Year-end Sale % OFF 
Abstract
The preparation of ωω′ bisfunctional oligoesters (unsaturated or not) is described. The oligoesters are characterised by NMR, end-group titration and tonometry. Their modification by transformation of acid to acid chloride end-group is reported. Their solution polycondensation with ωω′ dihydroxy polyethers is described. A statistical method has been used to optimize the reaction conditions. The properties of the poly (unsaturated esters-b-ethers) are studied. Examination by thermal differential analysis shows that the two blocks are compatible.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: 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.
