Spectral-Luminescent and Ionochromic Properties of Azomethine Imine-Coumarin Conjugates
O. G. Nikolaeva, O. S. Popova, I. V. Dubonosova, O. Yu. Karlutova, A. D. Dubonosov, V. A. Bren, V. I. Minkin
Российский журнал общей химии
https://doi.org/10.1134/S1070363222050139
Azomethine imine-coumarin mono- and bis-conjugates have been synthesized for the first time. The obtained compounds represent multifunctional chromogenic and fluorescent species capable of detecting fluoride, acetate, dihydrophosphate, and cyanide anions as well as d-metal cations (Zn2+, Pb2+, Hg2+, and Cu2+) owing to the ionochromism (the naked-eye effect) and enhancing/quenching of initial ESIPT emission with anomalous Stokes shift. The monoconjugate based on 6,7-dihydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde has been found capable of selective detection of CN– anions in the presence of competing F–, AcO–, H2PO4–, Cl–, NO3–, and HSO4–ions. It has exhibited selective sensor activity towards Hg2+ cations in the presence of Na+, K+, Ca2+, Ba2+, Zn2+, Cu2+, Cd2+, Ni2+, Cu2+, and Pb2+ ions.
- Institute of Physical and Organic Chemistry, Southern Federal University, 344090, Rostov-on-Don, RussiaO. G. Nikolaeva, O. S. Popova, I. V. Dubonosova, O. Yu. Karlutova, V. A. Bren & V. I. Minkin
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