Abstract
Aggregation of Fe(III)-tetra-(4-sulfonatophenyl)-porphyrin (Fe(III)TPPS) was studied in the presence of block copolymers, poly(ethylene glycol)-block-poly(4-vinylpyridine) (PEG-b-P4VP), poly(ethylene glycol)-block-poly(2-(dimethylamino)ethyl methylacrylate) (PEG-b-PDMAEMA), and poly(ethylene glycol)-block-poly(β-cyclodextrin) (PEG-b-PCD). The interaction between the iron porphyrin and the blocks, P4VP, PDMAEMA, and PCD, led to the formation of copolymers/Fe(III)TPPS complex micelles with a PEG shell and determined the species of Fe(III)TPPS. The electrostatic interaction of protonated P4VP and PDMAEMA with Fe(III)TPPS remarkably decreased the apparent pKd of Fe(III)TPPS and led to a micellar μ-oxo dimer of the iron porphyrin. At pH above the pKa of P4VP, Fe(III)TPPS was kept inside the hydrophobic P4VP core and formed an encapsulated μ-oxo dimer. However, when above the pKa of PDMAEMA, Fe(III)TPPS escaped from the hydrophobic PDMAEMA core, existing as a free μ-oxo dimer. PCD caused the monomer of the porphyrin because of the inclusion complexation between the β-cyclodextrin residues and Fe(III)TPPS. The two micellar monomer species Fe(III)TPPS(H2O)2 and Fe(III)TPPS(OH) were obtained with an equilibrium pKa ~ 6.4.
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