首页> 外文期刊>Turkish journal of chemistry >Template Synthesis and Structural Characterization of Homo Binuclear Chromium(III),Manganese (III),Iron(III),Cobalt (III),and Ruthenium (III) Complexes with Octaazamacrocyclic Ligands
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Template Synthesis and Structural Characterization of Homo Binuclear Chromium(III),Manganese (III),Iron(III),Cobalt (III),and Ruthenium (III) Complexes with Octaazamacrocyclic Ligands

机译:八氮杂大环配体的同核双价铬(III),锰(III),铁(III),钴(III)和钌(III)配合物的模板合成和结构表征

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摘要

The Schiff base octaazamacrocyclic ligands derived from primary diamines and 3,6-dimethyl/diphenyl-4,5-diazaocta-3,5-diene-2,7-dione,and their binuclear complexes [M2LCl4]Cl2 [M = Cr(III),Fe(III),Co(III),or Ru(III)] and [Mn2L(AcO)4](AcO)2 were synthesized by template condensation reactions.Attempts to synthesize the corresponding metal-free macrocyclic ligands did not prove successful.The overall geometry and stereochemistry of these complexes were elucidated by elemental analyses,magnetic susceptibilities,electronic spectra,infrared spectra,molar conductance measurements,1H NMR,and thermogravimetric analysis.All the trivalent metal ion complexes appear to be 1:2 electrolytes.An octahedral geometry is proposed for all the complexes.
机译:衍生自伯二胺和3,6-二甲基/二苯基-4,5-二氮杂八-3,5-二烯-2,7-二酮的席夫碱八氮杂大环配体及其双核络合物[M2LCl4] Cl2 [M = Cr(III ),Fe(III),Co(III)或Ru(III)]和[Mn2L(AcO)4](AcO)2的合成通过模板缩合反应进行。没有尝试合成相应的无金属大环配体通过元素分析,磁化率,电子光谱,红外光谱,摩尔电导测量,1H NMR和热重分析,阐明了这些配合物的整体几何结构和立体化学。所有三价金属离子配合物似乎都是1:2电解质。建议为所有配合物使用八面体几何形状。

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