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Molecular to supramolecular structure: Influence of coordination environment in azo-dye complexes

机译:分子至超分子结构:配位环境对偶氮染料络合物的影响

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The mixed donor ligand 2-(phenylazo)imidazole (L-1) forms a family of seven different metal complexes of varying coordination environments at the molecular level. The presence of hydrogen bonding sites along with metal coordination sites results in the formation of three-dimensional (3D) self-assembled supramolecular architectures. Variation of the 3D architecture is a consequence of fine-tuning of the coordination behavior of the mixed donor ligand. Compatibility of the hard-soft nature of the metal ion and the mixed donor L-1 controls the long-range 3D order in the solid-state. The solid-state structures of L, and their complexes were identified by single crystal X-ray structure analysis. The optical, electrochemical, and thermal properties of azo-dyes and their metal complexes were studied in detail and compared with their molecular structures.
机译:混合的供体配体2-(苯基偶氮)咪唑(L-1)在分子水平上形成了七种不同配位环境的金属配合物。氢键合位点以及金属配位点的存在导致形成三维(3D)自组装超分子体系结构。 3D结构的变化是混合供体配体配位行为的微调的结果。金属离子和混合供体L-1的硬软性质的兼容性控制固态的远程3D顺序。通过单晶X射线结构分析鉴定了L的固态结构及其配合物。详细研究了偶氮染料及其金属配合物的光学,电化学和热学性质,并将其与分子结构进行了比较。

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