NMR investigation of Pd(II)-Pd(0) reduction in the presence of mono- and ditertiary phosphines

被引：114

作者：

Csákai, Z

Skoda-Földes, R

Kollár, L

机构：

[1] Univ Veszprem, Dept Organ Chem, H-8201 Veszprem, Hungary

[2] Univ Pecs, Dept Inorgan Chem, H-7601 Pecs, Hungary

来源：

INORGANICA CHIMICA ACTA | 1999年 / 286卷 / 01期

基金：

匈牙利科学研究基金会;

关键词：

reduction; palladium complexes; phosphine complexes; nuclear magnetic resonance;

D O I：

10.1016/S0020-1693(98)00366-1

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The reduction of Pd(II) to Pd(0) was investigated in the presence of both monodentate (PPh3) and bidentate (dppp = 1,3-bis(diphenylphosphino)propane) phosphines. It was shown by P-31 NMR measurements that triphenylphosphine can reduce Pd(OAc)(2) to zerovalent palladium in toluene and dppp is mainly responsible for the reduction in dmf resulting in dppp hemioxide and dppp dioxide. Both mono- and bidentate coordinations of dppp in intermediate species are proposed on the basis of in situ NMR studies. In the presence of two equivalents of silver triflate, the formation of the [Pd(dppp)(PPh3)(2)](2+) square-planar complex cation has been observed without any reduction of Pd(II) to Pd(0) species. (C) 1999 Elsevier Science S.A. All rights reserved.

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页码：93 / 97

页数：5

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