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First dicadmium(II)complex of tripodal amide ligand with one edge-sharing monocapped octahedral geometry

机译:具有一个边缘共享的单封八面体几何结构的三脚架酰胺配体的第一镉(II)配合物

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摘要

A new dicadmium(II)complex[Cd2(L)2(H2O)2](NO3)4·8H2O(1)with the tripodal amide ligand L(tris[3-aza-2-oxo-4-(2-pyr-idyl)butyl]amine)was synthesized and structurally characterized.Complex 1 is revealed as a dinuclear 2:2(Cd:L)complex,in which each cadmium(II)ion is hepta-coordinated with the coordination surrounding of distorted monocapped octahedral geometry.Two cad-mium(II)ions are dibridged by two carbonyl mu-O atoms forming a Cd2(mu-O)2 parallelogram-type moiety.Interestingly,the dinuclear coordination sphere can be seen as resulting from the fusion of two distorted monocapped octahedral[Cd(L)(H2O)f+units through sharing one edge originated from the two carbonyl mu-O atoms as a first example.Comparative NMR,IR and FAB-mass data of 1 are also discussed.
机译:具有三脚架酰胺配体L(tris [3-aza-2-oxo-4-(2-pyr)]的新型络合物[Cd2(L)2(H2O)2](NO3)4·8H2O(1)化合物1揭示为双核2:2(Cd:L)络合物,其中每个镉(II)离子都是七配位的,且扭曲的单封八面体的配位周围两个镉(II)离子被两个羰基mu-O原子双桥形成一个Cd2(mu-O)2平行四边形类型的部分。有趣的是,双核配位域可以看作是两个扭曲的融合产生的作为一个第一实例,通过共享源自两个羰基mu-O原子的一个单封端的八面体[Cd(L)(H2O)f +单元]。还讨论了1的比较NMR,IR和FAB质量数据。

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