Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives

Detalhes bibliográficos
Autor(a) principal: Barreto, Fabiano
Data de Publicação: 2015
Outros Autores: Jank, Louíse, Stefani, Valter
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/141523
Resumo: In this work, the synthesis, characterization and photophysical study of new derivatives of triazinyl-benzazoles with fluorescence by excited-state intramolecular proton transfer (ESIPT) are presented. It regards the synthesis of cyanuric chloride with different 2-(2’-hydroxyphenyl) benzazoles, two quite attractive groups from the synthetic and technological point of view. These new compounds have several potential applications such as biological markers and new photoluminescent materials. The derivatives were characterized by 1H and 13C nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), high-resolution mass spectrometry (HRMS), UV-Vis absorption and fluorescence emission. The dyes are fluorescent by an excited-state ESIPT in the blue-orange region, with a large Stokes’ shift.
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spelling Barreto, FabianoJank, LouíseStefani, Valter2016-05-21T02:09:02Z20150103-5053http://hdl.handle.net/10183/141523000991466In this work, the synthesis, characterization and photophysical study of new derivatives of triazinyl-benzazoles with fluorescence by excited-state intramolecular proton transfer (ESIPT) are presented. It regards the synthesis of cyanuric chloride with different 2-(2’-hydroxyphenyl) benzazoles, two quite attractive groups from the synthetic and technological point of view. These new compounds have several potential applications such as biological markers and new photoluminescent materials. The derivatives were characterized by 1H and 13C nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), high-resolution mass spectrometry (HRMS), UV-Vis absorption and fluorescence emission. The dyes are fluorescent by an excited-state ESIPT in the blue-orange region, with a large Stokes’ shift.application/pdfengJournal of the Brazilian Chemical Society. Campinas. Vol. 26, no. 12 (Dec. 2015), p. 2496-2506Transferencia protonica intramolecular no estado excitadoCorantes fluorescentes : Benzazolas : Síntese orgânicaCorantes fluorescentes : Transferência protônica : Síntese orgânicaFluorescênciaCloreto cianúricoFotofísicaBenzazoleCyanuric chlorideESIPTReactive dyeLarge Stokes’ shiftFluorescenceSynthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivativesinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000991466.pdf000991466.pdfTexto completo (inglês)application/pdf4231481http://www.lume.ufrgs.br/bitstream/10183/141523/1/000991466.pdf8e78da5888e1c12605d41378e9b4b4a1MD51TEXT000991466.pdf.txt000991466.pdf.txtExtracted Texttext/plain42829http://www.lume.ufrgs.br/bitstream/10183/141523/2/000991466.pdf.txt04f14cea8a303281ee6a05d3a0b4200fMD52THUMBNAIL000991466.pdf.jpg000991466.pdf.jpgGenerated Thumbnailimage/jpeg1712http://www.lume.ufrgs.br/bitstream/10183/141523/3/000991466.pdf.jpg89c1b358582e2a251ea5e31131111b45MD5310183/1415232021-09-18 04:54:15.289854oai:www.lume.ufrgs.br:10183/141523Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:54:15Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
title Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
spellingShingle Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
Barreto, Fabiano
Transferencia protonica intramolecular no estado excitado
Corantes fluorescentes : Benzazolas : Síntese orgânica
Corantes fluorescentes : Transferência protônica : Síntese orgânica
Fluorescência
Cloreto cianúrico
Fotofísica
Benzazole
Cyanuric chloride
ESIPT
Reactive dye
Large Stokes’ shift
Fluorescence
title_short Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
title_full Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
title_fullStr Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
title_full_unstemmed Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
title_sort Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
author Barreto, Fabiano
author_facet Barreto, Fabiano
Jank, Louíse
Stefani, Valter
author_role author
author2 Jank, Louíse
Stefani, Valter
author2_role author
author
dc.contributor.author.fl_str_mv Barreto, Fabiano
Jank, Louíse
Stefani, Valter
dc.subject.por.fl_str_mv Transferencia protonica intramolecular no estado excitado
Corantes fluorescentes : Benzazolas : Síntese orgânica
Corantes fluorescentes : Transferência protônica : Síntese orgânica
Fluorescência
Cloreto cianúrico
Fotofísica
topic Transferencia protonica intramolecular no estado excitado
Corantes fluorescentes : Benzazolas : Síntese orgânica
Corantes fluorescentes : Transferência protônica : Síntese orgânica
Fluorescência
Cloreto cianúrico
Fotofísica
Benzazole
Cyanuric chloride
ESIPT
Reactive dye
Large Stokes’ shift
Fluorescence
dc.subject.eng.fl_str_mv Benzazole
Cyanuric chloride
ESIPT
Reactive dye
Large Stokes’ shift
Fluorescence
description In this work, the synthesis, characterization and photophysical study of new derivatives of triazinyl-benzazoles with fluorescence by excited-state intramolecular proton transfer (ESIPT) are presented. It regards the synthesis of cyanuric chloride with different 2-(2’-hydroxyphenyl) benzazoles, two quite attractive groups from the synthetic and technological point of view. These new compounds have several potential applications such as biological markers and new photoluminescent materials. The derivatives were characterized by 1H and 13C nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), high-resolution mass spectrometry (HRMS), UV-Vis absorption and fluorescence emission. The dyes are fluorescent by an excited-state ESIPT in the blue-orange region, with a large Stokes’ shift.
publishDate 2015
dc.date.issued.fl_str_mv 2015
dc.date.accessioned.fl_str_mv 2016-05-21T02:09:02Z
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dc.relation.ispartof.pt_BR.fl_str_mv Journal of the Brazilian Chemical Society. Campinas. Vol. 26, no. 12 (Dec. 2015), p. 2496-2506
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