BODIPY- and Porphyrin-Based Sensors for Recognition of Amino Acids and Their Derivatives

Molecules. 2020 Oct 2;25(19):4523. doi: 10.3390/molecules25194523.

Abstract

Molecular recognition is a specific non-covalent and frequently reversible interaction between two or more systems based on synthetically predefined character of the receptor. This phenomenon has been extensively studied over past few decades, being of particular interest to researchers due to its widespread occurrence in biological systems. In fact, a straightforward inspiration by biological systems present in living matter and based on, e.g., hydrogen bonding is easily noticeable in construction of molecular probes. A separate aspect also incorporated into the molecular recognition relies on the direct interaction between host and guest with a covalent bonding. To date, various artificial systems exhibiting molecular recognition and based on both types of interactions have been reported. Owing to their rich optoelectronic properties, chromophores constitute a broad and powerful class of receptors for a diverse range of substrates. This review focuses on BODIPY and porphyrin chromophores as probes for molecular recognition and chiral discrimination of amino acids and their derivatives.

Keywords: BODIPY; chiral discrimination; covalent recognition; molecular recognition; porphyrin tweezers.

Publication types

  • Review

MeSH terms

  • Amino Acids / analysis*
  • Boron Compounds / chemistry*
  • Ions
  • Models, Molecular
  • Molecular Probes / chemistry
  • Porphyrins / chemistry*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Amino Acids
  • Boron Compounds
  • Ions
  • Molecular Probes
  • Porphyrins