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

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• 作者：Ottó ; Horvá ; th^a ; ^{otto@mk.uni-pannon.hu} ; ^{otto@vegic.uni-pannon.hu} ; Zsolt Valicsek^a ; Gergely Harrach^a ; Gyö ; rgy Lendvay^a ; ^b ; Melinda A. Fodor^a
• 关键词：Photochemistry ; Porphyrins ; Out-of-plane ; Silver ; Gold ; Cadmium ; Bismuth ; Manganese ; LMCT ; Photodissociation
• 刊名：Coordination Chemistry Reviews
• 出版年：2012
• 期刊代码：27_00108545
• 类别：ch
• 出版时间：August, 2012
• 卷：256
• 期：15-16
• 页码：1531-1545
• 文件大小：1886 K

摘要

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⁺ (r_ion = 94 pm) formed in the reaction of the Ag⁺ ion and the TSPP^{6鈭?/sup> ligand (H₂TSPP4鈭?/sup> = 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin anion) displays OOP features, the corresponding complex also of open-shell Au3+ (r_ion = 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+ (r_ion = 95 pm), octabromination of the TSPP6鈭?/sup> 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鈭?/sup> ligand further increases the distortion and photoreactivity. The efficiency for the photoinduced LMCT reaction of the cationic complex of Bi3+ (r_ion = 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鈭?/sup>, 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.}