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通过消除过程由取代的1,4 - 二氨基配体形成的一种意外的铂π配合物的合成与结构。

Synthesis and structure of an unexpected platinum pi complex formed from substituted 1,4-diamino ligands through an elimination process.

作者信息

Gay Marina, Montaña Angel M, Moreno Virtudes, Font-Bardia Mercè, Solans Xavier

机构信息

Departamento de Química Orgánica, Universidad de Barcelona, Facultad de Química c/Martí i Franquès 1-11, 08028, Barcelona, Spain.

出版信息

Chemistry. 2005 Mar 18;11(7):2130-4. doi: 10.1002/chem.200401228.

Abstract

An unusual reactivity of cis-1,2-bis[(N,N-dimethylamino)methyl] cyclohexane with PtCl(2) was observed, resulting in the formation of a platinum(II) pi-olefin complex instead of the conventional square-planar cis Pt(II) coordination complex with the diamino ligand. This behavior was interpreted on the basis of the steric hindrance of the dimethylamino groups whose electron lone pairs are barely accessible to a platinum atom, which can make it difficult for both dimethylamino groups to bind platinum at the same time. This complex has been physically and spectroscopically characterized and its structure has been confirmed by using X-ray diffraction analyses on single crystals.

摘要

观察到顺式-1,2-双[(N,N-二甲基氨基)甲基]环己烷与PtCl₂具有异常的反应活性,结果形成了一种铂(II) π-烯烃配合物,而不是与二氨基配体形成传统的平面正方形顺式Pt(II)配位配合物。这种行为是基于二甲基氨基的空间位阻来解释的,其孤对电子几乎无法接近铂原子,这使得两个二甲基氨基难以同时与铂结合。该配合物已通过物理和光谱方法进行了表征,其结构已通过对单晶进行X射线衍射分析得以确认。

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