Hydrogen bonded 2,2′-biimidazolate transition metal complexes as a tool of crystal engineering

被引:218
|
作者
Tadokoro, M
Nakasuji, K
机构
[1] Osaka City Univ, Grad Sch Sci, Dept Chem, Sumiyoshi Ku, Osaka 5588585, Japan
[2] Osaka Univ, Grad Sch Sci, Dept Chem, Toyonaka, Osaka 5600043, Japan
关键词
crystal engineering; hydrogen bond; metal complex; nanostructure; supramolecular chemistry;
D O I
10.1016/S0010-8545(99)00223-4
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the field of crystal engineering, many attempts have been made to control the molecular arrangements in crystal by simultaneous use of coordination bonds of a transition metal ion and complementary intermolecular hydrogen bonds. We obtained the first crystal structure of the hydrogen bonded metal complex of 2,2'-biimidazolate monoanion ligand Hbim(-) with Cu(II) as a neutral dimer metal complex. The hydrogen-bonded dimer structure indicates that the Hbim(-) ligand controls the crystal structure using not only the coordination to a transition metal ion as a bidentate chelate but simultaneously the formation of complementary intermolecular hydrogen bonds. We also found that the Hbim(-) ligand gave [Ni(Hbim)(3)](-) as a new building block for hydrogen-bonded self-assembling networks by one-pot synthesis to mix Ni(II) ion, counter cation and the ligand. The networks form zero-dimensional, one-dimensional, two-dimensional, and three-dimensional structures depending upon the kind of counter cations. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:205 / 218
页数:14
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