Three novel lanthanide complexes with imidazole-4,5-dicarboxylate ligand: Hydrothermal syntheses, structural characterization, and properties

被引:26
|
作者
Li, Zhao-Yang [1 ]
Zhang, Zhi-Min [1 ]
Dai, Jing-Wei [1 ]
Huang, Hui-Zhen [1 ]
Li, Xiao-Xu [1 ]
Yue, Shan-Tang [1 ]
Liu, Ying-Liang [2 ]
机构
[1] S China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
[2] Jinan Univ, Sch Chem, Guangzhou, Guangdong, Peoples R China
关键词
Hydrothermal synthesis; Lanthanide complex; Helical character; Chair conformation; Hydrogen bonds; METAL-ORGANIC FRAMEWORKS; CUBIC BUILDING-BLOCKS; ZEOLITE-LIKE TOPOLOGY; 1D OPEN CHANNELS; COORDINATION POLYMERS; HELICAL CHAINS; SUPRAMOLECULAR ISOMERISM; CRYSTAL-STRUCTURE; ACID; NETWORK;
D O I
10.1016/j.molstruc.2009.10.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three novel lanthanide complexes, namely, [Ce(Himdc)(H(2)imdc)(H2O)(3)]center dot H2O (1), {[Dy(Himdc)(Ox)(0.5)(H2O)(2)]center dot H2O}(n) (2), and {[Nd(Himdc)(Ox)(0.5)(H2O)(2)]center dot H2O}(n) (3) (H(3)imdc = imidazole-4,5-dicarboxylic acid, Ox = oxalate), have been successfully prepared by the assembly of lanthanicle ions and H(3)imdc ligand under different synthetic conditions. All of the complexes have been characterized by means of elemental analysis, IR, TG analysis, luminescence spectroscopy as well as single-crystal X-ray diffraction analysis. The 3D supramolecular structure of 1 is constructed from 1D zig-zag chains through the hydrogen bonding interactions. Complex 2 possesses the chair-shaped secondary building units (SBUs) with Dy-6(Himdc)(4)(Ox)(2) and meso-helical chains (P + M), resulting in a novel 2D structure based on the linkages of oxalate ligand. Complex 3 also presents 2D layer structure with uninodal 6-connected net topology, but crystallizes in the different space group and owns higher coordination number of the central metal atom than complex 2. The luminescence property of 2 is investigated in the solid state at room temperature. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 56
页数:7
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