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首页> 外文期刊>Inorganic Chemistry Communications >Molecular self-assembly of cadmium-triazolate complexes via hydrogen bonding:Synthesis, structures and photoluminescent properties
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Molecular self-assembly of cadmium-triazolate complexes via hydrogen bonding:Synthesis, structures and photoluminescent properties

机译:三唑镉镉配合物通过氢键的分子自组装:合成,结构和光致发光性能

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Two new cadmium coordination polymers namely [Cd(HAmTrz-COO)4(NH_4~+)2] 1; and [Cd(HAmTrz)2I2]n 2; (HAmTrz-COOH = 3-amino-1,2,4-triazole-5-carboxylic acid), have been prepared based on HAmTrz-COOH as ligand. The crystal structures of 1 and 2 have been determined by single-crystal X-ray diffraction technique. In coordination-complex 1 four triazole ligands coordinate via N1 nitrogen leading to a tetrahedral geometry around cadmium ion, while in 2 the ligand prefers to coordinate to the metal in a bidentate bridging mode. The structures of both the coordination polymers can be envisaged as 3D hydrogen bonded networks. Thermogravimetric analysis shows that 2 is more stable than 1 owing to different coordination numbers of cadmium atoms. Photoluminescence properties of both the compounds have been investigated in the solid state.
机译:两种新的镉配位聚合物为[Cd(HAmTrz-COO)4(NH_4〜+)2] 1;和[Cd(HAmTrz)2 I 2] n 2; (HAmTrz-COOH = 3-氨基-1,2,4-三唑-5-羧酸)是基于HAmTrz-COOH作为配体制备的。 1和2的晶体结构已经通过单晶X射线衍射技术确定。在配位化合物1中,四个三唑配体通过N1氮进行配位,导致镉离子周围为四面体几何形状,而在配位化合物2中,配位体更倾向于以双齿桥联方式与金属配位。两种配位聚合物的结构都可以设想为3D氢键网络。热重分析表明,由于镉原子的配位数不同,2比1更稳定。已经在固态下研究了两种化合物的光致发光性质。

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