A pillar[5]arene/imidazolium [2]rotaxane: solvent-and thermo-driven molecular motions and supramolecular gel formation

Based on the pillar[5]arene/imidazolium recognition motif, a [2]rotaxane was effectively prepared. Solvent/temperature triggered molecular motions of the pillar[5] arene ring on the imidazolium axle were successfully realized. By comparison of proton NMR spectra of the [2] rotaxane in different solvents, we found that if we increased the solvent polarity, the pillar[5] arene ring gradually moved away from the imidazolium part. In DMSO, we also could adjust the binding site of the pillar[5] arene ring by changing the temperature. Furthermore, in DMSO, the [2] rotaxane self-assembled to form a supramolecular gel, which showed multiple stimuli-responsiveness.