Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities

Detalhes bibliográficos
Autor(a) principal: Alipázaga,Maria V.
Data de Publicação: 2003
Outros Autores: Bonifácio,Rodrigo L., Kosminsky,Luis, Bertotti,Mauro, Coichev,Nina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532003000500003
Resumo: The oxidation of Cu(II) complexes with tetra, penta and hexaglycine in borate buffer aqueous solution, by dissolved oxygen is strongly accelerated by sulfite. The formation of Cu(III) complexes with maximum absorbances at 250 nm (e = 9000 mol-1 L cm-1) and 365 nm (e = 7120 mol-1 L cm-1) was also characterized by using rotating ring-disk voltammetry, whose anodic and cathodic components were observed in voltammograms recorded in solutions containing Cu(II). Voltammograms, obtained at various rotation speeds, showed that the Cu(III) species electrochemically generated is not stable over the entire time window of the experiment and in solutions containing tetraglycine the overall limiting current is controlled by the kinetics of an equilibrium involving Cu(II) species.The calculated first order rate constant of the decomposition was 4.37x10-3 s-1. Electrochemical experiments carried out in Cu(II) solutions after the addition of relatively small amounts of sulfite demonstrated that the Cu(III) species formed in the chemical reaction is the same as the one collected at the ring electrode when Cu(II) is oxidized at the disk electrode in ring-disk voltammetry. The concentration of Cu(III) complexes is proportional to the amount of added sulfite and the results indicated that indirect analytical methods for sulfite may be developed by means of spectrophotometric or amperometric detection of the chemically generated product.
id SBQ-2_72db896e825a1e986056b9031f086138
oai_identifier_str oai:scielo:S0103-50532003000500003
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialitiescopper (III)glycinessulfitecatalysisautoxidationrotating ring disc electrodeThe oxidation of Cu(II) complexes with tetra, penta and hexaglycine in borate buffer aqueous solution, by dissolved oxygen is strongly accelerated by sulfite. The formation of Cu(III) complexes with maximum absorbances at 250 nm (e = 9000 mol-1 L cm-1) and 365 nm (e = 7120 mol-1 L cm-1) was also characterized by using rotating ring-disk voltammetry, whose anodic and cathodic components were observed in voltammograms recorded in solutions containing Cu(II). Voltammograms, obtained at various rotation speeds, showed that the Cu(III) species electrochemically generated is not stable over the entire time window of the experiment and in solutions containing tetraglycine the overall limiting current is controlled by the kinetics of an equilibrium involving Cu(II) species.The calculated first order rate constant of the decomposition was 4.37x10-3 s-1. Electrochemical experiments carried out in Cu(II) solutions after the addition of relatively small amounts of sulfite demonstrated that the Cu(III) species formed in the chemical reaction is the same as the one collected at the ring electrode when Cu(II) is oxidized at the disk electrode in ring-disk voltammetry. The concentration of Cu(III) complexes is proportional to the amount of added sulfite and the results indicated that indirect analytical methods for sulfite may be developed by means of spectrophotometric or amperometric detection of the chemically generated product.Sociedade Brasileira de Química2003-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532003000500003Journal of the Brazilian Chemical Society v.14 n.5 2003reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532003000500003info:eu-repo/semantics/openAccessAlipázaga,Maria V.Bonifácio,Rodrigo L.Kosminsky,LuisBertotti,MauroCoichev,Ninaeng2004-02-05T00:00:00Zoai:scielo:S0103-50532003000500003Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2004-02-05T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
title Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
spellingShingle Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
Alipázaga,Maria V.
copper (III)
glycines
sulfite
catalysis
autoxidation
rotating ring disc electrode
title_short Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
title_full Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
title_fullStr Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
title_full_unstemmed Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
title_sort Sulfite induced autoxidation of Cu(II)/tetra/ penta and hexaglycine complexes: spectrophotometric and rotating-ring-disk glassy carbon electrode studies and analytical potentialities
author Alipázaga,Maria V.
author_facet Alipázaga,Maria V.
Bonifácio,Rodrigo L.
Kosminsky,Luis
Bertotti,Mauro
Coichev,Nina
author_role author
author2 Bonifácio,Rodrigo L.
Kosminsky,Luis
Bertotti,Mauro
Coichev,Nina
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Alipázaga,Maria V.
Bonifácio,Rodrigo L.
Kosminsky,Luis
Bertotti,Mauro
Coichev,Nina
dc.subject.por.fl_str_mv copper (III)
glycines
sulfite
catalysis
autoxidation
rotating ring disc electrode
topic copper (III)
glycines
sulfite
catalysis
autoxidation
rotating ring disc electrode
description The oxidation of Cu(II) complexes with tetra, penta and hexaglycine in borate buffer aqueous solution, by dissolved oxygen is strongly accelerated by sulfite. The formation of Cu(III) complexes with maximum absorbances at 250 nm (e = 9000 mol-1 L cm-1) and 365 nm (e = 7120 mol-1 L cm-1) was also characterized by using rotating ring-disk voltammetry, whose anodic and cathodic components were observed in voltammograms recorded in solutions containing Cu(II). Voltammograms, obtained at various rotation speeds, showed that the Cu(III) species electrochemically generated is not stable over the entire time window of the experiment and in solutions containing tetraglycine the overall limiting current is controlled by the kinetics of an equilibrium involving Cu(II) species.The calculated first order rate constant of the decomposition was 4.37x10-3 s-1. Electrochemical experiments carried out in Cu(II) solutions after the addition of relatively small amounts of sulfite demonstrated that the Cu(III) species formed in the chemical reaction is the same as the one collected at the ring electrode when Cu(II) is oxidized at the disk electrode in ring-disk voltammetry. The concentration of Cu(III) complexes is proportional to the amount of added sulfite and the results indicated that indirect analytical methods for sulfite may be developed by means of spectrophotometric or amperometric detection of the chemically generated product.
publishDate 2003
dc.date.none.fl_str_mv 2003-10-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532003000500003
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532003000500003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532003000500003
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.14 n.5 2003
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
_version_ 1750318165356707840