Effect of the interface on the photophysics of eosin-Y in reverse miceles
- Autores
- Arbeloa, Ernesto Maximiliano; Porcal, Gabriela Valeria; Bertolotti, Sonia Graciela; Previtali, Carlos Mario
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The photophysics of the xanthene dye eosin-Y (Eos) was studied in reverse micelles (RMs) of sodium 1,4-bis (2-ethylhexyl) sulfosuccinate (AOT) and benzylhexadecyldimethylammonium chloride (BHDC). Special interest was assigned to the effect of organization on the triplet state properties. In the reverse micellar media both the absorption and emission spectra of the dye present a red shift with respect to water. It is concluded that Eos in both reverse micellar systems is localized in the interface. Although this is predictable in BHDC due to the positive charge at the interface and the negative charge of the dye, it is notable in the case of the negative interface of AOT. In this case it may be concluded that Eos resides in the interface co-micellizing with the surfactant, although more exposed to water than in the case of BHDC.
Triplet state decay kinetics and absorption spectra were determined by laser flash photolysis. The triplet lives longer in RMs than in homogeneous solvents. The compartmentalization of the dye precludes the auto-quenching which shorts the lifetime in homogeneous solvents. The quenching by aliphatic amines was also investigated. The hydrophilic triethanolamine (TEOA) is localized in the water pool, and the triplet quenching is more efficient than in homogeneous solvents. On the other hand the quenching by tributylamine (TBA) which is located in the bulk organic solvent is much less efficient. The quenching by TEOA in RMs can be understood in terms of an exchange mechanism between micelles. Quantum yields of radicals produced in the triplet quenching process were determined.
Fil: Arbeloa, Ernesto Maximiliano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina
Fil: Porcal, Gabriela Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina
Fil: Bertolotti, Sonia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; 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. Centro Científico Tecnológico Conicet - Córdoba; Argentina - Materia
-
EOSIN-Y
PHOTOPHYSICS
TRIPLET STATE
REVERSE MICELLES - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/94116
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Effect of the interface on the photophysics of eosin-Y in reverse micelesArbeloa, Ernesto MaximilianoPorcal, Gabriela ValeriaBertolotti, Sonia GracielaPrevitali, Carlos MarioEOSIN-YPHOTOPHYSICSTRIPLET STATEREVERSE MICELLEShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The photophysics of the xanthene dye eosin-Y (Eos) was studied in reverse micelles (RMs) of sodium 1,4-bis (2-ethylhexyl) sulfosuccinate (AOT) and benzylhexadecyldimethylammonium chloride (BHDC). Special interest was assigned to the effect of organization on the triplet state properties. In the reverse micellar media both the absorption and emission spectra of the dye present a red shift with respect to water. It is concluded that Eos in both reverse micellar systems is localized in the interface. Although this is predictable in BHDC due to the positive charge at the interface and the negative charge of the dye, it is notable in the case of the negative interface of AOT. In this case it may be concluded that Eos resides in the interface co-micellizing with the surfactant, although more exposed to water than in the case of BHDC.<br />Triplet state decay kinetics and absorption spectra were determined by laser flash photolysis. The triplet lives longer in RMs than in homogeneous solvents. The compartmentalization of the dye precludes the auto-quenching which shorts the lifetime in homogeneous solvents. The quenching by aliphatic amines was also investigated. The hydrophilic triethanolamine (TEOA) is localized in the water pool, and the triplet quenching is more efficient than in homogeneous solvents. On the other hand the quenching by tributylamine (TBA) which is located in the bulk organic solvent is much less efficient. The quenching by TEOA in RMs can be understood in terms of an exchange mechanism between micelles. Quantum yields of radicals produced in the triplet quenching process were determined.Fil: Arbeloa, Ernesto Maximiliano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; ArgentinaFil: Porcal, Gabriela Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; ArgentinaFil: Bertolotti, Sonia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; 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. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaElsevier Science Sa2013-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/94116Arbeloa, Ernesto Maximiliano; Porcal, Gabriela Valeria; Bertolotti, Sonia Graciela; Previtali, Carlos Mario; Effect of the interface on the photophysics of eosin-Y in reverse miceles; Elsevier Science Sa; Journal of Photochemistry and Photobiology A: Chemistry; 252; 1-2013; 31-361010-6030CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1010603012005424info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotochem.2012.11.003info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:48:23Zoai:ri.conicet.gov.ar:11336/94116instacron: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:34982025-09-03 09:48:24.035CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
title |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
spellingShingle |
Effect of the interface on the photophysics of eosin-Y in reverse miceles Arbeloa, Ernesto Maximiliano EOSIN-Y PHOTOPHYSICS TRIPLET STATE REVERSE MICELLES |
title_short |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
title_full |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
