Erkus, BetulOzcan, HafizeZaim, Omer2024-06-122024-06-1220200022-152X1943-5193https://doi.org/10.1002/jhet.3922https://hdl.handle.net/20.500.14551/25431Four new macrocyclic compounds with thiophene (L1 and L2) and furan (L3 and L4) rings were synthesized and characterized by IR, H-1 NMR, C-13 NMR, and Q-TOF spectral data. Macrocyclic amides (L1, L2, L3, and L4) were tested for ion transportation with Na+ and K+ ions, and also, antimicrobial activities were investigated against the Gram-negative Escherichia coli ATCC 25922, Gram-positive Staphylococcus aureus ATCC 25923, Gram-negative Listeria monocytogenes ATCC 19115, Gram-negative Salmonella typhimurium ATCC 14028, Bacillus cereus bacteria, and Candida albicans ATCC 10231 for all amides.en10.1002/jhet.3922info:eu-repo/semantics/closedAccessStructural AspectsPhane NomenclatureMacrocyclic LigandCyclic PolyethersCrown-EthersFt-IrPeptidesDerivativesPartComplexesSynthesis, antimicrobial activity, and ion transportation investigation of four new [1+1] condensed furan and thiophene-based cycloheterophane amidesArticle57419561962Q3WOS:0005255449000402-s2.0-85079460911Q3