Harnessing Nitrous Oxide for Sustainable Methane Activation: A Computational Exploration of CNC-Ligated Iron Catalysts

This study employs DFT at the APFD/def2-TZVP level, with SMD solvation in THF, to investigate the catalytic activation of methane by [(κ<sup>3</sup>-CNC)Fe(N₂O)]<sup>2+</sup> cation complexes. The catalytic mechanism encompasses three key steps: oxygen atom transfer (OAT), hy...

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Bibliographic Details
Main Author: Bruce M. Prince
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Methane
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Online Access:https://www.mdpi.com/2674-0389/4/1/6
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Summary:This study employs DFT at the APFD/def2-TZVP level, with SMD solvation in THF, to investigate the catalytic activation of methane by [(κ<sup>3</sup>-CNC)Fe(N₂O)]<sup>2+</sup> cation complexes. The catalytic mechanism encompasses three key steps: oxygen atom transfer (OAT), hydrogen atom abstraction (HAA), and oxygen radical rebound (ORR). The computational results identify OAT as the rate-determining step, with activation barriers of −10.2 kcal/mol and 5.0 kcal/mol for κ<sup>1</sup>-O- and κ<sup>1</sup>-N-bound intermediates in the gas and solvent phases, respectively. Methane activation proceeds via HAA, with energy barriers of 16.0–25.2 kcal/mol depending on the spin state and solvation, followed by ORR, which occurs efficiently with barriers as low as 6.4 kcal/mol. The triplet (S = 1) and quintet (S = 2) spin states exhibit critical roles in the catalytic pathway, with intersystem crossing facilitating optimal reactivity. Spin density analysis highlights the oxyl radical character of the Fe<sup>IV</sup>=O intermediate as being essential for activating methane’s strong C–H bond. These findings underscore the catalytic potential of CNC-ligated iron complexes for methane functionalization and demonstrate their dual environmental benefits by utilizing methane and reducing nitrous oxide, a potent greenhouse gas.
ISSN:2674-0389