Copolymerization of e-caprolactone and morpholine-2,5-dione derivatives

P.J.A. in 't Veld, Ye Wei-Ping, Richard Klap, Pieter J. Dijkstra, Jan Feijen

Research output: Contribution to journalArticleAcademic

44 Downloads (Pure)

Abstract

Novel biodegradable poly(ester-amide)s were prepared by ring-opening copolymerization of -caprolactone and 3- and/or 6-alkyl-substituted morpholine-2,5-dione derivatives. The copolymerizations were carried out in the bulk using stannous octoate as an initiator. Molecular weights of the copolymers ranged from 1,0 · 104 to 8,3 · 104 and decreased with increasing mole fractions of morpholine-2,5-dione derivatives in the feed. 13C NMR sequence analysis indicated that the copolymers had a random distribution of -oxycaproyl and depsipeptide units, which resulted from the occurrence of transesterification reactions during copolymerization. The results of the DSC measurements and 13C NMR sequence analysis showed a close relationship between the crystallinity and average length of ε-oxycaproyl blocks. Copolymers with a mole fraction of depsipeptide units smaller than 0,20 were semi-crystalline, whereas incorporation of larger amounts of depsipeptide units resulted in amorphous copolymers. The melting point depression as a function of the molar composition of the semi-crystalline copolymers was in good agreement with the melting point depression predicted by the Baur equation, which indicated the rejection of depsipeptide units from crystals consisting of ε-oxycaproyl units.
Original languageEnglish
Pages (from-to)1927-1942
Number of pages16
JournalMakromolekulare Chemie
Volume193
Issue number8
DOIs
Publication statusPublished - 1992

Keywords

  • METIS-105253
  • IR-70994

Fingerprint Dive into the research topics of 'Copolymerization of e-caprolactone and morpholine-2,5-dione derivatives'. Together they form a unique fingerprint.

Cite this