“…In our previous papers, we synthesized and characterized polymer-linked halogenated tetraphenylporphyrin derivatives and covalently linked porphyrin dimers, in which transmembrane electron transfer between porphyrins catalyzed by manganese porphyrins was observed, depending on the structure of the porphyrin derivative. 1f,,3a,b,d Moreover, transmembrane electron transfer catalyzed by phospholipid-linked manganese tetraphenylporphyrin derivatives with separated methylene groups (PE-C n -MnTTP and PE-C n -MnPFPP) ( n = 0, 5, 11) (Chart ) which can be easily immersed into the lipid bilayer is reported. 1c,3c The phospholipid-linked manganese porphyrins caused an enhanced electron transfer, depending upon the length of the spacer methylene group (C n ) and also the structure of manganese porphyrins. Alternatively, a large number of chemists have identified that electroactive species such as porphyrins, myoglobin, flavins, viologens, ferrocenes, and quinones can be immobilized on electrode surfaces. 1g,− However, there has been little study of electron transfer between porphyrin complexes on an electrode modified with lipid bilayers 1g. In the previous paper, 1g, enhanced electron transfer between porphyrins in polypeptide membranes cast on a galssy carbon electrode or in those membranes was observed especially in hydrophilic polypeptide membranes and also when mesoporphyrin derivatives were used.…”