Update and challenges in organo-mediated polymerization reactions
dc.rights.license | open | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
dc.contributor.author | OTTOU, Winnie Nzahou | |
hal.structure.identifier | Institute for Polymer Materials [POLYMAT] | |
dc.contributor.author | SARDON, Haritz | |
dc.contributor.author | MECERREYES, David | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
dc.contributor.author | VIGNOLLE, Joan | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
dc.contributor.author | TATON, Daniel | |
dc.date.accessioned | 2020 | |
dc.date.available | 2020 | |
dc.date.issued | 2016 | |
dc.identifier.issn | 0079-6700 | |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/20024 | |
dc.description.abstractEn | Organocatalysis has become a very powerful tool for precision macromolecular chemistry, as judged by the number of articles published in this field in the past decade. A variety of small organic molecules, including Bronsted/Lewis bases and acids, based on amines, phosphines or carbenes, but also on bi-component systems, have been employed as a means to catalyze the polymerization of miscellaneous monomers. Not only can organocatalysts be employed to promote the ring-opening polymerization of various heterocyclics (e.g. lactones, lactide, cyclic carbonates, epoxides, lactams, cyclocarbosiloxanes), but some of them also allow activating vinylic monomers such as (meth)acrylics, or triggering the step growth polymerization of monomers such as diisocyanates and diols for polyurethane synthesis. The reduced toxicity of organocatalysts in comparison to their metallic counterparts is also driving their development in some sensitive applications, such as biomedical or microelectronics. Overall, organocatalysts display specific monomer activation modes, thereby providing a unique opportunity to control the polymerization of various functional monomers, under mild conditions. This review article focuses on advances of the past 4 years (>150 publications) in polymerization reactions utilizing small organic molecules either as direct initiators or as true catalysts, with a special emphasis on monomer activation modes, as well as polymerization mechanism aspects. | |
dc.description.sponsorship | POLYMERISATIONS ORGANOCATALYSEES PAR LES CARBENES : VERS UNE PLATEFORME CATALYTIQUE MULTI-TACHE - ANR-11-BS08-0011 | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.subject.en | Bifunctional activation | |
dc.subject.en | Direct initiation | |
dc.subject.en | Organic catalyst | |
dc.subject.en | Ring-opening polymerization | |
dc.subject.en | Step-growth polymerization | |
dc.subject.en | Group transfer polymerization | |
dc.subject.en | Acid catalysis | |
dc.subject.en | Basic catalysis | |
dc.title.en | Update and challenges in organo-mediated polymerization reactions | |
dc.type | Article de revue | |
dc.identifier.doi | 10.1016/j.progpolymsci.2015.12.001 | |
dc.subject.hal | Chimie/Polymères | |
dc.description.sponsorshipEurope | European Joint Doctorate in Organocatalysis and Sustainable Polymers | |
bordeaux.journal | Progress in Polymer Science | |
bordeaux.page | 64-115 | |
bordeaux.volume | 56 | |
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-01366512 | |
hal.version | 1 | |
hal.origin.link | https://hal.archives-ouvertes.fr//hal-01366512v1 | |
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