Electrochemical properties of Langmuir-Blodgett films of polyesters derived from oligothiophenes
Identifieur interne : 017237 ( Main/Repository ); précédent : 017236; suivant : 017238Electrochemical properties of Langmuir-Blodgett films of polyesters derived from oligothiophenes
Auteurs : RBID : Pascal:98-0223208Descripteurs français
- Pascal (Inist)
- Propriété électrochimique, Conducteur électrique, Thiophène dérivé polymère, Ester polymère, Solution chimique, Couche Langmuir Blodgett, Electrode disque, Platine, Electrode optiquement transparente, Indium Oxyde, Etain Oxyde, Solvant organique, Acétonitrile, Electrode ITO, Ammonium(tétrabutyl) perchlorate, Thiophène(3-décyl) polymère.
- Wicri :
- concept : Platine.
English descriptors
- KwdEn :
Abstract
The electrochemical properties of polyesters derived from oligothiophenes have been studied in solution, and as Langmuir-Blodgett (LB) and cast films. Polyesters with four or five thiophene units exhibited a well-defined voltammetric response and good LB transfer characteristics. Mono and multilayer LB films were electroactive with clear symmetrical peaks, better developed than for the cast films. These films can be p- or n-doped electrochemically.
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Electrochemical properties of Langmuir-Blodgett films of polyesters derived from oligothiophenes</title>
<author><name sortKey="Goldenberg, L M" uniqKey="Goldenberg L">L. M. Goldenberg</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>School of Engineering and Centre for Molecular Electronics, University of Durham</s1>
<s2>Durham DH1 3LE</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Royaume-Uni</country>
<wicri:noRegion>Durham DH1 3LE</wicri:noRegion>
</affiliation>
<affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Institute of Chemical Physics in Chernoglovka, Russian Academy of Science, CHernagolovka, 142432</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
<country>Russie</country>
<placeName><settlement type="city">Moscou</settlement>
<region>District fédéral central</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Donat Bouillud, A" uniqKey="Donat Bouillud A">A. Donat-Bouillud</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Chemistry, University of Montreal</s1>
<s2>Montreal, Que., H3C 3J7</s2>
<s3>AGO</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Angola</country>
<wicri:noRegion>Montreal, Que., H3C 3J7</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Leclerc, M" uniqKey="Leclerc M">M. Leclerc</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Chemistry, University of Montreal</s1>
<s2>Montreal, Que., H3C 3J7</s2>
<s3>AGO</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Angola</country>
<wicri:noRegion>Montreal, Que., H3C 3J7</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Petty, M C" uniqKey="Petty M">M. C. Petty</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>School of Engineering and Centre for Molecular Electronics, University of Durham</s1>
<s2>Durham DH1 3LE</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Royaume-Uni</country>
<wicri:noRegion>Durham DH1 3LE</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="inist">98-0223208</idno>
<date when="1998">1998</date>
<idno type="stanalyst">PASCAL 98-0223208 INIST</idno>
<idno type="RBID">Pascal:98-0223208</idno>
<idno type="wicri:Area/Main/Corpus">017246</idno>
<idno type="wicri:Area/Main/Repository">017237</idno>
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<seriesStmt><title level="j" type="main">Journal of electroanalytical chemistry:(1992)</title>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acetonitrile</term>
<term>Chemical solution</term>
<term>Disk electrode</term>
<term>Electrical conductor</term>
<term>Electrochemical properties</term>
<term>Ester polymer</term>
<term>Indium Oxides</term>
<term>Langmuir Blodgett layer</term>
<term>Optically transparent electrode</term>
<term>Organic solvent</term>
<term>Platinum</term>
<term>Thiophene derivative polymer</term>
<term>Tin Oxides</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Propriété électrochimique</term>
<term>Conducteur électrique</term>
<term>Thiophène dérivé polymère</term>
<term>Ester polymère</term>
<term>Solution chimique</term>
<term>Couche Langmuir Blodgett</term>
<term>Electrode disque</term>
<term>Platine</term>
<term>Electrode optiquement transparente</term>
<term>Indium Oxyde</term>
<term>Etain Oxyde</term>
<term>Solvant organique</term>
<term>Acétonitrile</term>
<term>Electrode ITO</term>
<term>Ammonium(tétrabutyl) perchlorate</term>
<term>Thiophène(3-décyl) polymère</term>
</keywords>
<keywords scheme="Wicri" type="concept" xml:lang="fr"><term>Platine</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The electrochemical properties of polyesters derived from oligothiophenes have been studied in solution, and as Langmuir-Blodgett (LB) and cast films. Polyesters with four or five thiophene units exhibited a well-defined voltammetric response and good LB transfer characteristics. Mono and multilayer LB films were electroactive with clear symmetrical peaks, better developed than for the cast films. These films can be p- or n-doped electrochemically.</div>
</front>
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<inist><standard h6="B"><pA><fA05><s2>443</s2>
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<fA06><s2>2</s2>
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<fA08 i1="01" i2="1" l="ENG"><s1>Electrochemical properties of Langmuir-Blodgett films of polyesters derived from oligothiophenes</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>GOLDENBERG (L. M.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>DONAT-BOUILLUD (A.)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>LECLERC (M.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>PETTY (M. C.)</s1>
</fA11>
<fA14 i1="01"><s1>School of Engineering and Centre for Molecular Electronics, University of Durham</s1>
<s2>Durham DH1 3LE</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Institute of Chemical Physics in Chernoglovka, Russian Academy of Science, CHernagolovka, 142432</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Department of Chemistry, University of Montreal</s1>
