Abstract
Biodegradable polyester resins were prepared via photo crosslinking of functional polyesters obtained by copolymerization of ε-caprolactone and the functional cyclic esters γ-acryloyloxy-ε-caprolactone (ACL) and γ-methacryloyloxy-ε-caprolactone (MCL). The cyclic esters were prepared via Baeyer-Villiger oxidation of the corresponding 4-acyloyloxy- cyclohexanone derivatives. Copolymers with different content of either acryloyloxy or methacryloyloxy functional groups were prepared via catalyzed ring-opening polymerization (ROP) of γ-acyloyloxy-ε-caprolactones and ε-caprolactone using Al(OiPr)3 as catalyst and initiator. 2D- and 3D-micropatterning of the copolymers was performed via UV-crosslinking of polymer films on a suitable substrate and by UV replica molding on both rigid and elastic masters, showing the processability of these novel functional polyesters and their potential as substrates for biomedical devices.
| Original language | English |
|---|---|
| Pages (from-to) | 6789-6800 |
| Number of pages | 12 |
| Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
| Volume | 46 |
| Issue number | 20 |
| DOIs | |
| State | Published - 15 Oct 2008 |
| Externally published | Yes |
Keywords
- Biodegradable polyesters
- Micropatterning
- Photo crosslinking
- Resins
- Ring-opening polymerization
- UV replica molding