POTENTIOMETRIC DETERMINATION OF ANIMAL STABILITY-CONSTANTS

Potentiometric titration was used to determine the logarithms of the stepwise equilibrium constants for the species formed between morpholine and formaldehyde in aqueous solution, ionic strength 0.5 and 2.5M (KCl) at 25 degrees C. The instrumental and computational techniques developed for metal-ligand stability constant determination were applied. Formaldehyde is equivalent to the metal-ion and is represented by M while neutral morpholine is equivalent to the ligand and is represented by L. The stability constants of the following equilibria were determined by non-linear regression (figures in parentheses are at ionic strength 2.5M KCl): M + L reversible arrow ML (hemi-aminal) log K-1 = 2.90+/-0.02 (2.980+/-0.004); ML + L reversible arrow ML(2) (bis-animal); log K-2 = 1.3+/-0.2 (1.41+/-0.07); MLH reversible arrow ML + H+ (protonated hemi-aminal) pK(a) = 5.87+/-0.01 (6.411+/-0.005); ML(2)H reversible arrow ML(2) + H+ (protonated bis-aminal) pK(a) = (7.6+/-0.2). The pK(a) of the protonated bis-aminal could only be determined at the higher ionic strength. The results are in good agreement with reported values determined using the classic formol titration. The automated titration system acquired the full time course of the pH change upon each titrant addition allowing a kinetic analysis to be performed as well as an equilibrium analysis. The forward and reverse rate constants for M + L reversible arrow ML were 0.77M(-1) sec(-1) and 8.1 x 10(-4) sec(-1), respectively.