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81.
Miguel Clemente-LeónEugenio Coronado José R. Galán-MascarósCarlos Giménez-Saiz Carlos J. Goémez-Garc?&#x;aJean M. Fabre G.A. MousdisG.C. Papavassiliou 《Journal of solid state chemistry》2002,168(2):616-625
The synthesis, structure and physical characterization of three new radical salts formed by the organic donor bis(ethylenediseleno)tetrathiafulvalene (BEDS-TTF or BEST) and the paramagnetic hexacyanoferrate(III) anion [Fe(CN)6]3− or the photochromic nitroprusside anion [Fe(CN)5NO]2− are reported: (BEST)4[Fe(CN)6] (1), (BEST)3[Fe(CN)6]2·H2O (2) and (BEST)2[Fe(CN)5NO] (3). Salts 1 and 3 show a layered structure with alternating organic (β-type packing) and inorganic slabs. Salt 2 shows an original interpenetrated structure probably due to the unprecedented presence of (BEST)2+ dications. The three salts are semiconductors although salt 1 exhibits a high room temperature conductivity and a semiconducting-semiconducting transition at ca. 150 K which has been attributed to a dimerization in the organic sublattice. 相似文献
82.
AbstractL-Ascorbic acid (AA), known as vitamin C, can form browning products by a non-enzymatic process during storage and the browning products cause deterioration of agricultural products. In the browning reaction, a red pigment, 2,2´-nitrilodi-2(2´)-deoxy-L-ascorbic acid ammonium salt (NDA), is generated from AA via L-scorbamic acid (SCA) as an intermediate. However, the biological activities of SCA and NDA have not yet been clarified. In this study, we assayed the antioxidant activities of SCA and NDA using ABTS radical cation and their neurite outgrowth-enhancing activities in PC12 cells. SCA showed stronger radical-scavenging activity than that of AA, while NDA hardly showed any activity. SCA and NDA enhanced the neurite outgrowth induced by dibutyryl cyclic AMP after their incorporation into cells in the same manner as that of AA. The results indicated that SCA has antioxidant activity and that SCA and NDA have neurite outgrowth-enhancing activity. 相似文献
83.
A.?P.?LeushinaEmail author L.?A.?Kolesnikova E.?V.?Makhanova V.?P.?Zlomanov 《Russian Journal of Electrochemistry》2005,41(6):639-645
Optimum compositions of ion-selective membranes in quasi-binary systems CuCl-CdCl2, LiCl-CdCl2, and In2S3-InCl3 are selected by a method of coulometric titration in cells with solid electrolytes. Transport numbers for ions are close to unity for the optimum compositions; transport numbers for electrons are vanishingly small (
≺10−3 to 10−4); the electroconductivity is equal to ≈ 10−3 S cm−1 at 200°C; the diffusion coefficients for the current-producing component are on the order of 10−6 to 10−7 cm2 s−1. When using a solid electrolyte of the composition CuCl-CdCl2, which contains 30 mol % CdCl2, methods of emf and electroconduction reveal that the region of homogeneity of copper(I) selenide falls in the region of compositions Cu1.33Se-Cu2.67Se.__________Translated from Elektrokhimiya, Vol. 41, No. 6, 2005, pp. 721–727.Original Russian Text Copyright © 2005 by Leushina, Kolesnikova, Makhanova, Zlomanov.Published on the basis of a report delivered at the VII Meeting on Fundamental Problems in Solid-State Ionics (Chernogolovka-2004). 相似文献
84.
Ângela F. S. S. Mendonça Dina T. R. Formigo Isabel M. S. Lampreia 《Journal of solution chemistry》2002,31(8):653-670
Solubilities of triethylamine in aqueous tetraethylammonium chloride solutions were measured at 20, 25, and 35°C. The molalities in Et4NCl of the aqueous solvents ranged from 0.03 to 1 mol-kg–1. The data were evaluated from density measurements using a vibrating-tube densimeter. At each temperature, least-squares method was used to fit experimental density data points to double polynomial equations of various degrees. Triethylamine molalities of the saturated aqueous phases were estimated by extrapolation from those equations. Experimental data were interpreted in terms of hydrophobic and electrostatic perturbed domains in the hydration shells of the noneleceory and of the cation of the salt, as a function of temperature and salt concentration. The conclusions obtained are consistent with previous volumetric studies. 相似文献
85.
