Synthesis and characterization of linear 1,4-diazine-triphenylamine–based selective chemosensors for recognition of nitroaromatic compounds and aliphatic amines

Novel 1,4-diazine-based dyes of the D–π–A type, possessing triphenylamine as an electron-donating group, have been developed. Fluorescence studies have demonstrated that emission of these fluorophores is sensitive towards different nitroaromatic compounds and aliphatic amines, both in solutions and...

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Published in:Dyes and pigments 2020-07, Vol.178, p.108344, Article 108344
Main Authors: Verbitskiy, Egor V., Kvashnin, Yuriy A., Baranova, Anna A., Khokhlov, Konstantin O., Chuvashov, Roman D., Schapov, Il'ya E., Yakovleva, Yuliya A., Zhilina, Ekaterina F., Shchepochkin, Aleksandr V., Makarova, Nadezhda I., Vetrova, Elena V., Metelitsa, Anatoly V., Rusinov, Gennady L., Chupakhin, Oleg N., Charushin, Valery N.
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Language:eng
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Summary:Novel 1,4-diazine-based dyes of the D–π–A type, possessing triphenylamine as an electron-donating group, have been developed. Fluorescence studies have demonstrated that emission of these fluorophores is sensitive towards different nitroaromatic compounds and aliphatic amines, both in solutions and in a vapor phase. Moreover, these compounds can be considered as "naked-eye" fluorescent probes for solution polarity because they possess pronounced solvatochromic properties. Therefore, these compounds have to be regarded as potential multifunctional chemosensors for monitoring hazardous organic substances. [Display omitted] •A novel pyrazine and quinoxaline based D–(π)–A type dyes were characterization.•The observed photophysical properties have shown these as potential polarity and pH probes.•Fluorophores could also serve as a potential chemosensors to detect NACs and aliphatic amines on-site.
ISSN:0143-7208
1873-3743