title_fullStr |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
title_full_unstemmed |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
title_sort |
Effect of the interface on the photophysics of eosin-Y in reverse miceles |
dc.creator.none.fl_str_mv |
Arbeloa, Ernesto Maximiliano Porcal, Gabriela Valeria Bertolotti, Sonia Graciela Previtali, Carlos Mario |
author |
Arbeloa, Ernesto Maximiliano |
author_facet |
Arbeloa, Ernesto Maximiliano Porcal, Gabriela Valeria Bertolotti, Sonia Graciela Previtali, Carlos Mario |
author_role |
author |
author2 |
Porcal, Gabriela Valeria Bertolotti, Sonia Graciela Previtali, Carlos Mario |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
EOSIN-Y PHOTOPHYSICS TRIPLET STATE REVERSE MICELLES |
topic |
EOSIN-Y PHOTOPHYSICS TRIPLET STATE REVERSE MICELLES |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The photophysics of the xanthene dye eosin-Y (Eos) was studied in reverse micelles (RMs) of sodium 1,4-bis (2-ethylhexyl) sulfosuccinate (AOT) and benzylhexadecyldimethylammonium chloride (BHDC). Special interest was assigned to the effect of organization on the triplet state properties. In the reverse micellar media both the absorption and emission spectra of the dye present a red shift with respect to water. It is concluded that Eos in both reverse micellar systems is localized in the interface. Although this is predictable in BHDC due to the positive charge at the interface and the negative charge of the dye, it is notable in the case of the negative interface of AOT. In this case it may be concluded that Eos resides in the interface co-micellizing with the surfactant, although more exposed to water than in the case of BHDC.<br />Triplet state decay kinetics and absorption spectra were determined by laser flash photolysis. The triplet lives longer in RMs than in homogeneous solvents. The compartmentalization of the dye precludes the auto-quenching which shorts the lifetime in homogeneous solvents. The quenching by aliphatic amines was also investigated. The hydrophilic triethanolamine (TEOA) is localized in the water pool, and the triplet quenching is more efficient than in homogeneous solvents. On the other hand the quenching by tributylamine (TBA) which is located in the bulk organic solvent is much less efficient. The quenching by TEOA in RMs can be understood in terms of an exchange mechanism between micelles. Quantum yields of radicals produced in the triplet quenching process were determined. Fil: Arbeloa, Ernesto Maximiliano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina Fil: Porcal, Gabriela Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina Fil: Bertolotti, Sonia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; 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. Centro Científico Tecnológico Conicet - Córdoba; Argentina |
description |
The photophysics of the xanthene dye eosin-Y (Eos) was studied in reverse micelles (RMs) of sodium 1,4-bis (2-ethylhexyl) sulfosuccinate (AOT) and benzylhexadecyldimethylammonium chloride (BHDC). Special interest was assigned to the effect of organization on the triplet state properties. In the reverse micellar media both the absorption and emission spectra of the dye present a red shift with respect to water. It is concluded that Eos in both reverse micellar systems is localized in the interface. Although this is predictable in BHDC due to the positive charge at the interface and the negative charge of the dye, it is notable in the case of the negative interface of AOT. In this case it may be concluded that Eos resides in the interface co-micellizing with the surfactant, although more exposed to water than in the case of BHDC.<br />Triplet state decay kinetics and absorption spectra were determined by laser flash photolysis. The triplet lives longer in RMs than in homogeneous solvents. The compartmentalization of the dye precludes the auto-quenching which shorts the lifetime in homogeneous solvents. The quenching by aliphatic amines was also investigated. The hydrophilic triethanolamine (TEOA) is localized in the water pool, and the triplet quenching is more efficient than in homogeneous solvents. On the other hand the quenching by tributylamine (TBA) which is located in the bulk organic solvent is much less efficient. The quenching by TEOA in RMs can be understood in terms of an exchange mechanism between micelles. Quantum yields of radicals produced in the triplet quenching process were determined. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01 |
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/11336/94116 Arbeloa, Ernesto Maximiliano; Porcal, Gabriela Valeria; Bertolotti, Sonia Graciela; Previtali, Carlos Mario; Effect of the interface on the photophysics of eosin-Y in reverse miceles; Elsevier Science Sa; Journal of Photochemistry and Photobiology A: Chemistry; 252; 1-2013; 31-36 1010-6030 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/94116 |
identifier_str_mv |
Arbeloa, Ernesto Maximiliano; Porcal, Gabriela Valeria; Bertolotti, Sonia Graciela; Previtali, Carlos Mario; Effect of the interface on the photophysics of eosin-Y in reverse miceles; Elsevier Science Sa; Journal of Photochemistry and Photobiology A: Chemistry; 252; 1-2013; 31-36 1010-6030 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1010603012005424 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotochem.2012.11.003 |
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 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Science Sa |
publisher.none.fl_str_mv |
Elsevier Science Sa |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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1842268921942507520 |
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13.13397 |