Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:

The development of fluorescence materials with switched on/off emission has attracted great attention owing to the potential pplication of these materials in chemical sensing. In this work, the photophysical properties of a series of original 2-(2′- hydroxyphenyl)pyrimidines were thoroughly studied....

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Autores: Plaza Pedroche, Rodrigo, Fernández Liencres, M. Paz, Jiménez Pulido, Sonia B., Illán Cabeza, Nuria A., Achelle, Sylvain, Navarro Rascón, Amparo, Rodríguez López, Julián
Formato: artículo
Fecha de publicación:2022
País:España
Recursos:Universidad de Castilla-La Mancha
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/36832
Acesso em linha:https://hdl.handle.net/10578/36832
Access Level:acceso abierto
Palavra-chave:Excited states
Fluorescence
Molecules
Pyrimidine
Reaction mechanisms
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spelling Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:Synthesis, Optical Properties, and Theoretical StudiesPlaza Pedroche, RodrigoFernández Liencres, M. PazJiménez Pulido, Sonia B.Illán Cabeza, Nuria A.Achelle, SylvainNavarro Rascón, AmparoRodríguez López, JuliánExcited statesFluorescenceMoleculesPyrimidineReaction mechanismsThe development of fluorescence materials with switched on/off emission has attracted great attention owing to the potential pplication of these materials in chemical sensing. In this work, the photophysical properties of a series of original 2-(2′- hydroxyphenyl)pyrimidines were thoroughly studied. The compounds were prepared by following well-established and straightforward methodologies and showed very little or null photoluminescence both in solution and in the solid state. This absence of emission can be explained by a fast proton transfer from the OH group to the nitrogen atoms of the pyrimidine ring to yield an excited tautomer that deactivates through a nonradiative pathway.American Chemical Society202420242022info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10578/36832reponame:RUIdeRA. Repositorio Institucional de la UCLMinstname:Universidad de Castilla-La ManchaInglésinfo:eu-repo/semantics/openAccessoai:ruidera.uclm.es:10578/368322026-05-27T07:36:41Z
dc.title.none.fl_str_mv Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
Synthesis, Optical Properties, and Theoretical Studies
title Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
spellingShingle Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
Plaza Pedroche, Rodrigo
Excited states
Fluorescence
Molecules
Pyrimidine
Reaction mechanisms
title_short Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
title_full Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
title_fullStr Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
title_full_unstemmed Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
title_sort Excited-State Intramolecular Proton Transfer in 2‑(2′- Hydroxyphenyl)pyrimidines:
dc.creator.none.fl_str_mv Plaza Pedroche, Rodrigo
Fernández Liencres, M. Paz
Jiménez Pulido, Sonia B.
Illán Cabeza, Nuria A.
Achelle, Sylvain
Navarro Rascón, Amparo
Rodríguez López, Julián
author Plaza Pedroche, Rodrigo
author_facet Plaza Pedroche, Rodrigo
Fernández Liencres, M. Paz
Jiménez Pulido, Sonia B.
Illán Cabeza, Nuria A.
Achelle, Sylvain
Navarro Rascón, Amparo
Rodríguez López, Julián
author_role author
author2 Fernández Liencres, M. Paz
Jiménez Pulido, Sonia B.
Illán Cabeza, Nuria A.
Achelle, Sylvain
Navarro Rascón, Amparo
Rodríguez López, Julián
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Excited states
Fluorescence
Molecules
Pyrimidine
Reaction mechanisms
topic Excited states
Fluorescence
Molecules
Pyrimidine
Reaction mechanisms
description The development of fluorescence materials with switched on/off emission has attracted great attention owing to the potential pplication of these materials in chemical sensing. In this work, the photophysical properties of a series of original 2-(2′- hydroxyphenyl)pyrimidines were thoroughly studied. The compounds were prepared by following well-established and straightforward methodologies and showed very little or null photoluminescence both in solution and in the solid state. This absence of emission can be explained by a fast proton transfer from the OH group to the nitrogen atoms of the pyrimidine ring to yield an excited tautomer that deactivates through a nonradiative pathway.
publishDate 2022
dc.date.none.fl_str_mv 2022
2024
2024
dc.type.none.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/10578/36832
url https://hdl.handle.net/10578/36832
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:RUIdeRA. Repositorio Institucional de la UCLM
instname:Universidad de Castilla-La Mancha
instname_str Universidad de Castilla-La Mancha
reponame_str RUIdeRA. Repositorio Institucional de la UCLM
collection RUIdeRA. Repositorio Institucional de la UCLM
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15.301603