Reaccion acido-base en estado excitado. Salicilamida en soluciones acuosas
Author
dc.contributor.author
Cortes, Victor Vargas
Admission date
dc.date.accessioned
2018-12-20T14:11:19Z
Available date
dc.date.available
2018-12-20T14:11:19Z
Publication date
dc.date.issued
1996
Cita de ítem
dc.identifier.citation
Boletin de la Sociedad Chilena de Quimica, Volumen 41, Issue 4, 2018, Pages 331-340
Identifier
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03661644
Identifier
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https://repositorio.uchile.cl/handle/2250/154558
Abstract
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In this work we propose a kinetic model for the reaction between the neutral and anionic species in the first singlet electronic excited state of salicylamide in aqueous solution. The radiative rate constants (k01, k02) and nonradiative transfer constants (k21 k12[H+]), are calculated employing the methodology of Global Analysis of lifetimes data of salicylamide in aqueous solution to pH 2.0,2.7 and 3.0, determined by means of the multifrequency of phase shift and modulation technique. The validity of the kinetics model is tested evaluating the lifetimes (τ1 and τ2)in function of the proton concentrations and the rate constants kjj determined by the model. The values τ1 and τ2 calculated agree with the experimental data in the pH (1.7 to 10) range studied. The acidity (K*a) of first excited electronic state is calculated by means of the ratio between the rate constants of transfer for the neutral and anionic species. The measured K*a agree with K*a determined by means of the thermodyna