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dc.rights.licenseopen
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorLEPOITTEVIN, Bénédicte
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorMATMOUR, Rachid
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorFRANCIS, Raju
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorGNANOU, Yves
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2005
dc.identifier.issn0141-8130
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20676
dc.description.abstractEnThe synthesis of dendrimer-like polystyrene (PS) of second and third generations by combination of atom transfer radical polymerization (ATRP) and chain end modifications is reported. Calixarene-based cores were used as initiators for ATRP of styrene yielding star polymers containing precisely 4, 6, or 8 arms. The latter were modified in two steps so as to generate PS stars carrying 8, 12, or 16 terminal bromoisobutyrate groups, respectively. These precursors served as multifunctional macroinitiators for the formation of the second generation of dendrimer-like PS. Reiteration of the aforementioned sequence of reactions allowed to derive dendrimer-like polystyrene of third generation that were constituted of 16, 24, or 32 outer arms, respectively. The chain end modification was monitored by H-1 NMR spectroscopy. The dendrimer-like PS were also characterized by size exclusion chromatography equipped with a multiangle laser light scattering detector (SEC/MALLS). The actual polymer architecture and the functionality of the stars were confirmed by analysis of the individual arms obtained upon hydrolysis of the ester links present at the core of the stars and at the branching points. The intrinsic viscosities of these dendrimer-like polystyrenes are similar to those reported for regular dendrimers.
dc.language.isoen
dc.publisherElsevier
dc.subject.enCOMBINATION
dc.subject.enARCHITECTURES
dc.subject.enMACROMOLECULES
dc.subject.enCONVENTIONAL MONOMERS
dc.subject.enBLOCK-COPOLYMER
dc.subject.enSTAR POLYMERS
dc.subject.enTERMINATOR MULTIFUNCTIONAL INITIATOR
dc.subject.enWELL-DEFINED POLYSTYRENE
dc.subject.enHYPERBRANCHED POLYMERS
dc.subject.enANIONIC-POLYMERIZATION
dc.title.enSynthesis of dendrimer-like polystyrene by atom transfer radical polymerization and investigation of their viscosity behavior
dc.typeArticle de revue
dc.identifier.doi10.1021/ma048106s
dc.subject.halChimie/Polymères
bordeaux.journalInternational Journal of Biological Macromolecules
bordeaux.page3120-3128
bordeaux.volume38
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue8
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00394293
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00394293v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International%20Journal%20of%20Biological%20Macromolecules&rft.date=2005&rft.volume=38&rft.issue=8&rft.spage=3120-3128&rft.epage=3120-3128&rft.eissn=0141-8130&rft.issn=0141-8130&rft.au=LEPOITTEVIN,%20B%C3%A9n%C3%A9dicte&MATMOUR,%20Rachid&FRANCIS,%20Raju&TATON,%20Daniel&GNANOU,%20Yves&rft.genre=article


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