Supramolecular Coordination Complexes with 5-Sulfoisophthalic Acid and 2,5-Bipyridyl-1,3,4-Oxadiazole: Specific Sensitivity to Acidity for Cd(II) Species

被引:103
作者
Li, Cheng-Peng [1 ]
Yu, Qian [1 ]
Chen, Jing [1 ]
Du, Miao [1 ]
机构
[1] Tianjin Normal Univ, Coll Chem & Life Sci, Tianjin Key Lab Struct & Performance Funct Mol, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; HYDROTHERMAL SYNTHESIS; STRUCTURAL-CHARACTERIZATION; BUILDING-BLOCKS; PH; POLYMERS; LIGANDS; SOLVENT; NETWORK;
D O I
10.1021/cg100144p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of Cd-II Co-II, Ni-II, and Pb-II mixed-ligand coordination complexes 1-8 based on 5-sulfoisophthalic acid (H(3)sip) and the bent dipyridyl ligand 2,5-bis(3-pyridyl)-1,3,4-oxadiazole (3-bpo) or its 4-pyridyl N-donor analogue (4-bpo) have been synthesized and fully characterized by IR spectra, microanalyses, and single crystal and powder X-ray diffraction techniques. The significant pH effect on assembly of the Cd-II complexes 1-4 has been demonstrated, which leads to the formation of distinct crystalline products, whereas the Co-II, and Pb-II systems 5-8 are independent to pH condition of the synthetic reaction. Complexes 1-8 display various coordination motifs with different existing forms, conformations, and coordination modes of the organic ligands. Further, extended supramolecular networks are constructed via secondary interactions such as hydrogen-bonding and aromatic stacking. Solid-state properties of thermal stability and fluorescence for these crystalline materials are also presented.
引用
收藏
页码:2650 / 2660
页数:11
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