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2,6-二乙酰基吡啶-双(R-硫代半卡巴腙)(R = H,苯基)的铁和钴配合物呈现出前所未有的配体偏离平面性。

Iron and Cobalt Complexes of 2,6-Diacetylpyridine-bis(R-thiosemicarbazone) (R=H, phenyl) Showing Unprecedented Ligand Deviation from Planarity.

作者信息

Panja Anangamohan, Campana Charles, Leavitt Christopher, Van Stipdonk Michael J, Eichhorn David M

机构信息

Department of Chemistry, Wichita State University, Wichita, KS 67260, USA.

出版信息

Inorganica Chim Acta. 2009 Mar 2;362(4):1348-1354. doi: 10.1016/j.ica.2008.06.031.

DOI:10.1016/j.ica.2008.06.031
PMID:20161238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2705211/
Abstract

The syntheses, characterization, and single-crystal X-ray crystal structures are reported for four complexes of iron and cobalt with the pentadentate ligands, 2,6-diacetylpyridinebis(thiosemicarbazone) (H(2)L(1)) and 2,6-diacetylpyridinebis-(phenylthiosemicarbazone) (H(2)L(2)), including a cobalt dimer displaying a deviation from planarity which is unprecedented for this class of ligands and allows the ligand to occupy five positions of a pseudo-octahedral coordination sphere. This dimer reacts with KCN to produce a mononuclear complex of relevance to the active site of cobalt nitrile hydratase.

摘要

报道了铁和钴与五齿配体2,6 - 二乙酰基吡啶双(硫代半卡巴腙)(H₂L₁)和2,6 - 二乙酰基吡啶双(苯硫代半卡巴腙)(H₂L₂)形成的四种配合物的合成、表征及单晶X射线晶体结构,其中包括一种钴二聚体,该二聚体显示出与平面性的偏差,这对于此类配体来说是前所未有的,并且使得配体能够占据伪八面体配位球的五个位置。这种二聚体与KCN反应生成一种与钴腈水合酶活性位点相关的单核配合物。

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