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通过氢转移促进的自组装过程合成手性超分子双膦亚胺钯配合物。

Synthesis of chiral supramolecular bisphosphinite palladacycles through hydrogen transfer-promoted self-assembly process.

机构信息

Aix-Marseille Univ, CNRS, Centrale Marseille, iSm2, Marseille, France.

出版信息

Chem Commun (Camb). 2018 Sep 6;54(72):10132-10135. doi: 10.1039/c8cc06283h.

DOI:10.1039/c8cc06283h
PMID:30131990
Abstract

P-Chiral secondary phosphine oxides react with Pd2(dba)3 in an acidic medium to provide chiral supramolecular bisphosphinite palladacycles through a H-transfer-based self-assembly process prior to SPO-promoted oxidative addition of an acid to a Pd(0) centre. The one-pot methodology allows variations of the X-type ligand as desired. Eight complexes have been characterised by X-ray diffraction.

摘要

手性 P-手性次膦氧化物在酸性介质中与 Pd2(dba)3 反应,通过基于 H 转移的自组装过程,提供手性超分子双膦亚胺钯配合物,然后 SPO 促进酸对 Pd(0)中心的氧化加成。该一锅法允许根据需要改变 X 型配体。通过 X 射线衍射对 8 个配合物进行了表征。

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