4.7 Article

Highly Cis/Trans-Stereoselective (ONSO)CrCl-Catalyzed Ring-Opening Copolymerization of Norbornene Anhydrides and Epoxides

Journal

MACROMOLECULES
Volume 49, Issue 17, Pages 6232-6239

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.6b01099

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Funding

  1. National Natural Science Foundation of China [51373046, 51473045]
  2. National Natural Science Foundation of Hebei Province [B2014202013]

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A (ONSO)CrCl complex-based binary catalyst for efficient ring-opening copolymerization (ROCOP) of epoxide and norbornene anhydride (NA) in a stereoselective manner to afford polymers with variable stereoisomerism is reported. The role of (ONSO)CrCl complex on the cis/trans selectivity of resulting polyester as well as enhancement, of the reaction rate has been revealed. The formation of chelates between the endo-diester unit of the polyester chain and the metal center plays a determinate role in the stereoselectivity of the cis-(endo, endo)-polyester in solution copolymerization of endo-NA with epoxides in the presence of metal complex. Additionally, the stereo structure of resulting polyester is also dependent on the polymerization method, NA type, and the bulkiness of the substituent of the formed ester units in the polyester chain. Accordingly, a proposed mechanistic pathway for the stereostructure formation of polyesters is provided.

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