Journal of the Chemical Society Perkin Transactions 1 · 1994 · 26 citations · 19 references
Natural SciencesChemistryCatalysisInorganic ChemistryOrganometallic ChemistryCoordination ChemistryMetal CatalysisCatalyst MechanismsCatalytic ActivityManganese CatalysisManganese ChemistryManganese Oxide CatalystsManganese Redox ChemistryPorphyrin ComplexesPorphyrin Redox Chemistry
Improvements are described to the synthesis of the catalytically important 5,10,15,20-tetrakis(2,6-dichlorophenyl)porphyrin 1(R = H) and [2,3,7,8,12,13,17,18-octachloro-tetrakis(2,6-dichlorophenyl)porphyrinato]manganese(III)3(R = Cl) which enable large-scale preparation of such compounds to be carried out easily. A comparative study of the catalytic performance of the manganese complexes of these two porphyrins proved that, contrary to earlier expectations, the manganese complex of 5,10,15,20-tetrakis(2,6-dichlorophenyl)porphyrin is the most stable and efficient catalyst for epoxidation when using sodium hypochlorite as oxidant. With [2,3,7,8,12,13,17,18-octachloro-tetrakis(2,6-dichlorophenyl)porphyrinato]manganese(III)3, chlorinated products tend to be formed and these can be the dominant products for some substrates.
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