Ni(acac)2/Phosphine as an Excellent Precursor of Nickel(0) for Catalytic Systems

被引:49
作者
Ananikov, Valentine P. [1 ]
Gayduk, Konstantin A. [1 ]
Starikova, Zoya A. [2 ]
Beletskaya, Irina P. [3 ]
机构
[1] Russian Acad Sci, ND Zelinskii Organ Chem Inst, Moscow 119991, Russia
[2] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 119991, Russia
[3] Lomonosov Moscow State Univ Vorobevy Gory, Dept Chem, Moscow 119899, Russia
基金
俄罗斯基础研究基金会;
关键词
VINYL SULFIDES; COMPLEXES; EFFICIENT; HECK; MECHANISM; PHOSPHINE;
D O I
10.1021/om1003732
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The coordination of phosphine ligands to nickel acetylacetonate was studied in toluene solution, and the first X-ray structure of the unstable complex trans-[Ni(acac)(2)(PMe2Ph)(2)] has been reported. A convenient procedure was developed to generate Ni(0) species in situ in solution from a Ni(acac)(2) precursor, and their application in catalysis was demonstrated. A study of the reaction mechanism has suggested that water may play an important role in the formation of zerovalent nickel species. The nature of the Ni(0) species was confirmed by trapping with Ph2S2, and the structure of the resulting complexes trans-[Ni(SPh)(2)L-2] was established by X-ray analysis for L = PMe2Ph, PMePh2, PBu3.
引用
收藏
页码:5098 / 5102
页数:5
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