homeownership set-aside programs pursuant to the requirements...

  9. 12 CFR 1291.6 - Homeownership set-aside programs.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 9 2013-01-01 2013-01-01 false Homeownership set-aside programs. 1291.6... LOAN BANKS' AFFORDABLE HOUSING PROGRAM § 1291.6 Homeownership set-aside programs. (a) Establishment of program. A Bank may establish one or more homeownership set-aside programs pursuant to the requirements...

  10. 12 CFR 1291.6 - Homeownership set-aside programs.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 9 2012-01-01 2012-01-01 false Homeownership set-aside programs. 1291.6... LOAN BANKS' AFFORDABLE HOUSING PROGRAM § 1291.6 Homeownership set-aside programs. (a) Establishment of program. A Bank may establish one or more homeownership set-aside programs pursuant to the requirements...

  11. 12 CFR 1291.6 - Homeownership set-aside programs.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 10 2014-01-01 2014-01-01 false Homeownership set-aside programs. 1291.6... LOAN BANKS' AFFORDABLE HOUSING PROGRAM § 1291.6 Homeownership set-aside programs. (a) Establishment of program. A Bank may establish one or more homeownership set-aside programs pursuant to the requirements...

  12. 12 CFR 630.6 - Funding Corporation committees.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 7 2012-01-01 2012-01-01 false Funding Corporation committees. 630.6 Section 630.6 Banks and Banking FARM CREDIT ADMINISTRATION FARM CREDIT SYSTEM DISCLOSURE TO INVESTORS IN... oversee the Funding Corporation's preparation of the report to stockholders and investors; review...

  13. 12 CFR 630.6 - Funding Corporation committees.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 7 2014-01-01 2014-01-01 false Funding Corporation committees. 630.6 Section 630.6 Banks and Banking FARM CREDIT ADMINISTRATION FARM CREDIT SYSTEM DISCLOSURE TO INVESTORS IN... SAC must oversee the Funding Corporation's preparation of the report to stockholders and...

  14. 12 CFR 932.6 - Operations risk capital requirement.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... risk capital requirement if: (1) The Bank provides an alternative methodology for assessing and... 12 Banks and Banking 8 2012-01-01 2012-01-01 false Operations risk capital requirement. 932.6 Section 932.6 Banks and Banking FEDERAL HOUSING FINANCE BOARD FEDERAL HOME LOAN BANK RISK MANAGEMENT...

  15. 12 CFR 932.6 - Operations risk capital requirement.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... risk capital requirement if: (1) The Bank provides an alternative methodology for assessing and... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Operations risk capital requirement. 932.6 Section 932.6 Banks and Banking FEDERAL HOUSING FINANCE BOARD FEDERAL HOME LOAN BANK RISK MANAGEMENT...

  16. 12 CFR 932.6 - Operations risk capital requirement.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... risk capital requirement if: (1) The Bank provides an alternative methodology for assessing and... 12 Banks and Banking 8 2013-01-01 2013-01-01 false Operations risk capital requirement. 932.6 Section 932.6 Banks and Banking FEDERAL HOUSING FINANCE BOARD FEDERAL HOME LOAN BANK RISK MANAGEMENT...

  17. 12 CFR 1511.6 - Authority of Federal Reserve Banks.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Authority of Federal Reserve Banks. 1511.6... PROCEDURE § 1511.6 Authority of Federal Reserve Banks. (a) Each Federal Reserve Bank is hereby authorized as... Securities Documentation, and Federal Reserve Bank Operating Circulars; to service and maintain...

  18. 12 CFR 1511.6 - Authority of Federal Reserve Banks.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 9 2012-01-01 2012-01-01 false Authority of Federal Reserve Banks. 1511.6... PROCEDURE § 1511.6 Authority of Federal Reserve Banks. (a) Each Federal Reserve Bank is hereby authorized as... Securities Documentation, and Federal Reserve Bank Operating Circulars; to service and maintain...

  19. 12 CFR 1511.6 - Authority of Federal Reserve Banks.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 9 2013-01-01 2013-01-01 false Authority of Federal Reserve Banks. 1511.6... PROCEDURE § 1511.6 Authority of Federal Reserve Banks. (a) Each Federal Reserve Bank is hereby authorized as... Securities Documentation, and Federal Reserve Bank Operating Circulars; to service and maintain...

  20. 12 CFR 1511.6 - Authority of Federal Reserve Banks.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Authority of Federal Reserve Banks. 1511.6... PROCEDURE § 1511.6 Authority of Federal Reserve Banks. (a) Each Federal Reserve Bank is hereby authorized as... Securities Documentation, and Federal Reserve Bank Operating Circulars; to service and maintain...

  1. 12 CFR 1511.6 - Authority of Federal Reserve Banks.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 10 2014-01-01 2014-01-01 false Authority of Federal Reserve Banks. 1511.6... PROCEDURE § 1511.6 Authority of Federal Reserve Banks. (a) Each Federal Reserve Bank is hereby authorized as... Securities Documentation, and Federal Reserve Bank Operating Circulars; to service and maintain...

  2. 12 CFR 987.6 - Authority of Federal Reserve Banks.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Authority of Federal Reserve Banks. 987.6... CONSOLIDATED OBLIGATIONS § 987.6 Authority of Federal Reserve Banks. (a) Each Federal Reserve Bank is hereby... other duties as fiscal agent as may be requested by the Office of Finance. (b) Each Federal Reserve...

  3. 12 CFR 564.6 - Professional association membership; competency.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 6 2012-01-01 2012-01-01 false Professional association membership; competency... APPRAISALS § 564.6 Professional association membership; competency. (a) Membership in appraisal organizations... an assignment for a federally related transaction solely by virtue of membership or lack...

  4. 12 CFR 722.6 - Professional association membership; competency.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Professional association membership; competency... CREDIT UNIONS APPRAISALS § 722.6 Professional association membership; competency. (a) Membership in... consideration for an assignment for a federally related transaction solely by virtue of membership or lack...

  5. 12 CFR 722.6 - Professional association membership; competency.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 6 2011-01-01 2011-01-01 false Professional association membership; competency... CREDIT UNIONS APPRAISALS § 722.6 Professional association membership; competency. (a) Membership in... consideration for an assignment for a federally related transaction solely by virtue of membership or lack...

  6. 12 CFR 564.6 - Professional association membership; competency.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 6 2013-01-01 2012-01-01 true Professional association membership; competency... APPRAISALS § 564.6 Professional association membership; competency. (a) Membership in appraisal organizations... an assignment for a federally related transaction solely by virtue of membership or lack...

  7. 12 CFR 204.6 - Charges for reserve deficiencies.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... waives the penalty for failing to satisfy a liquidity requirement, the Reserve Bank in the District where... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Charges for reserve deficiencies. 204.6 Section 204.6 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE...

  8. 12 CFR 310.6 - Special procedures: Medical records.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Special procedures: Medical records. 310.6... PRIVACY ACT REGULATIONS § 310.6 Special procedures: Medical records. Medical records shall be disclosed on... transmission of the medical information directly to the requesting individual could have an adverse effect...

  9. 12 CFR 750.6 - Filing instructions; appeal.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 7 2013-01-01 2013-01-01 false Filing instructions; appeal. 750.6 Section 750.6 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS GOLDEN... nondiscriminatory severance plan payments pursuant to § 750.1(e)(2)(v) and golden parachute payments permitted...

  10. 12 CFR 630.6 - Funding Corporation committees.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Funding Corporation committees. 630.6 Section... Corporation committees. (a) System Audit Committee. The Funding Corporation must establish and maintain a... must be free from any relationship that, in the opinion of the Funding Corporation board,...

