Cyclopentadienyl-, Indenyl- and Fluorenyl-Functionalized N-Heterocyclic Carbene Metal Complexes: Synthesis and Catalytic Applications

被引:63
|
作者
Royo, Beatriz [1 ]
Peris, Eduardo [2 ]
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, EAN, P-2780157 Oeiras, Portugal
[2] Univ Jaume 1, Dept Quim Inorgan & Organ, Castellon de La Plana 12071, Spain
关键词
N-Heterocyclic carbenes; Cyclo-penta-dienyl ligands; Half-sandwich complexes; Homogeneous catalysis; STEREODIRECTING LIGANDS; ZIRCONIUM COMPLEXES; BORROWING HYDROGEN; BEARING; ACTIVATION; TITANIUM; COORDINATION; REACTIVITY; ROUTE; IRIDIUM;
D O I
10.1002/ejic.201100990
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This microreview focuses on the preparation of metal complexes with N-heterocyclic carbene ligands linked to cyclopentadienyl (and related indenyl and fluorenyl) rings. Since the description of the first Ti and V complexes in 2006, the field has grown to afford a large number of new complexes, in which the metals range from early to late transition metals. The ligands that are now available not only include a wide set of cyclopentadienyl-, indenyl- and fluorenyl-NHCs with a variety of tethers, but may even present chirality. Several catalytic applications of the new complexes are described, including borrowing hydrogen processes (transfer hydrogenation, beta-alkylation of secondary alcohols, alkylation of amines with primary alcohols), hydrosilylation of aldehydes, epoxidation and hydroformylation of olefins, among others.
引用
收藏
页码:1309 / 1318
页数:10
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