The interactions of a series of water-soluble dendritic: phthalocyanines co
ntaining terminal carboxylate functionality with a range of surfactants in
aqueous media have been investigated. Cationic surfactants, as compared wit
h neutral and anionic counterparts, are much more effective to disrupt the
molecular aggregation of phthalocyanines, in particular for the first gener
ation macrocycle, as demonstrated by the absorption and fluorescence spectr
oscopy. The interactions are mainly electrostatic in nature, arising from t
he cationic head of the surfactant and the anionic surface of the dendrimer
s which has been supported by the fluorescence quenching experiments using
the cationic porphyrin (TMePyP)(4+) as the quencher. The complex formation
between the first generation dendritic phthalocyanine and the cationic surf
actant CTAB has also been monitored by dynamic laser light scattering in 0.
01 mol dm(-3) NaBr aqueous media. As the concentration of CTAB increases, t
he apparent average hydrodynamic radius of the aggregates decreases signifi
cantly from 14.1 to 3.2 nm, showing that the aggregation of phthalocyanines
is greatly relieved by CTAB and eventually the anionic macrocycles, mainly
in monomeric form, are adsorbed onto the cationic micelle surfaces in a si
deways manner.