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91.
Rodríguez-Cea A de la Campa MR Sanz-Medel A 《Analytical and bioanalytical chemistry》2005,381(2):388-393
Cytochromes P-450 are members of a superfamily of hemoproteins involved in the oxidative metabolism of various physiological and xenobiotic compounds in eukaryotes and prokaryotes. The multiplicity of this group of enzymes has been widely studied by chromatographic techniques, mainly high-performance liquid chromatography (HPLC). Because these enzymes are membrane-bound proteins, sample preparation for chromatographic separation of P-450 enzymes requires a solubilization step. The sample-preparation procedures are critical, because detergents affect not only the efficiency of protein solubilization but also their further chromatographic resolution. Trout liver microsomes have been taken here as a model sample to investigate iron speciation in cytochrome P-450. Trouts were treated intraperitoneally with -naphthoflavone, a potent inducer of some P-450 enzymes, and a microsomal suspension containing 7.4±0.1 nmol mL–1 P-450 enzymes was obtained by ultracentrifugation. Lubrol PX was selected as detergent for solubilization, resulting in about 90% solubilization recovery. The solubilized cytochromes P-450 were further separated by AE–FPLC, with UV detection, or coupled to ICP–MS with an octapole reaction system, ICP–(ORS)MS (monitoring Fe signals at masses 54, 56, and 57). A sampling procedure and chromatographic conditions are developed and were successfully applied to iron speciation in trout liver P-450 enzymes. ICP–(ORS)MS detection of P-450 enzymes is Fe-specific and so will give accurate information on the prosthetic group of the protein, which can constitute an advantageous alternative to classical methods for detection of these hemoproteins. 相似文献
92.
I. V. Korol’kov A. I. Gubanov K. V. Yusenko I. A. Baidina S. A. Gromilov 《Journal of Structural Chemistry》2007,48(3):486-493
Several non-equilibrium solid solutions belonging to the platinum-osmium systems Os0.9Pt0.1, Os0.8Pt0.2, Os0.5Pt0.5, Os0.7Pt0.3, Os0.75Pt0.25 are prepared and studied. The thermal decomposition of [Pt(NH3)4][OsCl6] in the hydrogen and helium atmosphere is investigated. It is found that the Pt0.5Os0.5 solid solution develops through the formation of (NH4)2[OsCl6] and a metallic phase based on Pt. The crystal structure of a double complex salt [Pt(NH3)4][OsCl6] is studied (X8-APEX Bruker, 1508 independent reflections, R = 2.04%). Crystal data for PtOsN4Cl6H12 are: a = 11.6216(5) Å, b = 11.0016(5) Å, c = 10.3819(5) Å, V = 1327.4(1) Å3, space group Cmca, Z = 4, d x = 3.333 g/cm3. The coordination polyhedron around Os is octahedral: 〈Os-Cl〉 2.357 Å, ∠Cl-Os-Cl 89.5–90.5°, while around Pt it is square-planar: Pt-N 2.046 Å, ∠ N-Pt-N 89.59° and 90.41°. 相似文献
93.
O. LeynaudA. Lafond Y. MoëloP. Palvadeau A. Meerschaut 《Journal of solid state chemistry》2002,168(1):41-51
Crystal structures of two new misfit compounds, [SrGd0.5S1.5]1.16NbS2 and [Sr(Fe,Nb)0.5S1.5]1.13NbS2, were determined through the composite approach, i.e., by refining each subpart (Q, H-parts, and the common part) of these composite materials, separately. The Q-part is a three-atom-thick layer, with the NaCl-type structure, where external SrS planes enclose the inner GdS or (Fe,Nb)S plane; the structural difference between these two compounds lies in the central layer within the Q-part: Gd and S atoms are in special positions (octahedral coordination), while Fe and S atoms are statistically distributed on split (×4) positions (tetrahedral coordination) around a central unique site (=special position occupied by Nb). The H-part is a sandwich of sulfur planes enclosing the inner Nb plane as observed for the structure of the binary compound NbS2 itself. The Sr-Gd derivative shows a paramagnetic behavior in the whole studied temperature range (2-300 K). On the other hand, antiferromagnetic interactions occur in the Sr-Fe derivative; the complex magnetic behavior of this compound is related to the statistical distribution of Fe atoms which leads to frustration of the magnetic interactions. At room temperature, experimental values obtained from Mössbauer spectrum correspond to Fe3+ in tetrahedral sulfur environment: isomer shift δ=0.32 mm s−1, and quadrupole splitting ΔE=0.48 mm s−1. 相似文献
94.
A. M. Astakhov A. D. Vasiliev M. S. Molokeev L. A. Kruglyakova A. M. Sirotinin R. S. Stepanov 《Journal of Structural Chemistry》2004,45(3):537-540
The structure of 5-nitraminotetrazole sodium salt sesquihydrate was determined by X-ray diffraction. The crystals are monoclinic, space group P21/c;a = 3.551(1) Å, b = 21.834(4) Å, c = 9.075(2) Å; = 110.68(3)°; V = 658.3(2) Å3; Z = 4; calc = 1.807 g/cm3. The anion is planar and has an intramolecular hydrogen bond. The negative charge of the anion is localized on one of the oxygens of the nitro group. The sodium cation (c.n.6) is coordinated by three oxygen atoms of different anions and three oxygens of crystallization water. One of the crystallization water molecules is disordered in the unit cell. The anions are hydrogen-bonded with each other and with crystallization water molecules.Original Russian Text Copyright © 2004 by A. M. Astakhov, A. D. Vasiliev, M. S. Molokeev, L. A. Kruglyakova, A. M. Sirotinin, and R. S. StepanovTranslated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 3, pp. 562–565, May–June 2004. 相似文献
95.
