Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270925 | Tetrahedron Letters | 2010 | 5 Pages |
Abstract
The synthesis of a calix[4]arene scaffold persubstituted with four redox-active tetrathiafulvalene (TTF) moieties at the lower rim is described. This assembly strongly binds sodium cation, and the binding process is accompanied by a conformational change of the receptor, as shown from NMR titration and by an X-ray diffraction led on the complex. This dynamic behavior remarkably results in a modification of the electrochemical response of TTF probes, which behave independently after sodium complexation.
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Authors
Joël Lyskawa, David Canevet, Magali Allain, Marc Sallé,