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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2021 Volume 31, Issue 5, Pages 620–623 (Mi mendc1002)

This article is cited in 2 papers

Communications

Oxidation-promoted synthesis of ferrocenyl planar chiral rhodium(iii) complexes for C–H functionalization catalysis

J. Cabanesa, M. Odnoroha, C. Duhayona, Ch. Bijania, A. Sournia-Saqueta, R. Poliab, A. Labandea

a Université de Toulouse, Toulouse, France
b Institut Universitaire de France, Paris, France

Abstract: The chemical oxidation of rhodium(i) complexes [Rh(L)(COD)][BF4], where L is a ferrocenyl phosphine/N-heterocyclic carbene ligand, with 2 equiv. of a triaryl-aminium salt [(4-BrC6H4)3N][BF4] in acetonitrile gave planar chiral, air-stable [Rh(L–H)(MeCN)3][BF4]2 complexes where the ferrocene (C5H4CH2ImR or C5H4CH2BImCH2Mes) ring has been C–H activated at the position 2 in good to excellent yields. An important reactivity difference between our complexes and the ubiquitous [Cp*Rh(MeCN)3]X2 complex has been observed in the Grignard-type arylation of 4-nitrobenzaldehyde.

Keywords: rhodium, N-heterocyclic carbenes, Ferrocene, redox active ligands, catalysis.

Language: English

DOI: 10.1016/j.mencom.2021.09.010



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