This article reports the synthesis and copolymerization of 6-hydroxynon-8-enoic acid lactone. The ring-opening polymerization of this lactone-type monomer bearing a pendant allyl group led to new homopolymers and random copolymers with -caprolactone and L,L-lactide. The copolymerizations were carrie
Alternating Copolymers of Ethylene and Diolefins Containing Pendent Functional Groups
โ Scribed by Alex Williamson; Gerhard Fink
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 225 KB
- Volume
- 204
- Category
- Article
- ISSN
- 1022-1352
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โฆ Synopsis
Abstract
The catalyst [Me~2~C(Flu)(3โMeCp)ZrCl~2~] (1), activated by MAO, was used for the copolymerization of ethylene and 1,7โoctadiene (OD) to form copolymers with pendent double bonds. The properties of the copolymers were strongly dependent on the purity of the comonomer. Formation of ethyleneโrich sequences and increased levels of crosslinking were observed with highly purified 1,7โoctadiene. Catalysts 1 and [Me~2~Si(Flu)~2~ZrCl~2~] (2), activated by MAO, were used for the copolymerization of ethylene and 7โmethylโ1,6โoctadiene (MOD). In both cases, alternating copolymers were formed with unreacted pendent double bonds. The triad distributions were analyzed by Markovian firstโ and secondโorder statistics. Copolymers produced by catalyst 2 were significantly more alternating than copolymers produced by catalyst 1 despite the fact that catalyst 2 is highly symmetrical. Epoxidation of pendent double bonds was examined.
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