4.8 Article

Organocatalyzed Controlled Radical Copolymerization toward Hybrid Functional Fluoropolymers Driven by Light

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 12, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202215628

Keywords

Controlled Radical Polymerization; Copolymer; Fluorine; Photocatalysis; Synthetic Method

Funding

  1. NSFC [21971044, 22171051]
  2. STCSM
  3. Shanghai Pilot Program for Basic Research-Fudan University [21TQ1400100, 21TQ007]
  4. State Key Laboratory of Molecular Engineering of Polymers

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In this work, a light-driven organocatalyzed copolymerization method using TFVB was reported for the controlled synthesis of a variety of hybrid fluorine/boron polymers with low dispersities and good chain-end fidelity. The combination of fluorine and boron was shown to provide high-performance copolymer electrolytes with a high lithium-ion transference number, offering new opportunities for engineering high-performance materials for energy storage.
Photo-controlled polymerizations are attractive to tailor macromolecules of complex compositions with spatiotemporal regulation. In this work, with a convenient synthesis for trifluorovinyl boronic ester (TFVB), we report a light-driven organocatalyzed copolymerization of vinyl monomers and TFVB for the first time, which enabled the controlled synthesis of a variety of hybrid fluorine/boron polymers with low dispersities and good chain-end fidelity. The good behaviors of ON/OFF switch, chain-extension polymerizations and post-modifications further highlight the versatility and reliability of this copolymerization. Furthermore, we demonstrate that the combination of fluorine and boron could furnish copolymer electrolytes of high lithium-ion transference number (up to 0.83), bringing new opportunities of engineering high-performance materials for energy storage purposes.

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