Protolytic reactions in the ground and excited states for 2-naphthol and its sulfo derivatives were studied. It was revealed that in the presence of cationic polyelectrolyte, the acidity constant of the protolytic reaction in the ground state shifts to a more acidic region. It was also found that the value of the shift depends on the number of sulfo substituents in 2-naphthol derivatives. It reaches 1.2 units for the disodium salt of 2-naphthol-3,6,8-trisulfonic acid. At the same time, no significant effect of the polyelectrolyte on the acidity constant in the excited state pKa* was observed, and the photoprotolytic reaction proceeds in the same way as for an unimmobilized substance.
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