Issue 1, 2014

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

Abstract

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.

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

Supplementary files

Article information

Article type
Edge Article
Submitted
04 Sep 2013
Accepted
20 Sep 2013
First published
20 Sep 2013

Chem. Sci., 2014,5, 247-252

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

S. Dong, J. Yuan and F. Huang, Chem. Sci., 2014, 5, 247 DOI: 10.1039/C3SC52481G

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