Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5224387 | Tetrahedron | 2008 | 6 Pages |
Abstract
Efficient and mild reaction conditions were developed for the catalytic carbonylation of fluorinated epoxides to their corresponding β-lactones. Six new lactones with fluorinated side chains were prepared in high isolated yields. These lactones were polymerized to form a series of new poly(β-hydroxyalkanoate)s with fluorinated side chains, and their properties were examined with respect to their hydrocarbon analogs. Finally, copolymerizations were performed with fluorinated lactones and β-butyrolactone, which resulted in tapered copolymers rather than the expected random copolymers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
John W. Kramer, Geoffrey W. Coates,