Afficher la notice abrégée

dc.rights.licenseopen
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorOTTOU, Winnie Nzahou
dc.contributor.authorBOURICHON, Damien
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorVIGNOLLE, Joan
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorWIROTIUS, Anne-Laure
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorROBERT, Frédéric
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorLANDAIS, Yannick
dc.contributor.authorSOTIROPOULOS, Jean-Marc
dc.contributor.authorMIQUEU, Karinne
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2014
dc.identifier.issn0947-6539
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20194
dc.description.abstractEnThe activation behavior of two N-heterocyclic carbenes (NHCs), namely, 1,3-bis(isopropyl)imidazol-2-ylidene(NHCiPr) and 1,3-bis(tert-butyl) imidazol-2-ylidene (NHCtBu), as organic nucleophiles in the reaction with methyl methacrylate (MMA) is described. NHCtBu allows the polymerization of MMA in DMF at room temperature and in toluene at 50 degrees C, whereas NHCiPr reacts with two molecules of MMA, forming an unprecedented imidazolium-enolate cyclodimer (NHCiPr/MMA=1:2). It is proposed that the reaction mechanism occurs by initial 1,4-nucleophilic addition of NHCiPr to MMA, generating a zwitterionic enolate 2, followed by addition of 2 to a second MMA molecule, forming a linear imidazolium-enolate 3 (NHCiPr/MMA=1:2). Proton transfer, generating intermediate 5, followed by cyclization and release of methanol yielded the aforementioned zwitterionic cyclodimer 1:2 adduct 7, the molecular structure of which has been established by NMR spectroscopy, X-ray diffraction, and mass spectrometry. This unexpected difference between NHCtBu and NHCiPr in the reaction with MMA (polymerization and cyclodimerization, respectively) can be rationalized by using DFT calculations. In particular, the nature of the NHC strongly influences the cyclodimerization pathway, the cyclization of 5 and the release of methanol are the discriminating step and limiting step, respectively. In the case of NHCtBu, both steps are strongly disfavoured compared with that of NHCiPr (energetic difference of around 14 and 9kcalmol(-1), respectively), preventing the cyclization mechanism from a kinetic viewpoint. Moreover, addition of a third molecule of MMA in the polymerization pathway results in a lower activation barrier than that of the limiting step in the cyclodimerization pathway (difference of around 14kcalmol(-1)), in agreement with the formation of polymethyl methacrylate (PMMA) by using NHCtBu as nucleophile.
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.subject.enACRYLATES
dc.subject.enGAUSSIAN-TYPE BASIS
dc.subject.enTO-TAIL DIMERIZATION
dc.subject.enFRUSTRATED LEWIS PAIRS
dc.subject.enMOLECULAR-ORBITAL METHODS
dc.subject.enpolymerization
dc.subject.enorganocatalysis
dc.subject.enN-heterocyclic carbenes
dc.subject.enREACTIVITY
dc.subject.enORGANIC-MOLECULES
dc.subject.enUMPOLUNG
dc.subject.encyclodimerization
dc.subject.enDFT calculations
dc.subject.enMECHANISM
dc.subject.enMONOMERS
dc.title.enCyclodimerization versus Polymerization of Methyl Methacrylate Induced by N-Heterocyclic Carbenes: A Combined Experimental and Theoretical Study
dc.typeArticle de revue
dc.identifier.doi10.1002/chem.201304492
dc.subject.halChimie/Polymères
bordeaux.journalChemistry - A European Journal
bordeaux.page3989-3997
bordeaux.volume20
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue14
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01373035
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01373035v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Chemistry%20-%20A%20European%20Journal&rft.date=2014&rft.volume=20&rft.issue=14&rft.spage=3989-3997&rft.epage=3989-3997&rft.eissn=0947-6539&rft.issn=0947-6539&rft.au=OTTOU,%20Winnie%20Nzahou&BOURICHON,%20Damien&VIGNOLLE,%20Joan&WIROTIUS,%20Anne-Laure&ROBERT,%20Fr%C3%A9d%C3%A9ric&rft.genre=article


Fichier(s) constituant ce document

FichiersTailleFormatVue

Il n'y a pas de fichiers associés à ce document.

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée