Supramolecular systems formed by calix[4]resorcinarenes and surfactants in chlorophorm

Capacity titration and 1H NOESY 2D NMR were applied to investigation of intermolecular interactions and aggregation of amphiphilic calix[4]resorcinarenes (CRA 1, 2) modified with 1,2,4-triazine (1) and oxazine (2) functions in chloroform in the presence of cationic (3) and non-ionic (4) surfactants (SAA). Critical concentrations of micelle formation (CMC) indicate that the ability of CRA 1, 2 to form supramolecular aggregates like micelles or hybrid micelles with SAA 3, 4 only weakly depends on the constitution of CRA functional groups. In the case of the hybrid micelles, when CMC are defined by the nature of surfactants 3 or 4, the methyl and methylene groups of the hydrophobic fragments (CRA 1, 2) were found to interact with the hydroxy groups of SAA 3 and ethylene oxide moieties of SAA 4.