首页> 外文期刊>Journal of the American Chemical Society >Reactivity of an Aryl-Substituted Silicon−Silicon Triple Bond: Reactions of a 1,2-Diaryldisilyne with Alkenes
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Reactivity of an Aryl-Substituted Silicon−Silicon Triple Bond: Reactions of a 1,2-Diaryldisilyne with Alkenes

机译:芳基取代的硅-硅三键的反应性:1,2-二芳基二甲硅烷基与烯烃的反应

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摘要

The reactivity of a bulky, diaryl-substituted disilyne, Ar−Si≡Si−Ar, was examined for the first time. Reaction of the disilyne with ethylene yielded an ethylene-bridged bis(silacyclopropane), which is interpreted as a further reaction product of the initially formed 1,2-disilacyclobutene species with ethylene. A cyclohexane fused with a 1,2-disilacyclobutene was obtained in the reaction with cyclohexene. In the reaction with 2,3-dimethyl-1,3-butadiene, a tricyclo derivative was isolated from the complex product mixture
机译:首次检查了庞大的二芳基取代的二硅炔Ar-Si≡Si-Ar的反应性。二甲炔与乙烯的反应产生了乙烯桥联的双(硅杂环丙烷),其被解释为最初形成的1,2-二硅环丁烯物种与乙烯的另一反应产物。在与环己烯的反应中获得与1,2-二硅环丁烯稠合的环己烷。在与2,3-二甲基-1,3-丁二烯的反应中,从复杂的产物混合物中分离出三环衍生物

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