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 pyridine derivatives in ethanol-water mixtures
✍ Scribed by Esma Kiliç; Fitnat Köseogǧlu; Özlem Başgut
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 533 KB
- Volume
- 294
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
Protonation constants of a number of mono-and disubstituted pyridines were determined potentiometrically in 0, 10, 20, 30, 40, 50, 60, 70, 80% (v/v) ethanol-water mixtures at 25°C with an ionic strength of 0.1 M. Data were calculated by a computer programme. The logarithm of the protonation constants of pyridines linearly decreased with increase of ethanol contents but the values determined in water and 80% ethanol did not follow this linear trend. Furthermore, the effects of the substituents on the basicity of pyridine, the additivities of these effects and the applicability of the Hammett equation to the behaviour of substituents are discussed.
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