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Nonradiative Deactivation of Excited Hemicyanines Studied with Submolecular Spatial Resolution by Time-Resolved Surface Second Harmonic Generation at Liquid−Liquid Interfaces
The excited-state dynamics of aminostilbazolium dyes is known to be dominated by nonradiative deactivation through large-amplitude motion. In order to identify the coordinate(s) responsible for this process, the excited-state lifetimes of two dialkylaminostyryl-methylpyridinium iodides have been mea...
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Published in: | Journal of the American Chemical Society 2011-03, Vol.133 (8), p.2358-2361 |
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container_title | Journal of the American Chemical Society |
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creator | Martin-Gassin, Gaelle Villamaina, Diego Vauthey, Eric |
description | The excited-state dynamics of aminostilbazolium dyes is known to be dominated by nonradiative deactivation through large-amplitude motion. In order to identify the coordinate(s) responsible for this process, the excited-state lifetimes of two dialkylaminostyryl-methylpyridinium iodides have been measured at liquid−liquid interfaces using time-resolved surface second harmonic generation. We found that the decay time of the excited-states of both compounds was increasing with the viscosity of the apolar phase, consisting of n-alkanes of varying length, but was unaffected by that of the polar phase, made of water/glycerol mixtures. This indicates that the nonradiative deactivation is associated with the twist of the dialkylaniline group, which is located in the apolar part of the molecule. |
doi_str_mv | 10.1021/ja109813j |
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In order to identify the coordinate(s) responsible for this process, the excited-state lifetimes of two dialkylaminostyryl-methylpyridinium iodides have been measured at liquid−liquid interfaces using time-resolved surface second harmonic generation. We found that the decay time of the excited-states of both compounds was increasing with the viscosity of the apolar phase, consisting of n-alkanes of varying length, but was unaffected by that of the polar phase, made of water/glycerol mixtures. 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This indicates that the nonradiative deactivation is associated with the twist of the dialkylaniline group, which is located in the apolar part of the molecule.</description><subject>Fluorescent Dyes - chemistry</subject><subject>Glycerol - chemistry</subject><subject>Molecular Structure</subject><subject>Pyridinium Compounds - chemistry</subject><subject>Quinolinium Compounds - chemistry</subject><subject>Stereoisomerism</subject><subject>Styrenes - chemistry</subject><subject>Surface Properties</subject><subject>Time Factors</subject><subject>Water - chemistry</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNptkc1u1DAUhS0EokNhwQsgbxBikdY_SSZZolLaSiMqkbKObuxr4VFiT-24MG_AmifhmXgS3EnpitX90XfOlX0Iec3ZCWeCn26Bs7bhcvuErHglWFFxUT8lK8aYKNZNLY_Iixi3eSxFw5-TI8ElE60oV-T3Z-8CaAuzvUP6EUHlJg_eUW_o-Q9lZ9T0Eier9uCsw0i7OWmbl9_t_I12aZj8iCqNEGi3y0oY6ReMfkwHk2FPb-yExWF1l1VdCgYU0g6Vd9kZwuSdVfQCHYblMMx0Y2-T1X9-_loaeuVmPOjiS_LMwBjx1UM9Jl8_nd-cXRab64ursw-bAmTZzoVh66FmZa0MmKY2yCush8ooqDQKbJpW6zpXqbWoNFvzdtA1yqERDMpKGiaPybvFdxf8bcI495ONCscRHPoU-6aSbSsEazP5fiFV8DEGNP0u2AnCvuesv8-nf8wns28eXPO_oX4k_wWSgbcLACr2W5-Cy4_8j9FfJ-ycjQ</recordid><startdate>20110302</startdate><enddate>20110302</enddate><creator>Martin-Gassin, Gaelle</creator><creator>Villamaina, Diego</creator><creator>Vauthey, Eric</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110302</creationdate><title>Nonradiative Deactivation of Excited Hemicyanines Studied with Submolecular Spatial Resolution by Time-Resolved Surface Second Harmonic Generation at Liquid−Liquid Interfaces</title><author>Martin-Gassin, Gaelle ; Villamaina, Diego ; Vauthey, Eric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a349t-f07b6046cfaf86fe15e6b5fca5de2e889dd62e83dd25d0719bd6e3b820a453f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Fluorescent Dyes - chemistry</topic><topic>Glycerol - chemistry</topic><topic>Molecular Structure</topic><topic>Pyridinium Compounds - chemistry</topic><topic>Quinolinium Compounds - chemistry</topic><topic>Stereoisomerism</topic><topic>Styrenes - chemistry</topic><topic>Surface Properties</topic><topic>Time Factors</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martin-Gassin, Gaelle</creatorcontrib><creatorcontrib>Villamaina, Diego</creatorcontrib><creatorcontrib>Vauthey, Eric</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martin-Gassin, Gaelle</au><au>Villamaina, Diego</au><au>Vauthey, Eric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonradiative Deactivation of Excited Hemicyanines Studied with Submolecular Spatial Resolution by Time-Resolved Surface Second Harmonic Generation at Liquid−Liquid Interfaces</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2011-03-02</date><risdate>2011</risdate><volume>133</volume><issue>8</issue><spage>2358</spage><epage>2361</epage><pages>2358-2361</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>The excited-state dynamics of aminostilbazolium dyes is known to be dominated by nonradiative deactivation through large-amplitude motion. In order to identify the coordinate(s) responsible for this process, the excited-state lifetimes of two dialkylaminostyryl-methylpyridinium iodides have been measured at liquid−liquid interfaces using time-resolved surface second harmonic generation. We found that the decay time of the excited-states of both compounds was increasing with the viscosity of the apolar phase, consisting of n-alkanes of varying length, but was unaffected by that of the polar phase, made of water/glycerol mixtures. 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subjects | Fluorescent Dyes - chemistry Glycerol - chemistry Molecular Structure Pyridinium Compounds - chemistry Quinolinium Compounds - chemistry Stereoisomerism Styrenes - chemistry Surface Properties Time Factors Water - chemistry |
title | Nonradiative Deactivation of Excited Hemicyanines Studied with Submolecular Spatial Resolution by Time-Resolved Surface Second Harmonic Generation at Liquid−Liquid Interfaces |
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