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dc.rights.licenseopen
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorKOELLER, Sylvain
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorTHOMAS, Coralie
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorDEFFIEUX, Alain
hal.structure.identifierLaboratoire de Biologie cellulaire
dc.contributor.authorMASSIP, Stéphane
hal.structure.identifierLaboratoire de Biologie cellulaire
dc.contributor.authorLÉGER, Jean-Michel
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorDESVERGNE, Jean-Pierre
hal.structure.identifierDépartement de Chimie Moléculaire - Chimie Théorique [DCM - CT]
dc.contributor.authorMILET, Anne
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorBIBAL, Brigitte
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2014
dc.identifier.issn0947-6539
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20228
dc.description.abstractEnα-Halogenoacetanilides (X=F, Cl, Br) were examined as H-bonding organocatalysts designed for the double activation of CO bonds through NH and CH donor groups. Depending on the halide substituents, the double H-bond involved a nonconventional CH⋅⋅⋅O interaction with either a HCXn (n=1-2, X=Cl, Br) or a HCAr bond (X=F), as shown in the solid-state crystal structures and by molecular modeling. In addition, the catalytic properties of α-halogenoacetanilides were evaluated in the ring-opening polymerization of lactide, in the presence of a tertiary amine as cocatalyst. The α-dichloro- and α-dibromoacetanilides containing electron-deficient aromatic groups afforded the most attractive double H-bonding properties towards CO bonds, with a NH⋅⋅⋅O⋅⋅⋅HCX2 interaction. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.subject.enHydrocarbons
dc.subject.enBromine
dc.subject.enAcetanilides
dc.subject.enhydrogen bond
dc.subject.enchemistry
dc.subject.enchemical structure
dc.subject.enhalogenated hydrocarbon
dc.subject.enfluoride
dc.subject.enacetanilide derivative
dc.subject.enring-opening polymerization
dc.subject.enFluorine
dc.subject.enCatalysis
dc.subject.enChlorine
dc.subject.enFluorides
dc.subject.enhydrogen bonds
dc.subject.enlactide
dc.subject.ennoncovalent interactions
dc.subject.enorganocatalysis
dc.subject.enHalogenated
dc.subject.enHydrogen Bonding
dc.subject.enModels
dc.subject.enMolecular
dc.subject.enQuantum Theory
dc.title.enα-Halogenoacetanilides as hydrogen-bonding organocatalysts that activate carbonyl bonds: fluorine versus chlorine and bromine
dc.typeArticle de revue
dc.identifier.doi10.1002/chem.201303662
dc.subject.halChimie/Polymères
bordeaux.journalChemistry - A European Journal
bordeaux.page2849-2859
bordeaux.volume20
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue10
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01368968
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01368968v1
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=10&rft.spage=2849-2859&rft.epage=2849-2859&rft.eissn=0947-6539&rft.issn=0947-6539&rft.au=KOELLER,%20Sylvain&THOMAS,%20Coralie&PERUCH,%20Fr%C3%A9d%C3%A9ric&DEFFIEUX,%20Alain&MASSIP,%20St%C3%A9phane&rft.genre=article


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