N-Heterocyclic carbene/Lewis acid-mediated ring-opening polymerization of propylene oxide. Part 1: Triisobutylaluminum as an efficient controlling agent
| dc.rights.license | open | |
| hal.structure.identifier | South China University of Technology [Guangzhou] [SCUT] | |
| dc.contributor.author | SONG, Qilei | |
| hal.structure.identifier | South China University of Technology [Guangzhou] [SCUT] | |
| dc.contributor.author | ZHAO, Junpeng | |
| hal.structure.identifier | South China University of Technology [Guangzhou] [SCUT] | |
| dc.contributor.author | ZHANG, Guangzhao | |
| hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
| dc.contributor.author | TATON, Daniel | |
| hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
| dc.contributor.author | PERUCH, Frédéric
IDREF: 152900748 | |
| hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
| dc.contributor.author | CARLOTTI, Stéphane | |
| dc.date.accessioned | 2020 | |
| dc.date.available | 2020 | |
| dc.date.issued | 2020 | |
| dc.identifier.issn | 0014-3057 | |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/19574 | |
| dc.description.abstractEn | Ring-opening polymerization (ROP) of propylene oxide (PO) is achieved at 25 °C either in bulk or in solution, using N-heterocyclic carbenes (NHCs) and triisobutylaluminum (i-Bu3Al) as a bicomponent catalytic system. Transfer to monomer was not observed and poly(propylene oxide)s with predictable molar masses up to 60 000 g·mol−1 and low dispersities were obtained. In presence/absence of an alcohol as the initiator, the polymerization of PO follows anionic or zwitterionic ROP mechanisms, respectively. The addition of the Lewis acid strongly improves the efficiency of NHCs for the polymerization of substituted epoxides. It is established that i-Bu3Al is involved both in the formation of an initiating/propagating complex of moderate basicity/nucleophilicity and in the coordination of PO, enabling the activation of the monomer towards the complexed nucleophilic active species. Block copolyethers are also prepared by PPO chain extension experiments. All (co)polyethers were thoroughly characterized by 1H NMR spectroscopy, SEC and MALDI-TOF mass spectrometry as means to prove the control and benefit of this NHC approach for epoxides ROP. | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.subject.en | substituted epoxides | |
| dc.subject.en | anionic ring-opening polymerization | |
| dc.subject.en | N-heterocyclic carbene | |
| dc.subject.en | bicomponent catalyst | |
| dc.subject.en | block copolymers | |
| dc.title.en | N-Heterocyclic carbene/Lewis acid-mediated ring-opening polymerization of propylene oxide. Part 1: Triisobutylaluminum as an efficient controlling agent | |
| dc.type | Article de revue | |
| dc.identifier.doi | 10.1016/j.eurpolymj.2020.109819 | |
| dc.subject.hal | Chimie/Polymères | |
| bordeaux.journal | European Polymer Journal | |
| bordeaux.page | 109819 | |
| bordeaux.volume | 134 | |
| bordeaux.hal.laboratories | Laboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629 | * |
| bordeaux.institution | Bordeaux INP | |
| bordeaux.institution | Université de Bordeaux | |
| bordeaux.peerReviewed | oui | |
| hal.identifier | hal-02864560 | |
| hal.version | 1 | |
| hal.origin.link | https://hal.archives-ouvertes.fr//hal-02864560v1 | |
| bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=European%20Polymer%20Journal&rft.date=2020&rft.volume=134&rft.spage=109819&rft.epage=109819&rft.eissn=0014-3057&rft.issn=0014-3057&rft.au=SONG,%20Qilei&ZHAO,%20Junpeng&ZHANG,%20Guangzhao&TATON,%20Daniel&PERUCH,%20Fr%C3%A9d%C3%A9ric&rft.genre=article |
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