A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios
We report the emission wavelength tunability of an excited state intramolecular proton transfer (ESIPT) fluorophore, 2,4-dibenzothiazolylphenol (2,4-DBTP), and its application to white light generation. In a nonpolar solvent, yellow fluorescent 2,4-DBTP had a maximum emission around 560 nm, but did...
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Veröffentlicht in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2013-01, Vol.1 (47), p.7866-7871 |
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creator | Sakai, Ken-ichi Ishikawa, Takaaki Akutagawa, Tomoyuki |
description | We report the emission wavelength tunability of an excited state intramolecular proton transfer (ESIPT) fluorophore, 2,4-dibenzothiazolylphenol (2,4-DBTP), and its application to white light generation. In a nonpolar solvent, yellow fluorescent 2,4-DBTP had a maximum emission around 560 nm, but did not absorb light in the blue region (400-500 nm) because of its large Stokes shift. In a polar solvent, however, a phenol proton of 2,4-DBTP involving in ESIPT is dissociated by solvent molecules, giving rise to blue emission. By dissolving the fluorophore in a polar-nonpolar solvent mixture, we observed white emission with a broad band ranging from 400 to 650 nm, a consequence of the small overlap between the absorption spectrum of the yellow-emitting form and the fluorescence spectrum of the blue-emitting form. We also successfully fabricated a white-emitting polymer film using yellow-emitting 2,4-DBTP and a representative blue fluorescent dye (perylene) as dopants. Our fluorophore will be useful for environmentally sensitive fluorescent probes and white organic light-emitting diodes. |
doi_str_mv | 10.1039/c3tc31526f |
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In a nonpolar solvent, yellow fluorescent 2,4-DBTP had a maximum emission around 560 nm, but did not absorb light in the blue region (400-500 nm) because of its large Stokes shift. In a polar solvent, however, a phenol proton of 2,4-DBTP involving in ESIPT is dissociated by solvent molecules, giving rise to blue emission. By dissolving the fluorophore in a polar-nonpolar solvent mixture, we observed white emission with a broad band ranging from 400 to 650 nm, a consequence of the small overlap between the absorption spectrum of the yellow-emitting form and the fluorescence spectrum of the blue-emitting form. We also successfully fabricated a white-emitting polymer film using yellow-emitting 2,4-DBTP and a representative blue fluorescent dye (perylene) as dopants. Our fluorophore will be useful for environmentally sensitive fluorescent probes and white organic light-emitting diodes.</description><identifier>ISSN: 2050-7526</identifier><identifier>EISSN: 2050-7534</identifier><identifier>DOI: 10.1039/c3tc31526f</identifier><language>eng</language><subject>Band spectra ; Chemical compounds ; Emission ; Excitation ; Fluorescence ; Solvents ; Wavelengths ; White light</subject><ispartof>Journal of materials chemistry. 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C, Materials for optical and electronic devices</title><description>We report the emission wavelength tunability of an excited state intramolecular proton transfer (ESIPT) fluorophore, 2,4-dibenzothiazolylphenol (2,4-DBTP), and its application to white light generation. In a nonpolar solvent, yellow fluorescent 2,4-DBTP had a maximum emission around 560 nm, but did not absorb light in the blue region (400-500 nm) because of its large Stokes shift. In a polar solvent, however, a phenol proton of 2,4-DBTP involving in ESIPT is dissociated by solvent molecules, giving rise to blue emission. By dissolving the fluorophore in a polar-nonpolar solvent mixture, we observed white emission with a broad band ranging from 400 to 650 nm, a consequence of the small overlap between the absorption spectrum of the yellow-emitting form and the fluorescence spectrum of the blue-emitting form. We also successfully fabricated a white-emitting polymer film using yellow-emitting 2,4-DBTP and a representative blue fluorescent dye (perylene) as dopants. Our fluorophore will be useful for environmentally sensitive fluorescent probes and white organic light-emitting diodes.</description><subject>Band spectra</subject><subject>Chemical compounds</subject><subject>Emission</subject><subject>Excitation</subject><subject>Fluorescence</subject><subject>Solvents</subject><subject>Wavelengths</subject><subject>White light</subject><issn>2050-7526</issn><issn>2050-7534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpFkN1KAzEQhYMoWGpvfIJcVmE1P93srnel-FMoKFivl2w6oZE0qUm2tXc-g76hT-JqRedmDjNnDsyH0CklF5Tw6lLxpDjNmdAHqMdITrIi56PDP83EMRrE-Ey6KqkoRdVD72Pc2Bay7dIkyHZgrd9i5a0PWWqdbCxgeFXdboFjkgmwcSnIlbegWisDXgefvMPdzEUNAQ-vH6cP8zOsbeuDXy99gCscwUWTzMakHU4er313-fn24bz7kTh6uwGXcJDJ-HiCjrS0EQa_vY-ebq7nk7tsdn87nYxnmeKcpEw1esGFWDQVIUKoklMtOGOaFISTEoQmIidCqrxqNBWsFCNKSwqsZFLKBgreR8N9bvfDSwsx1SsTVUdAOvBtrGkuCkoZL0lnPd9bVfAxBtD1OpiVDLuakvqbff3Pnn8BX717Og</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Sakai, Ken-ichi</creator><creator>Ishikawa, Takaaki</creator><creator>Akutagawa, Tomoyuki</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130101</creationdate><title>A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios</title><author>Sakai, Ken-ichi ; Ishikawa, Takaaki ; Akutagawa, Tomoyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c330t-cbfd366db90066c831f6322f070308e6f06506ac59bf1628641181e282aaabe73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Band spectra</topic><topic>Chemical compounds</topic><topic>Emission</topic><topic>Excitation</topic><topic>Fluorescence</topic><topic>Solvents</topic><topic>Wavelengths</topic><topic>White light</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakai, Ken-ichi</creatorcontrib><creatorcontrib>Ishikawa, Takaaki</creatorcontrib><creatorcontrib>Akutagawa, Tomoyuki</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakai, Ken-ichi</au><au>Ishikawa, Takaaki</au><au>Akutagawa, Tomoyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios</atitle><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle><date>2013-01-01</date><risdate>2013</risdate><volume>1</volume><issue>47</issue><spage>7866</spage><epage>7871</epage><pages>7866-7871</pages><issn>2050-7526</issn><eissn>2050-7534</eissn><abstract>We report the emission wavelength tunability of an excited state intramolecular proton transfer (ESIPT) fluorophore, 2,4-dibenzothiazolylphenol (2,4-DBTP), and its application to white light generation. 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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Band spectra Chemical compounds Emission Excitation Fluorescence Solvents Wavelengths White light |
title | A blue-white-yellow color-tunable excited state intramolecular proton transfer (ESIPT) fluorophore: sensitivity to polar–nonpolar solvent ratios |
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