  11. Primary Eye Irritation Potential of Insect Repellents. Methyl N,N’-Dihexylethylenediaminemonocarbamate (CHR4), (E)-1,2,3,4-Tetrahydro-6-Methyl-1-(2-Methyl-1-Oxo-2-Butenyl) Quinoline (CHR5) and 1,2,3,4-Tetrahydro-6-Methyl-1-(3-Methyl-1-Oxo-2-Butenyl) Quinoline (CHR6).

    DTIC Science & Technology

    1983-08-01

    corneal opacity or iritis (Tables 5 and 6). Slight redness (score of 1) was seen in rabbits 82F145 and 82F138 at the 24-hour and 48-hour observation...animals tested in this group, none showed signs of corneal opacity or Iritis (Tables 9 and 10). Slight redness was seen in the eye of rabbit 82F142

  12. 12 CFR 1203.3 - Eligible parties.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... cooperative association as defined in section 15(a) of the Agricultural Marketing Act, 12 U.S.C. 1141j(a... 12 Banks and Banking 9 2012-01-01 2012-01-01 false Eligible parties. 1203.3 Section 1203.3 Banks... to business interests; (3) A charitable or other tax-exempt organization described in section...

  13. 12 CFR 3.1 - Authority.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Authority. 3.1 Section 3.1 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Authority and Definitions § 3.1 Authority. This part is issued under the authority of 12 U.S.C. 1 et...

  14. 12 CFR 3.1 - Authority.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Authority. 3.1 Section 3.1 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Authority and Definitions § 3.1 Authority. This part is issued under the authority of 12 U.S.C. 1 et...

  15. 12 CFR 3.1 - Authority.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Authority. 3.1 Section 3.1 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Authority and Definitions § 3.1 Authority. This part is issued under the authority of 12 U.S.C. 1 et...

  16. 12 CFR 3.1 - Authority.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Authority. 3.1 Section 3.1 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Authority and Definitions § 3.1 Authority. This part is issued under the authority of 12 U.S.C. 1 et...

  17. 12 CFR 931.6 - Transfer of capital stock.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 8 2012-01-01 2012-01-01 false Transfer of capital stock. 931.6 Section 931.6... STANDARDS FEDERAL HOME LOAN BANK CAPITAL STOCK § 931.6 Transfer of capital stock. A Bank in its capital plan may allow a member to transfer any excess capital stock of the Bank to another member of that Bank...

  18. 12 CFR 931.6 - Transfer of capital stock.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 8 2013-01-01 2013-01-01 false Transfer of capital stock. 931.6 Section 931.6... STANDARDS FEDERAL HOME LOAN BANK CAPITAL STOCK § 931.6 Transfer of capital stock. A Bank in its capital plan may allow a member to transfer any excess capital stock of the Bank to another member of that Bank...

  19. 12 CFR 931.6 - Transfer of capital stock.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 8 2014-01-01 2014-01-01 false Transfer of capital stock. 931.6 Section 931.6... STANDARDS FEDERAL HOME LOAN BANK CAPITAL STOCK § 931.6 Transfer of capital stock. A Bank in its capital plan may allow a member to transfer any excess capital stock of the Bank to another member of that Bank...

  20. 12 CFR 931.6 - Transfer of capital stock.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Transfer of capital stock. 931.6 Section 931.6... STANDARDS FEDERAL HOME LOAN BANK CAPITAL STOCK § 931.6 Transfer of capital stock. A Bank in its capital plan may allow a member to transfer any excess capital stock of the Bank to another member of that Bank...

  1. Optical spectra of Dy3+-doped GdVO4 and Ca3Sc2Ge3O12 crystals and evaluation of the Ω2/Ω6 ratio as a quality factor for the classification of Dy3+-activated crystalline hosts

    NASA Astrophysics Data System (ADS)

    Cavalli, Enrico

    2016-11-01

    The room temperature absorption spectra of Dy3+-doped GdVO4 and Ca3Sc2Ge3O12 crystals have been measured and analysed in the framework of the Judd-Ofelt Theory. The calculated intensity parameters have then been correlated with the intensities of the emission bands in the yellow and blue region. The analysis has then been extended to a number of host lattices using literature data, and a general empirical model has been proposed, correlating the Ω2/Ω6 and the yellow to blue (Y/B) ratio in order to define a criterion for predicting the visible luminescence properties of the Dy-activated crystalline materials.

  2. Magnetoelectric effect in lead free piezoelectric Bi1/2Na1/2TiO3-modified CFO based magnetostrictive (Co0.6Zn0.4Fe1.7 Mn0.3O4) particulate nanocomposite prepared by sol-gel method

    NASA Astrophysics Data System (ADS)

    Thakur, Megha; Sharma, Puneet; Kumari, Mukesh; Singh, Anoop Pratap; Tyagi, Mintu

    2017-03-01

    Lead free magnetoelectric composites that comprise Co0.6Zn0.4Fe1.7Mn0.3O4 (CZFMO) and Bi1/2Na1/2TiO3 (BNT) were synthesized using sol-gel method and it's structural, dielectric, magnetic, ferroelectric and magnetoelectric (ME) properties were studied. The X-ray diffraction displayed the single phase formation of parent phases and the presence of two phases in the composites. The temperature dependent dielectric spectra of samples indicates two anomalies at 220 °C and 320 °C were ascribed to ferroelectric to antiferroelectric, and anti-ferroelectric to paraelectric phase transitions respectively. Room temperature (RT) magnetic measurements show that composites are soft magnetic. The composite with x=0.2, showed the large value of ME voltage coefficient (αE) 58 mV/cmOe. Moreover, these ME composites provide a great opportunity as potential lead free systems for multifunctional devices.

  3. Molecular structure, spectroscopic (FT-IR, FT Raman, UV, NMR and THz) investigation and hyperpolarizability studies of 3-(2-Chloro-6-fluorophenyl)-1-(2-thienyl) prop-2-en-1-one

    NASA Astrophysics Data System (ADS)

    Kumar, Rajesh; Kumar, Amit; Deval, Vipin; Gupta, Archana; Tandon, Poonam; Patil, P. S.; Deshmukh, Prathmesh; Chaturvedi, Deepika; Watve, J. G.

    2017-02-01

    In the present work, a combined experimental and theoretical study on ground state molecular structure, spectroscopic and nonlinear optical properties of the chalcone derivative 3-(2-Chloro-6-fluorophenyl)-1-(2-thienyl) prop-2-en-1-one (2C6F2SC) is reported. Initial geometry generated from single crystal X-ray diffraction parameters was minimized at DFT level employing B3LYP/6-311++G (d,p) without any constraint to the potential energy surface. The molecule has been characterized using various experimental techniques FT-IR, FT-Raman, UV-Vis, 1H NMR, TD-THz and the spectroscopic data have been analyzed theoretically by Density Functional Theory (DFT) method. Harmonic vibrational frequencies were calculated theoretically using the optimized ground state geometry and the spectra were interpreted by means of potential energy distribution. Time Dependent Density Functional Theory (TD-DFT) has been used to calculate energies, absorption wavelengths, oscillator strengths of electronic singlet-singlet transitions. The calculated energy and oscillator strength complement with the experimental findings. The HOMO-LUMO energy gap explains the charge interaction taking place within the molecule. Good correlations between the experimental 1H NMR chemical shifts and calculated GIAO shielding tensors were found. Stability of the molecule, hyperconjugative interactions and charge delocalization has been analyzed by natural bond orbital (NBO) analysis. The first order hyperpolarizability (β) of this molecular system and related properties (μ, <α> and Δα) have been calculated using the finite-field approach.

