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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Ligand behavior of 2,6-pyridinediylbis(2-pyridinyl)methanone in solvent-controlled formation of iron(III) complexes: A novel asymmetric quasi-linear trinuclear core containing an eight-coordinate iron center
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Ligand behavior of 2,6-pyridinediylbis(2-pyridinyl)methanone in solvent-controlled formation of iron(III) complexes: A novel asymmetric quasi-linear trinuclear core containing an eight-coordinate iron center

机译:2,6-吡啶二基双(2-吡啶基)甲酮在铁(III)络合物的溶剂控制形成中的配体行为:包含八坐标铁中心的新型不对称准线性三核核

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摘要

The crystal structures of two polymorphic forms of 2,6-pyridinediylbis(2-pyridinyl)methanone (1) crystallized from different solvents have been determined by X-ray crystallography. Solvent-controlled reaction between FeCl3 and I yielded four crystalline iron(III) complexes exhibiting two structural types: an asymmetric quasi-linear triiron core with a rarely observed eight-coordinate iron(III) center and three mononuclear moieties. Ligand I is solvolyzed at both carbonyl groups in the trinuclear complex but hydrolysis/solvolysis occurs at only one carbonyl site in its mononuclear complexes. The variable-temperature magnetic susceptibilities of 2 were also measured. (c) 2005 Elsevier Ltd. All rights reserved.
机译:已经通过X射线晶体学测定了从不同溶剂中结晶的2,6-吡啶二基双(2-吡啶基)甲酮(1)的两种多晶型形式的晶体结构。 FeCl3和I之间的溶剂控制反应产生了四种结晶的铁(III)配合物,具有两种结构类型:不对称的准线性三铁核,很少观察到八坐标的铁(III)中心和三个单核部分。配体I在三核配合物中的两个羰基上均被溶剂化,但水解/溶剂分解仅发生在其单核配合物中的一个羰基位点上。还测量了2的可变温度磁化率。 (c)2005 Elsevier Ltd.保留所有权利。

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