Solution decomposition of platinum(II) fluoride cations;: single-crystal structure of [Pt(PPh3)2(C6H4PPh2)][SbF6]•CD2Cl2

被引:17
作者
Clark, HCS [1 ]
Fawcett, J [1 ]
Holloway, JH [1 ]
Hope, EG [1 ]
Peck, LA [1 ]
Russell, DR [1 ]
机构
[1] Univ Leicester, Dept Chem, Leicester LE1 7RH, Leics, England
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1998年 / 07期
关键词
D O I
10.1039/a709075g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An extended X-ray absorption fine structure (EXAFS) investigation of the metal co-ordination geometry in the cations [PtF(PR3)(3)](+) (R = Et or Ph) indicates that the Pt-F bond lengths are identical and only slightly longer than those typical for low-valent metal fluoride complexes. The solution decomposition of the complexes, [PtF(PPh3)(3)][X] (X = HF2, BF4 or SbF6), have been studied in both wet and dry chlorinated solvents and the only reactions observed have been due to the presence of water, producing, initially, [Pt(OH)(PPh3)(3)](+) and subsequently the ortho-metallated products [Pt(PPh3)(3)(C6H4PPh2)][X], which have been characterised by mass spectrometry, multinuclear NMR spectroscopy and, when X = SbF6, by single-crystal X-ray crystallography.
引用
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页码:1249 / 1252
页数:4
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