Synthesis of new hydrogels by copolymerization of poly(2-methyl-2-oxazoline) bis(macromonomers) and N-vinylpyrrolidone

Juan C. Rueda, Hartmut Komber, Juan C. Cedrón, Brigitte Voit, Galina Shevtsova

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

New non-ionic hydrogels were synthesized by radical homopolymerization of vinyl end-functionalized poly(2-methyl-2-oxazoline) bis(macromonomers), or by radical copolymerization of these bis(macromonomers) with N-vinyl-2-pyrrolidone (NVP). The poly(2-methyl-2-oxazoline) bis(macromonomers) were synthesized through "living" cationic ring-opening polymerization of 2-methyl-2-oxazoline (MeOXA), using, simultaneously, the known "initiating" and "end-capping" method for synthesis of macromonomers. Chloromethyl styrene was used as initiator and N-(4-vinylbenzyl)-piperazine was used as the terminating agent. Well defined poly(2-methyl-2-oxazoline) bis(macromonomers) were obtained with Pn = 4, 11, and 17. The hydrogel structures were characterized by high-resolution magic angle spinning NMR technique and their solvent absorption capacity was tested by swelling experiments in different solvents. The bis(macromonomers) were characterized by NMR spectroscopy and gel permeation chromatography.

Original languageEnglish
Pages (from-to)947-953
Number of pages7
JournalMacromolecular Chemistry and Physics
Volume204
Issue number7
DOIs
StatePublished - 7 May 2003

Keywords

  • High-resolution magic angle spinning NMR
  • Hydrogels
  • Polyoxazoline
  • Polypyrrolidone
  • Swelling

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