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Influence of reaction conditions on degree of branching in hyperbranched aliphatic polyethers from 3-ethyl-3-(hydroxymethyl)oxetane
KTH, Superseded Departments, Polymer Technology.
KTH, Superseded Departments, Polymer Technology.ORCID iD: 0000-0002-8348-2273
KTH, Superseded Departments, Polymer Technology.ORCID iD: 0000-0002-9372-0829
2001 (English)In: Macromolecules, ISSN 0024-9297, E-ISSN 1520-5835, Vol. 34, no 17, 5786-5791 p.Article in journal (Refereed) Published
Abstract [en]

The cationic ring-opening polymerization of 3-ethyl-3-(hydroxymethyl)oxetane to form hyperbranched polyethers has been studied. The polymerizations have been performed in bulk using sulfonium salt initiators. To produce polymers of different degrees of branching, the reaction conditions (reaction temperature and initiator) have been varied. Polymerizations have also been performed in the presence of a trifunctional core molecule, trimethylolpropane. The conversion of monomer turned out to be the main factor determining the degree of branching in the resulting polymer. Polymers with degrees of branching ranging from 0.15 to 0.41 were synthesized. When 3-ethyl-3-(hydroxymethyl)oxetane was polymerized by slow addition of monomer to a core molecule, a lower degree of branching was obtained compared to the one-step synthesis with full conversion of monomer. The polydispersity was generally slightly lower when a core molecule was used than in the one-step homopolymerization of 3-ethyl-3(hydroxymethyl)oxetane.

Place, publisher, year, edition, pages
2001. Vol. 34, no 17, 5786-5791 p.
Keyword [en]
ring-opening polymerization, multibranching polymerization, cationic polymerization, poly(ether amide)s, polymers, resins, blends, analog
National Category
Chemical Sciences
URN: urn:nbn:se:kth:diva-20861DOI: 10.1021/ma010495sISI: 000170370800013OAI: diva2:339558
QC 20100525Available from: 2010-08-10 Created: 2010-08-10 Last updated: 2010-10-26Bibliographically approved

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Magnusson, HeleneMalmström, EvaHult, Anders
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