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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorPARRENIN, Laurie
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorBROCHON, Cyril
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorHADZIIOANNOU, Georges
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorCLOUTET, Eric
IDREF: 151048681
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2015
dc.identifier.issn1022-1336
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20273
dc.description.abstractEnThe synthesis and formulation of organic semiconductors for the emerging technology of organic electronics requires the use of preparative methods and solvents being environment friendly. Today most of the active layer materials for the organic photovoltaic devices and modules are using chlorinated solvents, which are toxic and hazardous. In this work, the synthesis of poly[N-9-heptadecanyl-2,7-carbazole-alt-5,5-(4,7-di-2-thienyl-2,1,3-benzothiadiazole] (PCDTBT) in propan-1-ol is presented as the dispersant continuous phase in the presence of poly(vinylpyrrolidone) used as stabilizer. Suzuki-Miyaura polycondensation of 9-(9-heptadecanyl)-9H-carbazole-2,7-diboronic acid bis(pinacol) ester and 4,7-bis(2-bromo-5-thienyl)-2,1,3-benzothiadiazole in alcohol dispersion yields colloidally stable nanoparticles of PCDTBT with particles size of 330-1300 nm, depending on the stabilizer concentration. Other reaction parameters are also discussed such as the amount of base or Pd catalyst.
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.subject.enMINIEMULSION
dc.subject.enPOLYTHIOPHENE
dc.subject.enPOLYANILINE
dc.subject.enpi-conjugated polymers
dc.subject.enpolymer dispersions
dc.subject.ensemiconducting polymer particles
dc.subject.enorganic solar cells
dc.subject.enSOLAR-CELLS
dc.subject.enPOLY 3
dc.subject.en4-ETHYLENEDIOXYTHIOPHENE
dc.subject.enDERIVATIVES
dc.subject.enPARTICLES
dc.title.enLow Bandgap Semiconducting Copolymer Nanoparticles by Suzuki Cross-Coupling Polymerization in Alcoholic Dispersed Media
dc.typeArticle de revue
dc.identifier.doi10.1002/marc.201500324
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecular Rapid Communications
bordeaux.page1816-1821
bordeaux.volume36
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue20
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01361294
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01361294v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecular%20Rapid%20Communications&rft.date=2015&rft.volume=36&rft.issue=20&rft.spage=1816-1821&rft.epage=1816-1821&rft.eissn=1022-1336&rft.issn=1022-1336&rft.au=PARRENIN,%20Laurie&BROCHON,%20Cyril&HADZIIOANNOU,%20Georges&CLOUTET,%20Eric&rft.genre=article


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