Photophysical properties of three hydrofullerenes
Identifieur interne : 000499 ( Istex/Corpus ); précédent : 000498; suivant : 000500Photophysical properties of three hydrofullerenes
Auteurs : R. V. Bensasson ; E. Bienvenue ; J.-M. Janot ; S. Leach ; P. Seta ; D. I. Schuster ; S. R. Wilson ; H. ZhaoSource :
- Chemical Physics Letters [ 0009-2614 ] ; 1995.
Abstract
The ground state and lowest triplet state properties of three hydrofullerenes, C60H2, C60H4 and [1-methylsuccinate-4-methyl-cyclohexadiene-2,3]buckminsterfullerene, have been investigated in toluene at room temperature. Their visible ground state absorption spectra are compared to those of methanofullerenes and methanolfulleroids. The triplet properties, including the absorption spectrum between 300 and 800 nm, molar absorption coefficient, quantum yield of formation and quantum yield for the photosensitized production of O2(1Δg), are compared to those of other C60 derivatives.
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DOI: 10.1016/0009-2614(95)01065-H
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ISTEX:ED24CD2B85F0127DFAF38B5C17C6BCD44EC25C80Le document en format XML
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to="570">570</biblScope></imprint></monogr><idno type="istex">ED24CD2B85F0127DFAF38B5C17C6BCD44EC25C80</idno><idno type="DOI">10.1016/0009-2614(95)01065-H</idno><idno type="PII">0009-2614(95)01065-H</idno><idno type="ArticleID">9501065H</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1995</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>The ground state and lowest triplet state properties of three hydrofullerenes, C60H2, C60H4 and [1-methylsuccinate-4-methyl-cyclohexadiene-2,3]buckminsterfullerene, have been investigated in toluene at room temperature. Their visible ground state absorption spectra are compared to those of methanofullerenes and methanolfulleroids. The triplet properties, including the absorption spectrum between 300 and 800 nm, molar absorption coefficient, quantum yield of formation and quantum yield for the photosensitized production of O2(1Δg), are compared to those of other C60 derivatives.</p></abstract></profileDesc><revisionDesc><change when="1995">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/ED24CD2B85F0127DFAF38B5C17C6BCD44EC25C80/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla" xml:lang="en"><item-info><jid>CPLETT</jid><aid>9501065H</aid><ce:pii>0009-2614(95)01065-H</ce:pii><ce:doi>10.1016/0009-2614(95)01065-H</ce:doi><ce:copyright type="unknown" year="1995"></ce:copyright></item-info><head><ce:title>Photophysical properties of three hydrofullerenes</ce:title><ce:author-group><ce:author><ce:given-name>R.V.</ce:given-name><ce:surname>Bensasson</ce:surname><ce:cross-ref refid="AFF1"><ce:sup loc="post">a</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>E.</ce:given-name><ce:surname>Bienvenue</ce:surname><ce:cross-ref refid="AFF2"><ce:sup loc="post">b</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>J.-M.</ce:given-name><ce:surname>Janot</ce:surname><ce:cross-ref refid="AFF2"><ce:sup loc="post">b</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>S.</ce:given-name><ce:surname>Leach</ce:surname><ce:cross-ref refid="AFF3"><ce:sup loc="post">c</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF4"><ce:sup loc="post">d</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>P.</ce:given-name><ce:surname>Seta</ce:surname><ce:cross-ref refid="AFF2"><ce:sup loc="post">b</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>D.I.</ce:given-name><ce:surname>Schuster</ce:surname><ce:cross-ref refid="AFF5"><ce:sup loc="post">e</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>S.R.</ce:given-name><ce:surname>Wilson</ce:surname><ce:cross-ref refid="AFF5"><ce:sup loc="post">e</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>H.</ce:given-name><ce:surname>Zhao</ce:surname><ce:cross-ref refid="AFF5"><ce:sup loc="post">e</ce:sup></ce:cross-ref></ce:author><ce:affiliation id="AFF1"><ce:label>a</ce:label><ce:textfn>Laboratoire de Biophysique, Muséum National d'Histoire Naturelle, CNRS UA481, INSERM U201, 43 rue Cuvier, 75231 Paris Cedex 05, France</ce:textfn></ce:affiliation><ce:affiliation id="AFF2"><ce:label>b</ce:label><ce:textfn>Laboratoire des Matériaux et Procédés Membranaires, UMR 9987 du CNRS, 1919 Route de Mende, BP 5051, 34033 Montpellier Cedex 01, France</ce:textfn></ce:affiliation><ce:affiliation id="AFF3"><ce:label>c</ce:label><ce:textfn>Laboratoire de Photophysique Moléculaire du CNRS, Université de Paris-Sud, 91405 Orsay, France</ce:textfn></ce:affiliation><ce:affiliation id="AFF4"><ce:label>d</ce:label><ce:textfn>DAMAP, CNRS URA 812, Observatoire de Paris-Meudon, 92195 Meudon, France</ce:textfn></ce:affiliation><ce:affiliation id="AFF5"><ce:label>e</ce:label><ce:textfn>Department of Chemistry, New York University, Washington Square, New York, NY 10003, USA</ce:textfn></ce:affiliation></ce:author-group><ce:date-received day="3" month="7" year="1995"></ce:date-received><ce:date-accepted