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A synthesized amphiphilic porphyrin, 5,10,15-tri(p-hydroxyphenyl)-20-(p-hexadecyl-oxyphenyl) porphyrin, can take a transfer process for the porphyrin moiety from the inner core to the outer surface layer of cetyltrimethylammonium bromide (CTAB) micelle. The increasing of FWHH of the Soret band was attributed to the multiplicity of porphyrin monomers related with deprotonation degree, arrangement, orientation, and position of porphyrin moiety at the surface area rather than the aggregates associated with irregular orientation of neighboring porphyrins.
A synthesized amphiphilic porphyrin, 5,10,15-tri (p-hydroxyphenyl) -20- (p-hexadecyl-oxyphenyl) porphyrin, can take a transfer process for the porphyrin moiety from the inner core to the outer surface layer of cetyltrimethylammonium bromide (CTAB) micelle. The increasing of FWHH of the Soret band was attributed to the multiplicity of porphyrin monomers related with deprotonation degree, arrangement, orientation, and position of porphyrin moiety at the surface area rather than the aggregates associated with irregular orientation of near porphyrins .