Exchange coupling states of cobalt complexes to control proton-coupled electron transfer

The electrochemical proton reactivity of transition metal complexes receives significant attentions. A thorough understanding of proton-coupled electron transfer (PCET) pathways is essential for elucidating the mechanism behind a proton reduction reaction, and controlling the pathway is a key focus in the field of the catalyst development. Spin interactions within complexes, which arise during electron transfer, can affect significantly the PCET pathway. Herein, we explore the phenomenon of spin rearrangement during the electrochemical reorganization of high-spin cobalt complexes. Our findings reveal that opposing spin interactions, induced by different coordination environments, can alter the PCET pathway. Finally, detailed analysis of the PCET pathway allows us to propose mechanisms for proton reduction in high-spin cobalt complexes.

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Publication Details

Journal
Nature Communications
Published
2024-10-07
DOI
https://doi.org/10.1038/s41467-024-53099-3
Citations
12
Primary Topic
Metalloenzymes and iron-sulfur proteins
Type
article
Field-Weighted Citation Impact
1.23

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article

Exchange coupling states of cobalt complexes to control proton-coupled electron transfer

Junhyeok Seo, Junseong Lee, Jueun Lee
12 citations
Nature Communications
Metalloenzymes and iron-sulfur proteins
1.23
article

Exchange coupling states of cobalt complexes to control proton-coupled electron transfer

Junhyeok Seo, Junseong Lee, Jueun Lee
article en
12 citations

Abstract

The electrochemical proton reactivity of transition metal complexes receives significant attentions. A thorough understanding of proton-coupled electron transfer (PCET) pathways is essential for elucidating the mechanism behind a proton reduction reaction, and controlling the pathway is a key focus in the field of the catalyst development. Spin interactions within complexes, which arise during electron transfer, can affect significantly the PCET pathway. Herein, we explore the phenomenon of spin rearrangement during the electrochemical reorganization of high-spin cobalt complexes. Our findings reveal that opposing spin interactions, induced by different coordination environments, can alter the PCET pathway. Finally, detailed analysis of the PCET pathway allows us to propose mechanisms for proton reduction in high-spin cobalt complexes.

Nature CommunicationsVol. 15(1)
Chonnam National University (KR), Gwangju Institute of Science and Technology (KR)
National Research Foundation, Ministry of Oceans and Fisheries, National Research Foundation of Korea, Korea Institute of Marine Science and Technology promotion, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 23%
Metalloenzymes and iron-sulfur proteins
1.23
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