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991.
[reaction: see text] Hydrozirconation of alkynes followed by in situ transmetalation to dimethylzinc and 1,2-addition to activated ketones and N-diphenylphosphinoylimines leads to tertiary allylic alcohols and amines in high overall yield. With 8-phenylmenthol as the chiral auxiliary, si-face attack proceeds in good to excellent diastereoselectivities. 相似文献
992.
Mogilevkina M. F. Shipachev V. A. Tkachev S. V. Troshkova G. P. Martynets L. D. 《Russian Journal of Coordination Chemistry》2002,28(6):419-422
The reaction between cis-[Pt(NH3)2Cl2], N1-(2"-tetrahydrofuranyl)-5-fluorouracil (HL), and NaOH (taken in a molar ratio of 1 : 1 : 1) or between cis-[Pt(NH3)2Cl2], HL, and Ag2O (taken in the molar ratio of 1 : 1 : 0.5) was used to synthesize complexes Ia (in the case of NaOH) or Ib (in the case of Ag2O) with composition Pt(NH3)2LCl. The model complex [Pt(NH3)3L]NO3 (II) was synthesized by the reaction between [Pt(NH3)3Cl]Cl, HL, AgNO3, and Ag2O (1 : 1 : 1 : 0.5). The obtained compounds were characterized by chemical analysis, chromatography, thermogravimetry, conductometry, potentiometry, IR, electronic, and NMR spectroscopies. Complexes Ia and Ib were found to have both similar and different properties. The structures of the compounds and the type of L– coordination to platinum(II) were suggested. Cytotoxic properties of Iaand Ib were studied. 相似文献
993.
Catalytic bipotentiometric and biamperometric methods for determining silver(I) with the use of the new manganese(IV)-arsenic(III) indicator reaction catalyzed by iodide ions in the presence of sulfuric acid have been developed. The effects of the sulfuric acid concentration of some ionic species, of the mole ratio of manganese(IV) to arsenic(III) in the solution titrated, and of the titrand temperature, as well as of the current and potential difference, respectively, used for polarization of the indicator electrodes on the conditions for determinations of silver(I) of various concentrations were investigated. The error in the determination of 1.0 g/cm3 silver(I) do not exceed 2%, and the precision of the results is high for both methods. 相似文献
994.
L.J. del Valle D. Aradilla F. Sepulcre E. Armelin F. Estrany 《European Polymer Journal》2007,43(6):2342-2349
Cell adhesion and proliferation in poly(3,4-ethylenedioxythiophene), an electroactive polythiophene derivative generated by anodic polymerization, has been investigated. Results show that epithelial cells Hep-2 present significant activity on the surface of poly(3,4-ethylenedioxythiophene) electrodeposited on stainless steel electrodes, no sign of cytotoxicity being detected for this conducting polymer. Indeed, seeded and cultured cells bound better to poly(3,4-ethylenedioxythiophene) than to uncoated stainless steel, the latter substrate being used as a control. Furthermore, the electrochemical characteristics of poly(3,4-ethylenedioxythiophene) covered with cells was determined in different biological media using cyclic voltammetry experiments. Results reveal a significant increase in the electroactivity of this material when it is covered with a cellular monolayer. The overall of the results evidences not only the biocompatibility of poly(3,4-ethylenedioxythiophene) with Hep-2 cells but also their electrocompatibility. 相似文献
995.
L. Moens F. De Corte A. De Wispelaere J. Hoste A. Simonits A. Elek E. Szabo 《Journal of Radioanalytical and Nuclear Chemistry》1984,82(2):385-452
Recommended k0-factors and related nuclear data for use in (n, γ) activation analysis are given for 72 isotopes. In addition the basic nuclear constants and experimental parameters needed in the k0 standardization method are reviewed. For convenient data reduction, computer programs were developed. 相似文献
996.
997.
The stereochemistry of the hydrogenolysis of benzyl-N bonds was studied using S(+)-2-dimethylamino-2-phenyl-propionic acid (I) and its derivatives, and R(?)-2-anilino-2-phenyl-propionic acid (II). The configuration of I was confirmed, that of II established by ORD. measurements, after transformation of the phenyl into cyclohexyl groups. On a palladium catalyst the hydrogenolysis of I, its methyl and ethyl esters and its amide proceeded with 72 to 99% inversion of configuration, that of II with at least 66% inversion. The ester of the quaternary ammonium derivative of I gave as much inversion as retention (= racemisation). 相似文献
998.
The coulometric electrolytic principle is utilized for the measurement of moisture sorbed on sintered thorium dioxide. Moisture is removed from the sample by heating and is swept by dry argon gas through a hygrometer. The resulting hygrometer output is converted into frequency pulses and counted cumulatively. The instrument is calibrated by use of standard hydrated chemicals. The number of counts/mu;g of water obtained from standards compares favourably with the theoretical number of counts/mu;g calculated from performance specifications of the components employed. The error is <5% for 1-350mu;g of water. A high sensitivity and low operating blank recommends application of this method to materials other than thorium dioxide, having very low moisture contents. 相似文献
999.
The complexes CoH(PF3)4?n (PPh3)n (n = 1–3) have been prepared by low from the reaction between CoH(PF3)(PPh3)3 and butadiene. The hydrido complexes are active catalysts for the isomerisation of 1-octene to 2-octene under hydrogen or nitrogen. 相似文献
1000.
The crystal structure of the title compound has been determined from X-ray diffractometer data by direct methods, and refined by full matrix least squares techniques to R = 0·057 for 1231 reflections. The crystals are monoclinic, space group C2/C, cell dimensions a = 1665, b = 987, c = 1443 pm, β = 107·37° and Z = 8. The conformation of the tetrahydro-1,2-oxazine ring is a chair with the N-substituent equatorial. There is evidence of significantly greater torsional angles around the N and O atoms than around the ring C atoms, showing the ring to be more puckered than cyclohexane. The hydrogen bond is between the acid group on one molecule and the ring nitrogen on its neighbour. 相似文献