“…Finally, the cavity of the molecule is non-polar in nature and surrounded by the polar wide rim, a feature that equips resorcin [4]arenes for micellar behavior. [20,21] Looking at these properties it is not surprising that these compounds have found their way into a number of applications such as molecular receptor systems, [22,23] photo resists, [24,25] selective membranes, molecular sensing, [26,27] drug delivery, [28,29] ion channel mimics, [30] metal ion extraction agents, [31,32] molecular switches, [33,34] stationary phases in GC and HPLC, [35][36][37][38] ligands for organometallic catalysts, [39][40][41] host-guest chemistry, [14,42] and starting materials in synthesis of supramolecular compounds. [43] Several relatives of these molecules have been developed and studied such as the closely related cavitands, [44] carcerands and hemicarcerands; [45] also pyrogallol [4]arenes, [46] catechol [4]arenes, [47] pillar [4]arenes, [48] pyridin [4]arenes; [49] calix [4]arenes, [50] and other structurally similar compounds.…”