Favorable protonation of the (μ-edt)[Fe2(PMe 3)4(CO)2(H-terminal)]+ hydrogenase model complex over its bridging μ-H counterpart: A spectroscopic and DFT study

Mary Grace I. Galinato, C. Matthew Whaley, Dean Roberts, Peng Wang, Nicolai Lehnert

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Abstract

The mechanism of hydrogen production in [FeFe] hydrogenase remains elusive. However, a species featuring a terminal hydride bound to the distal Fe is thought to be the key intermediate leading to hydrogen production. In this study, density functional theory (DFT) calculations on the terminal (H-term) and bridging (μ-H) hydride isomers of (μ-edt)-[Fe2(PMe 3)4(CO)2H]+ are presented in order to understand the factors affecting their propensity for protonation. Relative to H-term, μ-H is 12.7 kcal/mol more stable, which contributes to its decreased reactivity towards an acid. Potential energy surface (PES) calculations for the reaction of the H-term isomer with 4-nitropyridinium, a proton source, further reveal a lower activation energy barrier (14.5 kcal/mol) for H-term than for μ-H (29 kcal/mol). Besides these energetic considerations, the H-term isomer displays a key molecular orbital (MO <139>) that has a relatively strong hydride (1s) contribution (23%), which is not present in the μ-H isomer. This indicates a potential orbital control of the reaction of the hydride complexes with acid. The lower activation energy barrier and this key MO together control the overall catalytic activity of (μ-edt)[Fe2(PMe3)4(CO)2(H-term)] +. Lastly, Raman and IR spectroscopy were performed in order to probe the ν(Fe-H) stretching mode of the two isomers and their deuterated counterparts. A ν(Fe-H) stretching mode was observed for the μ-H complex at 1220 cm-1. However, the corresponding mode is not observed for the less stable H-term isomer.

Original languageEnglish (US)
Pages (from-to)1147-1154
Number of pages8
JournalEuropean Journal of Inorganic Chemistry
Issue number7
DOIs
StatePublished - Mar 2011

All Science Journal Classification (ASJC) codes

  • Inorganic Chemistry

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