Water-recyclable and reusable fluorescent sensors for nerve gas mimetic detection.

Herein, the serendipitous discovery of two water-recyclable and reusable fluorescent sensors IMPC (cyan-blue-cyan) and IMPC-OH (green-blue-green) is reported for sensing nerve agent simulants diethylcyanophosphonate and diethylchlorophosphate, respectively, with high sensitivity, short response time, and low detection limits. The unique features of these probes are their regeneration with the addition of a green and cheap solvent, namely water in CHCl3, and ease of fabrication into a portable paper-strip system that can also be regenerated. Various spectroscopic studies were employed to understand the mechanism of sensing and regeneration of both probes; the results reveal that water plays a critical role in the hydrolysis of the adduct formed with DCNP and DCP, which enables the retrieval of the probe with its original fluorescence.

Simple and efficient PET and AIEE mechanism-based fluorescent probes for sensing Tabun mimic DCNP.

The highly sensitive, selective, easy-to-prepare, aqueous media based on two novel probes 2-(pyren-1-yl)imidazo[1,2-a]pyridine (IMP-Py) and (2-(pyren-1-yl)imidazo[1,2-a]pyridin-3-yl)methanol (IMP-Py-OH) are synthesized for the detection of toxic chemical warfare nerve agent mimic diethylcyanochlorophosphonate (DCNP). Both probes are found effective in the detection of DCNP but comparatively, IMP-Py shows better properties in terms of instantaneous response, specificity, selectivity and a low detection limit of 16.9 nM. A significant enhancement of fluorescence intensity of IMP-Py due to aggregation-induced emission enhancement (AIEE) and photoinduced electron transfer (PET) phenomenon was inhibited due to phosphorylation of the hydroxy group of IMP-Py-OH in presence of DCNP has been observed. Taking the advantages of good sensitivity and fast response, probe IMP-Py has been fabricated into a viable paper strips portable product, tested for its potential for the detection of DCNP in tap water as well as with its vapor and response is visible under a UV lamp of 365 nm wavelength.

Progress in the Development of Imidazopyridine-Based Fluorescent Probes for Diverse Applications.

Different classes of Imidazopyridine i.e., Imidazo[1,2-a]pyridine, Imidazo[1,5-a] pyridine, Imidazo[4,5-b]pyridine, have shown versatile applications in various fields. In this review, we have concisely presented the usefulness of the fluorescent property of imidazopyridine in different fields such as imaging tools, optoelectronics, metal ion detection, etc. Fluorescence mechanisms such as excited state intramolecular proton transfer, photoinduced electron transfer, fluorescence resonance energy transfer, intramolecular charge transfer, etc. are incorporated in the designed fluorophore to make it for fluorescent applications. It has been widely employed for metal ion detection, where selective metal ion detection is possible with triazole-attached imidazopyridine, ß-carboline imidazopyridine hybrid, quinoline conjugated imidazopyridine, and many more. Also, other popular applications involve organic light emitting diodes and cell imaging. This review shed a light on recent development in this area especially focusing on the optical properties of the molecules with their usage which would be helpful in designing application-based new imidazopyridine derivatives.