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.

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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

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article

Mechanistic Insights into Light-Driven Acceptorless Dehydrogenation Reactions

Caroline J. Verhoef, J. Chris Slootweg, Runxuan Ma
Chemical Reviews
Radical Photochemical Reactions
article

Mechanistic Insights into Light-Driven Acceptorless Dehydrogenation Reactions

Caroline J. Verhoef, J. Chris Slootweg, Runxuan Ma
article en

Abstract

-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.

Chemical Reviews
Institute for Molecular Science (JP), University of Amsterdam (NL)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Openalex Percentile: Top 15%
Radical Photochemical Reactions
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