Switching-On Fluorescence by Copper (II) and Basic Anions: A Case Study with a Pyrene-Functionalized Squaramide

Molecules. 2021 Feb 28;26(5):1301. doi: 10.3390/molecules26051301.

Abstract

The new symmetric acyclic N,N'-bis(1-pyrenyl) squaramide (H2L) functionalized with the pyrene moiety as a fluorogenic fragment has been designed and its ability to selectively detect specific anions and metals investigated. H2L selectively binds Cl- both in solution (DMSO 0.5% H2O and MeCN) and in the solid state, and allows to selectively detect Cu2+ in MeCN with the formation of a 2:1 metal-receptor complex, with a green intense emission appreciable by naked eye under the UV lamp. The H2L copper complex preserves its emission properties in the presence of Cl-. The addition of basic anions (OH-, CN-, and F-) up to 10 equivalents caused the deprotonation of the squaramide NHs and a dramatic change of the emission properties of the H2L copper complex.

Keywords: DFT; anion recognition; metal sensing; squaramides; supramolecular chemistry.

MeSH terms

  • Acetonitriles / chemistry
  • Anions / chemistry
  • Coordination Complexes / chemistry*
  • Copper / chemistry*
  • Density Functional Theory
  • Models, Molecular
  • Molecular Conformation
  • Pyrenes / chemistry*
  • Quinine / analogs & derivatives*
  • Quinine / chemistry
  • Spectrometry, Fluorescence

Substances

  • Acetonitriles
  • Anions
  • Coordination Complexes
  • Pyrenes
  • squaramide
  • Copper
  • Quinine
  • acetonitrile