The host-guest complexation behaviour of beta -cyclodextrin 6-O-mono-2-naph
thoate (1) and 6-[(N-2-naphthoyl-2-aminoethyl) amino]-6-deoxy-beta -cyclode
xtrin (2) have been studied by the circular dichroism method. The exciton c
oupling band of 1 suggests that two naphthoyl moieties are partly included
in one beta -CD cavity. Host 1 could form a dimer in a more polar solvent a
nd the dimer could be dissociated in a less polar solvent or by adding a gu
est. Solvent-induced, concentration induced, and guest-induced circular dic
hroism variations were examined. No exciton coupling was observed for host
2.