Synthesis of End-group Functionalized Poly(octadecyl vinyl ether)
โ Scribed by Lievens, Serge S.; Goethals, Eric J.
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 405 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0959-8103
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โฆ Synopsis
The cationic polymerization of octadecyl vinyl ether (ODVE) initiated by trimethylsilyl iodide and 1,l-diethoxyethane in the presence of ZnI, in toluene at 0ยฐC and 10ยฐC has been investigated. For molecular weights lower than 6000, a linearity of M,, with conversion was observed, but for higher molecular weights a strong deviation from calculated values, assuming a living mechanism, was found. Kinetic analysis of the polymerization and the variation of molecular weight as a function of conversion was in agreement with a transfer to monomer with k,,/k, 0.006 at 10ยฐC. Analysis of the polymers obtained by termination with methanol provided evidence that the alkenyl ether end-groups formed by the transfer reaction lead to the same acetal end-groups as the active species. As a consequence, it is possible to prepare functionalized polyODVE polymers by end-capping with alcohols. This was confirmed by the synthesis of polyODVE macromonomers by end-capping with 2-hydroxyethyl methacrylate.
๐ SIMILAR VOLUMES
Poly(vinyl alcohol) (PVA) was cyanoethylated by reaction with acrylonitrile in the presence of sodium hydroxide and quaternary ammonium halide. Quaternary ammonium halide, acting as a phase transfer catalyst, increases the degree of substitution (DS) of PVA. The DS also increased with increasing acr
Water-soluble amphiphilic diblock copolymers were synthesized by the living cationic polymerization of methyl vinyl ether (hydrophilic block) and its subsequent termination with n-alcohols of chain lengths varying from one to eight, and three n-alkyl carboxylic acids with 10, 12, and 18 carbon atoms