Imprinted polymers were synthesized for the recognition of small nitrogen heterocycles such as pyridine and quinoline using a new variant of the sacrificial spacer methodology employing silyl ether derivatized templates designed to act as N-H-O 'isosteres' for binding the targets. The cleavage of the labile silyl ether bond led to the formation of sites bearing phenolic residues. The polymers prepared with DVB as the cross-linker were capable of discriminating between pyridine, quinoline and acridine in hexane but the effect did not exceed 20%. In order to improve the recognition properties of these materials, a post-imprinting modification of the polymers was performed using acyl chlorides of varying size. This simple approach, carried out after the removal of the templates, resulted in an enhanced selectivity (by factors of up to 5-fold) for binding of pyridine and quinoline by the modified polymers. Similar effects were observed with EGDMA-based imprinted polymers. The results obtained suggest that post-imprinting chemical modification can be an effective tool to engender 'size' selectivity in binding of even small molecules containing a paucity of functional groups.