A convenient access to N-phosphonio-substituted NHC metal complexes [M = Ag(I), Rh(I), Pd(II)]

被引:19
|
作者
Benaissa, Idir [1 ]
Taakili, Rachid [1 ]
Lugan, Noel [1 ]
Canac, Yves [1 ]
机构
[1] Univ Toulouse, LCC CNRS, INPT, UPS, 205 Route Narbonne, F-31077 Toulouse 4, France
关键词
HETEROCYCLIC CARBENE COMPLEXES; ALPHA-CATIONIC PHOSPHINES; CHELATING LIGANDS; COORDINATION CHEMISTRY; ELECTRONIC-PROPERTIES; STABLE CARBENES; H BOND; SALTS; YLIDE; DIAMINOCARBENE;
D O I
10.1039/c7dt02759a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of NHC pre-ligands featuring a pendant phosphonium moiety attached to N' position through a propyl linker was readily obtained upon quaternization of N-mesityl-and N-methyl-imidazole, or N-mesityl-imidazoline using (3-bromo-propyl)-triphenylphosphonium bromide. Reactions of the resulting dicationic salts with [PdCl(allyl)] 2 in the presence of K2CO3 afforded the anticipated NHC-ligated Pd(II) metal complexes in high yields. Further treatment of the latter complexes with tBuOK induced a deprotonation of the carbon atom adjacent to the phosphonium moiety and the formation of the corresponding C, C-chelating NHC-phosphonium ylide Pd(II) complexes. Investigation of an alternative synthetic route involving a silver transmetallation reaction incidentally allowed isolation and full characterization of an unusual dimeric tetranuclear NHC Ag(I) complex of general formula [(NHC similar to P+)(2)(Ag4Br6)(2-)].
引用
收藏
页码:12293 / 12305
页数:13
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