一种具有绿色光致发光的锌配位化合物

Yu-Shu Zhu, Cui-Er Deng, Xue-Chun Zhang, Kun-Lin Huang, Xi Liu
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摘要

摘要以四羧酸配体h4l (h4l = 1,3,6,8-四基(4-羧基苯基)芘)、z2l (h2o) 2·2DEF (1) (DEF = N, N′-二乙基甲酰胺)为溶剂热合成了一种新型三维配位化合物。每个Zn离子由来自4个l4 -配体的4个羧酸氧原子和来自水分子的1个氧原子配位,形成扭曲的方锥体结构。相邻的Zn阳离子被4个不同l4 -配体的羧酸基团桥接,形成桨轮[zn2 (COO) 4 (h2o) 2]二级构建单元(SBU)。每个SUB进一步连接到四个l4 -配体,以提供具有cds型(cdso4型)拓扑结构的三维框架。通过单晶x射线衍射确定了晶体结构,并通过元素分析和热分析、红外光谱、粉末x射线衍射和固态光致发光测量对化合物进行了表征。
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A zinc coordination compound showing green photoluminescence
Abstract A novel three-dimensional coordination compound has been solvothermally synthesized based on a tetracarboxylate ligand H 4 L (H 4 L = 1,3,6,8-tetrakis(4-carboxylphenyl)pyrene), Zn 2 L(H 2 O) 2 ·2DEF ( 1 ) (DEF = N , N ′-diethylformamide). Each Zn ion is coordinated by four carboxylate oxygen atoms from four L 4− ligands and one oxygen atom from a water molecule to provide a distorted square-pyramidal geometry. Pairs of adjacent Zn cations are bridged by four carboxylate groups of four different L 4− ligands to generate a paddle-wheel [Zn 2 (COO) 4 (H 2 O) 2 ] secondary building unit (SBU). Each SUB is further linked to four L 4− ligands to give a three-dimensional framework with cds-type (CdSO 4 -type) topology. The crystal structure has been determined via single-crystal X-ray diffraction, and the compound was characterized by elemental and thermal analysis, infrared spectroscopy, powder X-ray diffraction, and solid-state photoluminescence measurements.
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