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Article Abstract

The rising challenge of developing effective antimicrobial agents to combat a broad spectrum of bacterial infections, while mitigating the risk of drug resistance, has prompted extensive exploration into alternative treatment strategies. This paper focuses on the synthesis and characterization of imidazolium-based dicationic ionic liquids with the aim of addressing this crucial healthcare need. A total of 16 distinct compounds were successfully synthesized and systematically characterized using Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) techniques. The investigation into the antibacterial activity of these ionic liquids showcased their potential as promising antimicrobial agents. Drawing on the advantageous properties of ionic liquids, such as reduced toxicity and outstanding antimicrobial efficacy. Our study specifically explores dicationic imidazolium-based ionic liquids with two different spacers: 1,3-dibromopropane and (E)-1,4-dibromobut-2-ene. Thorough analysis using H NMR, C NMR, FTIR, and TGA techniques provided valuable insights into the molecular structures and thermal properties of the synthesized compounds. Antibacterial assays were conducted to evaluate the efficacy of various combinations of these ionic liquids against bacterial strains, including Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, and Methicillin-resistant Staphylococcus aureus. Remarkably, the ionic liquids containing the bisulphate anion exhibited exceptional antibacterial results compared to other combinations. The structure-activity relationship of the most prominent ionic liquids identified in the antibacterial assays was analyzed by DFT studies. Additionally, molecular docking was employed to investigate the molecular interactions involved in the antibacterial activities. ILs can be utilized as effective candidates against infections to avoid disabilities.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12285118PMC
http://dx.doi.org/10.1186/s13065-025-01574-3DOI Listing

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