Gradient copolymers of ε‐caprolactone and δ‐valerolactone via solvent‐free ring‐opening copolymerization with a pyridyl‐urea/MTBD system. Issue 15 (9th July 2020)

• Record Type: Journal Article
• Authors: Feng, Rui; Jie, Suyun; Braunstein, Pierre; Li, Bo‐Geng
• Is Part Of: Journal of polymer science. Volume 58:Issue 15(2020)
• Page Start: 2108
• Page End: 2115
• Publication Date: 2020-07-09
• Subjects: gradient copolymer -- pyridyl‐urea -- ring‐opening copolymerization -- δ‐valerolactone -- ε‐caprolactone; Polymers -- Periodicals; Polymerization -- Periodicals; Polymerization; Polymers; Periodicals; 547.7
• DOI: 10.1002/pol.20200174
• Languages: English
• ISSNs: 2642-4150

Abstract

Abstract: The ring‐opening copolymerization of ε‐caprolactone and δ‐valerolactone was carried out under solvent‐free conditions with a pyridyl‐urea (6C‐PU )/7‐methyl‐1, 5, 7‐triazabicyclo[4.4.0]dec‐5‐ene catalytic system by premixing two monomers, yielding gradient copolyesters with cyclic and linear structures in the absence or presence of an initiator, respectively. The random and block copolyesters of these two monomers were also prepared for comparison. The results of 1 H and 13 C NMR spectra determined the linear and cyclic structure of copolymers. The kinetic experiment was used to determine the consuming rates of two monomers during the polymerization. The topologies and thermal properties of all the copolymers were characterized and compared by NMR and DSC. Abstract : Gradient copolymers with cyclic and linear topologies have been prepared via the ring‐opening copolymerization of ε‐caprolactone and δ‐valerolactone in the absence or presence of BnOH catalyzed by a pyridyl‐urea (6C‐PU )/7‐methyl‐1, 5, 7‐triazabicyclo[4.4.0]dec‐5‐ene system. The structure and thermal properties of copolymers with different composition or different sequential distribution were also investigated.