Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study

Detalhes bibliográficos
Autor(a) principal: Machado, N. F. L.
Data de Publicação: 2011
Outros Autores: Ruano, C., Castro, J. L., Marques, M. P. M., Otero, J. C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/45099
https://doi.org/10.1039/c0cp01174f
https://doi.org/10.1039/C0CP01174F
Resumo: A SERS study of chromone 3-carboxylic acid adsorbed on silver colloids was undertaken, in order to assess the ability of this compound to accept electrons in charge transfer (CT) processes. Theoretical SERS intensities under photoinduced CT resonant conditions have been carried out for both the neutral and the deprotonated species allowing to conclude, by comparison with the experimental data, that the recorded SER corresponds to the anionic form of the acid linked to the metal. It was shown that the SERS-CT mechanism predominates for this particular compound, thus explaining the strong enhancement of the band at ca. 1600 cm(-1) assigned to the 8a ring stretching mode. The identification of CT processes is of the utmost importance for understanding the mechanism through which these benzopyranes may act as antioxidants.
id RCAP_f00b6354561954ff36ecf6b66c08c299
oai_identifier_str oai:estudogeral.uc.pt:10316/45099
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering studyAntioxidantsBenzopyransCarboxylic AcidsChromonesColloidsElectronsSilverSpectrum Analysis, RamanA SERS study of chromone 3-carboxylic acid adsorbed on silver colloids was undertaken, in order to assess the ability of this compound to accept electrons in charge transfer (CT) processes. Theoretical SERS intensities under photoinduced CT resonant conditions have been carried out for both the neutral and the deprotonated species allowing to conclude, by comparison with the experimental data, that the recorded SER corresponds to the anionic form of the acid linked to the metal. It was shown that the SERS-CT mechanism predominates for this particular compound, thus explaining the strong enhancement of the band at ca. 1600 cm(-1) assigned to the 8a ring stretching mode. The identification of CT processes is of the utmost importance for understanding the mechanism through which these benzopyranes may act as antioxidants.2011-01-21info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/45099http://hdl.handle.net/10316/45099https://doi.org/10.1039/c0cp01174fhttps://doi.org/10.1039/C0CP01174FengMachado, N. F. L.Ruano, C.Castro, J. L.Marques, M. P. M.Otero, J. C.info: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:RCAAP2021-10-07T08:07:44Zoai:estudogeral.uc.pt:10316/45099Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:56:08.328673Repositório 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 Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
title Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
spellingShingle Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
Machado, N. F. L.
Antioxidants
Benzopyrans
Carboxylic Acids
Chromones
Colloids
Electrons
Silver
Spectrum Analysis, Raman
title_short Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
title_full Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
title_fullStr Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
title_full_unstemmed Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
title_sort Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
author Machado, N. F. L.
author_facet Machado, N. F. L.
Ruano, C.
Castro, J. L.
Marques, M. P. M.
Otero, J. C.
author_role author
author2 Ruano, C.
Castro, J. L.
Marques, M. P. M.
Otero, J. C.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Machado, N. F. L.
Ruano, C.
Castro, J. L.
Marques, M. P. M.
Otero, J. C.
dc.subject.por.fl_str_mv Antioxidants
Benzopyrans
Carboxylic Acids
Chromones
Colloids
Electrons
Silver
Spectrum Analysis, Raman
topic Antioxidants
Benzopyrans
Carboxylic Acids
Chromones
Colloids
Electrons
Silver
Spectrum Analysis, Raman
description A SERS study of chromone 3-carboxylic acid adsorbed on silver colloids was undertaken, in order to assess the ability of this compound to accept electrons in charge transfer (CT) processes. Theoretical SERS intensities under photoinduced CT resonant conditions have been carried out for both the neutral and the deprotonated species allowing to conclude, by comparison with the experimental data, that the recorded SER corresponds to the anionic form of the acid linked to the metal. It was shown that the SERS-CT mechanism predominates for this particular compound, thus explaining the strong enhancement of the band at ca. 1600 cm(-1) assigned to the 8a ring stretching mode. The identification of CT processes is of the utmost importance for understanding the mechanism through which these benzopyranes may act as antioxidants.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-21
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://hdl.handle.net/10316/45099
http://hdl.handle.net/10316/45099
https://doi.org/10.1039/c0cp01174f
https://doi.org/10.1039/C0CP01174F
url http://hdl.handle.net/10316/45099
https://doi.org/10.1039/c0cp01174f
https://doi.org/10.1039/C0CP01174F
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799133846643408897