Halogen-Bonding Strapped Porphyrin BODIPY Rotaxanes for Dual Optical and Electrochemical Anion Sensing

Chemistry. 2021 Oct 19;27(58):14550-14559. doi: 10.1002/chem.202102493. Epub 2021 Sep 6.

Abstract

Anion receptors employing two distinct sensory mechanisms are rare. Herein, we report the first examples of halogen-bonding porphyrin BODIPY [2]rotaxanes capable of both fluorescent and redox electrochemical sensing of anions. 1 H NMR, UV/visible and electrochemical studies revealed rotaxane axle triazole group coordination to the zinc(II) metalloporphyrin-containing macrocycle component, serves to preorganise the rotaxane binding cavity and dramatically enhances anion binding affinities. Mechanically bonded, integrated-axle BODIPY and macrocycle strapped metalloporphyrin motifs enable the anion recognition event to be sensed by the significant quenching of the BODIPY fluorophore and cathodic perturbations of the metalloporphyrin P/P+. redox couple.

Keywords: BODIPY; anion sensing; electrochemical sensing; optical sensing; porphyrins; rotaxanes.

MeSH terms

  • Anions
  • Boron Compounds
  • Halogens
  • Hydrogen Bonding
  • Porphyrins*
  • Rotaxanes*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Anions
  • Boron Compounds
  • Halogens
  • Porphyrins
  • Rotaxanes