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[Display omitted] • Fe-DP was first applied in the detection of organophophonates. • Fe-DP had highly selectivity and sensitivity for trace determination of DTPMP. • The micro-mechanism of fluorescence quenching was revealed. Diethylenetriamine pentamethylene phosphonic acid (DTPMP) is one of the most commonly used amino organic phosphonates. The existing methods for DTPMP detection are complicated, time-consuming, and cannot detect trace DTPMP in the natural environment. In the present work, the Fe-based 3,5-dimethyl pyrazole fluorescent sensor (Fe-DP) was constructed. The addition of Fe3+ to DP solution can greatly decrease the fluorescent intensity of DP, while the addition of different concentrations of DTPMP will restore the fluorescence intensity of DP to different degrees, to achieve quantitative detection of DTPMP, and the detection limit (LOD) of DTPMP was lower as 0.105 μΜ. The Fe-DP fluorescent sensor exhibited excellent anti-interference ability and good stability. Moreover, the fluorescence quenching mechanism of DP by Fe3+ was revealed by UV absorption spectrum and Multiwfn wavefunction analysis based on density function theory (DFT). The results revealed that the excitation of DP belonged to local excitation, in which the electrons were donated primarily by the N atom with double bond and redistributed within the pyrazole ring. The fluorescence quenching of adding Fe3+ was not caused by resonance energy transfer or charge transfer, which did not belong to dynamic quenching, but due to the ground state complex formed by the coordination of Fe3+ and the double bond N atom on the DP pyrazole ring. [ABSTRACT FROM AUTHOR]

[Display omitted] • The prepared Tb-MOF emits stable Tb characteristic fluorescence at 545 nm in water. • The prepared Tb-MOF can be easily recycled after the OTC detection. • Based on the fluorescence detection of OTC by Tb-MOF, a test paper that can be easily carried, monitored in real time and has a clear color change was prepared. • Tb-MOF performed excellent in detecting the concentration of OTC in actual water samples. Oxytetracycline hydrochloride (OTC) is a commonly used over-the-counter antibiotic, valued for its potent antibacterial properties. However, the inappropriate and excessive use of OTC can result in the accumulation of the drug in both the environment and human body, causing significant harm to ecosystems and human health. Therefore, the development of a fast and sensitive method for detecting OTC is of great significance. Lanthanide metal–organic frameworks (LnMOFs) can effectively excite lanthanide metals to emit long-lifetime, narrow and stable fluorescence based on the antenna effect, but their application in fluorescence sensing is rarely reported. In this work, a strongly fluorescent material Tb-MOF was synthesized by a facile solvothermal method using 1,2,4,5-phenylenetetracarboxylic acid (H 4 btec) and 1,10-phenanthroline (1,10-phen) as organic ligands and lanthanide metal Tb as the luminescent center. Tb-MOF is a stable material in water and shows excellent linearity with OTC in the concentration range of 0 ∼ 70 μM, with low detection limit (0.12 μM) and luminescence color transition from bright green to dark green during the detection process. X-ray diffraction, UV–vis absorption and fluorescence lifetime analyses revealed that the fluorescence quenching of Tb-MOF by OTC is caused by the inner filter effect in static quenching. Test strips for OTC detection were successfully prepared using Tb-MOF. These strips are not only low cost and easy to prepare but can also be used as portable sensing devices that can be easily distinguished by the naked eye during OTC testing. This study not only presents a fluorescent probe for the detection of OTC in water but also offers a practical method for converting fluorescent luminescent materials into functional devices for OTC detection. [ABSTRACT FROM AUTHOR]

