Synthesis and photophysical characterization of novel ESIPT triazinyl-benzazole derivatives
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , |
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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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 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
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info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/141523 |
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0103-5053 |
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000991466 |
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http://hdl.handle.net/10183/141523 |
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eng |
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eng |
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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info:eu-repo/semantics/openAccess |
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openAccess |
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