Mechanistic Insights into Light-Driven Acceptorless Dehydrogenation Reactions
-hybridized C-C bonds in hydrocarbon substrates via oxidative C-H addition with subsequent β-hydride elimination. Second, binary homogeneous photocatalytic systems, consisting of a photosensitizer and a transition-metal-based proton reduction catalyst, enable all four types of dehydrogenation reactions via SET. Third, heterogeneous catalysts employed in light-driven dehydrogenation reactions often comprise a semiconductive support material integrated with a transition-metal-based active site, functioning via Mott-Schottky type photoinduced charge separation.
Authors
- Caroline J. Verhoef
- J. Chris Slootweg (ORCID: https://orcid.org/0000-0001-7818-7766)
- Runxuan Ma
Institutions
- Institute for Molecular Science (JP)
- University of Amsterdam (NL)
Publication Details
- Journal
- Chemical Reviews
- Published
- 2026-04-17
- DOI
- https://doi.org/10.1021/acs.chemrev.5c00904
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek