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hal.structure.identifierInstitut de Science des Matériaux de Mulhouse [IS2M]
dc.contributor.authorTELITEL, Sofia
hal.structure.identifierInstitut de Chimie Radicalaire [ICR]
dc.contributor.authorDUMUR, Frédéric
dc.contributor.authorTELITEL, Siham
hal.structure.identifierInstitut de Science des Matériaux de Mulhouse [IS2M]
dc.contributor.authorSOPPERA, Olivier
hal.structure.identifierInstitut Lavoisier de Versailles [ILV]
dc.contributor.authorLEPELTIER, Marc
hal.structure.identifierInstitut de Chimie Radicalaire [ICR]
dc.contributor.authorGUILLANEUF, Yohann
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorPOLY, Julien
hal.structure.identifierInstitut de Science des Matériaux de Mulhouse [IS2M]
dc.contributor.authorMORLET-SAVARY, Fabrice
dc.contributor.authorFIOUX, Philippe
hal.structure.identifierInstitut de Science des Matériaux de Mulhouse [IS2M]
dc.contributor.authorFOUASSIER, Jean Pierre
hal.structure.identifierInstitut de Chimie Radicalaire [ICR]
dc.contributor.authorGIGMES, Didier
dc.contributor.authorLALEVÉEE, Jacques
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2014
dc.identifier.issn1759-9954
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20167
dc.description.abstractEnA new iridium complex (nIr) was designed and investigated as a photoinitiator catalyst for radical and cationic polymerizations upon very soft irradiations (lights ranging from 457 to 532 nm). A ring-opening polymerization (ROP) of an epoxy monomer was easily promoted through the interaction between nIr and an iodonium salt (Iod) upon light. The addition of N-vinylcarbazole (NVK) enhances the performance. In radical polymerization, nIr can be efficient in combination with phenacyl bromide (PBr) and optionally an amine: these photoinitiating systems work according to an original oxidative cycle and a regeneration of nIr is observed. A control of the methyl methacrylate polymerization (conducted under a 462 nm light) with 1.2–1.6 polydispersity indexes was displayed. Surface modifications by direct laser write was also easily carried out for the first time through surface re-initiation experiments, i.e. the dormant species being reactivated by light in the presence of nIr; the polymer surfaces were analyzed by XPS. The chemical mechanisms were examined through laser flash photolysis, NMR, ESR and size exclusion chromatography experiments
dc.language.isoen
dc.publisherRoyal Society of Chemistry - RSC
dc.title.enPhotoredox catalysis using a new iridium complex as an efficient toolbox for radical, cationic and controlled polymerizations under soft blue to green lights
dc.typeArticle de revue
dc.identifier.doi10.1039/C4PY01358A
dc.subject.halChimie/Matériaux
bordeaux.journalPolymer Chemistry
bordeaux.page613-624
bordeaux.volume6
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01406394
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01406394v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Polymer%20Chemistry&rft.date=2014&rft.volume=6&rft.spage=613-624&rft.epage=613-624&rft.eissn=1759-9954&rft.issn=1759-9954&rft.au=TELITEL,%20Sofia&DUMUR,%20Fr%C3%A9d%C3%A9ric&TELITEL,%20Siham&SOPPERA,%20Olivier&LEPELTIER,%20Marc&rft.genre=article


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