Synthesis of New Hydrogels by Copolymerization of Poly(2-methyl-2-oxazoline) Bis(macromonomers) and N-Vinylpyrrolidone
✍ Scribed by Juan C. Rueda; Hartmut Komber; Juan C. Cedrón; Brigitte Voit; Galina Shevtsova
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 139 KB
- Volume
- 204
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
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 P~n~ = 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.
Schematic of polymerization
magnified imageSchematic of polymerization
📜 SIMILAR VOLUMES
## Abstract poly[isobutene‐__co__‐(__p__,__m__‐chloromethylstyrene)]‐__graft__‐poly(2‐methyl‐2‐oxazoline) graft copolymers (GP) were prepared by the “grafting from” method throught the cationic polymerization of 2‐methyl‐2‐oxazoline (MeOXA) initiated by a statistical copolymer is isobutene and chlo