Partial molar volumes for a homologous series of amino acids and peptides have been measured in aqueous 1M sodium acetate, sodium thiocyanate, and sodium sulfate at 25°C. These data have been utilized in conjunction with the data in water to deduce partial molar volumes of transfer V
2,m
0(tr) from water to these aqueous salt solutions. The volumes of transfer for the amino acids and peptides are found to be positive. The interpretation is that this result arises from the dominant interaction of the sodium salts with the charged centers of amino acids and peptides. Thermal denaturation of the structurally homologous proteins lysozyme and -lactalbumin has been studied in the presence of these salts. Significant thermal stabilization of hen egg-white lysozyme has been observed in the presence of sodium acetate and sodium sulfate. However, the thermal stabilization observed for -lactalbumin is very small in the presence of these salts and sodium thiocyanate leads to a lowering of its thermal denaturation temperature. The rise in the surface tension of aqueous salt solutions with salt concentration has been correlated with the calorimetric and volumetric measurements. The results show that V
2,m
0(tr) depends less on the type of electrolyte than on the ionic strength of the solution. The V
2,m
0(tr) values correlate very well with the increase in the surface tension of aqueous salt solutions, indicating significant role of surface tension in interactions of amino acids, peptides, or protein with the salts. 相似文献
86.
Eri Yoshida Kazuaki Nakamura Toshikazu Takata Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》1993,31(6):1505-1512
Oxoaminium salt ( 1 ), derived from 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO, 2 ) by one-electron oxidation, could be an initiator for cationic polymerization of vinyl monomers such as isobutyl vinyl ether (IBVE), 2,3-dihydrofuran, p-methoxystyrene, N-vinyl pyrrolidone, etc., to give the corresponding polymers, when 1 had a low nucleophilic counter anion. Formation of the adducts of 1 and IBVE as well as 1H-NMR and IR data suggested the formation of polymers containing N? O? C structure as the polymer head group. In the polymerization of IBVE, the effects of solvent and concentration of 1 were little observed, however the polymerization rate was dependent on temperature. Furthermore, the thermal reaction of the polymers obtained, which were regarded as prepolymers for block copolymerization and polymeric initiators for radical polymerization, was studied. For example, poly(2-benzylidene-1,3-dioxane) obtained by the polymerization of 2-benzylidene-1,3-dioxane with oxoaminium hexafluoroantimonate ( 1, X = SbF6) was employed as an initiator for radical polymerization of MMA to give its block copolymer with PMMA. © 1993 John Wiley & Sons, Inc. 相似文献
87.
CHANG Kai-Guo LU Xiang-Ping DU Fu-Ying ZHAO Min-ShouChangchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun Jilin China 《中国化学》1994,(6)
The apparent standard potential of Dy/Dy(III) system in the LiCl-KCl eutectic has been determined by the logarithmic analysis of the semi-integrals of voltammograms, logarithmic analysis of chronopotentiograms and the open circuit potentiometry. The dysprosium equilibrium potentiab for various concentration of dysprosium chloride in the LiCl-KCl eutectic melt between 400-500℃ were first determined experimentally, and the apparent standard potential of this system and its temperature dependance have been calculated. 相似文献
88.
Different physical chemical methods were used to study the thermochemical processes in a system involving a natural phosphate and complex acid salts of ammonium sulphate. The products of decomposition of the double ammonium salt and the products of their interactions with the phosphate were identified. The formation of ammonium and calcium polyphosphates and the disproportionation of P3O 10 5? and P2O 7 4? to PO 4 3? and PO 3 ? were found to depend on the circumstances of the thermal interactions. 相似文献
89.
90.