Synthesis and structure of cobalt(II) iodide bearing a bulky N-heterocyclic carbene ligand, and catalytic activation of bromoalkanes

被引:16
作者
Matsubara, Kouki [1 ]
Kumamoto, Aya [1 ]
Yamamoto, Hitomi [1 ]
Koga, Yuji [1 ]
Kawata, Satoshi [1 ]
机构
[1] Fukuoka Univ, Dept Chem, Jonan Ku, Fukuoka 8140180, Japan
基金
日本学术振兴会;
关键词
Cobalt(II) iodide; N-Heterocyclic carbene; beta-Elimination; Heck reaction; Homocoupling; Kumada coupling; CROSS-COUPLING REACTIONS; ARYL GRIGNARD-REAGENTS; ALKYL-HALIDES; COMPLEXES; IRON;
D O I
10.1016/j.jorganchem.2012.12.025
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A divalent cobalt iodine complex bearing 1,3-bis(mesityl) imidazol-2-ylidene and pyridine ligands was synthesized and its structure was determined. The cobalt center has a typical d(7)-tetrahedral geometry, as expected. Catalytic application of this cobalt complex with bromoalkanes and Grignard reagents demonstrated high-yield formation of alkenes as a result of beta-hydrogen elimination; in sharp contrast, the activation of alkyl halides was not successful using the larger N-heterocyclic carbene ligand, 1,3-bis(2,6-diisopropyl-phenyl)imidazol-2-ylidene. In the presence of styrene, Heck reaction proceeded with trans selectivity. The reaction of a substrate containing a bromobenzyl moiety yielded a homocoupling product. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 49
页数:6
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