A series of complex with a general formula of M(Fc₂Ph₂P) [Fc₂Ph₂P = 5, 10-bisferrocenyl-15,20-bisphenylporphyrin (2−); M = Fe(III)Cl Fe(III)(ClO₄) and Cu(II)] have been synthesized and characterized. The single crystal X-ray structure of Cu^II(Fc₂Ph₂P) has been reported in which two ferrocene moieties are in anti form with respect to each other. The ferrocenyl groups of Cu^II(Fc₂Ph₂P) are more easily oxidized via a single two-electron quasi-reversible process compared to the free base ligand in which two 1e-oxidative response separated by 0.23 V are observed. Electrochemical study of Fe^III(Fc₂Ph₂P)Cl revealed ferrocenebased two-electron quasi-reversible oxidation at 0.72 V indicating no observable coupling of the ferrocene moieties. The higher oxidation state of Fe(III) reduces the electron releasing tendency of the porphyrin ring and thus make the ferrocene oxidation difficult. The porphyrin, however, lack substituents at the 𝛽-pyrrolic positions, and the ferrocenyl moieties are therefore free to rotate. The observed electrochemical analyses thus demonstrate that the oxidation of the ferrocene subunit is strongly affected by porphyrin ring as well as the central metal through extended 𝜋-conjugation.