The Positional Isomeric Effect on the Structural Diversity of Cd(II) Coordination Polymers, Using Flexible Positional Isomeric Ligands Containing Pyridyl, Triazole, and Carboxylate Fragments

位置异构体效应对 Cd(II) 配位聚合物结构多样性的影响,使用含有吡啶基、三唑和羧酸酯片段的灵活位置异构配体

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作者:Jonathan Cisterna, Catherine Araneda, Pilar Narea, Alejandro Cárdenas, Jaime Llanos, Iván Brito

Abstract

To systematically investigate the influence of the positional isomeric effect on the structures of polymer complexes, we prepared two new polymers containing the two positional isomers ethyl 5-methyl-1-(pyridin-3-yl)-1H-1,2,3-triazole-3-carboxylate (L1) and ethyl-5-methyl-1-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylate (L2), as well as Cd(II) ions. The structures of the metal⁻organic frameworks were determined by a single crystal XRD analysis. The compound [Cd(L1)&sub2;·4H&sub2;O] (1), is a hydrogen bond-induced coordination polymer, whereas the compound [Cd(L2)&sub4;·5H&sub2;O]n (2) is a three-dimensional (3-D) coordination polymer. Their structures and properties are tuned by the variable N-donor positions of the ligand isomers. This work indicates that the isomeric effect of the ligand isomers plays an important role in the construction of the Cd(II) complexes. In addition, the thermal and luminescent properties are reported in detail.

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