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自由基阴离子 2,2'-联吡啶配体的第 3 族金属配合物。

Group 3 metal complexes of radical-anionic 2,2'-bipyridyl ligands.

机构信息

Department of Chemistry & Biochemistry, University of California, Los Angeles, California 90095, United States.

出版信息

Inorg Chem. 2010 Dec 20;49(24):11493-8. doi: 10.1021/ic101493k. Epub 2010 Nov 15.

Abstract

A new method for generating group 3 metal complexes containing radical-anionic 2,2'-bipyridyl (bipy) ligands is described that relies on hydrogen-atom abstraction from dearomatized biheterocyclic complexes. This method does not involve electron transfer to neutral 2,2'-bipyridyl or salt metathesis between the lithium salt of the 2,2'-bipyridyl radical anion and group 3 metal halides. The new metal complexes were characterized by single-crystal X-ray diffraction, electron paramagnetic resonance, and absorption spectroscopy. Density functional theory (DFT) calculations were used to probe the electronic structure of these compounds. All these methods support the radical-anionic character of bipy in all bipy compounds presented.

摘要

一种生成含自由基阴离子 2,2'-联吡啶(bipy)配体的第 3 族金属配合物的新方法被描述出来,该方法依赖于从去芳构化的双杂环配合物中提取氢原子。该方法不涉及向中性 2,2'-联吡啶进行电子转移,也不涉及 2,2'-联吡啶自由基阴离子的锂盐与第 3 族金属卤化物之间的盐交换。新的金属配合物通过单晶 X 射线衍射、电子顺磁共振和吸收光谱进行了表征。密度泛函理论(DFT)计算被用于探测这些化合物的电子结构。所有这些方法都支持所呈现的所有 bipy 化合物中 bipy 的自由基阴离子特性。

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