The investigation by FT-IR and Raman spectroscopy of several cyclodext
rin inclusion complexes reveals structural features not readily access
ible by other spectroscopic methods. Thus, the cis conformation of ter
ephthalaldehyde dominates within the alpha-cyclodextrin cavity. The lo
cked and unlocked acetate group of hydroquinone diacetate in beta-cycl
odextrin can be easily distinguished, while p-benzenedimethanol diacet
ate displays the features of a ''solid solution''. Finally, the detect
ion of hydrogen bonding in the alpha-cyclodextrin inclusion compound o
f butanediol diacetate brings to light even more complex supramolecula
r structures.