The apparent rate constants of formation and hydrolysis of the Schiff bases formed between pyridoxal and polyallylamine has been fitted to a kinetic scheme that involve the different protonated species in the reaction medium and the individual rate constants of formation (k and hydrolysis (k ). The
Determination of the rates of formation and hydrolysis of the Schiff bases of pyridoxal with polyallylamine
✍ Scribed by M.Angeles García del Vado; Angel F.Rodríguez Cardona; Gerardo R.Echevarría Gorostidi; M.Carolina González Martinez; JoséG.Santos Blanco; Francisco García Blanco
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 511 KB
- Volume
- 101
- Category
- Article
- ISSN
- 1381-1169
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✦ Synopsis
The rate constants of formation (k,) and hydrolysis ( k2 of the Schiff bases formed between pyridoxal (PL) and polyallylamine were determined as a function of pH at a temperature of 25°C and an ionic strength I = 0.1 M. The k, values obtained at every pH studied exceeded those for the Schiff bases of PL with poly-L-lysine and n-hexylamine, which is consistent with a favoured intramolecular acid catalysis of the dehydration of the intermediate carbinolamine formed in the process. The Schiff bases examined in this work lie in a hydrophobic environment and the pK for their imine group is smaller than 9.2.
📜 SIMILAR VOLUMES
The formation constants of the Schiff bases of pyridoxal %-phosphate with polyallylamine were determined over the pH range of the acetic-acetate buffer (3.9-5.5) a t an ionic strength of 0.1 M and a temperature of 25°C. The results were consistent with the rapid formation of an ionized carbinolamine