Abstract

A coumarin coupled electron donor–acceptor dyad (HL) has been synthesized and characterized by different conventional techniques. Details spectroscopic investigation has been carried out to understand the photophysical behavior of as-prepared HL. The UV–visible spectral behavior of HL is found to be intramolecular charge transfer in nature and shows broadband, having maxima at 432 nm with a shoulder peak around 348 nm in DMF. The emission spectrum of HL also gives broadband, having maxima located at 480 nm in DMF. Further, HL is employed for the cascade detection of Al3+ ions (ON) and picric acid (PA, OFF) in DMF-H2O (7:3, v/v) media. A colorimetric change from yellow to colorless is observed in the presence of Al3+ ions. A significant fluorescence enhancement is observed due to the well coordination of Al3+ ions with HL. A visual bluish-green color could be seen under 365 nm UV light irradiation, which is also well supported by the color chromaticity diagram. The fluorescence of the HL-Al3+ complex is quenched in the presence of PA among all the tested nitroaromatic compounds. The sensitivity of HL and HL-Al3+ complex towards detection of Al3+ ions and PA can be possible down to 0.638 μM and 0.623 µM, respectively. The developed chemosensor is employed for the practical application for mapping Al3+ ions in the living cell. The performance of HL toward Al3+ ions proved that it could be exploited as a signal tool for environmental and biological samples.

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