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hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorBABIN, Jerome
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierInstitut Charles Sadron [ICS]
dc.contributor.authorBRINKMANN, Martin
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLECOMMANDOUX, Sebastien
dc.date.accessioned2020
dc.date.available2020
dc.date.created2008
dc.date.issued2008
dc.identifier.issn0141-8130
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20789
dc.description.abstractEnBoth AB linear-type and AB(2) miktoarm star-type amphiphilic block copolymers based on polystyrene (PS) as A block and poly(glutamic acid) (PGA) as B block were obtained by a four-step synthetic approach combining (i) atom transfer radical polymerization of styrene and (ii) chemical modification of the bromo end groups of ATRP-derived precursors into many or twice as many primary amino groups, followed by (iii) ring-opening polymerization of gamma-benzyl-L-glutamate N-carboxyanhydride and (iv) a final step of hydrolysis. The self-assembly properties in bulk of these linear PS-b-PGA and miktoarm star PS-b-(PGA)(2) block copolymers were subsequently investigated by different analytical means, including Fourier transform infrared spectroscopy (FTIR), wide and small-angle X-ray scattering (WAXS and SAXS) and atomic force microscopy (AFM). FTIR analysis revealed that the PGA block systematically adopted a rodlike alpha-helix conformation, even for degree of polymerization as low as 18. The very high immiscibility between PS and PGA blocks (conformational asymmetry) drove all of these rod-coil block copolymers to self-assemble in a hexagonal in lamellar (HQ morphology in the nanometer size range, whatever their composition and architecture. In addition, WAXS and SAXS results evidenced the effect of the macromolecular architecture on the local organization of PGA helices: the linear block copolymers showed an internal lamellar structure with PGA helices stacked, inter-digitated or folded depending on the weight fraction of the rodlike PGA blocks, whereas miktoarm stars exhibited a stacked microstructure, independently of the PGA content
dc.language.isoen
dc.publisherElsevier
dc.subject.enPOLYMERS
dc.subject.enPOLYPEPTIDE BLOCK
dc.subject.enSUPRAMOLECULAR MATERIALS
dc.subject.enLIVING POLYMERIZATION
dc.subject.enTRANSFER RADICAL POLYMERIZATION
dc.subject.enROD-COIL
dc.subject.enDIBLOCK COPOLYMERS
dc.subject.enTRIBLOCK COPOLYMERS
dc.subject.enN-CARBOXYANHYDRIDES
dc.subject.enMORPHOLOGY
dc.title.enSynthesis and self-assembly in bulk of linear and Mikto-arm star block copolymers based on polystyrene and poly(glutamic acid)
dc.typeArticle de revue
dc.identifier.doi10.1021/ma70
dc.subject.halChimie/Polymères
bordeaux.journalInternational Journal of Biological Macromolecules
bordeaux.page1384-1392
bordeaux.volume41
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue4
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00338966
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00338966v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International%20Journal%20of%20Biological%20Macromolecules&rft.date=2008&rft.volume=41&rft.issue=4&rft.spage=1384-1392&rft.epage=1384-1392&rft.eissn=0141-8130&rft.issn=0141-8130&rft.au=BABIN,%20Jerome&TATON,%20Daniel&BRINKMANN,%20Martin&LECOMMANDOUX,%20Sebastien&rft.genre=article


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