| Literature DB >> 35132222 |
Michael G Pfeffer1, Carolin Müller2,3, Evelyn T E Kastl1, Alexander K Mengele1, Benedikt Bagemihl1, Sven S Fauth1, Johannes Habermehl1, Lydia Petermann1, Maria Wächtler3,4, Martin Schulz2, Daniel Chartrand5, François Laverdière5, Phillip Seeber2, Stephan Kupfer2, Stefanie Gräfe2, Garry S Hanan5, Johannes G Vos6, Benjamin Dietzek-Ivanšić7,8,9, Sven Rau10.
Abstract
The molecular apparatus behind biological photosynthesis retains its long-term functionality through enzymatic repair. However, bioinspired molecular devices designed for artificial photosynthesis, consisting of a photocentre, a bridging ligand and a catalytic centre, can become unstable and break down when their individual modules are structurally compromised, halting their overall functionality and operation. Here we report the active repair of such an artificial photosynthetic molecular device, leading to complete recovery of catalytic activity. We have identified the hydrogenation of the bridging ligand, which inhibits the light-driven electron transfer between the photocentre and catalytic centre, as the deactivation mechanism. As a means of repair, we used the light-driven generation of singlet oxygen, catalysed by the photocentre, to enable the oxidative dehydrogenation of the bridging unit, which leads to the restoration of photocatalytic hydrogen formation.Entities:
Mesh:
Substances:
Year: 2022 PMID: 35132222 DOI: 10.1038/s41557-021-00860-6
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274