A pyridine bridged dicarbene ligand and its silver(I) and palladium(II) complexes: synthesis, structures, and catalytic applications

被引:159
作者
Nielsen, DJ
Cavell, KJ
Skelton, BW
White, AH
机构
[1] Cardiff Univ, Dept Chem, Cardiff CF10 3TB, S Glam, Wales
[2] Univ Western Australia, Dept Chem, Nedlands, WA 6907, Australia
[3] Univ Tasmania, Sch Chem, Hobart, Tas 7001, Australia
基金
澳大利亚研究理事会;
关键词
palladium; silver; carbene complexes; catalysis; Heck reaction;
D O I
10.1016/S0020-1693(01)00677-6
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The potentially tridentate ligand 2,6-bis[(3-methylimidazolium-1-yl)methyl]pyridine dibromide reacts readily with silver(I) oxide in dichloromethane or dimethylsulfoxide to give a dinuclear silver(I)-carbene complex that was isolated as the tetrafluoroborate salt. Single crystal X-ray crystallography shows that each silver(l) ion is bridged by two ligands bonding through the carbene donors. Treatment of the silver(l) complex with suitable palladium(II) precursors gave the complexes PdCl[(CNC)BF4 and [PdMe(CNC]BF4 (CNC = 2,6-bis[(3-methylimidazolin-2-yliden-1-yl)methyl]pyridine), in which the pyridyl and both carbene moieties are coordinated to a single palladium(II). The palladium(11) complexes have been fully characterised, including X-ray crystallography, and exhibit good activities in the Heck coupling reaction of 4-bromoacetophenone and n-butyl acrylate. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:116 / 125
页数:10
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