Mostrar el registro sencillo del ítem

N-Heterocyclic carbene/Lewis acid-mediated ring-opening polymerization of propylene oxide. Part 2: Toward dihydroxytelechelic polyethers using triethylborane

dc.rights.licenseopen
hal.structure.identifierSouth China University of Technology [Guangzhou] [SCUT]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorSONG, Qilei
hal.structure.identifierSouth China University of Technology [Guangzhou] [SCUT]
dc.contributor.authorZHAO, Junpeng
hal.structure.identifierSouth China University of Technology [Guangzhou] [SCUT]
dc.contributor.authorZHANG, Guangzhao
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorCARLOTTI, Stéphane
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2020
dc.identifier.issn0014-3057
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19573
dc.description.abstractEnPropylene oxide (PO) is polymerized by metal-free ring-opening 11 polymerization (ROP) at 25 °C using N-heterocyclic carbenes (NHCs) and 12 triethylborane (Et 3 B) as a bicomponent catalytic system. Poly(propylene oxide)s with 13 predictable molar mass up to 60 000 g.mol-1 and low dispersity (Ð < 1.10) were 14 obtained without the occurrence of undesirable transfer reaction to the monomer. In 15 presence of an alcohol as the initiator, the ROP of PO follows an anionic mechanism 16 assisted by monomer activation improving the efficiency of NHCs for the 17 polymerization of substituted epoxides. Et 3 B is involved both in the formation of a 18 complexed active center and in the activation of PO. Interestingly, 19 dihydroxytelechelic PPOs can be readily synthesized not only using 1,4-20 benzenedimethanol but also water, both serving as difunctional initiators. Block
dc.language.isoen
dc.publisherElsevier
dc.title.enN-Heterocyclic carbene/Lewis acid-mediated ring-opening polymerization of propylene oxide. Part 2: Toward dihydroxytelechelic polyethers using triethylborane
dc.typeArticle de revue
dc.identifier.doi10.1016/j.eurpolymj.2020.109839
dc.subject.halChimie/Polymères
bordeaux.journalEuropean Polymer Journal
bordeaux.page109839
bordeaux.volume134
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-02882256
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-02882256v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=European%20Polymer%20Journal&amp;rft.date=2020&amp;rft.volume=134&amp;rft.spage=109839&amp;rft.epage=109839&amp;rft.eissn=0014-3057&amp;rft.issn=0014-3057&amp;rft.au=SONG,%20Qilei&amp;ZHAO,%20Junpeng&amp;ZHANG,%20Guangzhao&amp;TATON,%20Daniel&amp;PERUCH,%20Fr%C3%A9d%C3%A9ric&amp;rft.genre=article


Archivos en el ítem

ArchivosTamañoFormatoVer

No hay archivos asociados a este ítem.

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem