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About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions

Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity fo...

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Detalles Bibliográficos
Autores principales: Beil, Sebastian B., Breiner, Manuel, Schulz, Lara, Schüll, Aaron, Müller, Timo, Schollmeyer, Dieter, Bomm, Alexander, Holtkamp, Michael, Karst, Uwe, Schade, Wolfgang, Waldvogel, Siegfried R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052091/
https://www.ncbi.nlm.nih.gov/pubmed/35498499
http://dx.doi.org/10.1039/d0ra02673e
Descripción
Sumario:Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity for dehydrogenative coupling reactions of this novel active anode increases when the electrolyte is not stirred during electrolysis. Besides the aryl–aryl coupling, a dehydrogenative arylation reaction of benzylic nitriles was found while stirring the mixture providing quick access to synthetically useful building blocks.