Paired Pulsed Decarboxylative Hydroxylation Designed by Online Electrochemistry–Mass Spectrometry

We present a novel strategy for optimizing paired pulsed electrosynthesis by real-time monitoring of redox processes at the electrode interface using voltammetry-electrospray ionization mass spectrometry (VESI-MS). VESI-MS provides molecular insight into interfacial events, enabling the rational design of voltage pulses and synchronization of redox reactions, facilitating the discovery of new alternating current (AC) electrochemical transformations. We apply this approach to develop a selective decarboxylative hydroxylation by coupling oxygen reduction with the oxidative decarboxylation of a carboxylic acid. The pilot study with 2-phenylpropionic acid yields 1-phenylethanol with excellent selectivity using only molecular oxygen, KPF<sub>6</sub>, water, and carbon electrodes. This work opens new possibilities for the design of pulsed electrosynthetic reactions.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-02
DOI
https://doi.org/10.1021/jacs.5c12895
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Paired Pulsed Decarboxylative Hydroxylation Designed by Online Electrochemistry–Mass Spectrometry

Jana Roithová, Adarsh Koovakattil Surendran
1 citations
Journal of the American Chemical Society
Radical Photochemical Reactions
0.94
article

Paired Pulsed Decarboxylative Hydroxylation Designed by Online Electrochemistry–Mass Spectrometry

Jana Roithová, Adarsh Koovakattil Surendran
article en
1 citations

Abstract

We present a novel strategy for optimizing paired pulsed electrosynthesis by real-time monitoring of redox processes at the electrode interface using voltammetry-electrospray ionization mass spectrometry (VESI-MS). VESI-MS provides molecular insight into interfacial events, enabling the rational design of voltage pulses and synchronization of redox reactions, facilitating the discovery of new alternating current (AC) electrochemical transformations. We apply this approach to develop a selective decarboxylative hydroxylation by coupling oxygen reduction with the oxidative decarboxylation of a carboxylic acid. The pilot study with 2-phenylpropionic acid yields 1-phenylethanol with excellent selectivity using only molecular oxygen, KPF<sub>6</sub>, water, and carbon electrodes. This work opens new possibilities for the design of pulsed electrosynthetic reactions.

Journal of the American Chemical SocietyVol. 147(41)
Radboud University Nijmegen (NL)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Openalex Percentile: Top 21%
Radical Photochemical Reactions
0.94
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Paired Pulsed Decarboxylative Hydroxylation Designed by Online Electrochemistry–Mass Spectrometry — Jana Roithová, Adarsh Koovakattil Surendran · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS