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A new spectrofluorimetric method has been developed for the selective detection of Cu²⁺ ions based on a benzimidazole-containing Schiff base ligand. In this study, three structurally related Schiff bases (L1, L2, and L3) were synthesized and comparatively investigated for their fluorescence response in the presence of various cations. Among them, only L3 bearing ortho-hydroxyl groups on the aromatic rings exhibited a notable fluorescence quenching effect upon interaction with Cu²⁺, while L1 (para-hydroxyl substituted) and L2 (N, N-dimethylamino substituted) showed limited or no selectivity. The structure-function relationship revealed that the spatial orientation of donor groups plays a key role in metal coordination and signal transduction. The proposed method good sensitivity and selectivity toward Cu²⁺, with a linear response in the concentration range of 0-32 µg/L and a low detection limit of 0.98 µg/L, enabling quantification at relatively low concentrations. Furthermore, the method was tested with tap water samples. This work offers a potentially useful approach for Cu²⁺ determination but also highlights the importance of ligand geometry in fluorescent probe design.
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http://dx.doi.org/10.1007/s10895-025-04543-0 | DOI Listing |
Pol Merkur Lekarski
September 2025
I. HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY, TERNOPIL, UKRAINE.
Objective: Aim: To evaluate the state of oxidation processes and morphological changes in the heart of rats with chronic hypodynamia during the development of epinephrine heart damage (EHD)..
Patients And Methods: Materials and Methods: The study was performed on 144 white male Wistar rats.
J Phys Chem Lett
September 2025
National Laboratory of Solid State Microstructures (NLSSM), Collaborative Innovation Center of Advanced Microstructures, Frontiers Science Center for Critical Earth Material Cycling, College of Engineering and Applied Sciences, Nanjing University, Nanjing 210093, China.
The production of HO via the two-electron pathway of ORR has been widely studied. We pioneered the use of a Zn-Schiff base conductive polymer nanorod as an electrocatalyst for HO production, leveraging the Schiff base's ability to enhance electron transfer and catalytic efficiency. This novel catalyst achieved an unprecedented >98% HO selectivity with >90% stability after 1000 h.
View Article and Find Full Text PDFJ Biochem Mol Toxicol
September 2025
Department of Molecular Biology and Genetics, Faculty of Science, Bartin University, Bartin, Turkey.
Schiff bases containing sulfonyl units are important compounds because of their potential biological properties in the therapeutical field. In this study, three novel ligands (L1, L2, and L3) containing the sulfonyl groups, a derivative of Schiff base, were synthesized, and their molecular structures were characterized by FT-IR, H-NMR, C NMR, and elemental analysis results. The antiproliferative activities of these Schiff base ligands were evaluated against human colon cancer (HT-29 and Caco-2) and mouse fibroblast (L929) cells by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method.
View Article and Find Full Text PDFACS Omega
September 2025
Department of Chemistry, Faculty of Arts and Sciences, Kafkas University, 36040 Kars, Turkey.
In this study, we synthesized a series of novel -acetyl Schiff bases (-) containing 1,2,4-triazole moiety and evaluated their potential as anticancer agents through both experimental and computational approaches. Cytotoxicity assays on prostate cancer (PC) (DU145) and normal epithelial cells (PNT1a) demonstrated selective inhibition, particularly for compounds , , and , with IC values of 73.25, 49.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Polymer Institute of the Slovak Academy of Sciences, Dúbravská Cesta 9, 845 41 Bratislava, Slovakia; Polymer Materials Research Department, Advanced Technology and New Materials Research Institute (ATNMRI), City of Scientific Research and Technological Applications (SRTA-City), New Borg El-Arab Ci
This study involves the synthesis of a novel 7-ethoxy-3-formyl-2-morpholino quinoline (MQ) derivative, which was hybridized with aminated chitosan (AMCH) to yield a new AMCH-MQ Schiff base. Structural characterization via H NMR, FTIR, electronic spectra, XRD, and TGA confirmed successful hybridization. Ion exchange capacity decreased from 28.
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