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三-8-氨基喹啉三脚配体的合成与配位化学。

The synthesis and coordination chemistry of a tris-8-aminoquinoline tripodal ligand.

机构信息

Department of Chemistry, Cardiff University, PO Box 912, Cardiff, UKCF10 3TB.

出版信息

Dalton Trans. 2009 Oct 21(39):8356-62. doi: 10.1039/b909122j. Epub 2009 Aug 21.

Abstract

A tripodal tris-8-aminoquinoline ligand was synthesised in high yield via the Bucherer reaction. The septa-dentate ligand was found to give isolable complexes when coordinated with transition metals. Complexes of zinc(ii), cadmium(ii) and cobalt(iii) were isolated and their solid state structures were determined by single crystal X-ray diffraction. The solid state structures of these complexes were compared to the solution (1)H NMR data which was obtained for each complex. The two first row metals both gave octahedral six coordinate structures, although the two metals were coordinated by a differing donor set of heteroatoms. The cadmium complex was found to contain a seven coordinate cadmium centre in the solid state. DFT calculations were carried out in order to give an indication as to why the two different six coordinate binding modes were encountered.

摘要

一种三足三-8-氨基喹啉配体通过 Bucherer 反应高产率合成。发现该七齿配体与过渡金属配位时可得到可分离的配合物。分离得到锌(ii)、镉(ii)和钴(iii)的配合物,并通过单晶 X 射线衍射确定其固体结构。将这些配合物的固体结构与每种配合物获得的溶液 (1)H NMR 数据进行比较。前两个过渡金属都给出了八面体六配位结构,尽管两种金属由不同的杂原子供体组配位。在固态下,发现镉配合物含有一个七配位的镉中心。进行了 DFT 计算,以说明为什么会遇到两种不同的六配位结合模式。

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