化学
硅氢加成
催化作用
产量(工程)
选择性
分子内力
氢化物
烷基
水解
组合化学
三氯氢硅
光化学
氘
级联反应
均相催化
催化循环
反应中间体
烯烃
高分子化学
氰化
动力学分辨率
有机化学
作者
Xiaoming Xu,Yaxin Feng,Fen Wang,Yuhong Liu,Xiufang Xu,Shou‐Fei Zhu,Jianfeng Li,Chunming Cui
摘要
Catalytic hydrosilylation of iminocyclopropanes (ICPs) may selectively yield intriguing silicon-nitrogen heterocycles. Rare-earth alkyl complexes bearing silyl-binaphthyldiamide ligands have been synthesized and employed as catalysts for the hydrosilylation of ICPs with primary silanes. The catalytic reactions selectively yielded a series of azasilacyclopentanes in excellent yields (93-98%) with high selectivity (>99%) at room temperature. The catalytic reactions could be scaled up to the gram scale with 0.5 mol·% loadings of the catalysts. Notably, the azasilacyclopentanes could undergo facile alcoholysis and hydrolysis to give amine-functionalized siloxanes and silanols. The deuterium labeling and kinetic isotopic effect experiments as well as DFT calculations disclosed a catalytic cascade inter- and intramolecular hydrosilylation mechanism. The catalytic key intermediate silyl-binaphthyldiamine rare-earth hydride has been isolated and structurally characterized.
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