SET-LRP in biphasic mixtures of fluorinated alcohols with water

dc.bibliographicCitation.firstPage2313eng
dc.bibliographicCitation.issue17eng
dc.bibliographicCitation.journalTitlePolymer chemistryeng
dc.bibliographicCitation.lastPage2327eng
dc.bibliographicCitation.volume9eng
dc.contributor.authorMoreno, Adrian
dc.contributor.authorLiu, Tong
dc.contributor.authorDing, Liang
dc.contributor.authorBuzzacchera, Irene
dc.contributor.authorGalià, Marina
dc.contributor.authorMöller, Martin
dc.contributor.authorWilson, Christopher J.
dc.contributor.authorLligadas, Gerard
dc.contributor.authorPercec, Virgil
dc.date.accessioned2022-04-12T05:18:41Z
dc.date.available2022-04-12T05:18:41Z
dc.date.issued2018
dc.description.abstractBiphasic-binary mixtures of 2,2,2-trifluoroethanol (TFE) or 2,2,3,3-tetrafluoropropanol (TFP) with water were used as reaction media to synthesize well-defined poly(methyl acrylate) (PMA) with chain end functionality close to 100% by SET-LRP. Non-activated Cu(0) wire was used as a catalyst, taking advantage of the Cu(0)-activation property that these fluorinated alcohols possess. Biphasic-binary mixtures of water, containing a ligand and Cu(II)Br2 either generated by disproportionation of Cu(I)Br or externally added, and an organic solvent, containing a monomer and a polymer, were studied. Two N-ligands were investigated: the classic tris(2-dimethylaminoethyl)amine (Me6-TREN) and tris(2-aminoethyl)amine (TREN), as a more economically attractive alternative for technological purposes. The results reported here support the replacement of Me6-TREN by TREN, taking into account the fact that the latter requires small loadings of an externally added Cu(II)Br2 deactivator and a ligand in the water phase to mediate a living radical polymerization process. Both catalytic systems ensure efficient SET-LRP processes with first order kinetics to high conversion, linear dependence of experimental Mn on conversion, narrow molecular weight distribution, and near-quantitative chain end functionality.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8633
dc.identifier.urihttps://doi.org/10.34657/7671
dc.language.isoengeng
dc.publisherCambridge : RSC Publ.eng
dc.relation.doihttps://doi.org/10.1039/c8py00062j
dc.relation.essn1759-9962
dc.rights.licenseCC BY-NC 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/eng
dc.subject.ddc540eng
dc.subject.otherChainseng
dc.subject.otherCopper compoundseng
dc.subject.otherLigandseng
dc.subject.otherLiving polymerizationeng
dc.subject.otherMolecular weight distributioneng
dc.subject.other2 ,2 ,2-trifluoroethanoleng
dc.subject.otherDisproportionationseng
dc.subject.otherFirst order kineticseng
dc.subject.otherLiving radical polymerizationeng
dc.subject.otherNarrow molecular weight distributionseng
dc.subject.otherPoly(methyl acrylate)eng
dc.subject.otherTris(2-aminoethyl) amineeng
dc.subject.otherTris(2-dimethylami-noethyl) amineseng
dc.subject.otherBinary mixtureseng
dc.titleSET-LRP in biphasic mixtures of fluorinated alcohols with watereng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorDWIeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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