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首页> 外文期刊>Inorganic Chemistry Communications >Unusual structural features in tetrabromocatechol-chelated dinuclear manganese(II complex: Synthesis, electrochemistry and thermally induced valence tautomerism
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Unusual structural features in tetrabromocatechol-chelated dinuclear manganese(II complex: Synthesis, electrochemistry and thermally induced valence tautomerism

机译:四溴邻苯二酚螯合的双核锰的异常结构特征(II配合物:合成,电化学和热诱导价互变异构

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摘要

A novel dinuclear manganese(III) complex derived from tetrabromocatechol is reported. X-ray crystal structure reveals a bipyrimidine-bridged dinuclear manganese(III) complex in which both the metal ions are sit uated on the crystallographic inversion center. The most important feature of the crystal structure is that the geometrically rigid bidentate tetrabromocatechol ligand stretches one arm to coordinate axially elongated position. Moreover, the complex was found to exhibit thermally induced valence tautomerism accompanied by optical absorption spectral changes. As far as 1 am aware this is the first structural characterization of a dinuclear manganese(III) complex that consists exclusively of rigid bidentate ligands.
机译:报道了一种衍生自四溴邻苯二酚的新型双核锰(III)配合物。 X射线晶体结构揭示了双嘧啶桥联的双核锰(III)络合物,其中两种金属离子均位于结晶反转中心。晶体结构的最重要特征是几何刚性的双齿四溴邻苯二酚配体伸展了一只手臂以协调轴向伸长的位置。而且,发现该复合物表现出伴随光吸收光谱变化的热诱导价互变异构。据我所知,这是仅由刚性双齿配体组成的双核锰(III)配合物的第一个结构表征。

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