Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , |
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. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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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 |
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1799133846643408897 |