Cucurbit[6]uril (CB[6]) with a substituent attached solely to one methylene bridge was prepared for the first time. The monosubstituted CB[6] undergoes self-assembly to form a cyclic tetramer in the solid state. The affinity of the monosubstituted CB[6] to a series of alkylammonium salts was measured revealing a minor effect of the substituent on the binding properties of the macrocycle.

RECETOX and ‡Department of Chemistry Masaryk University Kamenice 5 625 00 Brno Czech Republic

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Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents