Synthesis of Ir(III) complexes improves detection of trinitrophenols in water, suggesting effective monitoring strategies.
Three fluorophenyl-substituted cyclometalated Ir(III) complexes (Ir1–Ir3) have been synthesized by changing the position of the fluorine atom. All complexes exhibit distinct aggregation-induced phosphorescence emission (AIPE) characteristics in CH3CN/H2O and demonstrate satisfactory detection performance for 2,4,6-trinitrophenols (TNPs) with limits of detection of 124 nM, 101 nM, and 127 nM, respectively. In addition, Ir1–Ir3 possess excellent selectivity and anti-interference capability for TNP detection, showing outstanding performance even in different common water samples. The ultraviolet–visible absorption spectra and luminescence lifetimes of the complexes show that their quenching processes include both a static process and dynamic process, and the detection mechanism may be assigned to a combination of photo-induced electron transfer and an inner-filter effect.
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Du et al. (2025) studied this question.
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