Two different Schiff base derivatives of p-tert butylcalix[4]arene 3, 6 in which one of them carrying two oxime groups, while the other has a 1,8-octylenediimino bridge, are synthesized. Treatment of these monomers with triethylene ditosylate provided corresponding copolymers 5, 7. Their complexing properties with selected alkali and transition metals are reported here. It has been concluded that the binding ability of Schiff base-calix-arene derivatives in transferring the metal cations is due to the presence of soft π-donor systems in the macrocyclic structure.