Characteristics and sorptive properties of three series of chelating resins having incorporated calixpyrrole ligands within their structures is reported. Two sets of resins were obtained by immobilization of calix[4]pyrrole or calix[4]pyrrole[2]thiophene on the beads of crosslinked (vinylbenzyl chloride)/divinylbenzene copolymer. The third series was synthesized by condensation of calix[4]pyrrole with formaldehyde. All resins displayed sorptive properties towards halide anions and cyanides in a non-aqueous medium (acetonitrile). The resins displayed superior selectivity for fluoride anions and the selectivity sequence for the uptake of other anions depended on their ionic radii. The bigger ligand, calix[4]pyrrole[2]thiophene, showed an enhanced affinity for bigger anions, including iodide, which was not observed in the case of calix[4]pyrroles. Thus, the resin containing the larger ligand complexes the whole range of anions, but with poorer selectivities.