| Literature DB >> 15762656 |
Estelle Renard1, Adrien Poux, Laurianne Timbart, Valérie Langlois, Philippe Guérin.
Abstract
The Poly(hydroxyalkanoate) (PHA) chemical modifications represent an alternative route to introduce functional groups, which cannot be introduced by bioconversion. PHAs containing unsaturated chains were readily converted into polyesters containing a terminal hydroxyl group on the side chains. With the use of the borane-tetrahydrofuran complex, the pendant side chain alkenes were quantitatively transformed into hydroxyl functions. The conversion proceeded to completion without a significant decrease in molecular weight. The introduction of hydroxyl groups in the products was confirmed from Fourier transform infrared and 1H NMR analysis. The presence of repeating units containing pendant hydroxyl groups in the proportion 25 mol % caused an increase in hydrophilicity of these new PHAs because they were soluble in polar solvents such as ethanol. Besides, these reactive PHAs can be used to bind bio-active molecules or to prepare novel graft copolymers with desired properties.Entities:
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Year: 2005 PMID: 15762656 DOI: 10.1021/bm049337+
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988