4.2 Article

Highly Active Bifunctional Cobalt-Salen Complexes for the Synthesis of Poly(ester-block-carbonate) Copolymer via Terpolymerization of Carbon Dioxide, Propylene Oxide, and Norbornene Anhydride Isomer: Roles of Anhydride Conformation Consideration

Journal

Publisher

WILEY
DOI: 10.1002/pola.27057

Keywords

block copolymer; carbon dioxide; copolymerization; poly(ester-b-carbonate); synthesis

Funding

  1. National Nature Science Foundation of China (NSFC) [51373046, 50973026]
  2. Program for New Century Excellent Talents in University [NCET-10-0125]
  3. Open Foundation of the State Key Laboratory of Fine Chemicals of Dalian University of Technology [KF013]
  4. Open Foundation of the State Key Laboratory of Molecular Engineering of Polymer (Fudan University, China)

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This article describes an efficient synthetic route of defined reactive polyester-block-polycarbonate copolymers, utilizing a bifunctional SalenCoNO(3) complex as catalyst for the single-step terpolymerization of norbornene anhydride (NA), propylene oxide, and carbon dioxide. The geometric isomer of NA plays an important role in polymerization efficacy and the resulting polymer microstructure, including carbonate content, sequence isomer of polycarbonate moiety, and molecular weight. A hydroxyl-functionalized polyester-polycarbonate block copolymer was synthesized by a thiol-ene reaction. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014, 52, 789-795

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