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Redox-ligand sustains controlled generation of CF(3) radicals by well-defined copper complex

A well-defined copper complex bearing iminosemiquinone ligands performs single electron reduction of an electrophilic CF(3)(+) source into CF˙3 radicals. This redox behavior is enabled by the ligand which shuttles through two different redox states (iminosemiquinone and iminobenzoquinone) while the...

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Detalles Bibliográficos
Autores principales: Jacquet, Jérémy, Blanchard, Sébastien, Derat, Etienne, Desage-El Murr, Marine, Fensterbank, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968567/
https://www.ncbi.nlm.nih.gov/pubmed/29899928
http://dx.doi.org/10.1039/c5sc03636d
Descripción
Sumario:A well-defined copper complex bearing iminosemiquinone ligands performs single electron reduction of an electrophilic CF(3)(+) source into CF˙3 radicals. This redox behavior is enabled by the ligand which shuttles through two different redox states (iminosemiquinone and iminobenzoquinone) while the copper center is preserved as a Cu(ii). This system was used in the trifluoromethylation of silyl enol ethers, heteroaromatics and in the hydrotrifluoromethylation of alkynes. This is the first example of cooperative redox catalysis for the controlled generation of CF˙3 radicals.