摘要:
                                The complexation properties of zinc 10,20-bis[5-(2,3,7,8,12,13,17,18-octaethylporphyrinate) ethynylphenyl]-5,5', 10', 15,15', 20'-hexamethylcalix[4]pyrrole toward halide ions, triethylenediamine, and 4,4'-bipyridyl were studied by spectrophotometric titration and (1)H NMR spectroscopy. The influence of binding of anions (F(-) and Cl(-)) by the calix[4]pyrrole fragment of zinc calixpyrrole-bisporphyrinate on the complexation properties of its interporphyrin cavity toward the bidentate organic ligand triethylenediamine.