A. Bohra et al., GROUND-STATE TRIPLE PROTON-TRANSFER IN 7-HYDROXYQUINOLINE .4. OBSERVATION IN ROOM-TEMPERATURE METHANOL AND AQUEOUS-SOLUTIONS, Journal of physical chemistry, 98(44), 1994, pp. 11424-11427
The stabilization of the ground-state keto tautomer of 7-hydroxyquinol
ine (7HQ) has been observed in room-temperature methanol and aqueous s
olutions. Concentration studies have shown that the 7HQ cyclic dimer i
s formed at high 7HQ concentrations in methanol and water, and either
the 7HQ-(MeOH)(2) or the 7HQ-water complex, presumably the cyclic 7HQ-
(H2O)(2) structure, is formed at low 7HQ concentrations in methanol or
water solvents, respectively. These species give rise to the keto-tau
tomer excitation band centered at 398 nm (7HQ dimer in water), 420 nm
(7HQ dimer in methanol), 377 nm (7HQ-water complex), and 387 nm (7HQ-m
ethanol complex). The emission band for all species appears at 520 nm.
This is the first report of the ground-state stabilized keto tautomer
spectrum in methanol at room temperature. The spectrum in water has b
een investigated in the past, but the interpretation differs from that
of this work.