Mechanistical Insights into the Ultrasensitive Detection of Radioactive and Chemotoxic UO₂²⁺ Ions by a Porous Anionic...

Development of a simple, cost-efficient, and portable UO₂²⁺ sensory probe with high selectivity and sensitivity is highly desirable in the context of monitoring radioactive contaminants. Herein, we report a luminescent Co-based metal-organic framework (MOF), {[Me₂NH₂]_0.5[Co(DATRz)_0.5(NH₂BDC)]·xG} (1), equipped with abundant amino functionalities for the selective detection of uranyl cations. The ionic structure consists of two types of channels decorated with plentiful Lewis basic amino moieties, which trigger a stronger acid-base interaction with the diffused cationic units and thus can selectively quench the fluorescence intensity in the presence of other interfering ions. Furthermore, the limit of detection for selective UO₂²⁺ sensing was achieved to be as low as 0.13 μM (30.94 ppb) with rapid responsiveness and multiple recyclabilities, demonstrating its excellent efficacy. Density functional theory (DFT) calculations further unraveled the preferred binding sites of the UO₂²⁺ ions in the tubular channel of the MOF structure. Orbital hybridization between NH₂BDC/DATRz and UO₂²⁺ together with its significantly large electron-accepting ability is identified as responsible for the luminescence quenching. More importantly, the prepared 1@PVDF {poly(vinylidene difluoride)} mixed-matrix membrane (MMM) displayed good fluorescence activity comparable to 1, which is of great significance for their practical employment as MOF-based luminosensors in real-world sensing application.