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Synthesis, Crystal Structure, and Properties of a Zn(II) Coordination Polymer Based on a Difunctional Ligand Containing Triazolyl and Carboxyl Groups

机译:基于含有三唑基和羧基的双官能配体的Zn(II)配位聚合物的合成,晶体结构和性质

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摘要

A new compound, namely, [Zn(L)2]n (1) was obtained by the reaction of 2-methyl-4-(4H-1,2,4-triazol-4-yl) benzoic acid (HL) with ZnSO4·7H2O, and the compound was characterized by single-crystal X-ray diffraction, infrared spectroscopy, elemental analysis, powder X-ray diffraction (PXRD), and thermogravimetric analysis. The linear HL ligands were deprotonated to be L− anions and act as two-connectors to link Zn2+ to form a two-dimensional (2D) lay structure with (4, 4) topology. The large vacancy of 2D framework allows another layer structure to interpenetrate, resulting in the formation of 2D + 2D → 2D parallel interpenetration in 1. The weak interactions, such as hydrogen bonding and π⁻π stacking interactions, connect the adjacent 2D layers into a three-dimensional (3D) coordination polymer. The solid-state UV-visible spectroscopy and luminescent property have also been studied.
机译:通过2-甲基-4-(4h-1,2,4-三唑-4-基)苯甲酸(HL)的反应得到新化合物,即[Zn(1)2] N(1)通过单晶X射线衍射,红外光谱,元素分析,粉末X射线衍射(PXRD)和热重分析,表征ZnSO4·7H 2 O,以及该化合物的特征在于。将线性HL配体剥夺以是伸张的,并用作连杆Zn2 +的两个连接器,以形成具有(4,4)拓扑的二维(2D)层结构。 2D框架的较大空位允许另一层结构渗透,导致形成2D + 2D→2D平行互通的晶体间隔。弱相互作用,例如氢键和π⁻π堆叠相互作用,将相邻的2D层连接到a中三维(3D)配位聚合物。还研究了固态的UV可见光谱和发光性。

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