Potentiometric determination of the dissociation constants of weak acids in 1 mol/l KNO3: pKA's of aliphatic acyclic monoamines

1993 ◽  
Vol 345 (6) ◽  
pp. 473-474 ◽  
Author(s):  
R. Garner ◽  
J. Yperman ◽  
J. Mullens ◽  
L. C. Van Poucke
Talanta ◽  
2008 ◽  
Vol 74 (4) ◽  
pp. 1008-1013 ◽  
Author(s):  
José M. Herrero-Martínez ◽  
Carme Repollés ◽  
Elisabeth Bosch ◽  
Martí Rosés ◽  
Clara Ràfols

1973 ◽  
Vol 62 (4) ◽  
pp. 656-659 ◽  
Author(s):  
Paul J. Niebergall ◽  
Roger L. Schnaare ◽  
Edwin T. Sugita

1982 ◽  
Vol 47 (4) ◽  
pp. 1203-1215 ◽  
Author(s):  
Vladimír Dostál ◽  
Zdeněk Stránský ◽  
Jan Slouka

The dissociation constants of nitrophenoxazines in isobutyl methyl ketone (MIBK) were determined and correlated with the HNP values in acetone. Of the derivatives studied, the strongest acid is 1,3,7-trinitrophenoxazine (pK = 19.8), the weakest, 1-nitrophenoxazine (pK > 26). The compounds have no tendency to homo- or heteroconjugation, and were used as indicators in determination of weak acids in MIBK. Some derivatives of malonic acid and of 1,2,4-triazine as well as the intermediates used in their synthesis were determined; their HNP and pK values were established. The shape of the potentiometric titration curves can be of assistance in solving some structure problems.


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