Photo-induced N-Center Radical Catalyzed Direct Hydrogen Atom Transfer Platform for Aliphatic C–H Functionalization

The introduction of diverse functionalities to omnipresent aliphatic C–H bonds is a challenge of notable value in catalysis. Herein, we report a universal platform using readily prepared 9-arylacridine catalysts−a class of neutral, N-centered photocatalysts−that engage aliphatic C–H bonds under mild conditions. This strategy enables the efficient generation of alkyl radicals, allowing various functionalizations of C–H bonds ranging from activated substrates to unativated, gaseous ethane. The platform features broad substrate scope, scalability, and compatibility with transition metal catalysis as well as multicomponent reactions. Its utility is demonstrated in streamlined synthesis of pharmaceutical synthons and late-stage functionalization of bioactive molecules. Detailed mechanistic studies highlight the crucial role of ortho-substituents (e.g. Cl atoms) on the 9-aryl moiety of catalysts, providing a rational basis for current and future catalyst design.

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Publication Details

Journal
ChemRxiv
Published
2025-08-18
DOI
https://doi.org/10.26434/chemrxiv-2025-r2760
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94

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article

Photo-induced N-Center Radical Catalyzed Direct Hydrogen Atom Transfer Platform for Aliphatic C–H Functionalization

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ChemRxiv
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article

Photo-induced N-Center Radical Catalyzed Direct Hydrogen Atom Transfer Platform for Aliphatic C–H Functionalization

Boya Feng, Timothy Noël, Joshua P. Barham, Michał Domański, Mattia Lepori, Guodong Zhang, Prakash C. Tiwari
article en
1 citations

Abstract

The introduction of diverse functionalities to omnipresent aliphatic C–H bonds is a challenge of notable value in catalysis. Herein, we report a universal platform using readily prepared 9-arylacridine catalysts−a class of neutral, N-centered photocatalysts−that engage aliphatic C–H bonds under mild conditions. This strategy enables the efficient generation of alkyl radicals, allowing various functionalizations of C–H bonds ranging from activated substrates to unativated, gaseous ethane. The platform features broad substrate scope, scalability, and compatibility with transition metal catalysis as well as multicomponent reactions. Its utility is demonstrated in streamlined synthesis of pharmaceutical synthons and late-stage functionalization of bioactive molecules. Detailed mechanistic studies highlight the crucial role of ortho-substituents (e.g. Cl atoms) on the 9-aryl moiety of catalysts, providing a rational basis for current and future catalyst design.

ChemRxiv
University of Strathclyde (GB), Chinese Academy of Sciences (CN), University of Regensburg (DE), University of Amsterdam (NL)
Alexander von Humboldt-Stiftung, National Natural Science Foundation of China, China Scholarship Council, Natural Science Foundation of Jiangsu Province, Horizon 2020, Elitenetzwerk Bayern
Openalex Percentile: Top 23%
Catalytic C–H Functionalization Methods
0.94
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