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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 593-597 
    ISSN: 0894-3230
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study of the acid-base behaviour of the three isomeric pyridinecarboxylic acids (picolinic, nicotinic and isonicotinic acid) was carried out using spectrophotometric and potentiometric measurements. The cationic form of picolinic acid converts partially into the corresponding zwitterion (pK1) within a borderline acidity range where neither the pH scale nor the acidity functions work satisfactorily. Protonation of the carboxyl groups (pK33) occurred at the highest acidity levels employed. The medium effects observed on the spectral curves were corrected by factor analysis. The potentiometric measurements gave values for pK1 and pK2 only, which were in good agreement with those determined spectrophotometrically.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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