(NHCMe)SiCl4: a versatile carbene transfer reagent synthesis from silicochloroform

被引:50
作者
Boettcher, Tobias [1 ]
Bassil, Bassem S. [1 ]
Zhechkov, Lyuben [1 ]
Heine, Thomas [1 ]
Roeschenthaler, Gerd-Volker [1 ]
机构
[1] Jacobs Univ Bremen, Sch Sci & Engn, D-28759 Bremen, Germany
关键词
N-HETEROCYCLIC CARBENES; ELECTRONIC-STRUCTURE; STABLE CARBENES; COMPLEXES; SILICON; CHEMISTRY; TRICHLOROSILANE; STABILITY; P-4; HEXACHLORODISILANE;
D O I
10.1039/c2sc21214e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new synthetic pathway for the N-heterocyclic carbene adduct (NHCMe)SiCl4 (2) (NHCMe = 1,3-dimethylimidazolidin-2-ylidene) using silicochloroform is presented. Supported by DFT calculations, the energy for dissociation of 2 into the carbene and the SiCl4 fragment was found to be comparable to carbene transfer reagents based on silver(I) chloride. Compound 2 was used to transfer the NHC ligand to three different phosphorus(III) chloro compounds, resulting in the neutral complexes (NHCMe)PCl3 (3a), (NHCMe)PCl2Ph (3b) and (NHCMe)PCl2Me (3c). The sterically non-demanding NHC ligand allowed the phosphorus(III) in complex 3a to be oxidized to phosphorus(V) without loss of the NHC ligand, and afford (NHCMe)PF4H (4). Furthermore, bis-carbene complexes of Ni(II) (5) and Pd(II) (6) were obtained by reacting 2 with the respective metal chlorides.
引用
收藏
页码:77 / 83
页数:7
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