Structure characterization of several oxalate-bridged transition-metal coordination polymers

被引:21
作者
Yu, Jie-Hui
Hou, Qin
Bi, Ming-Hui
Lu, Zheng-Liang
Zhang, Xiao
Qu, Xue-Jian
Lu, Jing
Xu, Ji-Qing [1 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130023, Peoples R China
[2] Jilin Univ, State Key Lab Inorgan Synthesis & Preparat Chem, Changchun 130023, Peoples R China
基金
中国国家自然科学基金;
关键词
oxalate; aromatic N-donor ligand; molecular structure; hydrothermal synthesis;
D O I
10.1016/j.molstruc.2006.03.079
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
Four oxalate-bridged transit ion-metal supramolecular compounds [Co-2(im)(4)(ox)(2)] 1, [Co(im)(2)(ox)] 2, [Mn(2,2'-bpy)(ox)] 3 and [Fe(H2O)(2)(ox)] 4 (im, imidazole.: ox, oxalate; bpy, bipyridine) were obtained from the simple hydrothermal reactions of Mn+-ox-L (M, transition metal; L, aromatic N-donor ligand) system. They all exhibit the 1-D chain structures, consisting of the ML22+ (or ML2+) units linked by oxalate bridges. Interestingly, the 1-D oxalate chains in the title compounds are further self-assembled into the 3-D supramolecular networks through the interchain various secondary bonding interactions. Because the ML22+ units adopt the different configuration, the oxalate chains show either zigzag type as in compounds 1-3 or linear type as in compound 4. Compounds I and 2 are isomeric, and only in packing modes of interchain im molecules there exists the difference. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 73
页数:5
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