Self-Assembly of Stereoisomers of p-tert-Butyl Thiacalix[4]arenes Tetrasubstituted at the Lower Rim by a Tertiary Amide Group with Cations of p- and d-Elements in the Organic Phase

The ability of p-tert-butyl thiacalix[4]arenes tetrasubstituted at the lower rim by morpholide and pyrrolidide groups in cone, partial cone, and 1,3-alternate conformations to recognize cations of p- (Al3+, Pb2+) and d- (Fe3+, Co3+, Ni2+, Cu2+, Cd2+, Hg2+) elements has been studied by the picrate extraction method, dynamic light scattering (DLS), and atomic force microscopy (AFM). The hydrodynamic diameters of supramolecular associates, polydispersity index of host−guest systems, and molecular weight of nanoscale aggregates consisting of p-tert-butyl thiacalix[4]arenes and metal nitrates have been determined by the correlation spectroscopy method. It was shown that the investigated macrocycles are effective extractants for metal cations. All the investigated thiacalix[4]arenes are able to form dimers of about 1 nm with metal cations and nanoscale particles of 238 and 212 nm with Ni2+ and Pb2+ cations, respectively.