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Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones

The electrocarboxylation of a series of benzophenones under galvanostatic conditions has been carried out in aprotic solvents using an undivided bulk electrolysis cell equipped with a Mg sacrificial anode. Systematic studies have been carried out in order to establish the qualitative relationships b...

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Autores principales: Zhao, Shu-Feng, Wang, Huan, Lan, Yang-Chun, Liu, Xiao, Lu, Jia-Xing, Zhang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Sequoia 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284772/
https://www.ncbi.nlm.nih.gov/pubmed/22368535
http://dx.doi.org/10.1016/j.jelechem.2011.11.001
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author Zhao, Shu-Feng
Wang, Huan
Lan, Yang-Chun
Liu, Xiao
Lu, Jia-Xing
Zhang, Jie
author_facet Zhao, Shu-Feng
Wang, Huan
Lan, Yang-Chun
Liu, Xiao
Lu, Jia-Xing
Zhang, Jie
author_sort Zhao, Shu-Feng
collection PubMed
description The electrocarboxylation of a series of benzophenones under galvanostatic conditions has been carried out in aprotic solvents using an undivided bulk electrolysis cell equipped with a Mg sacrificial anode. Systematic studies have been carried out in order to establish the qualitative relationships between the yield of carboxylation reaction and the operational and intrinsic parameters for the electrocarboxylation of benzophenones. For the diaryl ketones chosen for these studies, the yields of the target benzilic acids have been found to be strongly dependent on different parameters such as solvents, supporting electrolytes, cathode materials, current density, temperature and the nature of the substrates.
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spelling pubmed-32847722012-02-24 Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones Zhao, Shu-Feng Wang, Huan Lan, Yang-Chun Liu, Xiao Lu, Jia-Xing Zhang, Jie J Electroanal Chem (Lausanne Switz) Article The electrocarboxylation of a series of benzophenones under galvanostatic conditions has been carried out in aprotic solvents using an undivided bulk electrolysis cell equipped with a Mg sacrificial anode. Systematic studies have been carried out in order to establish the qualitative relationships between the yield of carboxylation reaction and the operational and intrinsic parameters for the electrocarboxylation of benzophenones. For the diaryl ketones chosen for these studies, the yields of the target benzilic acids have been found to be strongly dependent on different parameters such as solvents, supporting electrolytes, cathode materials, current density, temperature and the nature of the substrates. Elsevier Sequoia 2012-01-01 /pmc/articles/PMC3284772/ /pubmed/22368535 http://dx.doi.org/10.1016/j.jelechem.2011.11.001 Text en © 2012 Elsevier B.V. All rights reserved. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Article
Zhao, Shu-Feng
Wang, Huan
Lan, Yang-Chun
Liu, Xiao
Lu, Jia-Xing
Zhang, Jie
Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
title Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
title_full Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
title_fullStr Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
title_full_unstemmed Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
title_short Influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
title_sort influences of the operative parameters and the nature of the substrate on the electrocarboxylation of benzophenones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284772/
https://www.ncbi.nlm.nih.gov/pubmed/22368535
http://dx.doi.org/10.1016/j.jelechem.2011.11.001
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