Self-aggregation of light active barbituric acid derivatives and their self
-assembly with melamine derivatives through hydrogen-bonding, pi-aromatic s
tacking, and other weak interactions were studied by UV-visible absorption
and fluorescence spectroscopy. PB12Me has the same fluorescence behavior as
PB12 in chloroform though it cannot aggregate through a hydrogen-bond. AB(
12) and AB(1) lead to different degrees of fluorescence splitting. When bar
bituric acid molecular components were self-assembled with melamine a simil
ar splitting phenomenon was observed. It was shown that pi-aromatic stackin
g resulted in the exclusive fluorescence changes and H-aggregates were form
ed in solution. (C) 1998 Elsevier Science Limited. All rights reserved.