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Photosensitized oxidation of 4 chlorophenol (4CP) by the title complexes (AlPcS and ZnPcS) in aerated aqueous solution upon visible light irradiation ( λ ≥450 nm) has been investigated using methanol as a disassociating reagent. It is confirmed that the monomeric species of the sensitizer is more active than the corresponding dimer in singlet oxygen generation for 4CP oxidation. However, the monomer is also the main component found in the sensitizer’s photobleaching. In this regard, AlPcS is much more stable than ZnPcS, and the photobleaching is observed to proceed via singlet and triplet oxygen, respectively. The final products of 4CP oxidation in alkaline solution are carbon dioxide and chloride ions, while at pH=7 and pH=3 the p benzoquinone is the product. The temperature is found to have influence on both the photosensitized degradation of methyl orange and ZnPcS photobleaching, with an activation energy of 15 8 and 24 2 kJ/mol, respectively.
Photosensitized oxidation of 4 chlorophenol (4CP) by the title complexes (AlPcS and ZnPcS) in aerated aqueous solution upon visible light irradiation (λ ≥ 450 nm) has been investigated using methanol as a disassociating reagent. It is confirmed that the monomeric species of the However, the monomer is also the main component found in the sensitizer’s photobleaching. In this regard, AlPcS is much more stable than ZnPcS, and the photobleaching is observed to proceed via singlet and triplet oxygen, respectively. The final products of 4CP oxidation in alkaline solution are carbon dioxide and chloride ions, while at pH = 7 and pH = 3 the p benzoquinone is the product. The temperature is found to have influence on both the photosensitized degradation of methyl orange and ZnPcS photobleaching, with an activation energy of 15 8 and 24 2 kJ / mol, respectively.