ABSTRACT
Two rationally designed 4-nitrophenyl-based molecular clefts functionalized with thiourea (L 1 ) and urea (L 2 ) have been synthesized and studied for a variety of anions by UV-Vis and colorimetric techniques in DMSO. Results from the binding studies suggest that both L 1 and L 2 bind halides showing the order: fluoride > chloride > bromide > iodide; and oxoanions showing the order: dihydrogen phosphate > hydrogen sulfate > nitrate > perchlorate. Each receptor has been shown to form a 1:1 complex with an anion via hydrogen bonding interactions, displaying distinct color change for fluoride and dihydrogen phosphate in solution. As compared to the urea-based receptor L 2 , the thiourea-based receptor L 1 exhibits stronger affinity for anions due the presence of more acidic thiourea functional groups.
