Synthesis and properties of hydroxy-terminated poly(hydroxyalkanoate)s

Citation
Dt. Shah et al., Synthesis and properties of hydroxy-terminated poly(hydroxyalkanoate)s, MACROMOLEC, 33(8), 2000, pp. 2875-2880
Citations number
20
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULES
ISSN journal
00249297 → ACNP
Volume
33
Issue
8
Year of publication
2000
Pages
2875 - 2880
Database
ISI
SICI code
0024-9297(20000418)33:8<2875:SAPOHP>2.0.ZU;2-Y
Abstract
This paper describes the biosynthesis and properties of bacterial poly(hydr oxyalkanoate)s (PHA) with predominantly hydroxyl end groups. Hydroxy termin ation is achieved by the addition of low molecular weight diols to the cult ure. It is found that low molecular weight diols of various structures can be easily incorporated as chain ends, when used during fermentation, by a v ariety of microorganisms. Incorporation of a chiral diol does not appear to be stereospecific; both (R)- and (S)-1,2-propanediols were incorporated in to the polymer. Moreover, both primary and secondary hydroxyl groups of 1,2 -propanediol mere found to have reacted. It was found that an increase in t he hydroxy termination in P(3HB) leads to an increase in the thermal stabil ity, most likely by prolonging the condensation reaction and delaying the d egradation reaction.