The unusual conformational behaviour of a series of new cyclodextrin (
CD) dimers is studied by dedicated H-1-NMR techniques. In water some C
D-dimers form stable self-inclusion complexes, for which the aliphatic
linker is partially included in one of the two CD cavities. This phen
omenon affects the conformation of the substituted sugar ring of one C
D moiety. In the case of the alpha-beta heterodimer, the linker appear
s to be preferentially in the cavity of beta-CD, in contrast to what i
s known for intermolecular complexes where at ambient temperature a pr
eference for alpha-CD is observed. (C) 1998 Elsevier Science Ltd. All
rights reserved.