Electrochemical oxidation of propanil and related N-substituted amides

Detalhes bibliográficos
Autor(a) principal: Garrido, E. Manuela
Data de Publicação: 2001
Outros Autores: Lima, J. L. F. C., Delerue-Matos, Cristina, Borges, F., Silva, A. M. S., Oliveira-Brett, A. M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/2961
Resumo: The electrochemical behaviour of propanil and related N-substituted amides (acetanilide and N,N-diphenylacetamide) was studied by cyclic and square wave voltammetry using a glassy carbon electrode. Propanil has been found to have chemical stability under the established analytical conditions and showed an oxidation peak at +1.27V versus Ag/AgCl at pH 7.5. N,N-diphenylacetamide has a higher oxidation potential than the other compounds of +1.49V versus Ag/AgCl. Acetanilide oxidation occurred at a potential similar to that of propanil, +1.24V versus Ag/AgCl. These results are in agreement with the substitution pattern of the nitrogen atom of the amide. A degradation product of propanil, 3,4-dichloroaniline (DCA), was also studied, and showed an oxidation peak at +0.66V versus Ag/AgCl. A simple and specific quantitative electroanalytical method is described for the analysis of propanil in commercial products that contain propanil as the active ingredient, used in the treatment of rice crops in Portugal.
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spelling Electrochemical oxidation of propanil and related N-substituted amidesPropanilAnilide herbicidesSquare wave voltammetryN-substituted amidesThe electrochemical behaviour of propanil and related N-substituted amides (acetanilide and N,N-diphenylacetamide) was studied by cyclic and square wave voltammetry using a glassy carbon electrode. Propanil has been found to have chemical stability under the established analytical conditions and showed an oxidation peak at +1.27V versus Ag/AgCl at pH 7.5. N,N-diphenylacetamide has a higher oxidation potential than the other compounds of +1.49V versus Ag/AgCl. Acetanilide oxidation occurred at a potential similar to that of propanil, +1.24V versus Ag/AgCl. These results are in agreement with the substitution pattern of the nitrogen atom of the amide. A degradation product of propanil, 3,4-dichloroaniline (DCA), was also studied, and showed an oxidation peak at +0.66V versus Ag/AgCl. A simple and specific quantitative electroanalytical method is described for the analysis of propanil in commercial products that contain propanil as the active ingredient, used in the treatment of rice crops in Portugal.ElsevierRepositório Científico do Instituto Politécnico do PortoGarrido, E. ManuelaLima, J. L. F. C.Delerue-Matos, CristinaBorges, F.Silva, A. M. S.Oliveira-Brett, A. M.2013-11-26T15:54:05Z20012001-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/2961eng10.1016/S0003-2670(01)00817-0info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T12:42:35Zoai:recipp.ipp.pt:10400.22/2961Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:23:58.736737Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Electrochemical oxidation of propanil and related N-substituted amides
title Electrochemical oxidation of propanil and related N-substituted amides
spellingShingle Electrochemical oxidation of propanil and related N-substituted amides
Garrido, E. Manuela
Propanil
Anilide herbicides
Square wave voltammetry
N-substituted amides
title_short Electrochemical oxidation of propanil and related N-substituted amides
title_full Electrochemical oxidation of propanil and related N-substituted amides
title_fullStr Electrochemical oxidation of propanil and related N-substituted amides
title_full_unstemmed Electrochemical oxidation of propanil and related N-substituted amides
title_sort Electrochemical oxidation of propanil and related N-substituted amides
author Garrido, E. Manuela
author_facet Garrido, E. Manuela
Lima, J. L. F. C.
Delerue-Matos, Cristina
Borges, F.
Silva, A. M. S.
Oliveira-Brett, A. M.
author_role author
author2 Lima, J. L. F. C.
Delerue-Matos, Cristina
Borges, F.
Silva, A. M. S.
Oliveira-Brett, A. M.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Garrido, E. Manuela
Lima, J. L. F. C.
Delerue-Matos, Cristina
Borges, F.
Silva, A. M. S.
Oliveira-Brett, A. M.
dc.subject.por.fl_str_mv Propanil
Anilide herbicides
Square wave voltammetry
N-substituted amides
topic Propanil
Anilide herbicides
Square wave voltammetry
N-substituted amides
description The electrochemical behaviour of propanil and related N-substituted amides (acetanilide and N,N-diphenylacetamide) was studied by cyclic and square wave voltammetry using a glassy carbon electrode. Propanil has been found to have chemical stability under the established analytical conditions and showed an oxidation peak at +1.27V versus Ag/AgCl at pH 7.5. N,N-diphenylacetamide has a higher oxidation potential than the other compounds of +1.49V versus Ag/AgCl. Acetanilide oxidation occurred at a potential similar to that of propanil, +1.24V versus Ag/AgCl. These results are in agreement with the substitution pattern of the nitrogen atom of the amide. A degradation product of propanil, 3,4-dichloroaniline (DCA), was also studied, and showed an oxidation peak at +0.66V versus Ag/AgCl. A simple and specific quantitative electroanalytical method is described for the analysis of propanil in commercial products that contain propanil as the active ingredient, used in the treatment of rice crops in Portugal.
publishDate 2001
dc.date.none.fl_str_mv 2001
2001-01-01T00:00:00Z
2013-11-26T15:54:05Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.22/2961
url http://hdl.handle.net/10400.22/2961
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/S0003-2670(01)00817-0
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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