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• W2048693707 endingPage "686" @default.
• W2048693707 startingPage "678" @default.
• W2048693707 abstract "A series of novel Schiff's bases have been synthesized from 3-(1,3-benzothiazol-2-yl)-2-hydroxynaphthalene-1-carbaldehyde. The presence of hydroxyl group ortho to the benzothiazolyl group as well as the imine linkage lead to the occurrence of excited state intramolecular proton transfer process. The computational strategy was used to study the ESIPT process of the synthesized Schiff's bases, which revealed surprisingly that the keto form predominantly exists in the ground state contradicting the ESIPT process. Density functional theory and time dependent density functional theory have been used to investigate the structural parameters and photophysical properties in different solvents of one of the Schiff's bases. The experimental results correlate well with the computed results. All Schiff's bases show good thermal stability." @default.
• W2048693707 created "2016-06-24" @default.
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• W2048693707 date "2014-11-01" @default.
• W2048693707 modified "2023-09-25" @default.
• W2048693707 title "Photophysical properties of Schiff’s bases from 3-(1,3-benzothiazol-2-yl)-2-hydroxy naphthalene-1-carbaldehyde" @default.
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• W2048693707 doi "https://doi.org/10.1016/j.saa.2014.05.029" @default.
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• W2048693707 hasPublicationYear "2014" @default.
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