Abstract
The formation of complexes between Mo(VI) and 8-hydroxy-quinoline (oxine) and four oxine derivatives were investigated by multiwavelength molecular absorption spectrometry, potentiometry, and polarography. The following pKOH- and pKNH- values of the ligands and logK211-values of the complexes MoO2(OH)2Lx− (x=1 or 2) were obtained at 25° C and an ionic strength of 1M(NaClO4): 5,7-dinitro8-hydroxyquinoline 4.59, <0, 14.50; 7-nitro-8-hydroxyquinoline-5-sulfonic acid 5.34, 0.41, 15.70; 7-iodo-8-hydroxyquinoline-5-sulfonic acid 6.98, 2.62, 17.65; 8-hydroxyquinoline-5-sulfonic acid 8.33, 4.13, 18.71; and 8-hydroxyquinoline 9.62, 5.28, 19.69. A good linearity was found between logK211 and the sum of the pK-values of the OH- and NH+-groups. The dependence of the peak current of Mo(VI)-determinations by adsorption polarography of the 7-nitro-8-hydroxyquinoline-5-sulfonate complex of Mo(VI) MoO(OH)3L− can quantitatively be described at pH 0.8–2 using the corresponding pK-values and the log K311 of 18.54±0.03, determined by polarography.
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