Axial coordination of NHC ligands on dirhodium(II) complexes:: Generation of a new family of catalysts

被引:88
|
作者
Trindade, Alexandre F. [1 ,2 ]
Gois, Pedro M. P. [1 ,2 ,3 ,4 ]
Veiros, Luis F. [1 ,2 ]
Andre, Vania [1 ,2 ]
Duarte, M. Teresa [1 ,2 ]
Afonso, Carlos A. M. [1 ,2 ]
Caddick, Stephen [3 ]
Cloke, F. Geoffrey N. [4 ]
机构
[1] Inst Super Tecn, Dept Engn Quim & Biol, CQFM, P-1049001 Lisbon, Portugal
[2] Inst Super Tecn, Dept Engn Quim & Biol, CQE, P-1049001 Lisbon, Portugal
[3] UCL, Dept Chem, London WC1H 0AJ, England
[4] Univ Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QJ, E Sussex, England
来源
JOURNAL OF ORGANIC CHEMISTRY | 2008年 / 73卷 / 11期
关键词
D O I
10.1021/jo800087n
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient new methodology for the arylation of aldehydes is disclosed which uses dirhodium(II) catalysts and N-heterocyclic carbene (NHC) ligands. Complexes of Rh-2(OAc)(4) with one and two NHCs attached on the axial positions were successfully isolated, fully characterized, and used as catalysts in the reaction. The saturated monocomplex ((NHC 5)Rh-2(OAc)(4)) 31 was shown to be the most active catalyst and was particularly efficient in the arylation of alkyl aldehydes. DFT calculations support participation of complexes with one axial NHC in the reaction as the catalysts active species and indicate that hydrogen bonds involving dirhodium unit, reactants, and solvent (alcohol) play an important role on the reaction mechanism.
引用
收藏
页码:4076 / 4086
页数:11
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