A manganese(I) complex with a 190 ns metal-to-ligand charge transfer lifetime

Sandra Kronenberger, Robert Naumann, Christoph Förster, Nathan R. East, Jan Klett and Katja Heinze ()
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Sandra Kronenberger: Johannes Gutenberg University Mainz
Robert Naumann: Johannes Gutenberg University Mainz
Christoph Förster: Johannes Gutenberg University Mainz
Nathan R. East: Johannes Gutenberg University Mainz
Jan Klett: Johannes Gutenberg University Mainz
Katja Heinze: Johannes Gutenberg University Mainz

Nature Communications, 2025, vol. 16, issue 1, 1-11

Abstract: Abstract Application of photoactive transition metal complexes in lighting, imaging, sensing, and photocatalysis is usually based on the triplet metal-to-ligand charge transfer (3MLCT) excited state of precious metal complexes with 4/5d6 valence electron configurations. These photocatalysts exhibit excited state lifetimes exceeding hundreds of nanoseconds. Simple 3d6 transition metal complexes containing abundant metals exhibit lifetimes below 1–2 nanoseconds, and they require multistep ligand syntheses mitigating large-scale implementation. We report that a commercially available bis(imidazolium) pyridine pro-ligand [H2pbmi]2+ and a manganese(II) salt yield the tetracarbene manganese(I) complex [Mn(pbmi)2]+. This complex phosphoresces at room temperature in fluid solution from a 3MLCT state with a lifetime of 190 ns. In combination with the reversible [Mn(pbmi)2]2+/+ process, this translates to an excited state capable of reducing benzophenone. Combination of manganese(I) with rigid carbene/pyridine ligands expands key strategies for photoactive 3d6 metal complexes of earth-abundant metals with 3MLCT lifetimes rivalling those of precious metals and providing a conceptual starting point for a sustainable photochemistry.

Date: 2025
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DOI: 10.1038/s41467-025-63225-4

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