A novel calix[4]arene derivative 2 with amino functional groups at the lower rim was first prepared via introduction of nitro functional groups and amination of the dinitro derivative of calix[4]arene. The optically active monomers were synthesized by dehydration of L-leucine (and L-isoleucine) and 3

3'

4

4'-benzophenonetetracarboxylic-3

3'

4

4'-dianhydride (3) followed by reaction with thionyl chloride to form 5a and 5b. Two methods

polymerization under microwave irradiation and solution polymerization in CH2Cl2/TEA

were then employed to carry out the condensation polymerization of 2 with the optically active monomers 5a and 5b

respectively. The polymerization conditions affected the kind of resulting polymers

poly(amide-imide)s (PAIs) 6a and 6b and poly(ester-imide)s (PEIs) 6a' and 6b' were obtained selectively in good yields and moderate inherent viscosities. Sorption-extraction experiments were carried out using cram picrate extraction method and verified good binding ability of the resulting calixarene-based polymers towards silver

alkali metal and toxic heavy metal cations. Also thermogravimetric analysis indicated that the resulting PAIs and PEIs were thermally stable.