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Dehydrogenative silylation of alcohols catalysed by half-sandwich iron N-heterocyclic carbene complexes
被引:38
|作者:
Cardoso, Joao M. S.
[1
]
Lopes, Rita
[1
]
Royo, Beatriz
[1
]
机构:
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, EAN, P-2780157 Oeiras, Portugal
关键词:
Iron;
N-Heterocyclic carbene ligands;
Coupling of silanes with alcohols;
Silylethers;
EFFICIENT HYDROSILYLATION;
SELECTIVE HYDROSILYLATION;
HYDRIDE COMPLEX;
KETONES;
SILANES;
BEARING;
REDUCTION;
CHEMISTRY;
ALDEHYDES;
LIGANDS;
D O I:
10.1016/j.jorganchem.2014.06.005
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
A new series of tetramethylcyclopentadienyl-functionalised N-heterocyclic carbene complexes of iron bearing different wingtips of general type (Cp*-NHCR)Fe(CO)I (R = Bu-n, Bu-i, Et, CH2CH2OMe, CH2Ph) were prepared by direct reaction of Fe-3(CO)(12) and the corresponding imidazolium proligands. These new iron-NHC complexes have been found to be efficient catalysts for the dehydrogenative silylation of alcohols with silanes. Iron metal complexes bearing iso-butyl and n-butyl wingtips displayed slightly better catalytic performances than the related complexes (Cp*-NHCR)Fe(CO)I (R = Et, CH2CH2OMe, CH2Ph), affording quantitative yields of the corresponding silylethers in 8 h at 70 degrees C in acetonitrile. (C) 2014 Elsevier B.V. All rights reserved.
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页码:173 / 177
页数:5
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