首页> 外文期刊>Inorganica Chimica Acta >Iron and cobalt complexes of 2,6-diacetylpyridine-bis(R-thiosemicarbazone) (R = H, phenyl) showing unprecedented ligand deviation from planarity
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Iron and cobalt complexes of 2,6-diacetylpyridine-bis(R-thiosemicarbazone) (R = H, phenyl) showing unprecedented ligand deviation from planarity

机译:2,6-二乙酰基吡啶-双(R-硫代半脲)(R = H,苯基)的铁和钴络合物显示出前所未有的配体偏离平面性

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摘要

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) (H2L1) and 2,6-diacetylpyridinebis(phenylthiosemicarbazone) (H2L2), 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.
机译:报道了铁和钴与五齿配体的2,6-二乙酰吡啶双(硫代半碳a)(H2L1)和2,6-二乙酰吡啶双(苯基硫代半碳a)(H2L2)的四种配合物的合成,表征和单晶X射线晶体结构),包括显示出不同于平面度的钴二聚体,这对于此类配体来说是空前的,并允许配体占据伪八面体配位球的五个位置。该二聚体与KCN反应,产生与钴腈水合酶活性位点相关的单核复合物。

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