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 |
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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