Associative Photocatalysis: Activation of Inert Haloarenes by Interaction-Centric Design

The power of photoredox catalysis is constrained by the intrinsic properties of the individual catalyst molecules. This creates an energetic ceiling that prevents the activation of highly stable chemical bonds. This study introduces an “associative photocatalysis” strategy that circumvents this limitation by deriving photochemical function from transient intermolecular interactions. The selective excitation of a non-covalently bound electron donor–acceptor complex initiates a sequential two-photon process. This approach enables the functionalization of previously unreactive haloarenes, facilitating a range of efficient transformations. The gram-scale synthesis and late-stage diversification of loratadine are also performed. By shifting the design focus from static molecular scaffolds to dynamic interactions, associative photocatalysis provides a new blueprint for unlocking challenging chemical reactivities and advancing sustainable synthesis.

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Publication Details

Journal
ChemRxiv
Published
2025-08-22
DOI
https://doi.org/10.26434/chemrxiv-2025-1386d
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Associative Photocatalysis: Activation of Inert Haloarenes by Interaction-Centric Design

Sayaka Ohrui, Masanori Tayu, Masahiro Noji, Satoshi Hayashi et al.
ChemRxiv
Radical Photochemical Reactions
article

Associative Photocatalysis: Activation of Inert Haloarenes by Interaction-Centric Design

Sayaka Ohrui, Masanori Tayu, Masahiro Noji, Satoshi Hayashi, Nozomi Saito, Kakeru Matsukuma, K. Muto, Ryota Itai
article en

Abstract

The power of photoredox catalysis is constrained by the intrinsic properties of the individual catalyst molecules. This creates an energetic ceiling that prevents the activation of highly stable chemical bonds. This study introduces an “associative photocatalysis” strategy that circumvents this limitation by deriving photochemical function from transient intermolecular interactions. The selective excitation of a non-covalently bound electron donor–acceptor complex initiates a sequential two-photon process. This approach enables the functionalization of previously unreactive haloarenes, facilitating a range of efficient transformations. The gram-scale synthesis and late-stage diversification of loratadine are also performed. By shifting the design focus from static molecular scaffolds to dynamic interactions, associative photocatalysis provides a new blueprint for unlocking challenging chemical reactivities and advancing sustainable synthesis.

ChemRxiv
Meiji Pharmaceutical University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 84%
Radical Photochemical Reactions
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