day="25" month="8" year="1995"></ce:date-accepted><ce:abstract class="author"><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para view="all" id="simple-para.0010">The ground state and lowest triplet state properties of three hydrofullerenes, C<ce:inf loc="post">60</ce:inf>H<ce:inf loc="post">2</ce:inf>, C<ce:inf loc="post">60</ce:inf>H<ce:inf loc="post">4</ce:inf> and [1-methylsuccinate-4-methyl-cyclohexadiene-2,3]buckminsterfullerene, have been investigated in toluene at room temperature. Their visible ground state absorption spectra are compared to those of methanofullerenes and methanolfulleroids. The triplet properties, including the absorption spectrum between 300 and 800 nm, molar absorption coefficient, quantum yield of formation and quantum yield for the photosensitized production of <math altimg="si1.gif"><rm>O</rm><inf loc="post">2</inf>(<sup loc="pre">1</sup>Δ<inf loc="post"><rm>g</rm></inf>)</math>, are compared to those of other C<ce:inf loc="post">60</ce:inf> derivatives.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Photophysical properties of three hydrofullerenes</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Photophysical properties of three hydrofullerenes</title></titleInfo><name type="personal"><namePart type="given">R.V.</namePart><namePart type="family">Bensasson</namePart><affiliation>Laboratoire de Biophysique, Muséum National d'Histoire Naturelle, CNRS UA481, INSERM U201, 43 rue Cuvier, 75231 Paris Cedex 05, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E.</namePart><namePart type="family">Bienvenue</namePart><affiliation>Laboratoire des Matériaux et Procédés Membranaires, UMR 9987 du CNRS, 1919 Route de Mende, BP 5051, 34033 Montpellier Cedex 01, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J.-M.</namePart><namePart type="family">Janot</namePart><affiliation>Laboratoire des Matériaux et Procédés Membranaires, UMR 9987 du CNRS, 1919 Route de Mende, BP 5051, 34033 Montpellier Cedex 01, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S.</namePart><namePart type="family">Leach</namePart><affiliation>Laboratoire de Photophysique Moléculaire du CNRS, Université de Paris-Sud, 91405 Orsay, France</affiliation><affiliation>DAMAP, CNRS URA 812, Observatoire de Paris-Meudon, 92195 Meudon, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P.</namePart><namePart type="family">Seta</namePart><affiliation>Laboratoire des Matériaux et Procédés Membranaires, UMR 9987 du CNRS, 1919 Route de Mende, BP 5051, 34033 Montpellier Cedex 01, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D.I.</namePart><namePart type="family">Schuster</namePart><affiliation>Department of Chemistry, New York University, Washington Square, New York, NY 10003, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S.R.</namePart><namePart type="family">Wilson</namePart><affiliation>Department of Chemistry, New York University, Washington Square, New York, NY 10003, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H.</namePart><namePart type="family">Zhao</namePart><affiliation>Department of Chemistry, New York University, Washington Square, New York, NY 10003, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1995</dateIssued><copyrightDate encoding="w3cdtf">1995</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">The ground state and lowest triplet state properties of three hydrofullerenes, C60H2, C60H4 and [1-methylsuccinate-4-methyl-cyclohexadiene-2,3]buckminsterfullerene, have been investigated in toluene at room temperature. Their visible ground state absorption spectra are compared to those of methanofullerenes and methanolfulleroids. The triplet properties, including the absorption spectrum between 300 and 800 nm, molar absorption coefficient, quantum yield of formation and quantum yield for the photosensitized production of O2(1Δg), are compared to those of other C60 derivatives.</abstract><relatedItem type="host"><titleInfo><title>Chemical Physics Letters</title></titleInfo><titleInfo type="abbreviated"><title>CPLETT</title></titleInfo><genre type="journal">journal</genre><originInfo><dateIssued encoding="w3cdtf">19951110</dateIssued></originInfo><identifier type="ISSN">0009-2614</identifier><identifier type="PII">S0009-2614(00)X0037-1</identifier><part><date>19951110</date><detail type="volume"><number>245</number><caption>vol.</caption></detail><detail type="issue"><number>6</number><caption>no.</caption></detail><extent unit="issue pages"><start>519</start><end>699</end></extent><extent unit="pages"><start>566</start><end>570</end></extent></part></relatedItem><identifier type="istex">ED24CD2B85F0127DFAF38B5C17C6BCD44EC25C80</identifier><identifier type="DOI">10.1016/0009-2614(95)01065-H</identifier><identifier type="PII">0009-2614(95)01065-H</identifier><identifier type="ArticleID">9501065H</identifier><recordInfo><recordContentSource>ELSEVIER</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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