Synthesis of new luminescent bis-azo-linkage Schiff bases containing amino-phenol and its derivative. Part I: Studying of their tautomeric, acidochromic, thermochromic, ionochromic, and photolüminesence properties

[Display omitted] •A new azo-aldehyde compound (AZ-1) and two novel bis-azo-Schiff bases (H4L1 and H4L2) were synthesized and characterized elemental analysis, IR, 1H/13C NMR, UV-vis and mass methods.•The relation between tautomeric forms (azo-imine, hydrazone-imine and azo-amine) and the properties...

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Veröffentlicht in:Journal of photochemistry and photobiology. A, Chemistry. Chemistry., 2019-07, Vol.380, p.111868, Article 111868
1. Verfasser: Özdemir, Özlem
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Sprache:eng
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Zusammenfassung:[Display omitted] •A new azo-aldehyde compound (AZ-1) and two novel bis-azo-Schiff bases (H4L1 and H4L2) were synthesized and characterized elemental analysis, IR, 1H/13C NMR, UV-vis and mass methods.•The relation between tautomeric forms (azo-imine, hydrazone-imine and azo-amine) and the properties of acidochromism, thermochromism, ionochromism were investigated in solution by UV-vis spectra.•Photochromism was studied by photoluminescence spectra. H4L1 and H4L2 emitted strong green luminescence at room temperature (λemis = 505 and 523 nm).•H4L2 exhibited an excellent colorimetric and spectral response toward acid-base and anions.•They behaved thermochromically in solution, and azo-imine tautomer was stabilized by high temperature. In this work, two novel bis-azo-linkage Schiff bases (H4L1 and H4L2) containing conjugated group (phenol ring in H4L1 and nitro-phenol ring in H4L2) were synthesized by using new azo-aldehyde compound AZ-1 (3,3′-(4-nitro-1,2-phenylene)bis(diazene-2,1-diyl)bis(2-hydroxy-5-nitrobenzaldeyde). They were characterized by elemental analysis and IR, 1H/13C NMR, UV–vis, and masss pectral techniques. Prototropic tautomeric equilibrium (azo-imine ↔ hydrazone-imine or azo-imine ↔ azo-amine), and acido-, thermo-, ionochromism in these Schiff bases were investigated by UV–vis spectroscopy. Photochromism study indicated that DMSO solution of H4L1 and H4L2 exhibits strong green luminescence at room temperature upon photoexcitation, attributed to exist as hydrazone-imine form in the excited state. Emission wavelength was 505 and 523 nm in photoluminescence spectra. On the other hand, azo-imine tautomer was stabilized by increasing of temperature in the ground state in solution for both H4L1 and H4L2. As well, H4L2 showed a selective and sensitive colorimetric sensing toward acid-base and anions (F−, CH3COO−, C2O42- and SO32-).
ISSN:1010-6030
1873-2666
DOI:10.1016/j.jphotochem.2019.111868