A one-step solid-phase extraction procedure, based on a new silica gel adsorbent modified with cholesterol groups, has been
investigated for measurement of cotinine in urine. Cotinine is the main metabolite of nicotine in the human body and is analyzed
as a biomarker for assessment of direct or passive exposure to tobacco smoke. New cholesterol-modified adsorbents have been
obtained by chemical modification of silica gel of different porosity with cholesterol ligands. Although recovery by this
extraction procedure were optimum over a relatively broad range of sample pH (3.1–8.0), analytical conditions such as sample
loading, washing and elution conditions, concentration of cotinine to be extracted, and the type of adsorbent used for extraction
were found to affect the efficiency of the procedure and had to be controlled for optimum recovery. When these conditions
were controlled, recovery of cotinine from spiked human urine was reproducible and depended on compound ionization. Quantitative
analysis of cotinine was performed by reversed-phase high-performance liquid chromatography with UV detection.
Presented at: Conference of the Hyphenation of Liquid Chromatography–Nuclear Magnetic Resonance Spectroscopy, Liquid Chromatography–Mass
Spectrometry and Related Topics, Tuebingen, Germany, March 25–29, 2006. 相似文献
96.
Summary A global LSER model that relates HPLC retention to mobile phase composition and pH is tested for a varied group of solutes,
both neutral and ionizable, in a polymeric column and methanol-water mobile phases. It is compared to the local LSER model
developed only for a given mobile phase, i.e., a fixed organic modifier content, and to the global LSER model set only for
neutral solutes. The global LSER model for neutral and ionizable solutes requires a few supplementary parameters over the
other models tested, but it accounts for retention under any experimental conditions for a given column and methanol-water
mobile phases, describing properly the interactions established in the HPLC system (hydrophobicity, hydrogen-bond acidity
and basicity, dipolarity/polarizability…).
This paper is number 13 of a series with the same general title: “Retention of Ionizable Compounds on HPLC” published in various
journals. 相似文献
97.
D. M. Roitershtein K. A. Lyssenko P. A. Belyakov M. Yu. Antipin E. S. Petrov 《Russian Chemical Bulletin》1997,46(9):1590-1594
The reaction of the cyclopentadienyllutetium anthracenide, C5H5Lu(C14H10)2−(THF)2 (1), with azobenzene yielded the [C5H5(THF)Lu(μ−η2:η2−PhN—NPh)]2(THF)2 (2) binuclear complex. The structure of the reaction product was established by X-ray structural analysis. The dynamic behavior
of complex2 in a THF-d8 solution was studied by1H NMR spectroscopy in the temperature range of 265–330 K.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1667–1671, September, 1997. 相似文献
98.
D. Levy F. Del Monte X. Quintana J.M. Otón 《Journal of Sol-Gel Science and Technology》1997,8(1-3):1063-1066
Liquid crystal microdroplets trapped into silica gel-glasses by sol-gel processes may be used for display applications. Gel-glass
dispersed liquid crystals (GDLC) are switched between opaque and transparent states by applying external AC-voltage signals;
no polarizers are required. The feasibility of applying these materials to colored displays has been explored. A comparative
study of different dyes for GDLC color displays, which were either embedded in the sol-gel matrix or dissolved in the liquid
crystal microdroplets is presented. 相似文献
99.
Qian-Feng Zhang Yu-Jie Liu Richard D. Adams Alexander Rothenberger Dieter Fenske Wa-Hung Leung 《Journal of Cluster Science》2006,17(3):445-455
Treatment of tetracopper(I)-phosphonitocavitand [1·Cu4(μ-Cl)4(μ4-Cl)] (2) (1 = tetraphosphonitocavitand [rccc-2,8,14,20-tetrakis-(iso-butyl)-phosphonitocavitand (C44H48O8P4Ph4)]) with PhSeSiMe3 in THF at low temperature afforded a novel polyanionic cluster [pyH]6[(CuCl)9(μ3-SePh)5(μ4-SePh)] (4) as a major product along with a new tetracopper(I)-phosphonitocavitand (3) with a centered μ3-Cl. Molecular structure of anionic cluster in 4 consists of six PhSe− bridging ligands containing five μ3-SePh and one exceptional μ4-SePh bridging nine copper atoms, of which eight copper atoms have trigonal coordination geometry and the other has distorted
tetrahedral geometry.
Dedicated to Professor Han-Qin Liu on the occasion of his 70th birthday. 相似文献
100.
T. Kowalska 《Chromatographia》1991,31(3-4):119-122
Summary Intermolecular interactions between the solute and the moieties constituting the mobile phase significantly contribute to the overall retention pattern of a given solute in a given chromatographic system. In this paper retention of solute is discussed in the case of the B+AB1+AB2 type mobile phase, which, in a quasithermodynamic way, can be divided into seven individual moieties. One evaluates the influence of each moiety on solute retention, and refers these regularities to the polarity of the solutes. 相似文献