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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.
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页码:44 / 49
页数:6
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