The σ-CAM mechanism:: σ complexes as the basis of σ-bond metathesis at late-transition-metal centers

被引:490
作者
Perutz, Robin N. [1 ]
Sabo-Etienne, Sylviane
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[2] CNRS, Chim Coordinat Lab, F-31077 Toulouse 04, France
关键词
boranes; dihydrogen complexes; homogeneous catalysis; hydride ligands; silanes;
D O I
10.1002/anie.200603224
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Complexes in which a σ-H-E bond (E = H, B, Si, C) acts as a two-electron donor to the metal center are called σ complexes. Clues that it is possible to interconvert σ ligands without a change in oxidation state derive from C-H activation reactions effecting isotope exchange and from dynamic rearrangements of σ complexes (see Frontispiece). Through these pathways, metathesis of M-E bonds can occur at late transition metals. We call this process σ-complex-assisted metathesis, or σ-CAM, which is distinct from the familiar σ-bond metathesis (typical for d0 metals and requiring no intermediate) and from oxidative-reductive elimination mechanisms (inherently requiring intermediates with changed oxidation states and sometimes involving σ complexes). There are examples of σ-CAM mechanisms in catalysis, especially for alkane borylation and isotope exchange ofalkanes. It may also occur in silylation and alkene hydrogenation. © 2007 Wiley-VCH Verlag GmbH &. Co. KGaA.
引用
收藏
页码:2578 / 2592
页数:15
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