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Cyanopropyl functionalized benzimidazolium salts and their silver N-heterocyclic carbene complexes: Synthesis, antimicrobial activity, and theoretical analysis

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dc.contributor.author Türker, D.
dc.contributor.author Üstün, E.
dc.contributor.author Günal, S.
dc.contributor.author Yıldız, H.
dc.contributor.author D. Düşünceli, S.
dc.contributor.author Özdemir, İ.
dc.date.accessioned 2022-10-06T12:54:21Z
dc.date.available 2022-10-06T12:54:21Z
dc.date.issued 2022
dc.identifier.issn 03656233 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/72164
dc.description.abstract The reaction of N-substituted benzimidazole with 4-bromobutyronitrile gives the corresponding benzimidazolium salts as N-heterocyclic carbene (NHC) precursors. Silver(I) carbene complexes are synthesized by the reaction of the corresponding benzimidazolium salts with Ag2O in dichloromethane. These new NHC precursors and Ag–NHC complexes were characterized by spectroscopy techniques and also screened for their antibacterial activities against the standard bacterial strains Escherichia coli, Pseudomonas aeruginosa, Acinetobacter baumannii, Klebsiella pneumoniae, Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, and Enterococcus faecalis, and the standard fungal strains Candida albicans and Candida glabrata, and promising results were achieved. The compounds were also analyzed by density functional theory (DFT)/time-dependent DFT and docking methods. © 2022 Deutsche Pharmazeutische Gesellschaft.
dc.source Archiv der Pharmazie
dc.title Cyanopropyl functionalized benzimidazolium salts and their silver N-heterocyclic carbene complexes: Synthesis, antimicrobial activity, and theoretical analysis


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