Super Chirality Promotion of Helical Poly(Phenyl Isocyanide)s by Grafting onto Ethyl Cellulose

  • Xiaofei Shen
  • , Hailong Huang
  • , Hao Qian
  • , Longxiang Tang
  • , Yan Zhang
  • , Min Xu
  • , Huiqing Wang*
  • , Zhongkai Wang*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Chiral property of cellulose can be transferred to final materials, here artificial helical polymer, right-handed helical poly(phenyl isocyanide) (PPI) is grafted onto ethyl cellulose (EC) with expecting to enhance the chiral effect of PPI. EC-2,3-g-PPIn copolymers are prepared via “click” chemistry of copper-catalyzed alkyne-azide cycloaddition, and confirmed by high-resolution 1H and 13C NMR, Fourier transform infrared spectroscopy (FTIR), and gel permeation chromatography (GPC). The resulting EC-2,3-g-PPIn copolymer takes a right-handed helical structure with super circular dichroism intensity which is 302% higher than that of PPI, which indicates that EC backbone promotes the right-handed chirality of PPIn. Furthermore, EC-2,3-g-PPIn exhibits good chiral recognition ability of the D/L-Ala-DNSP fluorescent probe, and induces a uniquely visible blue shift for L-Ala-DNSP. Therefore, a novel facile strategy is provided to highly improve chiral property and chiral recognition ability of artificial helical polymers by grafting onto EC.

Original languageEnglish
Article number2100103
JournalMacromolecular Chemistry and Physics
Volume222
Issue number15
DOIs
StatePublished - Aug 2021

Keywords

  • chiral recognition
  • click chemistry
  • ethyl cellulose
  • poly(phenyl isocyanide)

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