4.8 Article

Development of Highly Active and Regioselective Catalysts for the Copolymerization of Epoxides with Cyclic Anhydrides: An Unanticipated Effect of Electronic Variation

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 138, Issue 22, Pages 7107-7113

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b03113

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Funding

  1. Center for Sustainable Polymers, an NSF Center for Chemical Innovation [CHE-1413862]
  2. NSF IGERT program
  3. NSF GRFP [DGE-1144153]
  4. Direct For Mathematical & Physical Scien
  5. Division Of Chemistry [1413862] Funding Source: National Science Foundation

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Recent developments in polyester synthesis have established several systems based on zinc, chromium, cobalt, and aluminum catalysts for the ring-opening alternating copolymerization of epoxides with cyclic anhydrides. However, to date, regioselective processes for this copolymerization have remained relatively unexplored. Herein we report the development of a highly active, regioselective system for the copolymerization of a variety of terminal epoxides and cyclic anhydrides. Unexpectedly, electron withdrawing substituents on the salen framework resulted in a more redox stable Co(III) species and longer catalyst lifetime. Using enantiopure propylene oxide, we synthesized semicrystalline polyesters via the copolymerization of a range of epoxide/anhydride monomer pairs.

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