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Mechanism of the Methane → Methanol Conversion Reaction Catalyzed by Methane Monooxygenase: A Density Functional Study
The hybrid density functional (DFT) method B3LYP was used to study the mechanism of the methane hydroxylation reaction catalyzed by a non-heme diiron enzyme, methane monooxygenase (MMO). The key reactive compound Q of MMO was modeled by (NH2)(H2O)Fe(μ-O)2(η2-HCOO)2Fe(NH2)(H2O), I. The reaction is sh...
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Published in: | Journal of the American Chemical Society 1999-08, Vol.121 (31), p.7249-7256 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The hybrid density functional (DFT) method B3LYP was used to study the mechanism of the methane hydroxylation reaction catalyzed by a non-heme diiron enzyme, methane monooxygenase (MMO). The key reactive compound Q of MMO was modeled by (NH2)(H2O)Fe(μ-O)2(η2-HCOO)2Fe(NH2)(H2O), I. The reaction is shown to take place via a bound-radical mechanism and an intricate change of the electronic structure of the Fe core is associated with the reaction process. Starting with I, which has a diamond-core structure with two FeIV atoms, L4FeIV(μ-O)2FeIVL4, the reaction with methane goes over the rate-determining H-abstraction transition state III to reach a bound-radical intermediate IV, L4FeIV(μ-O)(μ-OH(···CH3))FeIIIL4, which has a bridged hydroxyl ligand interacting weakly with a methyl radical and is in an FeIII−FeIV mixed valence state. This short-lived intermediate IV easily rearranges intramolecularly through a low barrier at transition state V for addition of the methyl radical to the hydroxyl ligand to give the methanol complex VI, L4FeIII(OHCH3)(μ-O)FeIIIL4, which has an FeIII−FeIII core. The barrier of the rate-determining step, methane H-abstraction, was calculated to be 19 kcal/mol. The overall CH4 oxidation reaction to form the methanol complex, I + CH4 → VI, was found to be exothermic by 39 kcal/mol. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja9906296 |