  4. 1,3-Bis(naphthalen-2-ylmeth­yl)-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione

    PubMed Central

    Afrakssou, Zahra; Rodi, Youssef Kandri; Capet, Frédéric; Essassi, El Mokhtar; Ng, Seik Weng

    2011-01-01

    The title compound, C37H24N2O3, is a 1H-anthra[2,1-d]imidazole-2,6,11(3H)-trione derivative having naphthyl­methyl substitutents attached to the imidazole N atoms. The anthraquinone part of the mol­ecule is somewhat folded along the the line connecting the carbonyl bonds. The dihedral angle between the two benzene rings is 7.8 (1)°. The two naphthyl systems of the substituents of the imidazole ring are positioned on the same side of the five-membered ring; these are approximately coplanar, the dihedral angle between the napthyl systems being 4.3 (2)°. PMID:22091155

  5. Solution combustion synthesis and enhanced electrochemical performance Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles by controlling NO{sub 3}{sup –}/CH{sub 3}COO{sup –} ratio of the precursors

    SciTech Connect

    Zhang, Qingtang; Mei, Juntao; Xie, Xiaolong; Wang, Xiaomei; Zhang, Junyan

    2015-10-15

    Highlights: • The size of Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles can be controlled by NO{sub 3}{sup −}/CH{sub 3}COO{sup −} ratio. • 35 nm Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles can be obtained with 3:1 NO{sub 3}{sup –}/CH{sub 3}COO{sup –} ratio. • 35 nm Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles shows excellent electrochemical performance. - Abstract: Lithium-rich layer oxide Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles were fabricated through solution combustion synthesis by controlling NO{sub 3}{sup –}/CH{sub 3}COO{sup –} ratio of the precursors. The relationships between the NO{sub 3}{sup –}/CH{sub 3}COO{sup –} ratio and structure as well as electrochemical performance of Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles are investigated. XRD reveals that Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} nanoparticles obtained with a suitable NO{sub 3}{sup –}/CH{sub 3}COO{sup –} ratio of 3:1 (LLO-3N1A) is composed of the smallest nanocrystallite of 18 nm. SEM reflects that the average primary particles of LLO-3N1A are the smallest with a size of 35 nm. Those unique characteristic guarantee the excellent electrochemical performance of LLO-3N1A. LLO-3N1A exhibits a specific capacity of 252.3 mA h g{sup −1} at 0.1 C. In addition, LLO-3N1A also shows best rate capability among the four prepared Li{sub 1.2}Ni{sub 0.2}Mn{sub 0.6}O{sub 2} samples.

  6. Ca2Mg(NO3)6×12H2O-structural investigations on a new compound retrieved from chimney deposits of a combined heat and power plant

    NASA Astrophysics Data System (ADS)

    Kahlenberg, Volker; Tessadri, Richard; Tribus, Martina; Schmidmair, Daniela; Perfler, Lukas; Haefeker, Udo

    2014-10-01

    Phase analysis of incrustations retrieved from chimney deposits of a combined heat and power plant in Malchow/Germany by X-ray powder diffraction gave evidence for the existence of a previously unknown hydrous calcium magnesium nitrate. Optical investigations of the sample showed the presence of colorless platy crystals with a maximum diameter of about 250 μm embedded in a partly polycrystalline and partly glassy matrix. Aided by EDX-analysis and Raman spectroscopy, a single-crystal diffraction study performed at ambient conditions demonstrated that the material represents a phase with composition Ca2Mg(NO3)6×12H2O. Basic crystallographic data are as follows: trigonal symmetry, space group type R , a = 10.5583(5) Å, c = 19.5351(10) Å, V = 1885.97(16) Å3, Z = 3, ( R(| F|) = 0.0248). The magnesium ions are coordinated by water molecules to form distorted Mg(H2O)6-octahedra. The calcium atoms are surrounded by nine ligands. The resulting CaO9 tricapped trigonal prisms involve oxygen atoms from additional water moieties as well as from three different bidentate nitrate groups, respectively. Hydrogen bonds link one octahedron with two adjacent prisms into trimers. The trimers in turn are stacked in columns running parallel to [001]. Further hydrogen bonding between neighboring columns results in the formation of a three-dimensional network. To our best knowledge, Ca2Mg(NO3)6×12H2O represents a new structure type. However, column-like topologies with rods consisting of different types of polyhedra have been also observed in other trigonal hydrous nitrates. The structural relationships between these compounds are discussed. It is interesting to note that in previous phase equilibrium studies on the ternary system Ca(NO3)2-Mg(NO3)2-H2O no other hydrous double salt has been described. Finally, the results of the structure analysis allowed a qualitative and quantitative phase analysis of the crystalline part of the chimney deposit by the Rietveld method.

  7. New lithium copper borates with BO3 triangles: Li6CuB4O10, Li3CuB3O7, Li8Cu7B14O32, and Li2Cu9B12O28.

    PubMed

    Kuratieva, N V; Bànki, M; Tsirlin, A A; Eckert, J; Ehrenberg, H; Mikhailova, D

    2013-12-16

    Crystal structures of three new lithium copper borates, Li3CuB3O7, Li8Cu7B14O32, and Li2Cu9B12O28, and a new Li6CuB4O10 polymorph were solved by single-crystal X-ray diffraction. In all of the structures, the boron cations form BO3 triangles, which are connected with each other and with copper polyhedra only via corners in Li6CuB4O10 and Li3CuB3O7 and via both corners and edges in Li8Cu7B14O32 and Li2Cu9B12O28. The Li3CuB3O7 and Li8Cu7B14O32 compounds were synthesized as pure samples with only trace amounts of impurities; hence, their magnetic properties could be investigated and analyzed in terms of underlying magnetic couplings. Other compositions always represented multiphase mixtures. Li3CuB3O7 features infinite Cu,O chains formed by Cu2O6 units consisting of edge-shared CuO4 squares. Together with two apical oxygen atoms with long interatomic Cu-O distances of 2.7-2.8 Å, the Cu2O6 units form chains extended along the a axis. These pseudochains are responsible for strong anisotropic thermal expansion behavior. The temperature dependence of the magnetization between 4 and 380 K for Li3CuB3O7 could be fit well by a spin-dimer model. The magnetic susceptibility of Li8Cu7B14O32 showed a more complex temperature dependence, with two different Curie-Weiss regimes in the temperature range of 2-380 K.

  8. Magnetic properties, microstructure and corrosion behavior of (Pr,nd)12.6Fe81.3B6.1-type sintered magnets doped with (Pr,nd)30Fe62Ga8

    NASA Astrophysics Data System (ADS)

    Ni, Junjie; Zhang, Zhenyu; Liu, Ying; Jia, Zhengfeng; Huang, Baoxu; Yin, Yibin

    2016-10-01

    NdFeB sintered magnets with (Pr,Nd)30Fe62Ga8 were prepared by a binary powder blending method and their magnetic properties, microstructure and corrosion behavior were investigated. Addition of 3 wt% (Pr,Nd)30Fe62Ga8 was found to be the most effective for improving (BH)max and iHc of the magnets. The increase in both magnetic parameters was related to the alteration in microstructure. However, in other samples the occurrence of micropore and the aggregation of intergranular phases harmed the magnetic properties. Such disadvantageous microstructure features also caused higher corrosion current density, thus decreasing the corrosion resistance of the sample with higher additive content. In addition, the Ga-containing intergranular phases that are more stable than the (Pr,Nd)-rich phase formed in the additive doped magnets, leading to better corrosion resistance of the 3 wt% additives doped sample in comparison with the contrastive sample.

  9. 12 CFR 3.5 - Applicability.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... written agreement or a temporary or final order pursuant to 12 U.S.C. 1818 (b) or (c), or as a condition... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Applicability. 3.5 Section 3.5 Banks and... Office determines, pursuant to the procedures set forth in subpart C, that different minimum...

  10. 12 CFR 3.5 - Applicability.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... written agreement or a temporary or final order pursuant to 12 U.S.C. 1818 (b) or (c), or as a condition... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Applicability. 3.5 Section 3.5 Banks and... Office determines, pursuant to the procedures set forth in subpart C, that different minimum...

  11. 36 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 1 2013-07-01 2013-07-01 false Definitions. 12.3 Section 12.3 Parks, Forests, and Public Property NATIONAL PARK SERVICE, DEPARTMENT OF THE INTERIOR NATIONAL... headstone placed in a memorial section of a national cemetery with the words “In Memory Of” inscribed...