<s2>Montreal, Que., H3C 3J7</s2>
<s3>AGO</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA20><s1>266-272</s1>
</fA20>
<fA21><s1>1998</s1>
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<fA23 i1="01"><s0>ENG</s0>
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<fA43 i1="01"><s1>INIST</s1>
<s2>1150</s2>
<s5>354000075143920140</s5>
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<fA44><s0>0000</s0>
<s1>© 1998 INIST-CNRS. All rights reserved.</s1>
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<fA45><s0>44 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>98-0223208</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i2="2"><s0>Journal of electroanalytical chemistry:(1992)</s0>
</fA64>
<fA66 i1="01"><s0>CHE</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>The electrochemical properties of polyesters derived from oligothiophenes have been studied in solution, and as Langmuir-Blodgett (LB) and cast films. Polyesters with four or five thiophene units exhibited a well-defined voltammetric response and good LB transfer characteristics. Mono and multilayer LB films were electroactive with clear symmetrical peaks, better developed than for the cast films. These films can be p- or n-doped electrochemically.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>001D09D04D</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Propriété électrochimique</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Electrochemical properties</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="GER"><s0>Elektrochemische Eigenschaft</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Propiedad electroquímica</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Conducteur électrique</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Electrical conductor</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="GER"><s0>Elektrischer Leiter</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Conductor eléctrico</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Thiophène dérivé polymère</s0>
<s2>NK</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Thiophene derivative polymer</s0>
<s2>NK</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Tiofeno derivado polímero</s0>
<s2>NK</s2>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Ester polymère</s0>
<s2>NK</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Ester polymer</s0>
<s2>NK</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Ester polímero</s0>
<s2>NK</s2>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Solution chimique</s0>
<s5>06</s5>
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<fC03 i1="05" i2="X" l="ENG"><s0>Chemical solution</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Solución química</s0>
<s5>06</s5>
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<fC03 i1="06" i2="X" l="FRE"><s0>Couche Langmuir Blodgett</s0>
<s5>07</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Langmuir Blodgett layer</s0>
<s5>07</s5>
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<fC03 i1="06" i2="X" l="SPA"><s0>Capa Langmuir Blodgett</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Electrode disque</s0>
<s5>09</s5>
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<fC03 i1="07" i2="X" l="ENG"><s0>Disk electrode</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Electrodo disco</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Platine</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Platinum</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="GER"><s0>Platin</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Platino</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Electrode optiquement transparente</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Optically transparent electrode</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Electrodo ópticamente transparente</s0>
<s5>12</s5>
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<fC03 i1="10" i2="X" l="FRE"><s0>Indium Oxyde</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>13</s5>
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<fC03 i1="10" i2="X" l="ENG"><s0>Indium Oxides</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Indio Óxido</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>13</s5>
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<fC03 i1="11" i2="X" l="FRE"><s0>Etain Oxyde</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>FX</s2>
<s2>NA</s2>
<s5>14</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Tin Oxides</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>FX</s2>
<s2>NA</s2>
<s5>14</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Estaño Óxido</s0>
<s1>ACT</s1>
<s2>NC</s2>
<s2>FX</s2>
<s2>NA</s2>
<s5>14</s5>
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<fC03 i1="12" i2="X" l="FRE"><s0>Solvant organique</s0>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>Organic solvent</s0>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="X" l="GER"><s0>Organisches Loesungsmittel</s0>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>Solvente orgánico</s0>
<s5>16</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Acétonitrile</s0>
<s1>SOL</s1>
<s2>NK</s2>
<s5>17</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>Acetonitrile</s0>
<s1>SOL</s1>
<s2>NK</s2>
<s5>17</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>Acetonitrilo</s0>
<s1>SOL</s1>
<s2>NK</s2>
<s5>17</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE"><s0>Electrode ITO</s0>
<s4>INC</s4>
<s5>62</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Ammonium(tétrabutyl) perchlorate</s0>
<s1>SOL</s1>
<s2>NK</s2>
<s4>INC</s4>
<s5>63</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE"><s0>Thiophène(3-décyl) polymère</s0>
<s2>NK</s2>
<s4>INC</s4>
<s5>64</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Métal transition</s0>
<s2>NC</s2>
<s5>11</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Transition metal</s0>
<s2>NC</s2>
<s5>11</s5>
</fC07>
<fC07 i1="01" i2="X" l="GER"><s0>Uebergangsmetalle</s0>
<s2>NC</s2>
<s5>11</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Metal transición</s0>
<s2>NC</s2>
<s5>11</s5>
</fC07>
<fN21><s1>145</s1>
</fN21>
</pA>
</standard>
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