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N‐Heterocyclic Carbene Dirhodium(II) Complexes as Catalysts for Allylic and Benzylic Oxidations
Author(s) -
Coelho Jaime A. S.,
Trindade Alexandre F.,
Wanke Riccardo,
Rocha Bruno G. M.,
Veiros Luis F.,
Gois Pedro M. P.,
Pombeiro Armando J. L.,
Afonso Carlos A. M.
Publication year - 2013
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201201300
Subject(s) - chemistry , carbene , allylic rearrangement , catalysis , medicinal chemistry , redox , ligand (biochemistry) , cyclohexene , ketone , cyclic voltammetry , solvent , electrochemistry , photochemistry , organic chemistry , biochemistry , receptor , electrode
The experimental conditions (solvent, base, temperature and oxidant) for allylic and benzylic oxidation reactions catalyzed by dirhodium(II)/N‐heterocyclic carbene (NHC) complexes were optimized for the first time in this work. The oxidations of cyclohexene and fluorene were used as model reactions. Two optimized experimental conditions for both types of oxidations were found, which resulted in their ketone [aerobic conditions, 40 °C, 1 equiv. t BuOOH (TBHP)] or tert ‐butyl peroxide derivatives (anaerobic conditions, 25 °C, 2 equiv. TBHP). The dirhodium(II) complexes undergo a single‐electron reversible oxidation by cyclic voltammetry in CH 2 Cl 2 , which is assigned to the Rh 2 4+ /Rh 2 5+ redox couple at an oxidation potential that is lowered upon sequential axial coordination of further ligands to the Rh–Rh centre. The oxidation potential is discussed in terms of the electron‐donor character of the NHC ligand, which was shown to act as an effective electron‐releaser to the Rh 2 4+ centre, and the electrochemical behaviour is compared to the observed catalytic activity.