“…Currently, various synthetic compounds capable of selective binding with dopamine through multiple non-covalent interactions, such as electrostatic interactions, hydrogen bonding, p-p-stacking, and hydrophobic forces, have been proposed as host molecules. The organophosphorus compounds, 9 calix[n]arenes (n = 4, 5, 6), [10][11][12][13][14][15][16] calix [4]resorcinarenes, 17 and pillar [5]arenes 18 with acidic, 10,12 quinone 11 and amide 8 groups, and charged fragments 14,18 as binding sites, show complexation ability toward dopamine.…”