ArticleJournal of fluorescence2026
Anisyl-methoxy Substituted Coumarin Derivatives as Fluorescent Sensors for Detection of Hazardous Nitroaromatics: High Selectivity Towards TNP.
Article in Journal of fluorescence, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
6 authors.
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Abstract
The detection of nitroaromatic compounds (NACs) is critically important due to their extensive use in explosive materials and the associated environmental and security risks. In this work, three structurally tailored coumarin derivatives 6-chloro-4-(4-methoxyphenoxymethyl)-chromen-2-one (S1), 1-(4-methoxyphenoxymethyl)-benzo[f]chromen-3-one (S2), and 6-methoxy-4-(4-methoxyphenoxymethyl)-chromen-2-one (S3) were explored as fluorescent probes for NAC sensing in Dimethyl sulfoxide (DMSO). Steady-state absorption, emission, and time-resolved spectroscopic investigations revealed significant fluorescence quenching upon gradual addition of nitrobenzene (NB), 2-nitrotoluene (2NT), 4-nitrotoluene (4NT), and 2,4,6-trinitrophenol (TNP). Stern-Volmer (S-V) analysis displayed positive deviations for NB, 2NT and 4NT, suggesting a combined dynamic and static quenching mechanism, whereas negative deviations observed for TNP indicates the major contribution from dynamic quenching mechanism. Fluorescence lifetime measurements confirmed dynamic quenching as the dominant pathway. Thermodynamic analysis revealed negative free energy change (ΔG
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