Abstract
AbstractPoly(3‐hydroxy undec‐10‐enoate) (PHU) was synthesized by feeding Pseudomonas oleovarans with 10‐undecenoic acid and nearly 100% hydroxylation of double bonds of PHU was achieved by hydroboration–oxidation reaction using 9‐borobicyclononane. The disappearance of vinyl signals of PHU in proton and 13C NMR spectra was observed. Acetylation of hydroxylated PHU was conducted for molecular weight measurements. Molecular weight and polydispersity of hydroxylated PHU were found to be 10,000 and 1.23, respectively, while that of the originals was 32,000 and 2.42. Decomposition temperatures of original and hydroxylated PHU were 280 and 200°C, respectively. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 2132–2139, 2005
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.