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1.
E. Sh. Finkel'shtein N. V. Ushakov N. A. Pritula E. A. Andreev N. A. Platé 《Russian Chemical Bulletin》1992,41(1):185-187
The thermally initiated and platinum-catalyzed polymerization of 1-silacyclobutanes with substitutents containing a trimethylsilyl group was carried out. Soluble, high-molecular-weight, heterochain siltrimethylene polymers were obtained, containing trimethylsilyl groups removed from the main chain by various bridges.A. V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 117912 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 1, pp. 223–225, January, 1992. 相似文献
2.
An estimate of the decomposition stability of the Poisson distribution is obtained under the condition that the components
are identical. The estimate is much sharper than that in the general case.
Supported in part by the International Science Foundation (grant No. NJY000).
Proceedings of the XVII Seminar on Stability Problems for Stochastic Models. Kazan, Russia, 1995, Part II. 相似文献
3.
4.
O. A. Kirichenko V. A. Ushakov V. A. Poluboyarov 《Reaction Kinetics and Catalysis Letters》1993,51(1):167-175
XPS, ESR and ESDR methods have been used for studying Al–Fe–O catalysts calcined at 620–1270 K. -Al2O3 interaction with impregnating solutions of iron oxalate complexes was shown to lead to the formation of isolated Fe3+ ions, and supported phases of solid solutions and associates at 620–820 K. 相似文献
5.
M. V. Alfimov S. P. Gromov O. B. Stanislavskii E. N. Ushakov O. A. Fedorova 《Russian Chemical Bulletin》1993,42(8):1385-1389
Styryl dyes containing a crown ether group and a heteroaromatic moiety with a sulfoalkylN-substituent (1a,b) undergo photocyclodimerization in acetonitrile in the presence of Mg(ClO4)2 to give only the typeA isomer of cyclobutane derivative (2a,b). The photochemical regio- and stereoselectivity of the cycloaddition is explained by self-organization of thetrans-isomers of the styryl dyes upon complexation with the Mg2+ cations into dimers with a fixed mutual arrangement of multiple bonds.For part 7, see ref. 1.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1449–1452, August, 1993. 相似文献
6.
Andriyankova L. V. Zhivet'ev S. A. Mal'kina A. G. Kudryakova P. N. Kositsyna E. I. Il'icheva L. N. Ushakov I. A. Afonin A. V. Trofimov B. A. 《Russian Journal of Organic Chemistry》2002,38(11):1681-1685
Reactions of nucleophilic addition of 2- and 4-mercaptopyridines to 3-phenyl-2-propynonitrile, 4-hydroxy-4-alkyl-2-alkynonitriles, and methyl 2-butynoate (triethylamine, 20-25 or 100°C) give rise to the corresponding S-adducts with Z-configuration (for cyanoethylenes), or to a mixture of E- and Z-isomers in 60:40 ratio for methyl 2-butynoate. 相似文献
7.
E. N. Ushakov L. G. Kuz’mina A. I. Vedernikov M. S. Kapichnikova J. A. K. Howard M. Wörner A. M. Braun M. V. Alfimov S. P. Gromov 《Russian Chemical Bulletin》2006,55(1):94-100
The structures of new butadienyl dyes of the benzothiazole series containing the dithia-15-crown-5 (2a) or dithia-18-crown-6 (2b) fragments were established by X-ray diffraction. Complexation of dyes 2a,b with Hg2+, Pb2+, Cd2+, Ag+, Zn2+, and alkaline-earth cations in aqueous-acetonitrile solutions was studied by spectrophotometry. At a high percentage of water
in solutions (P
w ≈ 50%), these dyes have a very low ability to bind Pb2+ cations (logK < 2) and virtually do not bind Cd2+, Zn2+, and alkaline-earth cations. At the same time, these dyes form stable 1: 1 complexes with Hg2+ and Ag+ cations at all P
w. The stability constants of complexes with the Ag+ cation increase with increasing P
w because the free energy of hydration of this cation is much lower than the free energy of solvation in acetonitrile. In the
P
w range from 0 to 75%, the stability constants of the complexes of dyes 2a,b with the Hg2+ cation are larger than those of the corresponding complexes with the Ag+ cation by more than four orders of magnitude.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 90–96, January, 2006. 相似文献
8.
A four-step synthesis of 1-(-ydroxyalkyl)- and 1-(4-hydroxyphenyl)silacyclobutanes was carried out. The influence of the structure of the initial compounds and the reaction conditions on the ratio of the reaction products formed was studied. The stability of the silacyclobutane alcohols and the hydrolysis of their trimethylsilyl ethers were investigated.For preliminary communication, see Ref. 6.Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 4, pp. 946–954, April, 1996. 相似文献
9.
10.
Tsykoza L. T. Ismagilov Z. R. Ushakov V. A. Kuznetsov V. V. Ovsyannikova I. A. 《Kinetics and Catalysis》2003,44(6):806-812
The phase composition of supported Mn–Al–O catalysts and their activity in the reaction of methane oxidation were studied depending on the composition of aluminum oxide supports (-Al2O3 with different -Al2O3 contents modified with individual Mg, La, and Ce oxides or Mg + La and Mg + Ce oxide mixtures) and calcination temperatures (500, 900, and 1300°C). It was found that the Mn–Al–O catalysts based on -alumina containing -Al2O3 and modified with Mg, La, or Ce additives are more active and thermally stable (up to 1300°C) than the samples based on pure -Al2O3. A conclusion was drawn that a higher degree of disorder of the structure of -Al2O3, compared to that of -Al2O3, is favorable for a deeper interaction of manganese and modifying additives with the support at the early stages of the synthesis and for the formation of Mn–Al compounds with complex composition (solid solutions and/or hexaaluminates) at 1300°C. These compounds are responsible for the stability and high activity of the catalysts in methane oxidation. 相似文献