The broadening reach of frustrated Lewis pair chemistry

被引:958
作者
Stephan, Douglas W. [1 ]
机构
[1] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S3H6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
METAL-FREE HYDROGENATION; FREE CATALYTIC-HYDROGENATION; H BOND ACTIVATION; ENANTIOSELECTIVE HYDROGENATION; ASYMMETRIC HYDROGENATION; DIHYDROGEN ACTIVATION; MOLECULAR-HYDROGEN; PROPARGYL ESTERS; BORENIUM CATIONS; CARBON-MONOXIDE;
D O I
10.1126/science.aaf7229
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
The revelation that combinations of Lewis acids and bases for which dative bonding is impeded can activate dihydrogen led to the concept of "frustrated Lewis pairs" (FLPs). Over the past decade, a range of FLP systems and substrate molecules have precipitated a paradigm change in main-group chemistry and metal-free catalysis. The FLP motif has also found application in a growing body of chemical problems in organic synthesis, transition metal and free radical chemistry, materials, enzymatic models, and surface chemistry. The current state of FLP chemistry is assessed herein, and the outlook for the future considered.
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页数:8
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