  12. 12 CFR 1203.3 - Eligible parties.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Eligible parties. 1203.3 Section 1203.3 Banks and Banking FEDERAL HOUSING FINANCE AGENCY ORGANIZATION AND OPERATIONS FREEDOM OF INFORMATION ACT... cooperative association as defined in section 15(a) of the Agricultural Marketing Act, 12 U.S.C....

  13. 46 CFR 12.40-3 - [Reserved

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 1 2010-10-01 2010-10-01 false 12.40-3 Section 12.40-3 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY MERCHANT MARINE OFFICERS AND SEAMEN REQUIREMENTS FOR RATING ENDORSEMENTS Non-resident Alien Unlicensed Members of the Steward's Department on U.S. Flag Large Passenger Vessels §...

  14. 18 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 18 Conservation of Power and Water Resources 1 2013-04-01 2013-04-01 false Definitions. 12.3 Section 12.3 Conservation of Power and Water Resources FEDERAL ENERGY REGULATORY COMMISSION, DEPARTMENT OF ENERGY REGULATIONS UNDER THE FEDERAL POWER ACT SAFETY OF WATER POWER PROJECTS AND PROJECT WORKS...

  15. 18 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 18 Conservation of Power and Water Resources 1 2010-04-01 2010-04-01 false Definitions. 12.3 Section 12.3 Conservation of Power and Water Resources FEDERAL ENERGY REGULATORY COMMISSION, DEPARTMENT OF ENERGY REGULATIONS UNDER THE FEDERAL POWER ACT SAFETY OF WATER POWER PROJECTS AND PROJECT WORKS...

  16. 18 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 18 Conservation of Power and Water Resources 1 2014-04-01 2014-04-01 false Definitions. 12.3 Section 12.3 Conservation of Power and Water Resources FEDERAL ENERGY REGULATORY COMMISSION, DEPARTMENT OF ENERGY REGULATIONS UNDER THE FEDERAL POWER ACT SAFETY OF WATER POWER PROJECTS AND PROJECT WORKS...

  17. 18 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 18 Conservation of Power and Water Resources 1 2011-04-01 2011-04-01 false Definitions. 12.3 Section 12.3 Conservation of Power and Water Resources FEDERAL ENERGY REGULATORY COMMISSION, DEPARTMENT OF ENERGY REGULATIONS UNDER THE FEDERAL POWER ACT SAFETY OF WATER POWER PROJECTS AND PROJECT WORKS...

  18. 18 CFR 12.3 - Definitions.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 18 Conservation of Power and Water Resources 1 2012-04-01 2012-04-01 false Definitions. 12.3 Section 12.3 Conservation of Power and Water Resources FEDERAL ENERGY REGULATORY COMMISSION, DEPARTMENT OF ENERGY REGULATIONS UNDER THE FEDERAL POWER ACT SAFETY OF WATER POWER PROJECTS AND PROJECT WORKS...

  19. CTC Sentinel. Volume 3, Issue 6

    DTIC Science & Technology

    2010-06-01

    executed multiple bomb attacks against the American banking giant Citibank in the Greek capital. The RS’ continued attacks on international targets led...for Revolution? The Life and Death of Greece’s Revolutionary Organization 17 RS attempted a second bombing, at a Citibank branch in Neo Psychico...communiqué on Citibank , dated March 12, 2009. 8 Ibid. 9 Ibid. juNe 2010 . VoL 3 . IssUE 6 “The group’s modus operandi incorporated high-profile

  20. 36 CFR 12.6 - Disinterments and exhumations.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...; (3) Recasketing the remains; (4) Rehabilitation of the gravesite according to conditions established... disinterment; and (6) Providing the superintendent a sworn statement, by a person having first hand...

  1. Crystal structure of (E)-2-[(2-bromopyridin-3-yl)methyl-idene]-6-meth-oxy-3,4-di-hydro-naphthalen-1(2H)-one and 3-[(E)-(6-meth-oxy-1-oxo-1,2,3,4-tetra-hydro-naphthalen-2-ylidene)meth-yl]pyridin-2(1H)-one.

    PubMed

    Zingales, Sarah K; Moore, Morgan E; Goetz, Andrew D; Padgett, Clifford W

    2016-07-01

    The title compounds C17H14BrNO2, (I), and C17H15NO3, (II), were obtained from the reaction of 6-meth-oxy-3,4-di-hydro-2H-naphthalen-1-one and 2-bromo-nicotinaldehyde in ethanol. Compound (I) was the expected product and compound (II) was the oxidation product from air exposure. In the crystal structure of compound (I), there are no short contacts or hydrogen bonds. The structure does display π-π inter-actions between adjacent benzene rings and adjacent pyridyl rings. Compound (II) contains two independent mol-ecules, A and B, in the asymmetric unit; both are non-planar, the dihedral angles between the meth-oxy-benzene and 1H-pyridin-2-one mean planes being 35.07 (9)° in A and 35.28 (9)°in B. In each mol-ecule, the 1H-pyridin-2-one unit participates in inter-molecular N-H⋯O hydrogen bonding to another mol-ecule of the same type (A to A or B to B). The structure also displays π-π inter-actions between the pyridyl and the benzene rings of non-equivalent mol-ecules (viz., A to B and B to A).

  2. Characterization of redox states of Ru(OH(2))(Q)(tpy)(2+) (Q = 3,5-di-tert-butyl-1,2-benzoquinone, tpy = 2,2':6',2''-terpyridine) and related species through experimental and theoretical studies.

    PubMed

    Tsai, Ming-Kang; Rochford, Jonathan; Polyansky, Dmitry E; Wada, Tohru; Tanaka, Koji; Fujita, Etsuko; Muckerman, James T

    2009-05-18

    The redox states of Ru(OH(2))(Q)(tpy)(2+) (Q = 3,5-di-tert-butyl-1,2-benzoquinone, tpy = 2,2':6',2''-terpyridine) are investigated through experimental and theoretical UV-vis spectra and Pourbaix diagrams. The electrochemical properties are reported for the species resulting from deprotonation and redox processes in aqueous solution. The formal oxidation states of the redox couples in the various intermediate complexes are systematically assigned using electronic structure theory. The controversy over the electronic assignment of ferromagnetic vs. antiferromagnetic coupling is investigated through comparison of ab initio methods and the broken-symmetry density functional theory (DFT) approach. The various pK(a) values and reduction potentials, including the consideration of proton-coupled electron-transfer (PCET) processes, are calculated, and the theoretical version of the Pourbaix diagram is constructed in order to elucidate and assign several previously ambiguous regions in the experimental diagram.

  3. New insights into the modification mechanism of Li-rich Li1.2Mn0.6Ni0.2O2 coated by Li2ZrO3.

    PubMed

    Zhang, Jicheng; Zhang, Heng; Gao, Rui; Li, Zhengyao; Hu, Zhongbo; Liu, Xiangfeng

    2016-05-21

    Lithium-rich Mn-based layered cathode materials have attracted wide attention due to their high specific capacity for lithium-ion batteries. However, some critical issues i.e. poor rate capability and voltage fade have limited their practical applications. Herein, we propose a synchronous lithiation strategy to coat Li-rich Li1.2Mn0.6Ni0.2O2 (LMNO) with a thin layer of Li(+)-conductive Li2ZrO3. The obtained syn-Li2ZrO3@LMNO integrates the advantages of the Li2ZrO3 coating and Zr(4+) doping, and shows a much higher rate capability and cycling stability than those of the counterpart post-Li2ZrO3@LMNO fabricated by a post-coating method. More importantly, the average voltage of syn-Li2ZrO3@LMNO has been enhanced by 0.15 V and the voltage decay has also been mitigated. New insights into the synergetic modification mechanism of the Li2ZrO3 coating and Zr(4+) doping have been proposed. The coating layer of Li(+)-conductive Li2ZrO3 alleviates the surface side reactions, suppresses the transition metal dissolution and enhances the Li-ion conductivity. Meanwhile, the doping and incorporation of Zr(4+) into the host structure accompanied by the Li2ZrO3 coating expands the interplanar spacing and decreases Li/Ni mixing which facilitates Li(+) diffusion. In addition, the integration of the Li2ZrO3 coating and Zr(4+) doping also further enhances the layered structure stability and mitigates the voltage fade during lithiation/delithiation cycles. Moreover, the proposed synchronous lithiation coating route avoids the duplicated high-temperature calcinations and can also be widely used to modify some other cathode materials.

