Dipartimento di Chimica

Osvaldo Lanzalunga is pleased to invite to the seminar:

Moving Beyond Sensitised Photocatalysis - Light Driven Oxidation of with Molecular Based non-heme Iron Catalysts

Prof. Wesley R.  Browne

The seminar will be held in Parravano Hall, S. Cannizzaro building CU014, Monday, 17th April at 2.30 p.m..

 

Abstract

The photophysics and photochemistry are seeing a recent resurgence in interest due to the need to supplant photoactive complexes based on Ir(III) and Ru(II). However, the low lying ³MC states of iron complexes has in large part lead to the conclusion that iron complexes are not generally photoactive in themselves. Recently, however, we have shown that non-heme iron(II) complexes such as those based on pentadentate ligands, e.g., N4Py (N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine), undergo visible light driven oxidation to their iron(III) state in the presence of O₂ without ligand degradation.^[1] Remarkably, however, the same complex in its higher oxidation states undergoes photochemical reduction with oxidation of solvent or organic substrates.[2] This opposing photochemical reactivity allows for a complete cycle to be achieved in the catalytic activation of oxygen to oxidize methanol.[3] Under mildly basic conditions, however, highly selective base catalysed ligand degradation with O₂, to form a well-defined pyridyl-imine iron(II) complex and an iron(III) picolinate complex, is accelerated photochemically.[4] Specifically a pyridyl-CH₂- moiety is lost from the ligand yielding a potentially N4 coordinating ligand containing an imine motif. The involvement of reactive oxygen species other than O₂ is excluded; instead deprotonation at the benzylic positions to generate an amine radical is proposed as the rate determining step. The selective nature of the transformation holds implications for efforts to increase catalyst robustness through liganddesign. Taken together these data open up new opportunities in photocatalysis without the need for light harvesting photosensitisers.

References

[1] A. Draksharapu, Q. Li, G. Roelfes, W. R. Browne, Dalton Trans. 2012, 41, 13180–13190.

[2] J. Chen, A. Draksharapu, E. Harvey, W. Rasheed, L. Que Jr., W. R. Browne, Chem. Commun. 2017, 53, 12357–12360

[3] J. Chen, S. Stepanovic, A. Draksharapu, M. Gruden, W. R. Browne, Angew. Chem. Int. Ed. 2018, 57, 3207-3211.

[4] J. Chen, D. Unjaroen, S. Stepanovic, A. van Dam, M. Gruden, Wesley R. Browne, Inorg. Chem. 2018, 57, 4510-4515