Preparation Characterization and Potentiometric Titrations of Some New Di 3 3 alkyl aryl 4 5 dihydro 1H 1 2 4 triazol 5 one 4 yl azomethinphenyl isophthalate terephthalate Derivatives
Yazarlar (2)
Yüksek Haydar
Gürsoy-Kol Özlem
| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Turkish Journal of Chemistry | ||
| Dergi ISSN | 1300-0527 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 12-2008 |
| Cilt / Sayı / Sayfa | 32 / 6 / 773–784 | DOI | – |
| Özet |
| 3-Alkyl(Aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) reacted with di-(3-formylphenyl) isoph-thalate (3) and di-(3-formylphenyl) terephthalate (6) to afford the corresponding 6 novel di-[3-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol~5-one-4-yl)-azomethinphenyl] isophthalates (4) and 6 novel di-[3-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethinphenyl] terephthalates (7), respectively. The acetylation reactions of compounds 4 and 7 were investigated, and 5 and 8 type compounds were obtained, respectively. The new compounds synthesized were characterized by using IR, $^1H-NMR$, $^{13}C-NMR$, and UV spectral data together with elemental analysis. In addition, to investigate the effects of solvents and molecular structure upon acidity, compounds 4 and 7 were titrated potentiometrically with tetrabutylammonium hydroxide in 5 non-aqueous solvents (isopropyl alcohol, tert-butyl alcohol, N,N-dimethylformamide, acetone, and dimethyl sulfoxide). The half-neutralization potential values and the corresponding pKa values were determined for all cases. |
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