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Schiff base complexes possess biological activity and electronic features, making them suitable for integration into both core and auxiliary components of bioelectronic technologies. However, integrated studies addressing their electrical, biological, and mechanical properties remain limited. This work investigates a Cu(II) complex based on a Schiff base ligand derived from 2-hydroxy-1-naphthaldehyde and 1,8-diaminonaphthalene. Comprehensive textural analyses using XRD, HRTEM, FESEM, AFM, and N₂ adsorption revealed high surface area, nanoscale morphology, and porosity, which are advantageous for antimicrobial and therapeutic bioelectronic platforms. Mechanical characterization via ultrasonic pulse-echo indicated auxetic behavior, a rare and valuable trait for flexible substrates. The complex also exhibited high ionic conductivity, facilitating charge transport in aqueous environments and contributing to antimicrobial efficacy through ionic disruption of microbial membranes. Thermal analyses showed a phase transition at 44 °C and decomposition onset at 70 °C. A temperature-induced insulator-to-metal transition was observed, suggesting potential for thermally activated sensing, temperature-triggered drug release, and adaptive signal modulation. Biological assays confirmed strong antimicrobial activity, with a 30 mm inhibition zone against Bacillus subtilis (agar well diffusion), and potent cytotoxicity against MCF-7 breast cancer cells, with an IC₅₀ of 18.4 μg/mL (MTT assay). These biological properties enhance the complex's biocompatibility and support its role in long-term bioelectronic device stability, particularly in applications where infection control is essential.
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http://dx.doi.org/10.1038/s41598-025-16628-8 | DOI Listing |
Chem Biodivers
September 2025
Department of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk, Republic of Korea.
One of the most significant problems facing the scientific community in the 21st century is diabetes mellitus. There is an urgent need to create new powerful compounds that can fight this terrible disease because the number of instances of diabetes and drug-resistant diabetes is rising. We have synthesized a novel series of thiazole-derived thiadiazole-based Schiff base derivatives (1-10) in an effort to identify potential antidiabetic agents.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Chemistry, Panskura Banamali College, Panskura RS, Purba Medinipur, WB 721152, India.
We report the synthesis and characterization of a new Schiff base ligand (HL), derived from 2-picolylamine and 2-hydroxy-3-methoxy-5-methylbenzaldehyde. Its reaction with Ni(NO)·6HO and Ln(NO)·HO (Ln = Gd, Tb, Dy) in the presence of triethylamine affords a carbonato-bridged family of heterobimetallic NiLn complexes: [NiLn(L)(L')(μ-CO)(NO)]·MeOH·HO (). During the complexation reaction, ligand HL undergoes an oxidation, followed by C-C coupling to generate a secondary ligand (HL').
View Article and Find Full Text PDFJ 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 PDFRSC Med Chem
August 2025
Department of Chemistry, National Institute of Technology Agartala Jirania-799046, West Tripura Tripura India.
The utility of bio-reductive prodrugs in cancer research has emerged as an attractive strategy. We synthesized and characterized a couple of cobalt(iii)-Schiff base complexes of general molecular formula Co(L)(L) and Co(L)(dox) , where L and L are ,-(ethane-1,2-diyl)bis(1-(pyridine-2-yl)methanimine) and 1-phenyl-1,3-butanedione, and dox = doxorubicin, as bio-reductive prodrugs. UV-vis and fluorescence spectroscopic assays confirmed the reductive release of doxorubicin from the complex in a GSH-dependent manner under physiological conditions, showing its potential for drug release.
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