# Detection of explosive picric acid via ESIPT-inhibited fluorescent chemosensor: theoretical insights, vapour phase detection and flexible indicator design

**Authors:** Pavithra S, Keshav Semwal, Vishnu S, Raksha D. Salian, Partha Kumbhakar, Avijit Kumar Das

PMC · DOI: 10.1039/d5ra05689f · RSC Advances · 2025-11-05

## TL;DR

A new fluorescent sensor detects picric acid by suppressing a proton transfer process, with potential for real-world explosive detection.

## Contribution

A novel fluorescent chemosensor for picric acid detection with vapor-phase and flexible solid-state sensing capabilities.

## Key findings

- BMP shows a 2-fold fluorescence decrease and 19-fold absorption increase upon picric acid binding.
- BMP-based polymer films enable visible fluorescence quenching for on-site explosive detection.
- The sensor has a detection limit of 4.87 μM and a Stern–Volmer constant of 14.059 M−1.

## Abstract

A fluorescent probe, (E)-2-((benzo[d]thiazol-2-ylimino)methyl)-5-(diethylamino)phenol (BMP), was designed and synthesized using 4-(diethylamino)-2-hydroxybenzaldehyde and benzothiazole-2-amine, and subsequently characterized for its selective turn-off response toward picric acid (PA). Upon the gradual addition of PA, significant changes in the absorption and fluorescence spectra were observed, marked by strong fluorescence quenching even in the presence of competing nitroaromatic compounds. BMP exhibited two absorption signals at 350 nm and 433 nm with a prominent emission band at 488 nm, attributed to excited-state intramolecular proton transfer (ESIPT), accompanied by a large Stokes shift of 138 nm. The interaction between PA and the hydroxyl group of BMP effectively suppressed the ESIPT process, leading to the observed spectral variations. The binding interactions were further confirmed through NMR spectroscopy and density functional theory (DFT) calculations. The ligand BMP has been utilized as a selective chemosensor for PA with a 2-fold reduction in fluorescence intensity and 19-fold increment in absorption intensity, showing a binding affinity of 2 × 104 M−1 and strong quenching efficiency toward picric acid, with a Stern–Volmer constant (Ksv) of 14.059 M−1 with a limit of detection (LOD) of 4.87 μM. For practical implementation, BMP was successfully employed in a dipstick-based detection format for vapor-phase sensing. Moreover, BMP-embedded polymer films demonstrated excellent potential as solid-state fluorescent sensors, exhibiting visible fluorescence quenching upon exposure to PA. Their rapid, time-dependent emission response under UV light allows for convenient, on-site detection using devices such as smartphones, making them highly promising for real-world applications in explosives detection and environmental monitoring.

A fluorescent probe, (E)-2-((benzo[d]thiazol-2-ylimino)methyl)-5-(diethylamino)phenol, was synthesized using 4-(diethylamino)-2-hydroxybenzaldehyde and benzothiazole-2-amine, and characterized for its selective turn-off response toward picric acid.

## Linked entities

- **Chemicals:** picric acid (PubChem CID 6954), 4-(diethylamino)-2-hydroxybenzaldehyde (PubChem CID 87293)

## Full-text entities

- **Chemicals:** PA (MESH:C005858), (E)-2-((benzo[d]thiazol-2-ylimino)methyl)-5-(diethylamino)phenol (-), polymer (MESH:D011108), 4-(diethylamino)-2-hydroxybenzaldehyde (MESH:C585236)

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12587293/full.md

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Source: https://tomesphere.com/paper/PMC12587293