## Abstract This contribution explores different strategies for the synthesis of side chain functional polydepsipeptides. First, the ring‐opening polymerization of side chain functional morpholine‐2,5‐diones is revisited and the optimized reaction conditions used for the polymerization of (Z)‐L‐Lys
AB2 Functional Polyesters via Ring Opening Polymerization: Synthesis and Characterization
✍ Scribed by Ingrid W. Velthoen; Pieter J. Dijkstra; Jan Feijen
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 415 KB
- Volume
- 210
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Aliphatic AB~2~ functional polyesters were conveniently prepared by the ring opening polymerization of ε‐caprolactone and L‐lactide in the presence of the AB~2~ functional initiator 2,2‐bis(hydroxymethyl)propionic acid (bis‐MPA) and Sn(Oct)~2~ as the catalyst. In L‐lactide polymerization, both bis‐MPA hydroxyl groups initiated the polymerization reaction, but for ε‐caprolactone polymerization this depended on the monomer to initiator to catalyst ratio. Initiation at two hydroxyl groups occurred at high monomer to initiator ([M]/[I]) ratio and at high Sn(Oct)~2~ to monomer ratio. The melting temperatures of the AB~2~‐functional PLLA and PCL polymers were comparable to linear polymers with a $\overline {DP}$ equal to the $\overline {DP}$ per arm in the polymer.
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📜 SIMILAR VOLUMES
## Abstract A new functional lactone, __α__‐iodo‐__ε__‐caprolactone (__α__I__ε__CL), was synthesized from __ε__‐caprolactone by anionic activation using a non‐nucleophilic strong base (lithium diisopropylamide) followed by an electrophilic substitution with iodine chloride. Ring‐opening (co)polymer
Caprolactone (-CL) has been mixed with ZnCl 2 at different mol ratios. The resulting complex was characterized through 1 H and 13 C NMR spectroscopy in bulk and in solutions, differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), and optical microscopy. Ring-opening polymeriza