The use of H-bonding to increase the dimensionality of coordination networks of Cu(I) and Cu(II)

被引:8
作者
Cordes, David B.
Hanton, Lyall R.
Spicer, Mark D.
机构
[1] Univ Otago, Dept Chem, Dunedin, New Zealand
[2] Univ Strathclyde, Dept Pure & Appl Chem, Glasgow G1 1XL, Lanark, Scotland
关键词
coordination-polymers; copper; interpenetration; H-bonding; network-topology;
D O I
10.1016/j.molstruc.2006.03.106
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
Two two-dimensional coordination networks were prepared by the reaction of a bent bridging ligand, bis(4-pyridyl)amine (bpa), with Cut and CuCl2. Both networks were formed by bpa ligands bridging between Cu2I2 dimers or six-coordinate trans CuCl2 moieties. The networks were isotopological and displayed (4,4) topology with nodes based on the midpoint of the Cu2I2 dimer or the Cu(II) ion, respectively. Reaction of a monoprotonated bpa ligand with CuSO4 resulted in the formation of a neutral discrete complex. H-bonding networks were formed in all three cases. The two coordination polymers were both extended to give related three-dimensional networks with the resulting CuI H-bonded network displaying twofold interpenetration. The discrete neutral complex formed a two-dimensional H-bonded network and when further H-bonding to H2O solvent molecules was considered, a highly complex three-dimensional network resulted with five different nodes of four different connectivities. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 159
页数:14
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