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Vibrational characterization of a diiron bridging hydride complex - a model for hydrogen catalysis.

ABSTRACT: A diiron complex containing a bridging hydride and a protonated terminal thiolate of the form [(μ,κ₂-bdtH)(μ-PPh₂)(μ-H)Fe₂(CO)₅]⁺ has been investigated through ⁵⁷Fe nuclear resonance vibrational spectroscopy (NRVS) and interpreted using density functional theory (DFT) calculations. We report the Fe-μH-Fe wagging mode, and indications for Fe-μD stretching vibrations in the D-isotopologue, observed by ⁵⁷Fe-NRVS. Our combined approach demonstrates an asymmetric sharing of the hydride between the two iron sites that yields two nondegenerate Fe-μH/D stretching vibrations. The studied complex provides an important model relevant to biological hydrogen catalysis intermediates. The complex mimics proposals for the binuclear metal sites in [FeFe] and [NiFe] hydrogenases. It is also an appealing prototype for the 'Janus intermediate' of nitrogenase, which has been proposed to contain two bridging Fe-H-Fe hydrides and two protonated sulfurs at the FeMo-cofactor. The significance of observing indirect effects of the bridging hydride, as well as obstacles in its direct observation, is discussed in the context of biological hydrogen intermediates.

SUBMITTER: Gee LB

PROVIDER: S-EPMC8159291 | biostudies-literature |

REPOSITORIES: biostudies-literature

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