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Synthesis and structural studies on the chiral phosphine-NHC rhodium and palladium complexes for their performances in the metal-catalyzed reactions

机译:手性膦-NHC铑和钯配合物在金属催化反应中的合成及结构研究

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摘要

Diverse chiral rhodium and palladium complexes ligated with phosphine-functionalized N-heterocyclic carbene ligands based on 1,10-binaphthyl backbone have been synthesized. The structures of these phosphine-NHC rhodium and palladium complexes have been confirmed by X-ray diffraction analysis. The different sizes of the N-substituents from the NHC-P rhodium complexes had an inverse relationship with their ability of chiral induction, which was accounted by the Rh-catalyzed asymmetric hydrosilylation of acetophenone to afford corresponding chiral alcohol with up to 72% ee. The NHC-P palladium complexes connected with different kinds of coordination anions were also applied in the Suzuki and Heck reactions. The acetate-coordinated NHC-P palladium complex exhibited better catalytic activity to give the products in excellent yield under mild conditions.
机译:已经合成了基于1,10-联萘骨架与膦官能化的N-杂环卡宾配体连接的不同手性铑和钯配合物。这些膦-NHC铑和钯配合物的结构已经通过X射线衍射分析确认。来自NHC-P铑配合物的N取代基的不同大小与它们的手性诱导能力呈反比关系,这是由Rh催化的苯乙酮的不对称氢化硅烷化得到相应的手性醇和高达72%ee所致。与不同种类配位阴离子连接的NHC-P钯配合物也用于Suzuki和Heck反应。乙酸盐配位的NHC-P钯配合物表现出更好的催化活性,在温和的条件下以优异的收率得到了产物。

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