Spectroscopic and photochemical properties of water-soluble metalloporphyrins of distorted structure

The location of the metal center in the porphyrin complexes strongly depends on its size, charge and spin multiplicity. Metal ions can form normal (in-plane) metalloporphyrins, or several of them, being too large to fit into the coordination cavity of the porphyrin ring, are located above the ligand plane, resulting in out-of-plane (OOP) complexes. The distorted structure of the latter type induces special photophysical and photochemical features that are characteristic of all OOP complexes. Efficient LMCT processes can take place upon excitation of these compounds. In this paper we review the results of recent studies on water-soluble (1:1) porphyrin complexes of several metal ions to reveal how the size (and partly the oxidation state) of the metal center influences their structure and photoinduced behavior. The effects of the pre-distortion (via bromination) and the charge of the porphyrin ligand on the structure and photoreactivity of these complexes are also discussed. While the porphyrin complex of Ag2+ (rion = 94 pm) formed in the reaction of the Ag+ ion and the TSPP6− ligand (H2TSPP4− = 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin anion) displays OOP features, the corresponding complex also of open-shell Au3+ (rion = 85 pm) is unambiguously of planar structure, and does not show any fluorescence and photoredox degradation. In the case of the anionic complex of Cd2+ (rion = 95 pm), octabromination of the TSPP6− ligand results in significant red-shifts in the absorption and emission spectra, dramatically diminishes the fluorescence quantum yield and lifetime, and turns the photodegradation into a very oxygen-sensitive reaction. The axial coordination of HO− ligand further increases the distortion and photoreactivity. The efficiency for the photoinduced LMCT reaction of the cationic complex of Bi3+ (rion = 103 pm) formed with the TMPyP2+ ligand (H2TMPyP4+ = 5,10,15,20-tetrakis(1-methyl-4-pyridinium)porphyrin cation) is significantly lower than that for anionic BiTSPP3−, due to the weaker Lewis-basicity of the positively charged porphyrin. DFT calculations of the geometrical structures show good correlation with the observed photophysical and photochemical properties. Deviating from the inner-sphere LMCT reaction of OOP complexes, the cationic ligand (such as TMPyP2+ and TAPP2+ (H2TAPP4+ = 5,10,15,20-tetrakis(4-trimethylammonium phenyl)porphyrin cation)) is favorable for the outer-sphere photoinduced reduction of the metal center in the in-plane manganese(III) porphyrins because the anionic porphyrin ligands of higher Lewis-basicity stabilize the +3 oxidation state. The cationic porphyrin ligands enhance the formation of manganese(II) complexes with OOP characteristics, and can be utilized in photocatalytic systems applicable for water splitting.

Water-soluble metalloporphyrins of distorted structure display peculiar photophysical and photochemical properties affected by the size of the metal center and the charge and pre-distortion of the ligand.Figure optionsDownload high-quality image (86 K)Download as PowerPoint slideHighlights
► Ag(II)TSPP4− exhibits the typical features of out-of-plane structure, deviating from the in-plane Au(III)TSPP3−.
► Pre-distortion of the porphyrin ligand by octabromination strongly modifies the photoinduced behavior of its Cd(II) complexes.
► Photoinduced LMCT reaction is more efficient for Bi(III)TSPP3− than for Bi(III)TMPyP5+.
► Cationic manganese(II/III) porphyrins can be utilized in photocatalytic cycles.