Synthesis, structures and properties of two lead halide coordination polymers based on pyridinedicarboxylate ligand

被引:1
|
作者
Liu, Dong-Sheng [1 ]
Qiu, Feng-Qing [1 ]
Xu, Yi-Xin [1 ]
Gu, Hua-Long [1 ]
Xi, Dong-Zheng [1 ]
Zhong, Hong [1 ]
Sui, Yan [1 ]
机构
[1] Jinggangshan Univ, Inst Appl Chem, Sch Chem & Chem Engn, Key Lab Coordinat Chem Jiangxi Prov, Jian 343009, Jiangxi, Peoples R China
关键词
Lead halides complex; Crystal structure; Fluorescence properties; TDDFT calculations; ORGANIC FRAMEWORK;
D O I
10.1016/j.jssc.2022.123161
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new lead halide coordination polymers, [Pb2(pydc)I2]n (1), [Pb2(pydc)ClI]n (2), (H2pydc 1/4 2,5-pyridinedicarboxylic acid) have been synthesized under hydrothermal condition, and structurally characterized by single-crystal X-ray diffraction. The results of X-ray crystallographic analysis reveal that both compounds are three-dimensional (3D) frameworks. For 1, 1D inorganic cation [Pb2I2]n2n thorn ribbons are fused by the carboxylate oxygen atoms to generate 2D layers. Then the 2D layers are sustained by pydc2- ligands and result in a 3D pillared framework. Remarkably, a novel 2D mixed-halide cation [Pb2ClI]n2n thorn layer is found in 2. The mixed-halide cation layers are further connected by pydc2- ligands and create a 3D network. In addition, solid-state properties of thermal stability and fluorescence for these crystalline materials are also presented. Time-dependent density functional theory (TDDFT) calculations reveal that the mechanism of the fluorescence emissions dominantly results from the ligand-to-metal charge transfer (LMCT) and partial the intraligand pi -> pi* and/or n ->pi* transitions for 1 and 2, which is in good agreement with their fluorescence spectra and crystal structures.
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页数:7
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