4.7 Article

Organocatalyzed Photoredox Polymerization from Aromatic Sulfonyl Halides: Facilitating Graft from Aromatic C-H Bonds

Journal

MACROMOLECULES
Volume 51, Issue 3, Pages 938-946

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.8b00134

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Funding

  1. NSFC [21704016]
  2. National Program for Thousand Young Talents of China, Fudan University
  3. State Key Laboratory of Polymer Physics and Chemistry

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Aromatic sulfonyl halides are readily accessible from many sources. With newly synthesized N-arylphenothiazine catalysts, organocatalyzed photoredox polymerization has been developed with arylsulfonyl halides initiators using white or purple LEDs light sources. This method allows the preparation of poly(meth)acrylates and poly(meth)acrylamides possessing a broad scope of (hetero)aryl chain ends without metal-contamination concern. Investigations such as MALDI-TOF analysis, chain extension, and ON/OFF control experiments confirmed the fidelity of the polymer structure and reliability of this method. Moreover, this method facilitates the two-step preparation of brush polymers from polystyrene through an electrophilic aromatic substitution/organocatalyzed photopolymerization sequence.

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