Development of tissue paper-based chemosensor and demonstration for the selective detection of Cu2+ and Hg2+ ions

Heavy metals emanate from natural and man-made sources, such as agricultural chemicals including fertilisers and pesticides, medical waste, and chemicals released from industries. Detection and monitoring toxic metal ions is one of the challenges confronting scientists in biological, environmental, and chemical systems. This study describes the design and synthesis of a new imidazole-based fluorescent and colourimetric chemosensor (DPICDT) for highly selective sensing of Hg2+ and Cu2+ ions in aqueous acetonitrile medium. The probe was synthesised by coupling benzil and substituted aldehyde using ethanolic ammonium acetate. The structure of DPICDT was confirmed via IR spectra, NMR, and HR-MS spectra. The DPICDT probe displayed a rapid naked-eye response towards Cu2+ ions from colourless to red-purple and significant fluorescence quenching response towards Hg2+ over other competitive metal ions in both solution and solid support. The binding modes of DPICDT with Cu2+ and Hg2+ ions were found to be at a 1 : 1 ratio as determined using Job plot, ESI HR-MS, and the sensing mechanism was evolved by H-1 NMR titrations, HR-MS spectra, and DFT calculations. The lower detection limit was 15.1 nM for Cu2+, eventually far less than the World Health Organization guideline for drinking water (Cu2+ - 31.5 mu M) and 1.17 mu M for Hg2+ (permissible concentration 2 ppb). Promisingly, the tissue paper-based DPICDT test strips and silica-supported DPICDT were developed and demonstrated for on-site application without resorting to expensive instruments.

Automated summary

This study presents the design and synthesis of a new chemosensor, DPICDT, for the selective detection of Hg2+ and Cu2+ ions. The binding modes of DPICDT with Cu2+ and Hg2+ ions were determined to be 1:1 using different experimental methods. The detection limits for Cu2+ and Hg2+ were found to be 15.1 nM and 1.17 mu M, respectively.