Novel benzimidazolium salts were synthesized as N-heterocyclic carbene (NHC) precursors, these NHC precursors were metallated with Ag2O in dichloromethane at room temperature to give novel silver(I)-NHC complexes. Structures of these benzimidazolium salts and silver(I)-NHC complexes were characterized on the basis of elemental analysis, (1)H NMR, (13)C NMR, IR and LC-MS spectroscopic techniques. A series of benzimidazolium salts and silver(I)-NHC complexes were tested against standard bacterial strains: Enterococcus faecalis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and the fungal strains: Candida albicans and Candida tropicalis. The results showed that benzimidazolium salts inhibited the growth of all bacteria and fungi strains and all silver(I)-NHC complexes performed good activities against different microorganisms.
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http://dx.doi.org/10.1016/j.bmc.2016.06.004 | DOI Listing |
Biochem Biophys Res Commun
December 2024
Suleyman Demirel University, Faculty of Pharmacy, Department of Basic Pharmaceutical Sciences, Isparta, 32260, Turkiye; Bahçeşehir University, Faculty of Engineering and Natural Sciences, Istanbul, 34353, Turkiye. Electronic address:
J Inorg Biochem
December 2024
Catalysis Research and Application Center, İnönü University, 44280 Malatya, Türkiye; Department of Chemistry, Faculty of Arts and Science, İnönü University, 44280 Malatya, Türkiye; Drug Application and Research Center, İnönü University, 44280 Malatya, Türkiye. Electronic address:
Herein, a series of new Ag(I)-NHC complexes containing 1,3-dioxane group were synthesized by the direct reaction of AgO and benzimidazolium salts in light-free conditions. All Ag(I)-NHC complexes were spectrally characterized using H, C NMR, FT-IR, LC-MS, and elemental analysis. Additionally, the structures of compounds 1a and 1e were elucidated by the single X-ray diffraction techniques.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2024
Department of Chemistry, Indian Institute of Technology Ropar (IIT Ropar), Rupnagar, Punjab 140001, India.
ACS Macro Lett
August 2024
Laboratoire de Chimie des Polymères Organiques (LCPO), UMR 5629, Université de Bordeaux, CNRS, Bordeaux-INP, UMR 5629, 16 Av. Pey Berland, 33607 Pessac Cedex, France.
The capability of some -heterocyclic carbenes (NHCs) to reversibly dimerize is exploited to access dynamic polymer networks. Benzimidazolium motifs serving as NHC precursors have thus been supported onto copolymer chains by reversible addition-fragmentation chain transfer (RAFT) copolymerization of styrene and up to 20 mol % of 4-vinylbenzyl-ethyl-benzimidazolium chloride. Molecular versions of 1,3-dialkyl benzimidazolium salts have been synthesized as models, the deprotonation of which with a strong base yields the NHC dimers in the form of tetraaminoalkenes.
View Article and Find Full Text PDFEnviron Res
July 2024
Center for Energy and Environment, School of Advanced Sciences, KLE Technological University, Hubballi, 580 031, India; School of Engineering, University of Petroleum and Energy Studies (UPES), Dehradun, Uttarakhand, 248 007, India; Korea University, Seoul, South Korea. Electronic address:
A novel method was used to synthesize benzimidazole-2-ones from the corresponding benzimidazolium salts. These salts were subsequently reacted with potassium tertiary butoxide (KOBu), followed by oxidation using tertiary butyl hydrogen peroxide (TBHP) at room temperature in tetrahydrofuran (THF) to obtain the desired products in 1 h with excellent yields. After optimizing the reaction conditions, the study focused on preparing benzimidazole-2-ones with diverse substituents at N1 and N3 positions, including benzyl, 2',4',6'-trimethyl benzyl groups, and long-chain aliphatic substituents (hexyl, octyl, decyl, and dodecyl).
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