Novel 5,5-diphenylpyrrolidineN-aroylthioureas,
containing 4-methylbenzoyl, 2-chlorobenzoyl,2,4-dichlorobenzoyl,
and2-naphthoyl, were synthesized and their structural analysis was performed
using 1H nuclear magnetic resonance (NMR), 13C
NMR, Fourier transform infrared spectroscopy, mass spectrometry (MS), and high-resolution
MS (HRMS) techniques. The acid dissociation constants of the
5,5-diphenylpyrrolidineN-aroylthiourea
derivative compounds were determined using Hyperquad computer program for data
obtained using potentiometric titration method in 25% (v/v) dimethyl
sulfoxide–water hydroorganic solvent in the presence of 0.1 mol×L-1 ionic strength of NaCl and in the acidic medium
at 25±0.1°C, using sodium hydroxide base as a titrant. Two acid dissociation
constants were obtained for 3a, 3b, and 3d, and it was suggested that
they were related to N-H and enol groups. Furthermore, three acid dissociation
constants obtained for 3a indicated
that they were related to N-H, enthiol, and enol groups, and four acid
dissociation constants obtained for 3c suggested
that they were related to N-H, enthiol, enol, and carboxyl groups.
Acid dissociation constant Aroylthiourea 5-Diphenylpyrrolidine Potentiometric titration
Birincil Dil | İngilizce |
---|---|
Konular | Mühendislik, Kimya Mühendisliği |
Bölüm | Makaleler |
Yazarlar | |
Yayımlanma Tarihi | 15 Ağustos 2017 |
Gönderilme Tarihi | 31 Temmuz 2017 |
Kabul Tarihi | 10 Ağustos 2017 |
Yayımlandığı Sayı | Yıl 2017 Cilt: 4 Sayı: 3 |