Merging Double Hydrogen Atom Transfer and Stepwise Proton-Coupled Electron Transfer for γ-C–H Hydrazination of Alcohols

A cobalt-(salen)-catalyzed γ-C-H hydrazination of alcohols is unveiled, merging a double hydrogen atom transfer (HAT) and a proton-coupled electron transfer (PCET) within a single catalytic cycle. The transformation harnesses metal-hydrogen atom transfer-induced radical translocation and electrophilic azodicarboxylate coupling to achieve remote C-H functionalization under mild and sustainable conditions. Mechanistic investigations (EPR, UV-vis, and spin-trapping) reveal cobalt oxidation state modulation and transient radical intermediates, while DFT analysis elucidates the double HAT/PCET pathway and site selectivity. This strategy offers an efficient and sustainable route from simple alcohols to γ-hydrazino and γ-amino alcohols.

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Publication Details

Journal
JACS Au
Published
2026-01-26
DOI
https://doi.org/10.1021/jacsau.5c01435
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Merging Double Hydrogen Atom Transfer and Stepwise Proton-Coupled Electron Transfer for γ-C–H Hydrazination of Alcohols

Luis Miguel Azofra, Olga S. Bokareva, Kosala N. Amarasinghe, Phong Dam et al.
JACS Au
Radical Photochemical Reactions
article

Merging Double Hydrogen Atom Transfer and Stepwise Proton-Coupled Electron Transfer for γ-C–H Hydrazination of Alcohols

Luis Miguel Azofra, Olga S. Bokareva, Kosala N. Amarasinghe, Phong Dam, Osama El-Sepelgy, Kaiming Zuo, Anke Spannenberg, Jabor Rabeah
article en

Abstract

A cobalt-(salen)-catalyzed γ-C-H hydrazination of alcohols is unveiled, merging a double hydrogen atom transfer (HAT) and a proton-coupled electron transfer (PCET) within a single catalytic cycle. The transformation harnesses metal-hydrogen atom transfer-induced radical translocation and electrophilic azodicarboxylate coupling to achieve remote C-H functionalization under mild and sustainable conditions. Mechanistic investigations (EPR, UV-vis, and spin-trapping) reveal cobalt oxidation state modulation and transient radical intermediates, while DFT analysis elucidates the double HAT/PCET pathway and site selectivity. This strategy offers an efficient and sustainable route from simple alcohols to γ-hydrazino and γ-amino alcohols.

JACS AuVol. 6(2)
Universidad de Las Palmas de Gran Canaria (ES), Leibniz Institute for Catalysis (DE), University of Rostock (DE)
Responsible consumption and production
Openalex Percentile: Top 77%
Radical Photochemical Reactions
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