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Stabilisation of Unusual Metal Co-Ordination Geometries Using an Oxo-Cubane Ligand; Syntheses and Structures of [{sn4(ntbu)3o}3licl]·3thf and [{Sn4(ntbu)3o}3fecl2]·3thf

C Brown, MEG Mosquera,JS Palmer,PR Raithby,A Steiner,DS Wright

Dalton(2000)

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摘要
Complexation of LiCl and FeCl2 with the oxo-cubane [Sn-4((NBu)-Bu-t)(3)O] 1 (3 equivalents) gave [{Sn-4((NBu)-Bu-t)(3)O}(3)LiCl]. 3thf 2 and [{Sn-4((NBu)-Bu-t)(3)O}(3)FeCl2]. 3thf 3, respectively; the co-ordination of three sterically demanding, 'ether-like' [Sn-4((NBu)-Bu-t)(3)O] ligands to the Li+ and Fe2+ centres of 2 and 3 results in unusual geometries for these metals. The geometry in 2 can be described as a distorted trigonal bipyramid with one vertex missing, while in 3 it is trigonal bipyramidal. Model semi-empirical calculations combined with the structural findings stress that although sterically encumbered 1 is a highly effective ligand for oxophilic metals.
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