  4. Spectral and quantum chemical studies on 1,3-bis(N(1)-4-amino-6-methoxypyrimidinebenzenesulfonamide-2,2,4,4-ethane-1,2-dithiol)-2,4-dichlorocyclodiphosph(V)azane and its erbium complex.

    PubMed

    Al-Mogren, Muneerah M; Alaghaz, Abdel-Nasser M A; El-Gogary, Tarek M

    2014-01-24

    Novel 1,3-bis(N(1)-4-amino-6-methoxypyrimidine-benzenesulfonamide-2,2,4,4-ethane-1,2-dithiol)-2,4-dichlorocyclodiphosph(V)azane (L), was prepared and their coordinating behavior towards the lanthanide ion Er(III) was studied. The structures of the isolated products are proposed based on elemental analyses, IR, UV-VIS., (1)H NMR, (13)C NMR, (31)P NMR, SEM, XRD, mass spectra, effective magnetic susceptibility measurements and thermogravimetric analysis (TGA). Computational studies have been carried out at the DFT-B3LYP/6-31G(d) level of theory on the structural and spectroscopic properties of L and its binuclear Er(III) complex. Different tautomers of the ligand were optimized at the ab initio DFT level. Keto-form structure is about 17.7 kcal/mol more stable than the enol form (taking zpe correction into account). Simulated IR frequencies were scaled and compared with that experimentally measured. TD-DFT method was used to compute the UV-VIS spectra which compared by the measured electronic spectra.

  5. Parallel Curriculum Units for Science, Grades 6-12

    ERIC Educational Resources Information Center

    Leppien, Jann H.; Purcell, Jeanne H.

    2011-01-01

    Based on the best-selling book "The Parallel Curriculum", this professional development resource gives multifaceted examples of rigorous learning opportunities for science students in Grades 6-12. The four sample units revolve around genetics, the convergence of science and society, the integration of language arts and biology, and the periodic…

  6. 6. Photographic copy of construction drawing, dated April 12, 1958, ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    6. Photographic copy of construction drawing, dated April 12, 1958, Germany S. Klees, Consulting Engineers, Detroit, in possession of Selfridge Base Museum, Mt. Clemens, Michigan. MODIFICATION TO BUILDING NO. 559, ARCHITECTURAL ELEVATIONS AND DETAILS. - Selfridge Field, Building No. 559, South of East Joy Boulevard, east of North-South Runway, Mount Clemens, Macomb County, MI

  7. 12 CFR 310.6 - Special procedures: Medical records.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... PRIVACY ACT REGULATIONS § 310.6 Special procedures: Medical records. Medical records shall be disclosed on... information to a medical doctor named by the requesting individual for release of the patient. ... 12 Banks and Banking 4 2011-01-01 2011-01-01 false Special procedures: Medical records....

  8. 12 CFR 310.6 - Special procedures: Medical records.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... PRIVACY ACT REGULATIONS § 310.6 Special procedures: Medical records. Medical records shall be disclosed on... information to a medical doctor named by the requesting individual for release of the patient. ... 12 Banks and Banking 5 2012-01-01 2012-01-01 false Special procedures: Medical records....

  9. Home Economics/Health Grades 6-12. Program Evaluation.

    ERIC Educational Resources Information Center

    Des Moines Public Schools, IA. Teaching and Learning Div.

    Home economics programs are offered to students in grades 6-12 in the Des Moines INdependent Community School District (Iowa). Programs at the middle school level are exploratory, leading to occupational training in family and consumer science, child care, food service, and textile and fashion arts at the high school level. Health education…

  10. 19 CFR 12.6 - Affidavits required to accompany entry.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...; DEPARTMENT OF THE TREASURY SPECIAL CLASSES OF MERCHANDISE Importation of Certain Cheeses § 12.6 Affidavits required to accompany entry. (a) Cheeses produced in the member states of the European Communities shall... (excluding Puerto Rico), of the producer or exporter that the cheese has not received and will not...

  11. 12. VIEW OF PUMPS NO. 6, 8, AND 7 (L ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    12. VIEW OF PUMPS NO. 6, 8, AND 7 (L TO R) WITH THEIR CANVAS COVERS, LOOKING NORTHEAST. NOTE CONCRETE CONSTRUCTION. THE FOUR LIGHT WINDOWS AND THE STEEL EAM FOR THE 10-TON HAND OPERATED TRAVELING CRANE. - Wyoming Valley Flood Control System, Woodward Pumping Station, East of Toby Creek crossing by Erie-Lackawanna Railroad, Edwardsville, Luzerne County, PA

  12. A Stress Control Workbook for Youth Grades 6-12.

    ERIC Educational Resources Information Center

    Trotter, Jennie C.

    Stress is an inevitable part of students' lives, but too much stress can have damaging consequences. Ways in which children can respond positively are covered in this stress booklet. Intended for students in grades 6-12, the booklet is divided into 20 lessons on stress. Each lesson features various activities, role plays, exercises, and checklists…

  13. 12 CFR 323.6 - Professional association membership; competency.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 5 2012-01-01 2012-01-01 false Professional association membership; competency... OF GENERAL POLICY APPRAISALS § 323.6 Professional association membership; competency. (a) Membership... membership or lack of membership in any particular appraisal organization. (b) Competency. All staff and...

  14. 12 CFR 722.6 - Professional association membership; competency.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 7 2012-01-01 2012-01-01 false Professional association membership; competency... CREDIT UNIONS APPRAISALS § 722.6 Professional association membership; competency. (a) Membership in... consideration for an assignment for a federally related transaction solely by virtue of membership or lack...

  15. 12 CFR 564.6 - Professional association membership; competency.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Professional association membership; competency... APPRAISALS § 564.6 Professional association membership; competency. (a) Membership in appraisal organizations... an assignment for a federally related transaction solely by virtue of membership or lack...

  16. 12 CFR 164.6 - Professional association membership; competency.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Professional association membership; competency... APPRAISALS § 164.6 Professional association membership; competency. (a) Membership in appraisal organizations... an assignment for a Federally related transaction solely by virtue of membership or lack...

  17. 12 CFR 323.6 - Professional association membership; competency.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 4 2011-01-01 2011-01-01 false Professional association membership; competency... OF GENERAL POLICY APPRAISALS § 323.6 Professional association membership; competency. (a) Membership... membership or lack of membership in any particular appraisal organization. (b) Competency. All staff and...

  18. 12 CFR 564.6 - Professional association membership; competency.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 5 2011-01-01 2011-01-01 false Professional association membership; competency... APPRAISALS § 564.6 Professional association membership; competency. (a) Membership in appraisal organizations... an assignment for a federally related transaction solely by virtue of membership or lack...

  19. 12 CFR 722.6 - Professional association membership; competency.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 7 2013-01-01 2013-01-01 false Professional association membership; competency... CREDIT UNIONS APPRAISALS § 722.6 Professional association membership; competency. (a) Membership in... consideration for an assignment for a federally related transaction solely by virtue of membership or lack...

  20. 12 CFR 323.6 - Professional association membership; competency.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Professional association membership; competency... OF GENERAL POLICY APPRAISALS § 323.6 Professional association membership; competency. (a) Membership... membership or lack of membership in any particular appraisal organization. (b) Competency. All staff and...

