Control of molecular architecture by steric and electronic factors: Dinuclear side-by-side vs. tetranuclear [2 × 2] grid-type silver(i) complexes
被引:31
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作者:
Department of Chemistry, University of Otago, P.O. Box 56, Dunedin, New Zealand
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机构:
Department of Chemistry, University of Otago, DunedinDepartment of Chemistry, University of Otago, Dunedin
Department of Chemistry, University of Otago, P.O. Box 56, Dunedin, New Zealand
[1
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机构:
Institute of Fundamental Sciences, Chemistry, Massey University, Palmerston North, P.O. BoxDepartment of Chemistry, University of Otago, Dunedin
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[2
]
机构:
[1] Department of Chemistry, University of Otago, Dunedin
[2] Institute of Fundamental Sciences, Chemistry, Massey University, Palmerston North, P.O. Box
来源:
Dalton Trans.
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2006年
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12卷
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1491-1494期
关键词:
17;
D O I:
10.1039/b516997f
中图分类号:
学科分类号:
摘要:
The molecular architecture of [2×2] grid-type silver(I) complexes by steric and electronic factors was controlled. Siver(I) complexes of the two closely related linear bis-bidentate pyridazine-based Schiff-based ligands 5 and 6 exhibit very different solid state molecular architectures. The coordination of relatively rigid bis-bidentate ligands to metal ions which prefer a tetrahedral geometry leads to the formation of [2×2] grid complexes. The X-ray crystal structure determination of the product of the 1:1 reaction of silver(I) tetrafluoroborate revealed two distinctly different [2×2] grids.