Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes
- Autores
- Montejano, Hernan Alfredo; Amat Guerri, Francisco; Costela, Angel; García Moreno, Inmaculada; Liras, Marta; Sastre, Roberto
- Año de publicación
- 2006
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The substituents at positions 2,6 and 8 in the commercial dye PM567 have been changed and their influence on the triplet state of each dye has been studied in terms of the absorption spectra, lifetimes, quantum yields and triplet-triplet extinction coefficients. The dyes have in position 8 the groups p-acetoxypolymethylene, p-(acetoxypropyl)phenyl or p-(acetoxymethyl)polyphenylene, or in positions 2 and 6 the groups tert-butyl (commercial dye PM597) or 3-acetoxypropyl. The triplet state spectroscopy results nearly independent on the molecular structure for the mono- and di-substituted aliphatic derivatives. However, the 8-aryl substitution increases both the triplet absorption over the fluorescence spectral region and the triplet state quantum yield, but reduces the triplet absorption coefficient.
Fil: Montejano, Hernan Alfredo. 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
Fil: Amat Guerri, Francisco. Consejo Superior de Investigaciones Científicas; España
Fil: Costela, Angel. Consejo Superior de Investigaciones Científicas; España
Fil: García Moreno, Inmaculada. Consejo Superior de Investigaciones Científicas; España
Fil: Liras, Marta. Universidad de Miguel Hernández; España
Fil: Sastre, Roberto. Consejo Superior de Investigaciones Científicas; España - Materia
-
Laser dyes
Dipyrromethene
Fluorescence
Triplet-state properties - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/279626
Ver los metadatos del registro completo
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Triplet-state spectroscopy of dipyrromethene·BF2 laser dyesMontejano, Hernan AlfredoAmat Guerri, FranciscoCostela, AngelGarcía Moreno, InmaculadaLiras, MartaSastre, RobertoLaser dyesDipyrrometheneFluorescenceTriplet-state propertieshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The substituents at positions 2,6 and 8 in the commercial dye PM567 have been changed and their influence on the triplet state of each dye has been studied in terms of the absorption spectra, lifetimes, quantum yields and triplet-triplet extinction coefficients. The dyes have in position 8 the groups p-acetoxypolymethylene, p-(acetoxypropyl)phenyl or p-(acetoxymethyl)polyphenylene, or in positions 2 and 6 the groups tert-butyl (commercial dye PM597) or 3-acetoxypropyl. The triplet state spectroscopy results nearly independent on the molecular structure for the mono- and di-substituted aliphatic derivatives. However, the 8-aryl substitution increases both the triplet absorption over the fluorescence spectral region and the triplet state quantum yield, but reduces the triplet absorption coefficient.Fil: Montejano, Hernan Alfredo. 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; ArgentinaFil: Amat Guerri, Francisco. Consejo Superior de Investigaciones Científicas; EspañaFil: Costela, Angel. Consejo Superior de Investigaciones Científicas; EspañaFil: García Moreno, Inmaculada. Consejo Superior de Investigaciones Científicas; EspañaFil: Liras, Marta. Universidad de Miguel Hernández; EspañaFil: Sastre, Roberto. Consejo Superior de Investigaciones Científicas; EspañaElsevier Science SA2006-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/279626Montejano, Hernan Alfredo; Amat Guerri, Francisco; Costela, Angel; García Moreno, Inmaculada; Liras, Marta; et al.; Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes; Elsevier Science SA; Journal of Photochemistry and Photobiology A: Chemistry; 181; 2-3; 12-2006; 142-1461010-6030CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotochem.2005.11.016info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1010603005005927info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-26T10:21:11Zoai:ri.conicet.gov.ar:11336/279626instacron: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:34982026-02-26 10:21:12.243CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| title |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| spellingShingle |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes Montejano, Hernan Alfredo Laser dyes Dipyrromethene Fluorescence Triplet-state properties |