  1. Career and Technology Education Grades 6-12. Program Evaluation.

    ERIC Educational Resources Information Center

    Des Moines Public Schools, IA. Teaching and Learning Div.

    Technology education programs are offered in 10 middle schools, 5 area high schools, 1 alternative high school, and at Central Campus in the Des Moines Independent Community School District. Programs in grades 6-12 consist of hands-on instruction using activities and projects as the medium for teaching modern technologies in the various trades.…

  2. 12 CFR 226.3 - Exempt transactions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Exempt transactions. 226.3 Section 226.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM TRUTH IN LENDING (REGULATION Z) General § 226.3 Exempt transactions. This regulation does not apply to...

  3. 12 CFR 269a.3 - Intervenor.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Intervenor. 269a.3 Section 269a.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM DEFINITIONS § 269a.3 Intervenor. The term intervenor means the party in a proceeding whose intervention has...

  4. 12 CFR 269a.3 - Intervenor.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Intervenor. 269a.3 Section 269a.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM DEFINITIONS § 269a.3 Intervenor. The term intervenor means the party in a proceeding whose intervention has...

  5. 12 CFR 225.3 - Administration.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 3 2012-01-01 2012-01-01 false Administration. 225.3 Section 225.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General Provisions § 225.3...

  6. 12 CFR 3.21 - Minority interest.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false Minority interest. 3.21 Section 3.21 Banks and... Capital § 3.21 Minority interest. (a) Applicability. For purposes of § 3.20, a national bank or Federal savings association is subject to the minority interest limitations in this section if: (1) A...

  7. A novel small heat shock protein 12.6 (HSP12.6) from Brugia malayi functions as a human IL-10 receptor binding protein.

    PubMed

    Gnanasekar, Munirathinam; Anandharaman, Veerapathran; Anand, Setty Balakrishnan; Nutman, Thomas B; Ramaswamy, Kalyanasundaram

    2008-06-01

    Phage display cDNA expression library of the third stage larvae (L3) of Brugia malayi was screened for identifying target(s) that bound to the human interleukin-10 receptor (huIL10R). This iterative screening identified an insert that showed significant homology to Caenorhabditis elegans HSP12.6. The gene was designated B. malayi HSP12.6 (BmHSP12.6) and has orthologues in several gastrointestinal nematode genome (Ancylostoma caninum, Ascaris lumbricoides and Ascaris suum) but the gene or gene product has not been studied further in these parasites. Structural analyses of BmHSP12.6 showed that it has a highly conserved alpha-crystallin central domain that is characteristic of other small heat shock proteins (HSPs). BmHSP12.6 has a short N-terminal domain and an unusually small C-terminal domain flanking the crystallin domain suggesting that this protein belongs to a novel class of small HSPs. BmHSP12.6 appears to be differentially transcribed with highest expression in the vertebrate stages of the parasite (L4, adult and mf) compared to its mosquito vector stage (L3). More importantly recombinant BmHSP12.6 bound to huIL10R in a dose dependent fashion and inhibited the binding of human IL-10 (huIL10) to huIL10R in vitro. rBmHSP12.6 also enhanced the growth and proliferation of MC/9 mast cells in vitro similar to huIL10. This study thus describes a novel small HSP from B. malayi that has the capacity to bind to huIL10R, block binding of huIL10 to huIL10R and function similar to huIL10.

  8. LIMS Version 6 Level 3 Dataset

    NASA Technical Reports Server (NTRS)

    Remsberg, Ellis E.; Lingenfelser, Gretchen

    2010-01-01

    This report describes the Limb Infrared Monitor of the Stratosphere (LIMS) Version 6 (V6) Level 3 data products and the assumptions used for their generation. A sequential estimation algorithm was used to obtain daily, zonal Fourier coefficients of the several parameters of the LIMS dataset for 216 days of 1978-79. The coefficients are available at up to 28 pressure levels and at every two degrees of latitude from 64 S to 84 N and at the synoptic time of 12 UT. Example plots were prepared and archived from the data at 10 hPa of January 1, 1979, to illustrate the overall coherence of the features obtained with the LIMS-retrieved parameters.

  9. A critical review of both the synthesis approach and the receptor profile of the 8-chloro-1-(2',4'-dichlorophenyl)-N-piperidin-1-yl-1,4,5,6-tetrahydrobenzo[6,7]cyclohepta[1,2-c]pyrazole-3-carboxamide and analogue derivatives.

    PubMed

    Lazzari, Paolo; Distinto, Rita; Manca, Ilaria; Baillie, Gemma; Murineddu, Gabriele; Pira, Marilena; Falzoi, Matteo; Sani, Monica; Morales, Paula; Ross, Ruth; Zanda, Matteo; Jagerovic, Nadine; Pinna, Gérard Aimè

    2016-10-04

    8-Chloro-1-(2',4'-dichlorophenyl)-N-piperidin-1-yl-1,4,5,6-tetrahydrobenzo[6,7]cyclohepta[1,2-c]pyrazole-3-carboxamide 9a was discovered as potent and selective CB1 antagonist by part of our group few years ago. In particular it was reported to have an affinity towards the CB1 cannabinoid receptor (CB1R), expressed as Ki, of 0.00035 nM. Nevertheless significantly divergent data were reported for the same compound from other laboratories. To unequivocally define the receptor profile of 9a, we have critically reviewed both its synthesis approach and binding data. Here we report that, in contrast to our previously reported data, 9a showed a Ki value for CB1R in the order of nanomolar rather than of fentomolar range. The new determined receptor profile of 9a was also ascertained for analogue derivatives 9b-i, as well as for 12. Moreover, the structural features of the synthesized compounds necessary for CB1R were investigated. Amongst the novel series, effects on CB1R intrinsic activity was highlighted due to the substituents at the position 3 of the pyrazole ring of the 1,4,5,6-tetrahydrobenzo[6,7]cyclohepta[1,2-c]pyrazole scaffold. Although the cannabinoid receptor profile of 9a was reviewed in this work, the relevance of this compound in CB1R antagonist based drug discovery is confirmed.

  10. 1,2-Dibromo-3-chloropropane (DBCP)

    Integrated Risk Information System (IRIS)

    1,2 - Dibromo - 3 - chloropropane ( DBCP ) ; CASRN 96 - 12 - 8 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessm

  11. [Oral hygiene customs in 6-12 year old schoolchildren].

    PubMed

    Hernández-Martínez, César Tadeo; Medina-Solís, Carlo Eduardo; Robles-Bermeo, Norma Leticia; Mendoza-Rodríguez, Martha; Veras-Hernández, Miriam; De la Rosa-Santillana, Rubén; Escoffié-Ramírez, Mauricio; Márquez-Rodríguez, Sonia

    2014-01-01

    OBJECTIVE. To characterize utilization of oral hygiene devices and customs in schoolchildren. MATERIAL AND METHODS. We performed a cross-sectional study in 1,404 schoolchildren (6- 12 year olds) from 14 public schools in Pachuca, Hidalgo, México, using a questionnaire for sociodemographic variables and 1) Tooth brushing frequency (<1/d vs. at least 1/d), 2) Use of toothpaste (not always vs. always), 3) Flossing (never, does not know vs. at least 1/week), 4) Use of mouthwash (never, does not know vs. at least 1/week). Analyses were performed with nonparametric tests. RESULTS. Mean age was 8.97 ± 1.99 years; 50.1% were male. Prevalence of utilization of oral hygiene devices and associated customs were 85.5% tooth brushing, 90.9% toothpaste, 19.4% flossing, and 28.2% mouthwash. Only 11.8% of participants reported utilization in all 4 categories. We observed differences (p < 0.05) across sexes only in the use of toothpaste, as women used it more often. Differences across age were observed (p < 0.05) for tooth brushing (younger children brushed more often) and flossing (older children flossed more often). CONCLUSIONS. Tooth brushing was the oral hygiene practice more often performed in this sample, with other frequencies being relatively low. There were differences by age and sex across some variables.

