The oxidative addition of diphenyl diselenide and ditelluride to tetrakis(triphenylphosphine)palladium

被引:73
作者
Oilunkaniemi, R
Laitinen, RS
Ahlgrén, M
机构
[1] Oulu Univ, Dept Chem, FIN-90014 Oulu, Finland
[2] Univ Joensuu, Dept Chem, FIN-80101 Joensuu, Finland
基金
芬兰科学院;
关键词
aromatic diselenides; aromatic ditellurides; palladium complexes; X-ray crystallography; NMR spectroscopy;
D O I
10.1016/S0022-328X(00)00829-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The oxidative addition of diphenyl diselenide to [Pd(PPh3)(4)] in dichloromethane results in the formation of a dinuclear complex [Pd-2(SePh)(4)(PPh3)(2)] (1) and a mononuclear complex [PdCl(SePh)(PPh3)(2)] (2) that have been identified and characterized structurally by X-ray crystallography and P-31-NMR spectroscopy. The analogous reaction involving diphenyl ditelluride leads to a mixture of products. [Pd6Cl2Te4(TePh)(2)(PPh3)(6)].1/2CH(2)Cl(2) (3) can be isolated and its X-ray structure determined. While the oxidative addition of Ph,Se, mainly involves the clevage of the Se-Se bond, that of Ph2Te2 indicates the rupture of both Te-Te and C-Te. Cumulative evidence shows that the choice of the central atom and the solvent also plays an important role in the oxidative addition. The final polynuclear complexes can be conceived to be formed from the mononuclear addition products by sequential condensation steps. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:168 / 175
页数:8
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