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Study advances understanding of two-state reactivity mechanism in iron-based catalysts

Study advances understanding of two-state reactivity mechanism in iron-based catalysts

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Significant breakthrough in understanding of the two-state reactivity mechanism
TSR model for iron(IV)-oxo complexes and calculated low-lying states for selected complexes. (A) Qualitative potential energy surface showing the proposed TSR model. (B) CASSCF-NEVPT2 calculated energies for low-lying singlet (gray), triplet (blue), and quintet (red) states. Arrows are highlighting the lowest vertical triplet to quintet excitation. Credit: Science Advances (2024). DOI: 10.1126/sciadv.ado1603

Iron-based catalysts are essential in various fields, including medicine, energy, and environmental science. They facilitate reactions that are vital for producing pharmaceuticals, clean fuels, and breaking down pollutants.

These catalysts operate by enabling the directed transformation of molecules into desired products, and can do so using energy efficient, environmentally friendly methods. The chemistry that these iron-based catalysts are capable of depends on the oxidation- and spin-state of the iron, and changes to either of these can result in very different reactivity and products.

A continuing challenge in catalysis is harnessing these differing states to increase reactivity, or the rate at which the transformation takes place, while maintaining specificity, in order to generate a majority of the desired products.

Specifically, iron(IV)-oxo complex are highly reactive intermediates involved in various oxidation reactions, such as the conversion of methane to methanol. The iron(IV)-oxo catalysts are known to have either S = 2 or S = 1 spin-states, with the S = 2 spin-states having been shown to generally be more reactive.

A long-standing theory known as the two-state reactivity model suggests that the catalysts with an S = 1 ground state can switch between different spin states to drive reactions. A component of this theory is that the energy separation between these two spin-states should be correlated with oxidative reactivity.

A large challenge in probing this mechanism has been that the energy difference between these spin states had never been measured experimentally. The difficulty of measuring this excitation energy is two-fold: the transitions between these states are spin-forbidden leading to low intensity, and they are expected to be low-energy placing them outside the range of standard spectroscopic techniques.

Researchers at the Max Planck Institute for Chemical Energy Conversion and MPI für Kohlenforschung have now made a significant breakthrough in understanding of the two-state reactivity mechanism.

Using a combination of advanced spectroscopic techniques: resonant inelastic X-ray scattering (collected at the PEAXIS beamline at the BESSY II Helmholtz-Zentrum Berlin für Materialien und Energie) and magnetic circular dichroism, the researchers were able to directly measure the elusive triplet-quintet excitation energy in these complexes.

The study is published in Science Advances. The implications are significant: With experimental measurements of this crucial excitation, scientists can now refine their theoretical models allowing for the design of more efficient and selective catalysts.

This work also demonstrates, to our knowledge, the first experimental methodology for measuring low-energy, spin-forbidden transitions in molecular catalysts.

More information:
Derek B. Rice et al, The spin-forbidden transition in iron(IV)-oxo catalysts relevant to two-state reactivity, Science Advances (2024). DOI: 10.1126/sciadv.ado1603

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Max Planck Society

Study advances understanding of two-state reactivity mechanism in iron-based catalysts (2024, July 1)
retrieved 1 July 2024

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