| Literature DB >> 27568984 |
Romain Liénard1,2, Nerea Zaldua3, Thomas Josse1, Julien De Winter2, Manuela Zubitur4, Agurtzane Mugica3, Amaia Iturrospe5, Arantxa Arbe5, Olivier Coulembier6, Alejandro J Müller7,8.
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.Entities:
Keywords: crystallization; cyclic block copolymers; poly(ε-caprolactone)
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Year: 2016 PMID: 27568984 DOI: 10.1002/marc.201600309
Source DB: PubMed Journal: Macromol Rapid Commun ISSN: 1022-1336 Impact factor: 5.734