Supramolecular Architectures and Hydrogen-Bond Directionalities of 4,4'-Biimidazole Metal Complexes Depending on Coordination Geometries
Supramolecular Architectures and Hydrogen-Bond Directionalities of 4,4'-Biimidazole Metal Complexes Depending on Coordination Geometries
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DOI:
10.1021/cg100958r
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发表时间:
2010-09
影响因子:
3.8
通讯作者:
T. Murata;Y. Yakiyama;K. Nakasuji;Y. Morita
中科院分区:
文献类型:
--
作者:
T. Murata;Y. Yakiyama;K. Nakasuji;Y. Morita
Assembled metal complexes of 4,4′-biimidazole (4,4′-H2Bim), a ligand exhibiting multidirectional hydrogen-bonds, were investigated in AgI, CuII, and NiII complexes. The most intriguing feature of this system is that the directionality of hydrogen-bonds varies depending on the cis/trans-conformations of the ligand and the coordination geometries of the metal atoms. The [AgI2(4,4′-H2Bim)3] complex included ligands of both cis- and trans-conformations, the latter of which linked two metal atoms to form a planar dinuclear complex. The triple N−H···X···H−N hydrogen-bonds across the counteranions (X) formed a one-dimensional hydrogen-bond chain. The [CuII(4,4′-H2Bim)2] complexes showed a square-planar coordination sphere by the chelating coordination of two 4,4′-H2Bim units having the cis-conformation. The complexes were linked by the double N−H···X···H−N hydrogen-bonds across counteranions or solvent molecules to form one-dimensional chains. The [CuII(4,4′-HBim−)2] including the monodeprotonated ligand had a s...