A Photorobust Mo(0) Complex Mimicking [Os(2,2'-bipyridine)3]2+ and its Application in Red-to-Blue Upconversion

Bilger, Jakob B. and Kerzig, Christoph and Larsen, Christopher B. and Wenger, Oliver S.. (2021) A Photorobust Mo(0) Complex Mimicking [Os(2,2'-bipyridine)3]2+ and its Application in Red-to-Blue Upconversion. Journal of the American Chemical Society, 143 (3). pp. 1651-1663.


Official URL: https://edoc.unibas.ch/81352/

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Osmium(II) polypyridines are a well-known class of complexes with luminescent metal-to-ligand charge-transfer (MLCT) excited states that are currently experiencing a revival due to their application potential in organic photoredox catalysis, triplet–triplet annihilation upconversion, and phototherapy. At the same time, there is increased interest in the development of photoactive complexes made from Earth-abundant rather than precious metals. Against this background, we present a homoleptic Mo(0) complex with a new diisocyanide ligand exhibiting different bite angles and a greater extent of π-conjugation than previously reported related chelates. This new design leads to deep red emission, which is unprecedented for homoleptic arylisocyanide complexes of group 6 metals. With a 3MLCT lifetime of 56 ns, an emission band maximum at 720 nm, and a photoluminescence quantum yield of 1.5% in deaerated toluene at room temperature, the photophysical properties are reminiscent of the prototypical [Os(2,2′-bipyridine)3]2+ complex. Under 635 nm irradiation with a cw-laser, the new Mo(0) complex sensitizes triplet–triplet annihilation upconversion of 9,10-diphenylanthracene (DPA), resulting in delayed blue fluorescence with an anti-Stokes shift of 0.93 eV. The photorobustness of the Mo(0) complex and the upconversion quantum yield are high enough to generate a flux of upconverted light that can serve as a sufficiently potent irradiation source for a blue-light-driven photoisomerization reaction. These findings are relevant in the greater contexts of designing new luminophores and photosensitizers for use in red-light-driven photocatalysis, photochemical upconversion, light-harvesting, and phototherapy.
Faculties and Departments:05 Faculty of Science > Departement Chemie > Chemie > Anorganische Chemie (Wenger)
UniBasel Contributors:Wenger, Oliver and Bilger, Jakob Benjamin and Kerzig, Christoph and Larsen, Christopher Bryan
Item Type:Article, refereed
Article Subtype:Research Article
Publisher:American Chemical Society
Note:Publication type according to Uni Basel Research Database: Journal article
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Last Modified:27 Jan 2022 02:30
Deposited On:02 Mar 2021 10:33

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