From structure to novel reactivity in frustrated Lewis pairs

被引:79
作者
Paradies, Jan [1 ]
机构
[1] Univ Paderborn, Dept Chem, Warburger Str 100, D-33098 Paderborn, Germany
关键词
HETEROLYTIC DIHYDROGEN ACTIVATION; METAL-FREE HYDROGENATION; PHOSPHINE OXIDES; STEREOSPECIFIC DEOXYGENATION; CATALYZED HYDROGENATION; ELECTRONIC CONTROL; BOND ACTIVATION; H-2; ACTIVATION; BORANE; CHEMISTRY;
D O I
10.1016/j.ccr.2018.09.014
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The coexistence of a strong Lewis acid and a Lewis base in solution, the so called frustrated Lewis pair, has led to the discovery of metal-free hydrogen activation. Since then, this observation has inspired numerous chemists to develop more examples. Metal-free hydrogenation is so far the most studied application of frustrated Lewis pairs in chemistry and highly efficient methodologies for a number of substrates have been developed. However, the targeted choice of a FLP-catalyst is yet rather intricate, due to the lack of an in depth understanding of FLP-reactivity. The presented structure-reactivity-relationship for hydrogenation reactions allowed the targeted development and optimization of unprecedented reactions using FLPs as catalysts. This article provides insight into FLP-reactivity by summarizing our mechanistic and synthetic work in this field. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:170 / 183
页数:14
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