Multidentate silyl ligands in transition metal chemistry

被引:40
|
作者
Simon, M. [1 ]
Breher, F. [1 ]
机构
[1] Karlsruhe Inst Technol, Inst Inorgan Chem, Devis Mol Chem, Engessetstr 15, D-76131 Karlsruhe, Germany
关键词
H BOND ACTIVATION; CATALYZED DEHYDROGENATIVE BORYLATION; POLYDENTATE PHOSPHINOALKYL-SILYL; TRINUCLEAR PALLADIUM COMPLEX; MOLYBDENUM HYDRIDO COMPLEXES; SILICON-CARBON BOND; PINCER-TYPE LIGAND; X-RAY CRYSTAL; SI-C BOND; RHODIUM COMPLEXES;
D O I
10.1039/c7dt02085f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Silyl ligands are of great interest in transition metal coordination chemistry since they exhibit a strong trans-influence and create electron rich metals centres, which are in turn eligible to activate reagents. This review presents and discusses the use of multidentate Si-based ligand systems in transition metal coordination chemistry. These include tri- and tetradentate pincer and scorpionate-type ligands, which have been developed in recent years in order to tailor both steric and electronic properties for achieving a defined control over the reactivity of a transition metal complex. A discussion of synthetic and structural aspects of several subgroups of ligand architectures is presented. Some compounds allow for a detailed insight into the activation process of silanes or are capable of activating small molecules.
引用
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页码:7976 / 7997
页数:22
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