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Developments in the Dehydrogenative Electrochemical Synthesis of 3,3',5,5'-Tetramethyl-2,2'-biphenol.
Gleede, Barbara; Selt, Maximilian; Franke, Robert; Waldvogel, Siegfried R.
Afiliación
  • Gleede B; Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
  • Selt M; Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
  • Franke R; Material Science IN MainZ (MAINZ), Graduate School of Excellence, Staudingerweg 9, 55128, Mainz, Germany.
  • Waldvogel SR; Evonik Performance Materials GmbH, Paul-Baumann-Straße 1, 45772, Marl, Germany.
Chemistry ; 27(32): 8252-8263, 2021 Jun 04.
Article en En | MEDLINE | ID: mdl-33453091
The symmetric biphenol 3,3',5,5'-tetramethyl-2,2'-biphenol is a well-known ligand building block and is used in transition-metal catalysis. In the literature, there are several synthetic routes for the preparation of this exceptional molecule. Herein, the focus is on the sustainable electrochemical synthesis of 3,3',5,5'-tetramethyl-2,2'-biphenol. A brief overview of the developmental history of this inconspicuous molecule, which is of great interest for technical applications, but has many challenges for its synthesis, is provided. The electro-organic method is a powerful, sustainable, and efficient alternative to conventional synthesis to obtain this symmetric biphenol up to the kilogram scale. Another section of this article is devoted to different process management strategies in batch-type and flow electrolysis and their respective advantages.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Alemania