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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Iron complexes of terdentate nitrogen ligands: formation and X-ray structure of three new dicationic complexes
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Iron complexes of terdentate nitrogen ligands: formation and X-ray structure of three new dicationic complexes

机译:齿状氮配体的铁配合物:三种新的双金属配合物的形成和X射线结构

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摘要

Dicationic iron complexes were obtained upon complexation of the ligands 6,6"-di(p-tolyl)-2,2':6',2"-terpyridine (L-1) or 2,6-bis(3-tnesitylpyrazol-1-yl)pyridine (L-2) with iron dichloride or iron trichloride. They were characterized by X-ray diffraction and FT-IR spectroscopy. Single crystal structure determinations of (L-1)(2)Fe2+(FeCl4-)(2), (L-2)(2)Fe2+FeCl42- and (L-2)(2)Fe2+(FeCl4-),(THF)(4) all show six-coordinate metal center. These complexes were obtained from (LFeCl2)-Fe-1 and (LFeCl2)-Fe-2 during recrystallization attempts. (L-1)(2)Fe2+ was shown to be a high-spin complex, whereas (L-2)(2)Fe2+ was shown to be low-spin. For (L-2)(2)Fe2+FeCl42-, two independent dications of very similar geometry but with distinctive distortion were observed by X-ray analysis. (C) 2004 Elsevier Ltd. All rights reserved.
机译:通过配体6,6“-二(对甲苯基)-2,2':6',2”-吡啶(L-1)或2,6-双(3-叔丁基吡唑- 1-基)吡啶(L-2)与二氯化铁或三氯化铁。它们通过X射线衍射和FT-IR光谱表征。 (L-1)(2)Fe2 +(FeCl4-)(2),(L-2)(2)Fe2 + FeCl42-和(L-2)(2)Fe2 +(FeCl4-),( THF)(4)均显示六坐标金属中心。这些配合物是在重结晶尝试期间从(LFeCl2)-Fe-1和(LFeCl2)-Fe-2获得的。 (L-1)(2)Fe2 +被证明是高自旋复合物,而(L-2)(2)Fe2 +被证明是低自旋。对于(L-2)(2)Fe2 + FeCl42-,通过X射线分析观察到两个非常相似的几何形状但具有独特变形的独立指示。 (C)2004 Elsevier Ltd.保留所有权利。

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