甲酰胺类
甲酰化
催化作用
化学
产量(工程)
小学(天文学)
过渡金属
二氧化碳
金属
药物化学
有机化学
材料科学
物理
天文
冶金
作者
Bi‐Xiang Leong,Yeow-Chuan Teo,Cloé Condamines,Ming‐Chung Yang,Ming‐Der Su,Cheuk‐Wai So
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-12-03
卷期号:10 (24): 14824-14833
被引量:56
标识
DOI:10.1021/acscatal.0c03795
摘要
This study describes the use of a silicon(II) complex, namely, the NHC-silyliumylidene cation complex [(IMe)2SiH]I (1, IMe = :C{N(Me)C(Me)}2), to catalyze the chemoselective N-formylation of primary and secondary amines using CO2 and PhSiH3 under mild conditions to afford the corresponding formamides as a sole product (average reaction time: 4.5 h; primary amines, average yield: 95%, average TOF: 8 h–1; secondary amines, average yield: 98%, average TOF: 17 h–1). The activity of 1 and product yields outperform the currently available non-transition-metal catalysts used for this catalysis. Mechanistic studies show that the silicon(II) center in complex 1 catalyzes the C–N bond formation via a different pathway in comparison with non-transition-metal catalysts. It sequentially activates CO2, PhSiH3, and amines, which proceeds via a dihydrogen elimination mechanism, to form formamides, siloxanes, and dihydrogen gas.
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