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Dostanić, J.; Lončarević, D.; Zlatar, M.; Vlahović, F.; Jovanović, D.M.
Journal of hazardous materials, 10/2016, Letnik: 316Journal Article
Display omitted •Electronic effects of para substituted arylazo pyridone dyes.•Linear relationship between Hammett σp constants and dyes photoreactivity.•The photocatalytic reactions facilitated by el.-acceptors and retarded by el.-donors.•Fukui functions to analyze the reactivity on concurrent sites within a molecule.•Hydroxyl radicals sustain attack from two reaction sites, depending on a substituent type. A series of arylazo pyridone dyes was synthesized by changing the type of the substituent group in the diazo moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The structural and electronic properties of the investigated dyes was calculated at the M062X/6-31+G(d,p) level of theory. The observed good linear correlations between atomic charges and Hammett σp constants provided a basis to discuss the transmission of electronic substituent effects through a dye framework. The reactivity of synthesized dyes was tested through their decolorization efficiency in TiO2 photocatalytic system (Degussa P-25). Quantitative structure-activity relationship analysis revealed a strong correlation between reactivity of investigated dyes and Hammett substituent constants. The reaction was facilitated by electron-withdrawing groups, and retarded by electron-donating ones. Quantum mechanical calculations was used in order to describe the mechanism of the photocatalytic oxidation reactions of investigated dyes and interpret their reactivities within the framework of the Density Functional Theory (DFT). According to DFT based reactivity descriptors, i.e. Fukui functions and local softness, the active site moves from azo nitrogen atom linked to benzene ring to pyridone carbon atom linked to azo bond, going from dyes with electron-donating groups to dyes with electron-withdrawing groups.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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