氯硅烷
化学
硅烷
硅
硅烷
有机化学
俘获
有机合成
高分子化学
药物化学
催化作用
生态学
生物
作者
Paul F. Hudrlik,Dai Donghua,Anne M. Hudrlik
标识
DOI:10.1016/j.jorganchem.2005.11.068
摘要
Reactions of 1,4-dilithiobutadienes (from 1,4-diiodo-1,2,3,4-tetraethylbutadiene (1) and 2,2′-dibromobiphenyl (7) with t-BuLi) with Me3SiCl gave siloles (3 and 9a) as the major products. No evidence for a disilylated butadiene was obtained. Use of higher molecular weight chlorosilanes ((allyl)Me2SiCl, BnMe2SiCl, and PhMe2SiCl) with dibromide 7 gave dimethylsilole 9a and a silane (10a, 10b, or 10c) resulting from trapping of the organic group by the chlorosilane.
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