  12. Determination of superoxide in seawater using 2-methyl-6-(4-methoxyphenyl)-3,7- dihydroimidazo[1,2-a]pyrazin-3(7H)-one chemiluminescence.

    PubMed

    Rose, Andrew L; Moffett, James W; Waite, T David

    2008-02-15

    Superoxide, the one-electron reduced form of dioxygen, is known to be generated in marine environments by photochemical and biological processes. Because of its selective reaction with only a few commonly occurring compounds, superoxide is expected to approach concentrations in the high picomolar or low nanomolar range in seawater. Most currently existing methods do not have both the necessary sensitivity and selectivity to measure naturally occurring concentrations. In contrast, we demonstrate here that the chemiluminescence reagent 2-methyl-6-(4-methoxyphenyl)-3,7-dihydroimidazo[l,2-a]pyrazin-3(7H)-one (MCLA) is selective for superoxide in seawater and can be used with a detection limit of around 50 pM. Although a wide range of potential interferences were shown not to react with MCLA directly, some care must be taken when analyzing samples containing nanomolar concentrations of Fe(II), Cu(I), Mo(V), V(III), or V(IV), since these compounds can react with oxygen to produce superoxide during analysis that is subsequently detected. We describe two methods for calibrating the system, one employing photochemically generated superoxide standards and the other employing the superoxide-generating xanthine/xanthine oxidase system and discuss limitations on the use of each. The method was successfully used in the field to determine steady-state superoxide concentrations in the water column in the eastern equatorial Pacific Ocean.

  13. 46 CFR 111.12-3 - Excitation.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... REQUIREMENTS Generator Construction and Circuits § 111.12-3 Excitation. In general, excitation must meet... generator unless it is provided with a permanent magnet or a residual-magnetism-type exciter that has...

  14. 46 CFR 111.12-3 - Excitation.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... REQUIREMENTS Generator Construction and Circuits § 111.12-3 Excitation. In general, excitation must meet... generator unless it is provided with a permanent magnet or a residual-magnetism-type exciter that has...

  15. 46 CFR 111.12-3 - Excitation.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... REQUIREMENTS Generator Construction and Circuits § 111.12-3 Excitation. In general, excitation must meet... generator unless it is provided with a permanent magnet or a residual-magnetism-type exciter that has...

  16. 46 CFR 111.12-3 - Excitation.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... REQUIREMENTS Generator Construction and Circuits § 111.12-3 Excitation. In general, excitation must meet... generator unless it is provided with a permanent magnet or a residual-magnetism-type exciter that has...

  17. 46 CFR 111.12-3 - Excitation.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... REQUIREMENTS Generator Construction and Circuits § 111.12-3 Excitation. In general, excitation must meet... generator unless it is provided with a permanent magnet or a residual-magnetism-type exciter that has...

  18. 12 CFR 3.14 - Remedies.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ..., whether required in subpart B of this part, in a decision pursuant to subpart C of this part, in a written agreement or temporary or final order under 12 U.S.C. 1818 (b) or (c), or in a condition for approval of an... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Remedies. 3.14 Section 3.14 Banks and...

  19. 12 CFR 3.14 - Remedies.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ..., whether required in subpart B of this part, in a decision pursuant to subpart C of this part, in a written agreement or temporary or final order under 12 U.S.C. 1818 (b) or (c), or in a condition for approval of an... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Remedies. 3.14 Section 3.14 Banks and...

  20. 12 CFR 219.3 - Cost reimbursement.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Cost reimbursement. 219.3 Section 219.3 Banks...) Reimbursement to Financial Institutions for Providing Financial Records § 219.3 Cost reimbursement. (a) Fees..., or other process shall reimburse the financial institution for reasonably necessary costs...

  1. 12 CFR 977.3 - Trustee powers.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Trustee powers. 977.3 Section 977.3 Banks and Banking FEDERAL HOUSING FINANCE BOARD MISCELLANEOUS FEDERAL HOME LOAN BANK OPERATIONS AND AUTHORITIES MISCELLANEOUS BANK AUTHORITIES § 977.3 Trustee powers. A Bank may act, and make reasonable charges for doing...

  2. 12 CFR 977.3 - Trustee powers.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 7 2011-01-01 2011-01-01 false Trustee powers. 977.3 Section 977.3 Banks and Banking FEDERAL HOUSING FINANCE BOARD MISCELLANEOUS FEDERAL HOME LOAN BANK OPERATIONS AND AUTHORITIES MISCELLANEOUS BANK AUTHORITIES § 977.3 Trustee powers. A Bank may act, and make reasonable charges for doing...

  3. 12 CFR 977.3 - Trustee powers.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 8 2013-01-01 2013-01-01 false Trustee powers. 977.3 Section 977.3 Banks and Banking FEDERAL HOUSING FINANCE BOARD MISCELLANEOUS FEDERAL HOME LOAN BANK OPERATIONS AND AUTHORITIES MISCELLANEOUS BANK AUTHORITIES § 977.3 Trustee powers. A Bank may act, and make reasonable charges for doing...

  4. 12 CFR 977.3 - Trustee powers.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 8 2012-01-01 2012-01-01 false Trustee powers. 977.3 Section 977.3 Banks and Banking FEDERAL HOUSING FINANCE BOARD MISCELLANEOUS FEDERAL HOME LOAN BANK OPERATIONS AND AUTHORITIES MISCELLANEOUS BANK AUTHORITIES § 977.3 Trustee powers. A Bank may act, and make reasonable charges for doing...

  5. 12 CFR 3.18 - Decision.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Decision. 3.18 Section 3.18 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Issuance of a Directive § 3.18 Decision. After the closing date of the bank's response period, or...

  6. 12 CFR 3.18 - Decision.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Decision. 3.18 Section 3.18 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY MINIMUM CAPITAL RATIOS; ISSUANCE OF DIRECTIVES Issuance of a Directive § 3.18 Decision. After the closing date of the bank's response period, or...

  7. 12 CFR 205.3 - Coverage.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Coverage. 205.3 Section 205.3 Banks and Banking... this paragraph (c)(7) remain subject to § 205.10(e) regarding compulsory use and sections 915 and 916... (REGULATION E) § 205.3 Coverage. (a) General. This part applies to any electronic fund transfer...

  8. 12 CFR 205.3 - Coverage.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 2 2012-01-01 2012-01-01 false Coverage. 205.3 Section 205.3 Banks and Banking... this paragraph (c)(7) remain subject to § 205.10(e) regarding compulsory use and sections 915 and 916... (REGULATION E) § 205.3 Coverage. (a) General. This part applies to any electronic fund transfer...

  9. 12 CFR 205.3 - Coverage.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 2 2014-01-01 2014-01-01 false Coverage. 205.3 Section 205.3 Banks and Banking... this paragraph (c)(7) remain subject to § 205.10(e) regarding compulsory use and sections 915 and 916... (REGULATION E) § 205.3 Coverage. (a) General. This part applies to any electronic fund transfer...

  10. 12 CFR 205.3 - Coverage.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 2 2013-01-01 2013-01-01 false Coverage. 205.3 Section 205.3 Banks and Banking... this paragraph (c)(7) remain subject to § 205.10(e) regarding compulsory use and sections 915 and 916... (REGULATION E) § 205.3 Coverage. (a) General. This part applies to any electronic fund transfer...

  11. 12 CFR 205.3 - Coverage.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 2 2011-01-01 2011-01-01 false Coverage. 205.3 Section 205.3 Banks and Banking... this paragraph (c)(7) remain subject to § 205.10(e) regarding compulsory use and sections 915 and 916... (REGULATION E) § 205.3 Coverage. (a) General. This part applies to any electronic fund transfer...

