Pyridyl thioureas as switchable anion receptors

Chem Commun (Camb). 2006 Nov 28:(44):4578-80. doi: 10.1039/b611138f. Epub 2006 Sep 26.

Abstract

The binding selectivity of simple pyridyl thioureas in acetonitrile can be completely switched by protonation; hence the neutral thiourea binds acetate, but not chloride or bromide, whereas the protonated thiourea binds strongly to chloride or bromide, but is deprotonated by acetate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / chemistry
  • Anions / chemical synthesis
  • Anions / chemistry
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Molecular Structure
  • Protons*
  • Pyridines / chemistry*
  • Sensitivity and Specificity
  • Stereoisomerism
  • Thiourea / analogs & derivatives*
  • Thiourea / chemical synthesis
  • Thiourea / chemistry*

Substances

  • Acetates
  • Anions
  • Protons
  • Pyridines
  • Thiourea