Three sorts of amphiphilic porphyrins(4-hydroxyphenyl porphyrins P0 and its alkoxy derivates P1
P2)were solublized in THF solutions and SDS micellar solutions.The position-made and aggregation behavi or were studied by means of UV-VIS and fluorescence spectra influenced by diffe rent side-chain substituents in varieties of microenvironments.The results ind icates that amphiphilic porphyrins exists as monomers in THF solutions
and the effects of the side-chain substituents on the electronic states of porphyrins a re negligible.The UV-VIS spectra's absorbance decreases
FWHH increases
fluo rescence quenching occurs in fluorescence spectra as amphiphilic porphyrin's si de-chain substituents increase.It demonstrates that amphiphilic porphyrin's s ide-chain substituents vary