Abstract
We report on a synthetic method where polyanhydride is used as starting material and the ester monomers are inserted through complete esterification, leading to an alternating ester-anhydride copolymer. The molar ratio of ricinoleic acid (RA) and sebacic acid (SA) was optimized until polysebacic acid is completely converted to carboxylic acid-terminated RA-SA and RA-SA-RA ester-dicarboxylic acids. These dimers and trimers were activated with acetic anhydride, polymerized under heat and vacuum to yield alternating RA-SA copolymer. The resulting alternating poly(ester-anhydride) have the RA at regular intervals. The regular occurrences of RA side chains prevent anhydride interchange, enhancing hydrolytic stability, which allows storage of the polymer at room temperature.
| Original language | English |
|---|---|
| Pages (from-to) | 2253-2259 |
| Number of pages | 7 |
| Journal | Biomacromolecules |
| Volume | 17 |
| Issue number | 6 |
| DOIs | |
| State | Published - 13 Jun 2016 |
Bibliographical note
Publisher Copyright:© 2016 American Chemical Society.
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