The interactions of two amphiphilic porphyrins with anionic surfactant sodium bis(2-ethylhexyl)sulfosuccinate (AOT) in aqueous solutions were studied by UV-vis absorption spectroscopy, fluorescence spectroscopy, resonance light scattering technique, fluorescence anisotropy and surface tension measurements. The two porphyrins, meso-tetra(4-hydroxyphenyl)porphyrin (THPP) and meso-tetra(3,5-dibromo-4-hydroxylphenyl)porphyrin (T(DBHP)P), exist as irregular aggregates in aqueous solutions with a broad and low absorption peak near the maximum of monomer peak. The interaction of THPP with AOT leads to the formation of a fluorescent aggregate of porphyrin which was assigned as J-type aggregate according to exciton theory. A long red-shifted Soret band together with a new strong Q-band, a broad emission peak and a sharply peaked resonance light scattering signal are observed for this J-aggregate. The formation of J-aggregate is independent of the initial THPP concentration and can be influenced greatly by ionic strength. The aggregation kinetics has been investigated by UV-vis absorption spectroscopy and fluorescence anisotropy. Conversion of the porphyrin monomers to J-aggregate is observed. The addition of THPP increases the surface tension of solution and changes the critical micelle concentration of AOT. J-aggregate was not observed for T(DBHP)P in AOT solutions which only shows solubilization. The mechanism of aggregation was discussed.
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