  12. 12 CFR 326.3 - Security program.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Security program. 326.3 Section 326.3 Banks and... SECURITY DEVICES AND PROCEDURES AND BANK SECRECY ACT 1 COMPLIANCE Minimum Security Procedures § 326.3 Security program. (a) Contents of security program. The security program shall: (1) Establish...

  13. 12 CFR 326.3 - Security program.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 5 2014-01-01 2014-01-01 false Security program. 326.3 Section 326.3 Banks and... SECURITY DEVICES AND PROCEDURES AND BANK SECRECY ACT 1 COMPLIANCE Minimum Security Procedures § 326.3 Security program. (a) Contents of security program. The security program shall: (1) Establish...

  14. 12 CFR 168.3 - Security program.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Security program. 168.3 Section 168.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY SECURITY PROCEDURES § 168.3 Security program. (a) Contents of security program. The security program shall: (1) Establish procedures...

  15. 12 CFR 326.3 - Security program.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Security program. 326.3 Section 326.3 Banks and... SECURITY DEVICES AND PROCEDURES AND BANK SECRECY ACT 1 COMPLIANCE Minimum Security Procedures § 326.3 Security program. (a) Contents of security program. The security program shall: (1) Establish...

  16. 12 CFR 391.3 - Security program.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 5 2014-01-01 2014-01-01 false Security program. 391.3 Section 391.3 Banks and... OF THRIFT SUPERVISION REGULATIONS Security Procedures § 391.3 Security program. (a) Contents of security program. The security program shall: (1) Establish procedures for opening and closing for...

  17. 12 CFR 168.3 - Security program.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 1 2014-01-01 2014-01-01 false Security program. 168.3 Section 168.3 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY SECURITY PROCEDURES § 168.3 Security program. (a) Contents of security program. The security program shall: (1) Establish procedures...

  18. 12 CFR 391.3 - Security program.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Security program. 391.3 Section 391.3 Banks and... OF THRIFT SUPERVISION REGULATIONS Security Procedures § 391.3 Security program. (a) Contents of security program. The security program shall: (1) Establish procedures for opening and closing for...

  19. 12 CFR 212.3 - Prohibitions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 2 2010-01-01 2010-01-01 false Prohibitions. 212.3 Section 212.3 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.3 Prohibitions. (a) Community. A management official of a depository organization may...

  20. 12 CFR 269a.3 - Intervenor.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 4 2014-01-01 2014-01-01 false Intervenor. 269a.3 Section 269a.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) DEFINITIONS § 269a.3 Intervenor. The term intervenor means the party in a proceeding whose intervention...

  1. 12 CFR 269a.3 - Intervenor.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 4 2012-01-01 2012-01-01 false Intervenor. 269a.3 Section 269a.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) DEFINITIONS § 269a.3 Intervenor. The term intervenor means the party in a proceeding whose intervention...

  2. 12 CFR 269a.3 - Intervenor.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 4 2013-01-01 2013-01-01 false Intervenor. 269a.3 Section 269a.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) DEFINITIONS § 269a.3 Intervenor. The term intervenor means the party in a proceeding whose intervention...

  3. 12 CFR 212.3 - Prohibitions.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 2 2014-01-01 2014-01-01 false Prohibitions. 212.3 Section 212.3 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.3 Prohibitions. (a) Community. A management official of a depository organization may...

  4. 12 CFR 212.3 - Prohibitions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 2 2012-01-01 2012-01-01 false Prohibitions. 212.3 Section 212.3 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.3 Prohibitions. (a) Community. A management official of a depository organization may...

  5. 12 CFR 212.3 - Prohibitions.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 2 2013-01-01 2013-01-01 false Prohibitions. 212.3 Section 212.3 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.3 Prohibitions. (a) Community. A management official of a depository organization may...

  6. 12 CFR 212.3 - Prohibitions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 2 2011-01-01 2011-01-01 false Prohibitions. 212.3 Section 212.3 Banks and Banking FEDERAL RESERVE SYSTEM BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM MANAGEMENT OFFICIAL INTERLOCKS § 212.3 Prohibitions. (a) Community. A management official of a depository organization may...

  7. 12 CFR 590.3 - Operation.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Operation. 590.3 Section 590.3 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY PREEMPTION OF STATE USURY LAWS § 590.3 Operation. (a) The provisions of the constitution or law of any state expressly limiting the rate or...

  8. 12 CFR 725.3 - Regular membership.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 7 2014-01-01 2014-01-01 false Regular membership. 725.3 Section 725.3 Banks... UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.3 Regular membership. (a) A natural person credit... stock subscription;1 and 1 A credit union which submits its application for membership prior to...

  9. 12 CFR 725.3 - Regular membership.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 7 2012-01-01 2012-01-01 false Regular membership. 725.3 Section 725.3 Banks... UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.3 Regular membership. (a) A natural person credit... stock subscription;1 and 1 A credit union which submits its application for membership prior to...

  10. 12 CFR 725.3 - Regular membership.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 7 2013-01-01 2013-01-01 false Regular membership. 725.3 Section 725.3 Banks... UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.3 Regular membership. (a) A natural person credit... stock subscription;1 and 1 A credit union which submits its application for membership prior to...

  11. 12 CFR 225.3 - Administration.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 3 2013-01-01 2013-01-01 false Administration. 225.3 Section 225.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General Provisions §...

  12. 12 CFR 225.3 - Administration.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 3 2014-01-01 2014-01-01 false Administration. 225.3 Section 225.3 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM (CONTINUED) BANK HOLDING COMPANIES AND CHANGE IN BANK CONTROL (REGULATION Y) Regulations General Provisions §...

  13. 12 CFR 13.3 - Business conduct.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Business conduct. 13.3 Section 13.3 Banks and....3 Business conduct. A bank that is a government securities broker or dealer shall observe high standards of commercial honor and just and equitable principles of trade in the conduct of its business as...

  14. 12 CFR 13.3 - Business conduct.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Business conduct. 13.3 Section 13.3 Banks and....3 Business conduct. A bank that is a government securities broker or dealer shall observe high standards of commercial honor and just and equitable principles of trade in the conduct of its business as...

  15. 12 CFR 368.3 - Business conduct.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Business conduct. 368.3 Section 368.3 Banks and... SECURITIES SALES PRACTICES § 368.3 Business conduct. A bank that is a government securities broker or dealer... conduct of its business as a government securities broker or dealer....

  16. 12 CFR 368.3 - Business conduct.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 5 2014-01-01 2014-01-01 false Business conduct. 368.3 Section 368.3 Banks and... SECURITIES SALES PRACTICES § 368.3 Business conduct. A bank that is a government securities broker or dealer... conduct of its business as a government securities broker or dealer....

  17. 12 CFR 368.3 - Business conduct.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Business conduct. 368.3 Section 368.3 Banks and... SECURITIES SALES PRACTICES § 368.3 Business conduct. A bank that is a government securities broker or dealer... conduct of its business as a government securities broker or dealer....

  18. 12 CFR 368.3 - Business conduct.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 4 2011-01-01 2011-01-01 false Business conduct. 368.3 Section 368.3 Banks and... SECURITIES SALES PRACTICES § 368.3 Business conduct. A bank that is a government securities broker or dealer... conduct of its business as a government securities broker or dealer....

  19. 12 CFR 13.3 - Business conduct.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 1 2013-01-01 2013-01-01 false Business conduct. 13.3 Section 13.3 Banks and....3 Business conduct. A bank that is a government securities broker or dealer shall observe high standards of commercial honor and just and equitable principles of trade in the conduct of its business as...

  20. 12 CFR 13.3 - Business conduct.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Business conduct. 13.3 Section 13.3 Banks and....3 Business conduct. A bank that is a government securities broker or dealer shall observe high standards of commercial honor and just and equitable principles of trade in the conduct of its business as...