硅氢加成
马尔科夫尼科夫法则
硅烷
烯烃
催化作用
化学
位阻效应
有机化学
铑
吡啶
氢化物
硼氢化
金属
均相催化
硅烷
组合化学
区域选择性
作者
Aaron M. Tondreau,Crisita Carmen Hojilla Atienza,Keith J. Weller,Susan A. Nye,Kenrick M. Lewis,Johannes G. P. Delis,Paul J. Chirik
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-02-02
卷期号:335 (6068): 567-570
被引量:550
标识
DOI:10.1126/science.1214451
摘要
Alkene hydrosilylation, the addition of a silicon hydride (Si-H) across a carbon-carbon double bond, is one of the largest-scale industrial applications of homogeneous catalysis and is used in the commercial production of numerous consumer goods. For decades, precious metals, principally compounds of platinum and rhodium, have been used as catalysts for this reaction class. Despite their widespread application, limitations such as high and volatile catalyst costs and competing side reactions have persisted. Here, we report that well-characterized molecular iron coordination compounds promote the selective anti-Markovnikov addition of sterically hindered, tertiary silanes to alkenes under mild conditions. These Earth-abundant base-metal catalysts, coordinated by optimized bis(imino)pyridine ligands, show promise for industrial application.
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