Iridium complexes with monodentate N-heterocyclic carbene ligands

被引:51
|
作者
Sipos, Gellert [1 ,2 ]
Dorta, Reto [1 ]
机构
[1] Univ Western Australia, Dept Chem, Sch Mol Sci, 35 Stirling Highway, Perth, WA 6009, Australia
[2] Innostudio Inc, Zahony Utca 7, H-1031 Budapest, Hungary
基金
澳大利亚研究理事会;
关键词
C-H ACTIVATION; HYDROGEN-ISOTOPE-EXCHANGE; OPPENAUER-TYPE OXIDATION; TRANSFER CATALYTIC-ACTIVITY; TRANSITION-METAL-COMPLEXES; DYNAMIC KINETIC RESOLUTION; NMR SIGNAL AMPLIFICATION; BOND ACTIVATION; ELECTRONIC-PROPERTIES; EFFICIENT CATALYSTS;
D O I
10.1016/j.ccr.2017.10.019
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Monodentate N-heterocyclic carbene (NHC) ligands have been an extremely successful class of ancillary ligands in transition metal chemistry over the last 3 decades. Particularly important developments during that period have seen the use of bulky, monodentate NHC ligands in late transition metal chemistry and catalysis. In this review, we have gathered results that present how these monodentate ligands have been used in iridium chemistry. A comprehensive overview on synthetic methods available to access NHC-Ir compounds, the stoichiometric activity of the resulting complexes as well as their use in catalysis and other applications is given in the following pages. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 68
页数:56
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