화학공학소재연구정보센터
Journal of Molecular Catalysis A-Chemical, Vol.290, No.1-2, 67-71, 2008
Carbene adduct of cyclopalladated ferrocenylimine: Efficient catalyst for the Suzuki coupling of sterically hindered aryl chlorides with a weaker base and low catalyst loading
One-pot synthesis of the N,N'-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr) adduct of cyclopalladated ferrocenylimine complex 1 has been described. This complex has been successfully applied to Suzuki coupling reaction. Various aryl chloride and boronic acids can be coupled efficiently with a mild base K3PO4 center dot 7H(2)O and low catalyst loadings. This system has been proven to be compatible with the sterically hindered aryl chlorides and some boronic acids leading to form di- and tri-ortho-substituted biaryls in high yields. (C) 2008 Elsevier B.V. All rights reserved.