Cargando…

Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores

Oxazolinyl- and arylchalcogenazolyl-substituted hydroxyfluorenes exhibiting excited-state intramolecular proton transfer (ESIPT) are described as potent and highly modular luminophores. Emission color tuning was achieved by varying the π-expansion and the insertion of different chalcogen atoms.

Detalles Bibliográficos
Autores principales: Göbel, Dominik, Rusch, Pascal, Duvinage, Daniel, Bigall, Nadja C., Nachtsheim, Boris J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517962/
https://www.ncbi.nlm.nih.gov/pubmed/33231590
http://dx.doi.org/10.1039/d0cc05780k
_version_ 1784584120070832128
author Göbel, Dominik
Rusch, Pascal
Duvinage, Daniel
Bigall, Nadja C.
Nachtsheim, Boris J.
author_facet Göbel, Dominik
Rusch, Pascal
Duvinage, Daniel
Bigall, Nadja C.
Nachtsheim, Boris J.
author_sort Göbel, Dominik
collection PubMed
description Oxazolinyl- and arylchalcogenazolyl-substituted hydroxyfluorenes exhibiting excited-state intramolecular proton transfer (ESIPT) are described as potent and highly modular luminophores. Emission color tuning was achieved by varying the π-expansion and the insertion of different chalcogen atoms.
format Online
Article
Text
id pubmed-8517962
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-85179622021-11-04 Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores Göbel, Dominik Rusch, Pascal Duvinage, Daniel Bigall, Nadja C. Nachtsheim, Boris J. Chem Commun (Camb) Chemistry Oxazolinyl- and arylchalcogenazolyl-substituted hydroxyfluorenes exhibiting excited-state intramolecular proton transfer (ESIPT) are described as potent and highly modular luminophores. Emission color tuning was achieved by varying the π-expansion and the insertion of different chalcogen atoms. The Royal Society of Chemistry 2020-11-10 /pmc/articles/PMC8517962/ /pubmed/33231590 http://dx.doi.org/10.1039/d0cc05780k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Göbel, Dominik
Rusch, Pascal
Duvinage, Daniel
Bigall, Nadja C.
Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores
title Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores
title_full Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores
title_fullStr Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores
title_full_unstemmed Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores
title_short Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores
title_sort emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (esipt)-based luminophores
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517962/
https://www.ncbi.nlm.nih.gov/pubmed/33231590
http://dx.doi.org/10.1039/d0cc05780k
work_keys_str_mv AT gobeldominik emissioncolortunableoxazolinylsubstitutedexcitedstateintramolecularprotontransferesiptbasedluminophores
AT ruschpascal emissioncolortunableoxazolinylsubstitutedexcitedstateintramolecularprotontransferesiptbasedluminophores
AT duvinagedaniel emissioncolortunableoxazolinylsubstitutedexcitedstateintramolecularprotontransferesiptbasedluminophores
AT bigallnadjac emissioncolortunableoxazolinylsubstitutedexcitedstateintramolecularprotontransferesiptbasedluminophores
AT nachtsheimborisj emissioncolortunableoxazolinylsubstitutedexcitedstateintramolecularprotontransferesiptbasedluminophores