Prediction of Setschenow constants of N-heteroaromatics in NaCl solutions based on the partial charge on the heterocyclic nitrogen atom

Environ Sci Pollut Res Int. 2016 Feb;23(4):3399-405. doi: 10.1007/s11356-015-5544-x. Epub 2015 Oct 21.

Abstract

The solubilities of 19 different kinds of N-heteroaromatic compounds in aqueous solutions with different concentrations of NaCl were determined at 298.15 K with a UV-vis spectrophotometry and titration method, respectively. Setschenow constants, Ks, were employed to describe the solubility behavior, and it is found that the higher ring numbers of N-heteroaromatics gave rise to the lower values of Ks. Moreover, Ks showed a good linear relationship with the partial charge on the nitrogen atom (QN) for either QN > 0 or QN < 0 N-heteroaromatics. It further revealed that QN was well-matched in the prediction of salting-out effect for N-heteroaromatics compared to the conventional descriptors such as molar volume (VH) and the octanol-water partition coefficient (Kow). The heterocyclic N in N-heteroaromatics may interact with Na(+) ions in NaCl solution for QN < 0 and with Cl(-) for QN > 0.

Keywords: N-heteroaromatics; Partial charge; Salting-out effect; Setschenow constant; Solubility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Octanol / chemistry
  • Heterocyclic Compounds / chemistry*
  • Nitrogen / chemistry*
  • Sodium Chloride / chemistry*
  • Solubility
  • Solutions
  • Water / chemistry

Substances

  • Heterocyclic Compounds
  • Solutions
  • Water
  • Sodium Chloride
  • Nitrogen
  • 1-Octanol