Synthesis and Characterization of Double Crystalline Cyclic Diblock Copolymers of Poly(ε-caprolactone) and Poly(l(d)-lactide) (c(PCL-b- PL(D)LA))

Macromol Rapid Commun. 2016 Oct;37(20):1676-1681. doi: 10.1002/marc.201600309. Epub 2016 Aug 29.

Abstract

The synthesis of symmetric cyclo poly(ε-caprolactone)-block-poly(l(d)-lactide) (c(PCL-b-PL(D)LA)) by combining ring-opening polymerization of ε-caprolactone and lactides and subsequent click chemistry reaction of the linear precursors containing antagonist functionalities is presented. The two blocks can sequentially crystallize and self-assemble into double crystalline spherulitic superstructures. The cyclic chain topology significantly affects both the nucleation and the crystallization of each constituent, as gathered from a comparison of the behavior of linear precursors and cyclic block copolymers. The stereochemistry of the PLA block does not have a significant effect on the nonisothermal crystallization of both linear and cyclo PCL-b-PDLA and PCL-b-PLLA copolymers.

Keywords: crystallization; cyclic block copolymers; poly(ε-caprolactone).

MeSH terms

  • Crystallization
  • Molecular Structure
  • Particle Size
  • Polyesters / chemical synthesis
  • Polyesters / chemistry*
  • Surface Properties

Substances

  • Polyesters
  • polycaprolactone
  • poly(lactide)