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Detecting antibiotic residues is crucial for monitoring their excessive use in healthcare and agricultural practices. Herein, a new 3D metal–organic framework (MOF) containing {[Cd (bpyp)(sdba)]·DMF·2H2O}n (1) (bpyp = 2,5‐bis (pyrid‐4‐yl)pyridine and H2sdba = 4,4′‐sulfonyldibenzoic acid) has been designed and synthesized. MOF 1 displays sensitive detection tetracycline (TCY) with a limit of detection below 7.67 × 10−6 M in an aqueous solution. The detection mechanism involves competitive absorption between MOF 1 and antibiotics, supported by UV–vis spectroscopy and fluorescence lifetime measurements. MOF 1 exhibits a visible fluorescence response to TCY under a 254 nm UV lamp. MOF 1 is applied in the quantitative detection of TCY in lake water with the recovery based on the sensing platform was 92.26–107.54% with RSD (%) less than 4.38%, indicating outstanding reliability. [ABSTRACT FROM AUTHOR]

A novel zinc‐based metal–organic framework (Zn‐MOF), designated as [Zn3(L)(bpyp)2(HCOO)3·2DMF·H2O] (1), was synthesized using 2,5‐bis(pyrid‐4‐yl)pyridine (bpyp), 1,3,5‐benzenetricarboxylic acid (H3L), and Zn(CH3COO)2·2H2O in a DMF solution. Single‐crystal X‐ray diffraction analysis revealed that MOF 1 crystallizes in the monoclinic system with a C2/c space group, featuring a (3,5)‐connected binodal network. The structural integrity and characteristics of MOF 1 were confirmed by Fourier transform infrared (FT‐IR), thermal gravimetric analysis (TGA), powder X‐ray diffraction (PXRD), and Brunauer–Emmett–Teller (BET) analyses, showing type IV isotherms indicative of microporous structures. The photocatalytic efficiency of MOF 1 was evaluated for the degradation of various antibiotics under UV light, with nitrofurantoin (NFT) demonstrating the highest degradation rate of 83.9% at an optimal concentration of 40 ppm and catalyst loading of 5 mg. The degradation process followed a pseudo‐first‐order kinetic model with a rate constant of 0.02492 min−1. Radical trapping experiments identified superoxide radicals (O2˙−) and holes (h+) as the predominant reactive species, while hydroxyl radicals (˙OH) played a negligible role. Reusability tests over four cycles confirmed the stability and durability of MOF 1, with consistent photocatalytic performance and unchanged structural morphology as evidenced by PXRD and SEM analyses. The proposed mechanism involves photoinduced electron–hole pair generation, with subsequent formation of reactive oxygen species (ROS) facilitating NFT degradation. This study highlights MOF 1 as a promising photocatalyst for environmental remediation, specifically for the efficient degradation of pharmaceutical contaminants in aquatic systems, providing insights into its structural properties, photocatalytic activity, and underlying degradation mechanisms. [ABSTRACT FROM AUTHOR]

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A new coordination polymer (CP) with composition [Zn3(bpyp)2(TCB)2(H2O)2]n (1) has been engendered by performing reaction of Zn(II) with 1,3,5‐tris‐(4‐carboxyphenyl)benzene (H3TCB) and 2,5‐bis(pyrid‐4‐yl)pyridine (bpyp) under solvothermal condition. The single crystal X‐ray diffraction analysis for 1 suggests kgd topological behavior having resemblance with a tessellation composed of diamond shapes arranged in a star pattern and represented by the Schläfli symbol {41}2{42·62·81}. This newly designed CP exhibits optical band gap of 2.92 eV and employed as photocatalyst for photodegradation of antibiotics, namely, nitrofurazone (NFZ), chloramphenicol (CAP), sulfasalazine (SLA), oxytetracycline (OXY), and furazolidone (FZD). Among these antibiotics, 1 displays best photocatalytic activity against the photodegradation of NFZ and under optimized conditions viz. photocatalyst dosage of 15 mg, and initial NFZ concentration of 40 ppm, the CP 1 displays best catalytic performance and photo‐decomposed 93.04% NFZ with pseudo first order rate constant k of 0.04502 min−1 in 1 h. The likely photocatalytic mechanism has been evaluated using theoretical calculations. [ABSTRACT FROM AUTHOR]

A new Zn(ii) metal–organic framework, formulated as {[Zn(L)]·2.7 DMF} (1), was synthesized using a multidentate ligand 1,4-bis(triazol-1-yl)terephthalic acid (H2L). The MOF 1 adopts 3D uninodal 4-c CdSO4 topology and behaves as a luminescent chemosensor for highly selective and sensitive detection of Fe3+ and nitro-aromatics, particularly 2,4,6-trinitrophenol (TNP). In addition, the thermal stability, UV/Vis diffuse-reflection spectra and photocatalytic behaviors of 1 against organic dyes have also been investigated. The possible mechanism associated with the alleviation in the emission intensity of 1 in the presence of nitro-aromatic compounds were addressed by theoretical calculations. In addition, the photocatalytic activity of 1 against organic dyes was addressed using density of states (DOS) calculations. [ABSTRACT FROM AUTHOR]