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Cobalt(II) and (I) Complexes of Diphosphine-Ketone Ligands: Catalytic Activity in Hydrosilylation Reactions

机译:二膦 - 酮配体的钴(II)和(I)复合物:氢化硅烷化反应中的催化活性

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The hydrosilylation of unsaturated compounds homogeneously catalyzed by cobalt complexes has gained considerable attention in the last years, aiming at substituting precious metal-based catalysts. In this study, the catalytic activity of well-characterized Co-II and Co-I complexes of the (pTol)dpbp ligand is demonstrated in the hydrosilylation of 1-octene with phenylsilane. The Co-I complex is the better precatalyst for the mentioned reaction under mild conditions, at 1 mol-% catalyst, 1 h, room temperature, and without solvent, yielding 84 % of octylphenylsilane. Investigation of the substrate scope shows lower performance of the catalyst in styrene hydrosilylation, but excellent results with allylbenzene (84 %) and acetophenone ( 99 %). This catalytic study contributes to the field of cobalt-catalyzed hydrosilylation reactions and shows the first example of catalysis employing the dpbp ligand in combination with a base metal.
机译:在过去几年中,通过钴络合物均匀催化的不饱和化合物的氢化硅烷化在旨在替代贵金属基催化剂的含量显着。 在该研究中,在用苯基硅烷的1-辛烯的氢化硅烷化中对(PTOL)DPBP配体的良好表征CO-II和CO-I复合物的催化活性在1-辛烯的氢化物中进行了说明。 CO-I复合物是在温和条件下更好的预催化剂,在温和的条件下,在1mol%催化剂,1小时,室温和没有溶剂,不产生84%的辛基苯基硅烷。 基材范围的研究显示苯乙烯氢化硅烷化催化剂的较低性能,但烯丙基苯(84%)和苯乙酮(& 99%)的优异结果。 该催化研究有助于钴催化的氢化硅化反应领域,并显示与基础金属组合使用DPBP配体的催化剂分析的第一个实施例。

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