Protonation constants of some substituted salicylideneanilines have been determined in ethanol-water mixtures at ionic strength of 0.1 M and at 25°C. A potentiometric method was used and calculation was done by Martell's and Motekaitis' PKAS computer programme. The trend in the values of protonation
Protonation constants of some substituted salicylideneanilines in dioxan—water mixtures
✍ Scribed by Turgut Gündüz; Esma Kiliç; Esin Canel; Fitnat Köseo > glu
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 543 KB
- Volume
- 282
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
Sixteen Schiffs bases have been prepared from sahcylaldehyde and substituted anilines and their stoichiometric protonation constants have been determined in dioxan-water mixtures of 30, 40, 50 and 60% dioxan (v/v) using a combined pH electrode at 25"C, under nitrogen atmosphere. The calculation of the constants has been carried out using a PRAS computer programme. The effects of the substituents on the protonation constants and the additivities of these effects are dhxussed. Furthermore, it was found that the log KOH value increases but the log Km value decreases for all Schiffs bases if the percentage of dioxan is increased.
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