Structural invariance in silver(I) coordination networks formed using flexible four-armed thiopyridine ligands

被引:45
作者
Cordes, David B. [1 ]
Hanton, Lyall R. [1 ]
机构
[1] Univ Otago, Dept Chem, Dunedin, New Zealand
关键词
D O I
10.1021/ic061867m
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new isomeric, flexible four-armed thioether pyridine-containing ligands 1,2,4,5-tetrakis(3-pyridylmethylsulfanylmethyl)benzene (3tet) and 1,2,4,5-tetrakis(4-pyridylmethylsulfanylmethyl)benzene (4tet) were prepared and characterized. The ligand 3tet gave rise to three isomorphous 3-D networks when reacted with AgClO4 (1), AgPF6 (2), and AgCF3CO2 (3). The topology of the resulting networks was that of the pyrite net. The ligand 4tet gave rise to two isotopological 3-D networks when reacted with AgClO4 (4 center dot 2MeCN center dot 2CHCl(3)) and AgPF6 (5 center dot 6MeCN). The topology of these networks was that of the rutile net. A third type of 3-D network of previously unknown topology was formed on reaction with AgCF3SO3 (6 center dot 3H(2)O). The network showed nodes with short topological terms 4(2).6 and 4(4).6(2).8(7).10(2). All six networks were binodal and based on three-connected Ag(I) nodes and six-connected ligand-centered nodes. In all of the networks the flexible ligands 3tet and 4tet showed two categories of ligand geometry which in all but one case gave rise to an interligand three-layered pi stack. The networks showed a remarkable lack of dependence on the nature of the counterion and solvent.
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页码:1634 / 1644
页数:11
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