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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorGERVAIS, Matthieu
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorBROCAS, Anne-Laure
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorDEFFIEUX, Alain
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorIBARBOURE, Emmanuel
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorCARLOTTI, Stéphane
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2012
dc.identifier.issn0033-4545
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20442
dc.description.abstractEnA series of polyethers was prepared by monomer-activated anionic polymerization. The combination of an ammonium salt with triisobutylaluminum allowed the polymerization of epoxides containing various aliphatic side chains (1,2-butene oxide (BO), 1,2-hexene oxide (HO), and 1,2-octadecene oxide (ODO)) or a fluorinated group (3,3,3-trifluoro-1,2-epoxypropane (TFEP)). Polymers of molar masses up to 35 000 g/mol with relatively narrow molar mass distribution could be synthesized. Polymer structures were analyzed by C-13 NMR, and the thermal behavior was studied by differential scanning calorimetry (DSC). The evolution of hydrophobicity was investigated according to the length and composition of the side chain. Using a long aliphatic side-chain epoxide (C16) imparted crystallinity to the resulting atactic polymer.
dc.language.isoen
dc.publisherDe Gruyter
dc.subject.enpolymerization
dc.subject.enring-opening
dc.subject.enhydrophobicity
dc.subject.enmonomer activation
dc.subject.enpolyether
dc.subject.enpoly(alkylene oxide)
dc.title.enRapid and controlled synthesis of hydrophobic polyethers by monomer activation
dc.typeArticle de revue
dc.identifier.doi10.1351/PAC-CON-11-11-1616
dc.subject.halChimie/Polymères
bordeaux.journalPure and Applied Chemistry
bordeaux.page2103-2111
bordeaux.volume84
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue10
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00817190
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00817190v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Pure%20and%20Applied%20Chemistry&rft.date=2012&rft.volume=84&rft.issue=10&rft.spage=2103-2111&rft.epage=2103-2111&rft.eissn=0033-4545&rft.issn=0033-4545&rft.au=GERVAIS,%20Matthieu&BROCAS,%20Anne-Laure&DEFFIEUX,%20Alain&IBARBOURE,%20Emmanuel&CARLOTTI,%20St%C3%A9phane&rft.genre=article


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