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 ±
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 pH conditions, the different
complex forms were formulated as ML2, MHL2, MH2L2,
MH3L2, MH4L2, MH5L2
and MH-4L2 between Pt2+/Ni2+ ions
and 5,5-diphenylpyrrolidine N-aroylthioureas. Stability
constants of the complexes show that the ligands 1a-e form complexes with Pt(II) and Ni(II) metals as 2:1. The
stability of the complexes formed by the ligands and platinum were found to
follow the order: 3d > 3a > 3e > 3c > 3b. The stability of the complexes
formed by the ligands and nickel were found to follow the order: 4d > 4c > 4a > 4b > 4e. As a result, generally the platinum complexes formed with these
ligands are more stable than their nickel complexes.
Acid dissociation constant Aroylthiourea 5 5-Diphenylpyrrolidine Nickel Platinum Stability constant
Subjects | Engineering |
---|---|
Journal Section | Articles |
Authors | |
Publication Date | March 30, 2017 |
Published in Issue | Year 2017 Volume: 13 Issue: 1 |