Solvation rules: aromatic interactions outcompete cation–π interactions in synthetic host–guest complexes in water

Abstract

Chemical double mutant cycles were used to measure the interaction of a N-methyl pyridinium cation with a π-box in a calix[4]pyrrole receptor. Although the cation–π interaction is attractive (−11 kJ mol⁻¹), it is 7 kJ mol⁻¹ less favourable than the corresponding aromatic interaction with the isosteric but uncharged tolyl group.