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Hydroboration of Phosphaalkynes by HB(C6F5)(2)

机译:HB(C6F5)(2)对磷炔烃进行硼氢化

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摘要

The hydroboration of phosphaalkynes with Piers' borane (HB(C6F5)(2)) generated unusual phosphaalkenylboranes [RCH=PB(C6F5)(2)](2) that persisted as dimers in both solution and the solid state. These P2B2 heterocycles underwent ring opening when subjected to nucleophiles, such as pyridine and tert-butylisocyanide, to yield monomeric phosphaalkenylborane adducts RCH=PB(C6F5)(2)(L). DFT calculations were performed to probe the nature of the interaction of phosphaalkynes with boranes.
机译:磷炔烃与Piers's硼烷(HB(C6F5)(2))的硼氢化生成了异常的磷烯基硼烷[RCH = PB(C6F5)(2)](2),在溶液和固态下均以二聚体形式存在。这些P2B2杂环在经历亲核试剂(例如吡啶和叔丁基异氰化物)时会发生开环反应,从而生成单体磷烯基硼烷加合物RCH = PB(C6F5)(2)(L)。进行DFT计算以探究磷炔与硼烷相互作用的性质。

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