| title_short |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| title_full |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| title_fullStr |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| title_full_unstemmed |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| title_sort |
Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes |
| dc.creator.none.fl_str_mv |
Montejano, Hernan Alfredo Amat Guerri, Francisco Costela, Angel García Moreno, Inmaculada Liras, Marta Sastre, Roberto |
| author |
Montejano, Hernan Alfredo |
| author_facet |
Montejano, Hernan Alfredo Amat Guerri, Francisco Costela, Angel García Moreno, Inmaculada Liras, Marta Sastre, Roberto |
| author_role |
author |
| author2 |
Amat Guerri, Francisco Costela, Angel García Moreno, Inmaculada Liras, Marta Sastre, Roberto |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
Laser dyes Dipyrromethene Fluorescence Triplet-state properties |
| topic |
Laser dyes Dipyrromethene Fluorescence Triplet-state properties |
| 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 substituents at positions 2,6 and 8 in the commercial dye PM567 have been changed and their influence on the triplet state of each dye has been studied in terms of the absorption spectra, lifetimes, quantum yields and triplet-triplet extinction coefficients. The dyes have in position 8 the groups p-acetoxypolymethylene, p-(acetoxypropyl)phenyl or p-(acetoxymethyl)polyphenylene, or in positions 2 and 6 the groups tert-butyl (commercial dye PM597) or 3-acetoxypropyl. The triplet state spectroscopy results nearly independent on the molecular structure for the mono- and di-substituted aliphatic derivatives. However, the 8-aryl substitution increases both the triplet absorption over the fluorescence spectral region and the triplet state quantum yield, but reduces the triplet absorption coefficient. Fil: Montejano, Hernan Alfredo. 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 Fil: Amat Guerri, Francisco. Consejo Superior de Investigaciones Científicas; España Fil: Costela, Angel. Consejo Superior de Investigaciones Científicas; España Fil: García Moreno, Inmaculada. Consejo Superior de Investigaciones Científicas; España Fil: Liras, Marta. Universidad de Miguel Hernández; España Fil: Sastre, Roberto. Consejo Superior de Investigaciones Científicas; España |
| description |
The substituents at positions 2,6 and 8 in the commercial dye PM567 have been changed and their influence on the triplet state of each dye has been studied in terms of the absorption spectra, lifetimes, quantum yields and triplet-triplet extinction coefficients. The dyes have in position 8 the groups p-acetoxypolymethylene, p-(acetoxypropyl)phenyl or p-(acetoxymethyl)polyphenylene, or in positions 2 and 6 the groups tert-butyl (commercial dye PM597) or 3-acetoxypropyl. The triplet state spectroscopy results nearly independent on the molecular structure for the mono- and di-substituted aliphatic derivatives. However, the 8-aryl substitution increases both the triplet absorption over the fluorescence spectral region and the triplet state quantum yield, but reduces the triplet absorption coefficient. |
| publishDate |
2006 |
| dc.date.none.fl_str_mv |
2006-12 |
| 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/11336/279626 Montejano, Hernan Alfredo; Amat Guerri, Francisco; Costela, Angel; García Moreno, Inmaculada; Liras, Marta; et al.; Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes; Elsevier Science SA; Journal of Photochemistry and Photobiology A: Chemistry; 181; 2-3; 12-2006; 142-146 1010-6030 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/279626 |
| identifier_str_mv |
Montejano, Hernan Alfredo; Amat Guerri, Francisco; Costela, Angel; García Moreno, Inmaculada; Liras, Marta; et al.; Triplet-state spectroscopy of dipyrromethene·BF2 laser dyes; Elsevier Science SA; Journal of Photochemistry and Photobiology A: Chemistry; 181; 2-3; 12-2006; 142-146 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/doi/10.1016/j.jphotochem.2005.11.016 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1010603005005927 |
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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 |
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Elsevier Science SA |
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Elsevier Science SA |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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