Abstract
Aggregation properties of meso-tetratolylporphyrins bearing cationic substituents of a lipophilic nature such as ammonium, pyridinium, phosphonium, sulfonium, and isothiouronium were studied by UV/vis and resonance light scattering spectroscopy. The exciton point−dipole approximation was used to predict the structural alignment of the porphyrin units within the aggregate. The contribution of various types of aggregates depends on the porphyrin substitution, ionic strength, and temperature of aqueous solution of the porphyrin. In general, the preferred structure of an aggregate formed by temperature-induced aggregation is the J-aggregate exhibiting the characteristically narrow, red-shifted Soret band indicating a parallel “side-by-side” arrangement of the porphyrin units. The formation of aggregates of cationic tetratolylporphyrins is controlled by both electrostatic and hydrophobic interactions. Observed aggregation properties of porphyrin derivatives bearing trimethylammonium, trimethylphosphonium, pyridinium, dimethylphenylphosphonium, and triphenylphosphonium substituents are in very good agreement with a theoretical model based solely on electrostatic interactions.
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