Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution

Detalhes bibliográficos
Autor(a) principal: Boldrin Zanoni, M. V. [UNESP]
Data de Publicação: 1997
Outros Autores: Rosa, I. L V, Pesquero, C. R., Stradiotto, Nelson Ramos [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0103-50531997000300007
http://hdl.handle.net/11449/65293
Resumo: The electrochemical behavior of aniline protected by a nitrobenzene sulphonyl group in aqueous solution at a mercury electrode is reported. At pH < 10 the compound was reduced in a single well-defined step. Reduction of the nitro group involving a preceding protonation step was postulated. Two reduction steps are present at higher pH (pH > 11). Controlled potential electrolysis confirms that the reduction of the nitro group in a four-electron step to N-phenyl-4-hydroxylamine sulphonamide is always the preponderant process. ©1997 Soc. Bras. Química.
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spelling Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solutionAmine improtectionCathodic cleavageNitrobenzenesulphonamideThe electrochemical behavior of aniline protected by a nitrobenzene sulphonyl group in aqueous solution at a mercury electrode is reported. At pH < 10 the compound was reduced in a single well-defined step. Reduction of the nitro group involving a preceding protonation step was postulated. Two reduction steps are present at higher pH (pH > 11). Controlled potential electrolysis confirms that the reduction of the nitro group in a four-electron step to N-phenyl-4-hydroxylamine sulphonamide is always the preponderant process. ©1997 Soc. Bras. Química.Depto. de Quim. Analítica Institute de Química UNESP, C.P.355, 14800-900 Araraquara - SPDepartamento de Química Faculdade de Filos., Cie. e Letras USP, C.P. 3900, 14040-901 Ribeirão Preta - SPDepto. de Quim. Analítica Institute de Química UNESP, C.P.355, 14800-900 Araraquara - SPUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Boldrin Zanoni, M. V. [UNESP]Rosa, I. L VPesquero, C. R.Stradiotto, Nelson Ramos [UNESP]2014-05-27T11:18:18Z2014-05-27T11:18:18Z1997-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article223-227application/pdfhttp://dx.doi.org/10.1590/S0103-50531997000300007Journal of the Brazilian Chemical Society, v. 8, n. 3, p. 223-227, 1997.0103-5053http://hdl.handle.net/11449/6529310.1590/S0103-50531997000300007S0103-50531997000300007WOS:A1997XG435000072-s2.0-00313509912-s2.0-0031350991.pdf0072173018005712Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,357info:eu-repo/semantics/openAccess2023-12-07T06:19:17Zoai:repositorio.unesp.br:11449/65293Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:43:53.706704Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
title Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
spellingShingle Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
Boldrin Zanoni, M. V. [UNESP]
Amine improtection
Cathodic cleavage
Nitrobenzenesulphonamide
title_short Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
title_full Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
title_fullStr Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
title_full_unstemmed Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
title_sort Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution
author Boldrin Zanoni, M. V. [UNESP]
author_facet Boldrin Zanoni, M. V. [UNESP]
Rosa, I. L V
Pesquero, C. R.
Stradiotto, Nelson Ramos [UNESP]
author_role author
author2 Rosa, I. L V
Pesquero, C. R.
Stradiotto, Nelson Ramos [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Boldrin Zanoni, M. V. [UNESP]
Rosa, I. L V
Pesquero, C. R.
Stradiotto, Nelson Ramos [UNESP]
dc.subject.por.fl_str_mv Amine improtection
Cathodic cleavage
Nitrobenzenesulphonamide
topic Amine improtection
Cathodic cleavage
Nitrobenzenesulphonamide
description The electrochemical behavior of aniline protected by a nitrobenzene sulphonyl group in aqueous solution at a mercury electrode is reported. At pH < 10 the compound was reduced in a single well-defined step. Reduction of the nitro group involving a preceding protonation step was postulated. Two reduction steps are present at higher pH (pH > 11). Controlled potential electrolysis confirms that the reduction of the nitro group in a four-electron step to N-phenyl-4-hydroxylamine sulphonamide is always the preponderant process. ©1997 Soc. Bras. Química.
publishDate 1997
dc.date.none.fl_str_mv 1997-12-01
2014-05-27T11:18:18Z
2014-05-27T11:18:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0103-50531997000300007
Journal of the Brazilian Chemical Society, v. 8, n. 3, p. 223-227, 1997.
0103-5053
http://hdl.handle.net/11449/65293
10.1590/S0103-50531997000300007
S0103-50531997000300007
WOS:A1997XG43500007
2-s2.0-0031350991
2-s2.0-0031350991.pdf
0072173018005712
url http://dx.doi.org/10.1590/S0103-50531997000300007
http://hdl.handle.net/11449/65293
identifier_str_mv Journal of the Brazilian Chemical Society, v. 8, n. 3, p. 223-227, 1997.
0103-5053
10.1590/S0103-50531997000300007
S0103-50531997000300007
WOS:A1997XG43500007
2-s2.0-0031350991
2-s2.0-0031350991.pdf
0072173018005712
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of the Brazilian Chemical Society
1.444
0,357
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 223-227
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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