The vinyl groups in the pendant substituents of a series of poly(3-hydroxyoctanoate-co-3-hydroxy-10-undecenoate)s, PHOUs, were completely converted into epoxide groups with m-chloroperbenzoic acid to produce a series of copolymers, poly(3hydroxyoctanoate-co-3-hydroxy-10,11-epoxyundecenoate)s, PHOEs
Epoxidation of bacterial polyesters with unsaturated side chains. II. Rate of epoxidation and polymer properties
β Scribed by Won Ho Park; Robert W. Lenz; Steve Goodwin
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 154 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
Poly(3-hydroxyoctanoate-co-3-hydroxy-10-undecenoate)s (PHOUs) with controlled amounts of unsaturated repeating units were epoxidized to various extents with m-chloroperbenzoic acid (MCPBA) in homogeneous solution. The epoxidation reaction was second order, with an initial rate constant of 1.1 Ο« 10 Οͺ3 Lmol Οͺ1. s Οͺ1 at 20Β°C, regardless of the unsaturated unit content in PHOU. No substantial change in either molecular weight or molecular weight distribution occurred as a result of epoxidation, but the melt transition temperature and enthalpy of melting both decreased as the unsaturated groups were increasingly converted into epoxide groups. In contrast, the glass transition temperature (T g ) increased by approximately 0.25 Β°C for each 1 mol % of epoxidation, irrespective of the composition of the PHOU.
π SIMILAR VOLUMES
Nine polymers with kinked aromatic structures in the main chain and biphenylene-type mesogenic groups in the side chain were synthesized by the polyaddition of bis(epoxide)s and thio-and O-esters. Tetrabutylphosphonium chloride and tetraphenylphosphonium chloride effectively catalyzed the polymeriza