Synthesis, Characterization, and Reactivities of Manganese(V)−Oxo Porphyrin Complexes
- 3 January 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 129 (5) , 1268-1277
- https://doi.org/10.1021/ja066460v
Abstract
The reactions of manganese(III) porphyrin complexes with terminal oxidants, such as m-chloroperbenzoic acid, iodosylarenes, and H2O2, produced high-valent manganese(V)−oxo porphyrins in the presence of base in organic solvents at room temperature. The manganese(V)−oxo porphyrins have been characterized with various spectroscopic techniques, including UV−vis, EPR, 1H and 19F NMR, resonance Raman, and X-ray absorption spectroscopy. The combined spectroscopic results indicate that the manganese(V)−oxo porphyrins are diamagnetic low-spin (S = 0) species with a longer, weaker Mn−O bond than in previously reported Mn(V)−oxo complexes of non-porphyrin ligands. This is indicative of double-bond character between the manganese(V) ion and the oxygen atom and may be attributed to the presence of a trans axial ligand. The [(Porp)MnVO]+ species are stable in the presence of base at room temperature. The stability of the intermediates is dependent on base concentration. In the absence of base, (Porp)MnIVO is generated instead of the [(Porp)MnVO]+ species. The stability of the [(Porp)MnVO]+ species also depends on the electronic nature of the porphyrin ligands: [(Porp)MnVO]+ complexes bearing electron-deficient porphyrin ligands are more stable than those bearing electron-rich porphyrins. Reactivity studies of manganese(V)−oxo porphyrins revealed that the intermediates are capable of oxygenating PPh3 and thioanisoles, but not olefins and alkanes at room temperature. These results indicate that the oxidizing power of [(Porp)MnVO]+ is low in the presence of base. However, when the [(Porp)MnVO]+ complexes were associated with iodosylbenzene in the presence of olefins and alkanes, high yields of oxygenated products were obtained in the catalytic olefin epoxidation and alkane hydroxylation reactions. Mechanistic aspects, such as oxygen exchange between [(Porp)MnV16O]+ and H218O, are also discussed.Keywords
This publication has 69 references indexed in Scilit:
- Laser Flash Photolysis Generation and Kinetic Studies of Corrole–Manganese(v)‐Oxo IntermediatesChemistry – A European Journal, 2005
- Synthesis, Characterization, and Physicochemical Properties of Manganese(III) and Manganese(V)−Oxo CorrolazinesInorganic Chemistry, 2005
- Oxoiron(IV) porphyrin π-cation radical complexes with a chameleon behavior in cytochrome P450 model reactionsJBIC Journal of Biological Inorganic Chemistry, 2005
- Oxidizing intermediates in cytochrome P450 model reactionsJBIC Journal of Biological Inorganic Chemistry, 2004
- One oxidant, many pathways: a theoretical perspective of monooxygenation mechanisms by cytochrome P450 enzymesJBIC Journal of Biological Inorganic Chemistry, 2004
- Multielectron Atom Transfer Reactions of Perchlorate and Other Substrates Catalyzed by Rhenium Oxazoline and Thiazoline Complexes: Reaction Kinetics, Mechanisms, and Density Functional Theory CalculationsInorganic Chemistry, 2004
- Remarkable axial ligand effect on regioselectivity towards terminal alkenes in epoxidation of dienes by a robust manganese porphyrinChemical Communications, 2003
- Epoxidation Catalysis by a Manganese Corrole and Isolation of an Oxomanganese(V) CorrolePublished by Wiley ,2000
- The High-Valent Compound of Cytochrome P450: The Nature of the Fe−S Bond and the Role of the Thiolate Ligand as an Internal Electron DonorPublished by Wiley ,2000
- Evidence for Compound I Formation in the Reaction of Cytochrome-P450cam with m-Chloroperbenzoic AcidBiochemical and Biophysical Research Communications, 1994