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Characterization of new amphiphilic block copolymers of N-vinyl pyrrolidone and vinyl acetate, 1 - analysis of copolymer composition, end groups, molar masses and molar mass distributions

  • New amphiphilic block copolymers consisting of N-vinyl pyrrolidone and vinyl acetate were synthesized via controlled radical polymerization using a reversible addition/fragmentation chain transfer (RAFT)/macromolecular design via the interchange of xanthates (MADIX) system. The synthesis was carried out in 1,4-dioxane as process solvent. In order to get conclusions on the mechanism of the polymerization the molecular structure of formed copolymers was analysed by means of different analytical techniques. 13C NMR spectroscopy was used for the determination of the monomer ratios. End groups were analysed by means of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. This technique was also used to determine possible fragmentations of the RAFT end groups. By means of a combination of size exclusion chromatography, 13C NMR and static light scattering molar mass distributions and absolute molar masses could be analysed. The results clearly show a non-ideal RAFTNew amphiphilic block copolymers consisting of N-vinyl pyrrolidone and vinyl acetate were synthesized via controlled radical polymerization using a reversible addition/fragmentation chain transfer (RAFT)/macromolecular design via the interchange of xanthates (MADIX) system. The synthesis was carried out in 1,4-dioxane as process solvent. In order to get conclusions on the mechanism of the polymerization the molecular structure of formed copolymers was analysed by means of different analytical techniques. 13C NMR spectroscopy was used for the determination of the monomer ratios. End groups were analysed by means of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. This technique was also used to determine possible fragmentations of the RAFT end groups. By means of a combination of size exclusion chromatography, 13C NMR and static light scattering molar mass distributions and absolute molar masses could be analysed. The results clearly show a non-ideal RAFT mechanism.zeige mehrzeige weniger

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Metadaten
Autoren/innen:Nick Fandrich, Jana Falkenhagen, Steffen Weidner, Dietmar Pfeifer, B. Staal, Andreas F. Thünemann, A. Laschewsky
Dokumenttyp:Zeitschriftenartikel
Veröffentlichungsform:Verlagsliteratur
Sprache:Englisch
Titel des übergeordneten Werkes (Englisch):Macromolecular chemistry and physics
Jahr der Erstveröffentlichung:2010
Verlag:Wiley-VCH Verl.
Verlagsort:Weinheim
Jahrgang/Band:211
Ausgabe/Heft:8
Erste Seite:869
Letzte Seite:878
Freie Schlagwörter:Amphiphiles; Block copolymers; Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-TOF MS); N-vinyl pyrrolidone; Reversible addition/fragmentation chain transfer (RAFT)
DOI:https://doi.org/10.1002/macp.200900466
ISSN:1022-1352
ISSN:1521-3935
Verfügbarkeit des Volltexts:Papiergebundenes Belegexemplar in der Bibliothek der BAM vorhanden ("Hard-copy Access")
Bibliotheksstandort:Sonderstandort: Publica-Schrank
Datum der Freischaltung:19.02.2016
Referierte Publikation:Ja
Datum der Eintragung als referierte Publikation:09.09.2010