𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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


Schiff bases of pyridoxal and polyallyla
✍ M. Angeles García Del Vado; Gerardo R. Echevarría Gorostidi; Andrea Basagoitía; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 146 KB 👁 2 views

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 rate of formation o
✍ M. Angeles Garcí Del Vado; Angel F. Rodríguez Cardona; Gerardo R. Echevarría; Jo 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 586 KB

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