Complete spectroscopic, structural, and anion-binding properties are reported for a special class of calixphyrins, namely, 5, 10-disubstituted porphodimethenes (PDMs). The crystal structure clearly shows that PDMs exhibit nonplanar (distorted) structures with both sp(2)- and sp(3)-hybridized meso carbon centers. We were able to obtain and characterize the diacid form [H-4(PDM)][X](2) upon addition of several acids to PDMs, where X denotes anions of different acids: HCl, HBr, MeSO3H, CF3CO2H, and HClO4. We found that the PDM dications generated were more conjugated and thus more stable than their corresponding porphyrms, Their potential to coordinate anions was clearly shown by using H-1 NMR spectroscopy. In addition, we found that when HClO4 was used to protonate PDMs, the conversion occurs through an intermediate species, which has been assigned to the elusive monoacid derivative on the basis of UV-vis and H-1 NMR experiments.