Abstract
Polythioesters have recently been attracted attention due to their interesting characteristics, such as poor solubility against organic solvents and higher heat stability compared to polyoxyesters. Polythioesters were synthesized by the direct polycondensation of 1,6-hexanedithiol and diacid diesters having a variety of methylene lengths using lipase CAas a catalyst. The obtained polythioesters showed a higher melting temperature compared to those of the corresponding polyoxyesters. The 1,6-hexanedithiol and diacid diesters were reacted in n-nonane using lipase CA to produce cyclic oligomers with an Mw of a few hundreds. Synthesis of polythioester was studied using these cyclic oligomers. A high-molecular weight polythioester having an M w of about 120,000 was produced through the ring-opening polymerization using lipase CA.
Original language | English |
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Number of pages | 1 |
Publication status | Published - 2006 Oct 19 |
Event | 55th SPSJ Annual Meeting - Nagoya, Japan Duration: 2006 May 24 → 2006 May 26 |
Other
Other | 55th SPSJ Annual Meeting |
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Country/Territory | Japan |
City | Nagoya |
Period | 06/5/24 → 06/5/26 |
Keywords
- Biodegradation
- Cyclic oligomers
- Enzymatic polymerization
- Polythioester
- Ring opening polymerization
ASJC Scopus subject areas
- Engineering(all)