Calixpyrrole derivatives bearing long n-alkyl ester chains have been synthesized from calixpyrroles containing carboxylic acid functional groups. These systems, which contain ester groups on either the meso- carbon atoms of the calixpyrrole ring or the beta-positions of individual pyrrole rings, were prepared from the corresponding carboxylic acids. Esterification was effected using dicyclohexylcarbodiimide/4-dimethylaminopyridine (DCC/DMAP) to obtain long alkyl chain substituted calixpyrroles. In the context of this work, several brominated calixpyrrole derivatives were prepared using N-bromosuccinimide (NBS) as the brominating agent. Anion binding studies carried out by isothermal titration calorimetry (ITC) in 1,2-dichloroethane with Cl- and CH3CO2- in the form of their respective tetrabutylammonium salts, revealed that the functionalized ester derivatives have anion binding affinities similar to those of the unsubstituted "parent" systems, octamethylcalixpyrrole (1) and beta-octabromocalixpyrrole (2). The new alkylated systems proved soluble in nonpolar solvents, such as hexanes. Structure identification studies, carried out by single crystal X-ray diffraction analyses, revealed that the control ester system 4 contains two unique crystal structures per asymmetric unit. These asymmetric units interact via intermolecular hydrogen bonds in the solid state to produce a continuous intermolecular structure. Such interactions are not present in the case of the corresponding brominated ester 5.