Synthesis of unsymmetrical 1,2-bis(diorganochlorosilyl)ethanes
摘要:
Unsymmetrical 1,2-bis(diorganylsilyl)ethanes were synthesized by two procedures. Hydrosilylation of chloro(vinyl)silanes were used to obtain compounds of the general formula ClMe2SiCH2CH2SiRMeCl with different substituents (R = Et, Vin, Ph) on the silicon atom. Chlorodealkylation of 1,2-bis(trialkylsilyl)ethanes gave compounds of the general formula ClAlk(2)SiCH(2)CH(2)SiAlk(2)Cl (Alk = Me, Et, Pr). It is established that the latter reaction provides high yields only with Me- and Et-substituted compounds, whereas Pr-substituted products are formed in poor yields. The mechamism of this reaction based on quantum-chemical calculations is offered.
Sheludyakov, V. D.; Zhun', V. I.; Vlasenko, S. D., Journal of general chemistry of the USSR, 1985, vol. 55, # 7, p. 1372 - 1381
作者:Sheludyakov, V. D.、Zhun', V. I.、Vlasenko, S. D.、Bochkarev, V. N.、Slyusarenko, T. F.、et al.
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Sheludyakov, V. D.; Zhun', V. I.; Vlasenko, S. D., Journal of general chemistry of the USSR, 1985, vol. 55, # 8, p. 1594 - 1597
作者:Sheludyakov, V. D.、Zhun', V. I.、Vlasenko, S. D.
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SHELUDYAKOV, V. D.;ZHUN, V. I.;VLASENKO, S. D., ZH. OBSHCH. XIMII, 1985, 55, N 8, 1795-1799
作者:SHELUDYAKOV, V. D.、ZHUN, V. I.、VLASENKO, S. D.
DOI:——
日期:——
Synthesis of unsymmetrical 1,2-bis(diorganochlorosilyl)ethanes
作者:V. G. Lakhtin、S. P. Knyazev、L. E. Gusel’nikov、E. N. Buravtseva、N. A. Kuyantseva、I. A. Zalomnova、L. A. Parshkova、V. G. Bykovchenko、A. V. Kisin、E. A. Chernyshev
DOI:10.1134/s1070363208090053
日期:2008.9
Unsymmetrical 1,2-bis(diorganylsilyl)ethanes were synthesized by two procedures. Hydrosilylation of chloro(vinyl)silanes were used to obtain compounds of the general formula ClMe2SiCH2CH2SiRMeCl with different substituents (R = Et, Vin, Ph) on the silicon atom. Chlorodealkylation of 1,2-bis(trialkylsilyl)ethanes gave compounds of the general formula ClAlk(2)SiCH(2)CH(2)SiAlk(2)Cl (Alk = Me, Et, Pr). It is established that the latter reaction provides high yields only with Me- and Et-substituted compounds, whereas Pr-substituted products are formed in poor yields. The mechamism of this reaction based on quantum-chemical calculations is offered.