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Understanding the Selective-Sensing Mechanism of Al3+ Cation by a Chemical Sensor Based on Schiff Base: A Theoretical Approach

dc.contributor.authorTreto-Suárez M.A.
dc.contributor.authorHidalgo-Rosa Y.
dc.contributor.authorSchott E.
dc.contributor.authorZarate X.
dc.contributor.authorPáez-Hernández D.
dc.date.accessioned2020-09-02T22:29:24Z
dc.date.available2020-09-02T22:29:24Z
dc.date.issued2019
dc.identifier10.1021/acs.jpca.9b03366
dc.identifier.citation123, 32, 6970-6977
dc.identifier.issn10895639
dc.identifier.urihttps://hdl.handle.net/20.500.12728/6443
dc.descriptionA methodology that allows us to explain the experimental behavior of a turn-on luminescent chemosensor is proposed and verified in 1-[(1H-1,2,4-triazole-3-ylimino)-methyl]-naphthalene-2-ol] (L1), selective to Al3+ cations. This sensor increases its emission when interacting with ions upon excitation at 442 nm, which is denoted as the chelation-enhanced fluorescence effect. Photoinduced electron transfer is responsible for the fluorescence quenching in L1 at 335 nm, in Ni2+/L1 at 385 nm, and in Zn2+/L1 at 378 nm. In Ni2+/L, ligand-to-metal charge transfer (LMCT), from the molecular orbital of the ligand to the Ni 3dx 2 - y2 orbital, can contribute to the quenching of fluorescence. Based on oscillator strength, the highest luminescence intensity of L1 at 401 nm and that of Al3+/L1 at 494 nm in relation to the others is evidenced. The consideration of the relative energies of the excited states and the calculation of the rate and lifetime of the electron transfer deactivation are necessary to get a good description of the sensor. Copyright © 2019 American Chemical Society.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.titleUnderstanding the Selective-Sensing Mechanism of Al3+ Cation by a Chemical Sensor Based on Schiff Base: A Theoretical Approach
dc.typeArticle


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