NMR approach for the identification of dinuclear and mononuclear complexes: The first detection of [Pd(SPh)2(PPh3)2] and [Pd2(SPh)4(PPh3)2] - The intermediate complexes in the catalytic carbon-sulfur bond formation reaction

被引:25
作者
Ananikov, Valentine P. [1 ]
Zalesskiy, Sergey S. [1 ]
Kachala, Vadim V. [1 ]
Beletskaya, Irina P. [2 ]
机构
[1] Russian Acad Sci, Zelinsky Inst Organ Chem, Moscow 119991, Russia
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
基金
俄罗斯基础研究基金会;
关键词
Catalysis; Palladium complexes; DOSY NMR; Diffusion; Mechanism; IONIZATION MASS-SPECTROMETRY; PALLADIUM COMPLEXES; OXIDATIVE ADDITION; ZEROVALENT PALLADIUM; INTERMOLECULAR HYDROALKOXYLATION; ASYMMETRIC 1,4-ADDITION; PROPARGYLIC ALCOHOLS; BINUCLEAR PALLADIUM; RHODIUM COMPLEXES; PGSE DIFFUSION;
D O I
10.1016/j.jorganchem.2010.10.012
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the present study we have analyzed the nature of palladium complexes in the catalytic system for selective carbon-sulfur bond formation via the addition of S-S and S-H bonds to alkynes. For the first time the mononuclear and dinuclear palladium complexes were clearly detected by DOSY NMR under the catalytic conditions. It was demonstrated that the concentration of these palladium complexes strongly depends on the amount of phosphine ligand available under reaction conditions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:400 / 405
页数:6
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