Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes

被引:465
作者
Tondreau, Aaron M. [1 ]
Atienza, Crisita Carmen Hojilla [1 ]
Weller, Keith J. [2 ]
Nye, Susan A. [2 ]
Lewis, Kenrick M. [3 ]
Delis, Johannes G. P. [4 ]
Chirik, Paul J. [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[2] Moment Performance Mat, Waterford, NY 12188 USA
[3] Moment Performance Mat, Tarrytown, NY 10591 USA
[4] Moment Performance Mat Bv, NL-4612 PX Bergen Op Zoom, Netherlands
关键词
TRANSITION-METAL-COMPLEXES; DINITROGEN;
D O I
10.1126/science.1214451
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
收藏
页码:567 / 570
页数:4
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