In this study, acid dissociation constants of 5,5-diphenylpyrrolidine N-aroylthiourea derivatives,
exhibiting anti(myco)bacterial activity, were determined by potentiometric titration in 30% (v/v)
acetonitrile-water hydroorganic solventat 25 ± 0.1 °C, at an ionic background of 0.1 mol / L of NaCl using the HYPERQUAD computer program. Three acid dissociation constants were determined for each
compound 1a-e and we suggest that these acid dissociation constants are related to the carboxyl, enol and enthiol groups. Stability constants of their Pt(II) and Ni(II) complexes were also determined by
potentiometric titration under the same conditions stated above using the HYPERQUAD computer
program. The ligands behave as bidentate and bind to the metal atom via the S and O atoms. In various
p...