
Tetrahedron Letters p. 5691 - 5694 (1997)
Update date:2022-08-05
Topics:
Ashton, Peter R.
Everitt, Simon R. L.
Gomez-Lopez, Marcos
Jayaraman, Narayanaswamy
Stoddart, J. Fraser
A [2]rotaxane self-assembles spontaneously by 'slippage' in D2O during one week at room temperature when a dumbbell-shaped compound, containing a hydroquinone ring recognition site and terminated by P-D-glucopyranose units, is mixed with cyclobis(paraquat-p-phenylene) tetrachloride. A [2]rotaxane with benzoylated D-glucopyranose residues is obtained when the dumbbell-shaped octabenzoate serves as a template for the formation of the cyclobis(paraquat-p-phenylene) tetracation in DMF.
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