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Thallium (Tl) has been identified as a priority contaminant because of its severe toxic effects. Exact measurement of Tl is a challenge because it is difficult to avoid altering the element's chemical speciation during sampling, transport, and storage. In situ measurement may be a good choice. Based on the in situ technique of diffusive gradients in thin films (DGT), new DGT devices equipped with novel laboratory-synthesized manganese oxide (δ-MnO 2 ) binding gels were developed and systematically validated for the measurement of Tl, including Tl(I) and Tl(III) species, in water. Comparison between Chelex binding gel and δ-MnO 2 gel on the uptake kinetics of Tl demonstrated that δ-MnO 2 binding gels could adsorb Tl rapidly and effectively. Removal of Tl from the δ-MnO 2 gels was achieved by use of 1 mol·L -1 oxalic acid, yielding elution efficiencies of 1.0 for Tl(I) and 0.86 for TI(III). Theoretical responses from DGT devices loaded with δ-MnO 2 gel (δ-MnO 2 -DGT) were obtained irrespective of pH (4-9) and ionic strength (0.1-200 mmol·L -1 NaNO 3 ). δ-MnO 2 -DGT showed good potential for long-term monitoring of Tl due to its high adsorption capacity of 27.1 μg·cm -2 and the stable performance of δ-MnO 2 binding gel kept in solution, containing only 10 mmol·L -1 NaNO 3 , for at least 117 days. Field deployment trials confirmed that δ-MnO 2 -DGT can accurately measure the time-averaged concentrations of Tl in fluvial watercourses. In summary, the newly developed δ-MnO 2 -DGT technique shows potential for environmental monitoring and biogeochemical investigation of Tl in waters.

Thallium (Tl) is an extremely toxic heavy metal and exists in very low concentrations in the environment, but its sensing is largely underexplored as compared to its neighboring elements in the periodic table (especially mercury and lead). In this work, we developed a ratiometric phosphorescent nanoprobe for thallium detection based on Mn-doped ZnSe quantum dots (QDs) and water-soluble carbon dots (C-dots). Upon excitation with 360 nm, Mn-doped ZnSe QDs and C-dots can emit long-lived and spectrally resolved phosphorescence at 580 and 440 nm, respectively. In the presence of thallium, the phosphorescence emission from Mn-doped ZnSe QDs could be selectively quenched, while that from C-dots retained unchanged. Therefore, a ratiometric phosphorescent probe was thus developed, which can eliminate the potential influence from both background fluorescence and other analyte-independent external environment factors. Several other heavy metal ions caused interferences to thallium detection but could be efficiently masked with EDTA. The proposed method offered a detection limit of 1 μg/L, which is among the most sensitive probes ever reported. Successful application of this method for thallium detection in biological serum as well as in environmental water and soil samples was demonstrated.

Thallium (Tl) is a highly toxic heavy metal situated between mercury and lead in the periodic table. While its neighbors have been thoroughly studied for DNA-based sensing, little is known about thallium detection. In this work, in vitro selection of RNA-cleaving DNAzymes is carried out using Tl(3+) as the target metal cofactor. Both normal DNA and phosphorothioate (PS)-modified DNA are tested for this purpose. While no Tl(3+)-dependent DNAzymes are obtained, a DNA oligonucleotide containing a single PS-modified RNA nucleotide is found to cleave by ∼7% by Tl(3+) at the RNA position. The remaining 93% are desulfurized. By hybridization of this PS-modified oligonucleotide with the Tm7 DNAzyme, the cleavage yield increases to ∼40% in the presence of Tl(3+) and Er(3+). Tm7 is an Er(3+)-dependent RNA-cleaving DNAzyme. It cleaves only the normal substrate but is completely inactive using the PS-modified substrate. Tl(3+) desulfurizes the PS substrate to the normal substrate to be cleaved by Tm7 and Er(3+). This system is engineered into a catalytic beacon for Tl(3+) with a detection limit of 1.5 nM, which is below its maximal contamination limit defined by the U.S. Environmental Protection Agency (10 nM).

A fluorogenic derivative of 1,3-alternate calix[4]arenebis(crown-6) (1) containing a dansyl group in the proton-ionizable side arm has been employed in selective sensing of Tl+ and Cs+ at low concentration levels in MeCN-H2O (1:1) mixed solvent. Optical recognition of these two metal cations by 1 occurs in contrasting modes. On the basis of the results of fluorescence, matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS), and 1H NMR studies, Tl+ and Cs+ react with 1 via formation of 1:1 complexes that differ in coordination arrangement around the metal ion.