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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Di- and tri-alkylphosphine adducts of S-donor palladacycles as catalysts in the Suzuki coupling of aryl chlorides
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Di- and tri-alkylphosphine adducts of S-donor palladacycles as catalysts in the Suzuki coupling of aryl chlorides

机译:S-供体palladacycles的二烷基和三烷基膦加合物作为芳基氯的Suzuki偶联反应的催化剂

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摘要

The reaction of tricyclohexylphosphine with the S-based palladacycle [{Pd(mu-OAc)(kappa(2)-S, C-C6H4CH2SMe)}(2)] gives several products, regardless of stoichiometry, one of which, [Pd(kappa(1)-OAc)(eta(1)-C6H4CH2SMe)(PCy3)(2)], has been characterised crystallographically. Despite this, catalysts formed in situ from di- and tri-alkylphosphines and [{Pd(mu-OAc)(kappa(2)-S, C-C6H4CH2SMe)}(2)] show excellent activity in the Suzuki coupling of a range of deactivated, non-activated and activated aryl chloride substrates.
机译:三环己基膦与基于S的Palladacycle [{Pd(mu-OAc)(kappa(2)-S,C-C6H4CH2SMe)}(2)]的反应可得到几种产物,无论化学计量如何,其中一种[Pd( kappa(1)-OAc)(eta(1)-C6H4CH2SMe)(PCy3)(2)]已通过结晶学表征。尽管如此,由二烷基和三烷基膦和[{Pd(mu-OAc)(kappa(2)-S,C-C6H4CH2SMe)}(2)]原位形成的催化剂在一定范围的Suzuki偶联中显示出优异的活性失活的,未活化的和活化的芳基氯底物。

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