Substituent effects in cation–π interactions. Recognition of tetramethylammonium chloride by uranyl-salophen receptors†
Massimo Cametti,Antonella Dalla Cort,Luigi Mandolini
Chemical Science Pub Date : 03/21/2012 00:00:00 , DOI:10.1039/C2SC00675H
Abstract

The binding affinities of tetramethylammonium chloride to uranyl salophen receptors decorated with X-substituted aromatic pendants (X = OCH3, CH3, H, Br, NO2) point to the importance of resonance effects in cation–π interactions, at variance with the view that field/inductive effects play a dominant role.

Graphical abstract: Substituent effects in cation–π interactions. Recognition of tetramethylammonium chloride by uranyl-salophen receptors