Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy

Autores
Broglia, Martin Federico; Previtali, Carlos Mario; Bertolotti, Sonia Graciela
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The interaction of the triplet state of the synthetic dye phenosafranine (3,7-diamino-5-phenylphenazinium chloride) with indolic compounds of biological relevance was investigated in water by means of laser flash photolysis. The rate constants for the triplet quenching were determined. The quenching process may be explained by an electron transfer from the indole to the dye in its triplet state. The rate constants present a typical dependence of an electron transfer process with the one-electron oxidation potential of the indole. Indole-3-acetic acid and its homologous indole propionic and indole butyric acids are the most effective quenchers with rate constants reaching the diffusion limit. Rate constants for indole itself, tryptophan and indole-3 carboxylic acid are one order of magnitude lower. The electron transfer nature of the quenching reaction is further confirmed by the detection of the semi-reduced form of the dye by its transient absorption. The absorption coefficients of the transient species were estimated, and the quantum yield of the charge separation process was determined. The efficiency of formation of radical species is between 60 and 90% of the triplets intercepted.
Fil: Broglia, Martin Federico. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Previtali, Carlos Mario. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Materia
Phenosafranine
Triplet state
Indolic compounds
Electron transfer
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/100187

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network_name_str CONICET Digital (CONICET)
spelling Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopyBroglia, Martin FedericoPrevitali, Carlos MarioBertolotti, Sonia GracielaPhenosafranineTriplet stateIndolic compoundsElectron transferhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The interaction of the triplet state of the synthetic dye phenosafranine (3,7-diamino-5-phenylphenazinium chloride) with indolic compounds of biological relevance was investigated in water by means of laser flash photolysis. The rate constants for the triplet quenching were determined. The quenching process may be explained by an electron transfer from the indole to the dye in its triplet state. The rate constants present a typical dependence of an electron transfer process with the one-electron oxidation potential of the indole. Indole-3-acetic acid and its homologous indole propionic and indole butyric acids are the most effective quenchers with rate constants reaching the diffusion limit. Rate constants for indole itself, tryptophan and indole-3 carboxylic acid are one order of magnitude lower. The electron transfer nature of the quenching reaction is further confirmed by the detection of the semi-reduced form of the dye by its transient absorption. The absorption coefficients of the transient species were estimated, and the quantum yield of the charge separation process was determined. The efficiency of formation of radical species is between 60 and 90% of the triplets intercepted.Fil: Broglia, Martin Federico. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Previtali, Carlos Mario. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaRoyal Society of Chemistry2015-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/100187Broglia, Martin Federico; Previtali, Carlos Mario; Bertolotti, Sonia Graciela; Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy; Royal Society of Chemistry; Photochemical and Photobiological Sciences; 14; 2; 2-2015; 407-4131474-905XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c4pp00365ainfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2015/PP/C4PP00365Ainfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:37:40Zoai:ri.conicet.gov.ar:11336/100187instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:37:40.553CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
title Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
spellingShingle Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
Broglia, Martin Federico
Phenosafranine
Triplet state
Indolic compounds
Electron transfer
title_short Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
title_full Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
title_fullStr Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
title_full_unstemmed Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
title_sort Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy
dc.creator.none.fl_str_mv Broglia, Martin Federico
Previtali, Carlos Mario
Bertolotti, Sonia Graciela
author Broglia, Martin Federico
author_facet Broglia, Martin Federico
Previtali, Carlos Mario
Bertolotti, Sonia Graciela
author_role author
author2 Previtali, Carlos Mario
Bertolotti, Sonia Graciela
author2_role author
author
dc.subject.none.fl_str_mv Phenosafranine
Triplet state
Indolic compounds
Electron transfer
topic Phenosafranine
Triplet state
Indolic compounds
Electron transfer
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The interaction of the triplet state of the synthetic dye phenosafranine (3,7-diamino-5-phenylphenazinium chloride) with indolic compounds of biological relevance was investigated in water by means of laser flash photolysis. The rate constants for the triplet quenching were determined. The quenching process may be explained by an electron transfer from the indole to the dye in its triplet state. The rate constants present a typical dependence of an electron transfer process with the one-electron oxidation potential of the indole. Indole-3-acetic acid and its homologous indole propionic and indole butyric acids are the most effective quenchers with rate constants reaching the diffusion limit. Rate constants for indole itself, tryptophan and indole-3 carboxylic acid are one order of magnitude lower. The electron transfer nature of the quenching reaction is further confirmed by the detection of the semi-reduced form of the dye by its transient absorption. The absorption coefficients of the transient species were estimated, and the quantum yield of the charge separation process was determined. The efficiency of formation of radical species is between 60 and 90% of the triplets intercepted.
Fil: Broglia, Martin Federico. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Previtali, Carlos Mario. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
description The interaction of the triplet state of the synthetic dye phenosafranine (3,7-diamino-5-phenylphenazinium chloride) with indolic compounds of biological relevance was investigated in water by means of laser flash photolysis. The rate constants for the triplet quenching were determined. The quenching process may be explained by an electron transfer from the indole to the dye in its triplet state. The rate constants present a typical dependence of an electron transfer process with the one-electron oxidation potential of the indole. Indole-3-acetic acid and its homologous indole propionic and indole butyric acids are the most effective quenchers with rate constants reaching the diffusion limit. Rate constants for indole itself, tryptophan and indole-3 carboxylic acid are one order of magnitude lower. The electron transfer nature of the quenching reaction is further confirmed by the detection of the semi-reduced form of the dye by its transient absorption. The absorption coefficients of the transient species were estimated, and the quantum yield of the charge separation process was determined. The efficiency of formation of radical species is between 60 and 90% of the triplets intercepted.
publishDate 2015
dc.date.none.fl_str_mv 2015-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/100187
Broglia, Martin Federico; Previtali, Carlos Mario; Bertolotti, Sonia Graciela; Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy; Royal Society of Chemistry; Photochemical and Photobiological Sciences; 14; 2; 2-2015; 407-413
1474-905X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/100187
identifier_str_mv Broglia, Martin Federico; Previtali, Carlos Mario; Bertolotti, Sonia Graciela; Triplet state quenching of phenosafranine dye by indolic compounds studied by transient absorption spectroscopy; Royal Society of Chemistry; Photochemical and Photobiological Sciences; 14; 2; 2-2015; 407-413
1474-905X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1039/c4pp00365a
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2015/PP/C4PP00365A
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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