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dc.rights.licenseopen
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorCLOUTET, Eric
IDREF: 151048681
hal.structure.identifierKing Abdullah University of Science and Technology [Saudi Arabia] [KAUST]
dc.contributor.authorGNANOU, Yves
hal.structure.identifierInstitut des Sciences Chimiques de Rennes [ISCR]
dc.contributor.authorFILLAUT, Jean-Luc
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorASTRUC, Didier
dc.date.accessioned2020
dc.date.available2020
dc.date.issued1996
dc.identifier.issn1359-7345
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19581
dc.description.abstractEnA hexaarm hexachloropolystyrene star polymer 1 ([M with combining macron]n= 18 000 g mol–1) is functionalized by reaction with Me3SiN3 to give the hexaazido star polymer 2; reduction of 2 by PPh3/H2O leads to the hexaamine star polymer 3, and reaction of 2 with a two-fold excess of C60 gives the hexafullerence star polymer 4, characterized by size-exclusion chromatography, NMR, thermal-gravimetry analysis and CV.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.title.enC60 end-capped polystyrene stars
dc.typeArticle de revue
dc.identifier.doi10.1039/CC9960001565
dc.subject.halChimie/Polymères
bordeaux.journalChemical Communications
bordeaux.page1565
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue13
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-02930414
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-02930414v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Chemical%20Communications&rft.date=1996&rft.issue=13&rft.spage=1565&rft.epage=1565&rft.eissn=1359-7345&rft.issn=1359-7345&rft.au=CLOUTET,%20Eric&GNANOU,%20Yves&FILLAUT,%20Jean-Luc&ASTRUC,%20Didier&rft.genre=article


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