Halide/pseudohalide-directed cadmium(II) coordination polymers based on 3-phenyl-5-(2-pyridyl)-4-(4-pyridyl)-4H-1,2,4-triazole

被引:10
|
作者
You, Wei [1 ]
Guo, Jian-Hua [1 ]
Li, Cheng-Peng [1 ]
Chen, Jing [1 ]
机构
[1] Tianjin Normal Univ, Tianjin Key Lab Struct & Performance Funct Mol, MOE Key Lab Inorgan Organ Hybrid Funct Mat Chem, Coll Chem, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金;
关键词
Coordination polymers; Crystal structures; Cd(II) complexes; Multidentate N-donor ligand; Halide/pseudohalide anions; METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; BUILDING-BLOCK; LIGANDS; COMPLEXES; NETWORKS; CHAIN;
D O I
10.1016/j.poly.2015.03.001
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new Cd(II) polymers [Cd-2(L-240)(2)I-4](n) (1) [Cd(L-240)(SCN)(2)](n) (2), and [Cd(L-240)(N-3)(2)](n) (3) have been synthesized via the reaction of 3-phenyl-5-(2-pyridyl)-4-(4-pyridyl)-4H-1,2,4-triazole (L-240) with CdI2 or in the presence of distinct pseudohalide anions (SCN- and N-3(-)). Single-crystal X-ray diffraction indicates that complex I features a 1D coordination chain and further forms a 2D supramolecular network extended via pi center dot center dot center dot pi stacking interactions. Complex 2 shows a 2D layered coordination network and complex 3 has a 3D diamond framework. In complexes 1-3, the Cd-II centers adopt the same octahedral geometry, whereas the L-240 ligands show distinct (mu(3), eta(2)), (mu(4), eta(3)), and (mu(2), eta(2)) binding modes, respectively. These results reveal that such polymeric networks can be well modulated by the halide anion (I-) and pseudohalide anions of SCN- and N-3(-). Thermal stability and fluorescence for complexes 1-3 have been studied. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 109
页数:6
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