Abstract

New copolyesters with designed architecture were obtained via anionic ring-opening copolymerization of β-butyrolactone with β-ethoxymethyl-β-propiolactone. The resulting copolyesters contained predominantly linear macromolecular chains terminated by acetate end groups derived from the used initiator regardless of the type or the composition. Similar behavior of β-alkoxy-substituted-β-lactone and β-alkyl-substituted-β-lactone (including side reactions leading to unsaturated end groups) was observed under the conditions of anionic ring-opening copolymerization. The application of ion trap ESI-MS/MS analysis for structural studies and investigation of the fragmentation product patterns of the individual molecular ions showed significant differences in the molecular structure at the level of individual molecular chains of random and diblock copolyesters. Thus, the sequence distribution of diblock and random copolyester was determined based on the investigation and comparison of the fragmentation product patte...

Full Text
Paper version not known

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 call

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.