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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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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
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author Beil, Sebastian B.
Breiner, Manuel
Schulz, Lara
Schüll, Aaron
Müller, Timo
Schollmeyer, Dieter
Bomm, Alexander
Holtkamp, Michael
Karst, Uwe
Schade, Wolfgang
Waldvogel, Siegfried R.
author_facet Beil, Sebastian B.
Breiner, Manuel
Schulz, Lara
Schüll, Aaron
Müller, Timo
Schollmeyer, Dieter
Bomm, Alexander
Holtkamp, Michael
Karst, Uwe
Schade, Wolfgang
Waldvogel, Siegfried R.
author_sort Beil, Sebastian B.
collection PubMed
description 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.
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spelling pubmed-90520912022-04-29 About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions Beil, Sebastian B. Breiner, Manuel Schulz, Lara Schüll, Aaron Müller, Timo Schollmeyer, Dieter Bomm, Alexander Holtkamp, Michael Karst, Uwe Schade, Wolfgang Waldvogel, Siegfried R. RSC Adv Chemistry 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. The Royal Society of Chemistry 2020-04-08 /pmc/articles/PMC9052091/ /pubmed/35498499 http://dx.doi.org/10.1039/d0ra02673e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Beil, Sebastian B.
Breiner, Manuel
Schulz, Lara
Schüll, Aaron
Müller, Timo
Schollmeyer, Dieter
Bomm, Alexander
Holtkamp, Michael
Karst, Uwe
Schade, Wolfgang
Waldvogel, Siegfried R.
About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
title About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
title_full About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
title_fullStr About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
title_full_unstemmed About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
title_short About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
title_sort about the selectivity and reactivity of active nickel electrodes in c–c coupling reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052091/
https://www.ncbi.nlm.nih.gov/pubmed/35498499
http://dx.doi.org/10.1039/d0ra02673e
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