Tuning and dissecting electronic and steric effects in ammonium receptors: nonactin vs artificial receptors

J Am Chem Soc. 2002 May 15;124(19):5374-9. doi: 10.1021/ja0174175.

Abstract

Ion selective electrodes (ISE) based on three different tripodal receptors (5, 6, and 7) have been investigated for sensing ammonium ion. Each receptor is based on three pyrazole groups that can accept three H-bonds from the bound ammonium ion. The receptor based on 4-bromo-3,5-dimethylpyrazole (6) is the most sensitive with a detection limit for ammonium ion of 2.5 x 10(-5) M at pH 8. The detection limits for the receptors based on 2,3-dimethylpyrazole (5) and unsubstitued pyrazole (7) are 1.0 x 10(-4) and 2.0 x 10(-4) M, respectively. The selectivities of the receptors 5, 6, and 7 for sensing ammonium ion over potassium ion (logK(NH)4+(/K)+) are -2.8, -2.3, and -1.7, respectively. In contrast, the detection limit and the selectivity of a nonactin-based ISE are 2.2 x 10(-5) M and -1.3, respectively. Crystallographic studies reveal that 6 accepts three H-bonds from the bound ammonium and singly protonated receptor 5 forms three H-bonds with the bound water molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry*
  • Crystallography, X-Ray
  • Electrodes
  • Hydrogen-Ion Concentration
  • Kinetics
  • Macrolides / chemistry*
  • Molecular Structure
  • Pyrazoles / chemistry*
  • Quaternary Ammonium Compounds / chemistry*
  • Receptors, Drug / chemistry*
  • Stereoisomerism

Substances

  • Anti-Bacterial Agents
  • Macrolides
  • Pyrazoles
  • Quaternary Ammonium Compounds
  • Receptors, Drug
  • nonactin