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M. G. Voronkov E. A. Grebneva O. M. Trofimova A. I. Albanov N. F. Chernov N. N. Chipanina 《Russian Journal of General Chemistry》2006,76(12):1851-1853
Reaction of tetrafluorosilane with tris(2-hydroxyethyl)-and tris(2-trimethylsiloxyethyl)amine results in formation of 1-fluorosilatrane and fluorosilatrane in 75 and 53% yield, respectively. Reaction of tetrafluorosilane with bis(2-trimethylsiloxyethyl)amine and its N-methyl derivative leads to the hitherto unknown 1,1-difluoroquasisilatranes (N → Si) F2Si(OCH2CH2)2NR (R = H, Me) containing donor-acceptor bond N → Si and pentacoordinate silicon atom. The structure of the synthesized compounds was proved by 1H, 13C, 15N, 19F, 29Si NMR and IR spectroscopy. 相似文献
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M. G. Voronkov S. G. D’yachkova I. P. Lebedeva A. V. Evart L. G. Shagun 《Russian Journal of General Chemistry》2007,77(4):604-606
Alkylthiochloroacetylenes react with geminal (in ether) and vicinal (in THF) dithiols to form, respectively, functional 1,3-dithiolenes (yield 43%) or 1,3-dithiolanes (yield 34%). 相似文献
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V. A. Titov V. I. Rakhlin A. A. Titov F. A. Kuznetsov M. G. Voronkov 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2006,80(12):1907-1910
The thermodynamic properties of several silicon-containing derivatives of asymmetric dimethylhydrazine were estimated by comparative methods. The CVD diagrams of the deposition of silicon nitride and dioxide from gas media containing these reagents were constructed. 相似文献
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The review summarizes and systematizes the authors' data on the synthesis and reactivity of halomethyl thioketones. Reactions involving the title compounds as intermediates are also considered. Mechanisms of formation of halomethyl thioketones are discussed in terms of the results of quantum-chemical calculations. 相似文献
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M. G. Voronkov N. N. Vlasova S. A. Bolshakova S. V. Kirpichenko 《Journal of organometallic chemistry》1980,190(4):335-341
The hydrosilylation of mono- and di-alkenyl sulphides of the type RS(CH2)nCH=CH2 (R = C2H5, CH2=CH, CH2=CHCH2, C3H7, n = 0, 1 and 4) by triethyl- and triethoxy-silane, catalyzed by H2PtCl6·6 H2O, (Ph3P)3RhCl and (PhCN)2PdCl2·Ph3P, has been studied. The addition of hydrosilane to the double bond of alkenyl sulphide leads to a mixture of two isomeric monoadducts. The hydrosilane can cleave the C---S bond of the initial sulphides giving the corresponding derivatives of thiosilanes, X3SiS(CH2)nCH=CH2 (X = C2H5, C2H5O). Hydrosilylation of alkenyl sulphides is accompanied by some side reactions such as dehydrocondensation, reduction and polymerization. The effect of the catalyst nature, the structure of hydrosilane and alkenyl sulphide on the reaction route has been investigated. 相似文献
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M. G. Voronkov V. I. Rakhlin S. N. Adamovich L. P. Petukhov R. G. Mirskov N. K. Yarosh A. L. Kuznetsov M. V. Sigalov 《Russian Chemical Bulletin》1986,35(4):819-821
Conclusions 1-Hydrosilatrane does not react with monosubstituted ethylenes (or acetylenes) either in the presence of platinum or rhodium complexes or upon initiation of the reactions using organic peroxides, UV irradiation, or thermal methods. By contrast, 2-methyl-6-ethyl-1,3-dioxa-6-aza-2-silacyclooctane readily takes part in hydrosilylation of the indicated unsaturated compounds when Rhacac (CO)2 is present.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khirnicheskaya, No. 4, pp. 899–901, April, 1986. 相似文献
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R. G. Mirskov S. V. Basenko V. Yu. Vitkovskii I. A. Gebel' N. K. Yarosh M. G. Voronkov 《Russian Chemical Bulletin》1989,38(3):597-600
Conclusions Alkoxychlorosilanes react with trimethylacyloxysilanes to give the difficultly accessible alkoxy(acyloxy)silanes of general formula (RO)nSi(OCOR)4-n (n=1–3) in 60–80% yields.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 671–674, March, 1989. 相似文献