摘要:
The binding of a series of nitrogen donor ligands (Piperazine (Pipz), Piperidine (Pip) and Pyrrolidine (Pyr)) to iron porphyrin, OEPFeClO4, where OEP is octaethylporphyrin, has been characterized by electronic spectroscopy in CH2Cl2. In nonaqueous media, in the presence of a neutral ligand, the equilibria observed are: OEPFeClO4 + 2L reversible arrow [OEPFeL2]+ClO4- (beta(2)) where the product is an ion pair and in some cases: OEPFeClO4 + L reversible arrow OEPFeLClO4 (K-1), where the product may either be the six-coordinate or the five-coordinate [OEPFeL]+ClO4- ion pair, that L denotes neutral N-donor ligands. This behavior for the nitrogen donor ligands (L = Pipz, Pip, Pyr) is confirmed by spectrophotometric titrations data and the binding constants for the substitution reaction have been reported.