[Display omitted] • Composition of dual-emitting fluorescent probes was achieved by utilizing Eu and Tb as bimetallic centers. • First proposed dual-emission ratio sensor constructed with diaminoterephthalic acid. • Emission color conversion by adjusting the doping ratio of Eu and Tb. • The probe enables ratiometric sensing of furacilin and has excellent sensitivity and low detection limits. Lanthanide metal–organic frameworks (LnMOFs) have substantial potential in luminescence due to their unique antenna effect. Nevertheless, the single emission is susceptible to pseudo-signals caused by external environmental conditions, which significantly threaten the accurate measurement of the concentration. In this case, we prepared a dual-emission fluorescent probe {Eu x Tb 1-x (NH 2 -BDC) 3 (DMF) 4 ·2DMF} ∞ (NH 2 -BDC = Diaminoterephthalic acid, DMF = N , N -dimethylformamide). The stable dual-emission signal provides a superior signal output for detecting nitrofurazone (NFZ), which is detected by the probe with excellent fluorescence for 0–10 μM NFZ. In the investigation of the detection mechanism, it is speculated that NFZ incorporates with probe to generate a novel complex. Furthermore, The UV absorption curves of the novel complexes and NFZ overlap extensively with those of the probe. The addition of NFZ attenuates the characteristic luminescence of Eu and Tb by competing for the absorption of the excitation light of the probe. The probe has exhibits rapid response, excellent sensitivity, visual detection and a meagre detection limit (LOD = 0.013 μ M) for the detection of NFZ. This work not only broadens the application of LnMOFs in the field of ratiometric detection but also provides a favorable fluorescent probe for the quantitative detection of NFZ. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fluorescent quantitative detection of Cu2+ realized by L-cysteine modified ZnS. • The formation of ground state complexes is verified by experiments and simulations. • Fluorescence quenching mechanism of the probe by Cu2+ revealed by simulation. L-cysteine (L-Cys) capped ZnS fluorescent probe (L-ZnS) were synthesized by binding ZnS nanoparticles in situ with L-Cys, the fluorescence intensity of L-ZnS increased more than 3.5 times than that of ZnS due to the cleavage of S–H bonds and the formation of Zn–S bonds between the thiol group of L-Cys and ZnS. The addition of copper ions (Cu2+) can effectively quench the fluorescence of L-ZnS to realize the rapid detection of trace Cu2+. The L-ZnS showed high sensitivity and selectivity to Cu2+. The LOD (limit of detection) of Cu2+ was as low as 7.28 nM and linearity in the concentration range of 3.5–25.5 μM. Meanwhile, for the first time, electron localization function (ELF), bond order density (BOD), and natural adaptive orbital (NAdO) analysis in the Multiwfn wavefunction program based on density functional theory were carried out to probe the binding sites and binding mode of L-Cys with Cu2+, it indicated that the deprotonated carboxyl oxygen atoms of L-Cys had the lowest electrostatic potential (ESP) and provided lone pair electrons to coordinate with Cu2+ to form non-luminescent ground state complexes, which led to fluorescence quenching of L-ZnS. From the microscopic point of view of atoms, the mechanism of fluorescence enhancement of L-Cys capped ZnS and the mechanism of fluorescence quenching after adding Cu2+ were revealed in depth, the theoretical analysis results were accordance with the experiments. [ABSTRACT FROM AUTHOR]

[Display omitted] • CuMnS as a fluorescent probe for the first time and used for the detection of OTC. • CuMnS performs excellently for OTC in actual river water and tap water detection. • Reveal the microscopic mechanism of fluorescence quenching of CuMnS by OTC. The novel CuMnS nanoflower fluorescent probe based on Mn-doped CuS was developed to achieve the fluorescence detection of oxytetracycline hydrochloride (OTC), the fluorescent sensor has good selectivity and stability. The doping of Mn significantly increased the fluorescence intensity of CuS, which was above 10 times that of CuS. When the predominant species of OTC molecule was zwitterionic OTC+/−at the solution pH of about 5.00, the fluorescence quenching efficiency of CuMnS by OTC reached the highest. Through fluorescence lifetime and UV absorption, the sensing mechanism between CuMnS and OTC was found to be static quenching. Moreover, Multiwfn wavefunction analysis program based on density function theory (DFT) calculation was applied to compare the interactions between different OTC species and CuMnS at different pH, to reveal the micromechanism of fluorescence quenching of CuMnS by OTC from the views of atoms. The molecular surface quantitative analysis and basin analysis of different OTC species demonstrated that the N atom and O atoms of tricarbonylamide moiety of zwitterionic OTC+/− can provide lone pair electrons to form a non-fluorescent ground state complex with CuMnS. Meanwhile, the electrostatic attraction of OTC+/− with negatively charged CuMnS was also beneficial to the interaction, resulting in the effective fluorescence quenching of CuMnS. This work offers a convenient method for sensitively detecting OTC and broadens the application of CuMnS in the field of fluorescence detection. [ABSTRACT FROM AUTHOR]

[Display omitted] • • A novel fluorescent probe based on Ag 2 S QDs/g-C 3 N 4 composites was developed to detect nitrofurazone (NFZ) sensitively. • • Excellent recognition ability could reach as low as 0.054 μM. • •The detection mechanism based on formation of non-fluorescent ground state complex was demonstrated. • • The fluorescent probe has been successfully applied to detect NFZ in real water samples. In the paper, a novel fluorescent probe based on Ag 2 S QDs/g-C 3 N 4 composite was synthesized by loading Ag 2 S quantum dots (Ag 2 S QDs) on the surface of g-C 3 N 4 through in-situ synthesis method and developed to detect Nitrofurazone (NFZ) sensitively. The results showed that the linear detection range of Ag 2 S QDs/g-C 3 N 4 to NFZ was 0–30 μM, with a low detection limit of 0.054 μM. The results of time-fluorescence-resolved spectroscopy and UV–vis absorption spectroscopy exhibited that the possible detection mechanism of Ag 2 S QDs/g-C 3 N 4 to NFZ was proposed to be Internal Filtration Effect (IFE). Moreover, Multiwfn wavefunction analysis was employed to uncover the possible interaction between the Ag 2 S QDs/g-C 3 N 4 and NFZ, thereby further revealing the fluorescence detection mechanism from the scale of atoms. Combining experiments and theoretical calculations, we proposed the sensing mechanism of the formation of non-fluorescent ground state complex linked by hydrogen bonds. This work indicated that the Ag 2 S QDs/g-C 3 N 4 composite processed the ability to detect NFZ efficiently and sensitively. [ABSTRACT FROM AUTHOR]