<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">JERA</journal-id><journal-title-group><journal-title>Journal of Electronic Research and Application</journal-title></journal-title-group><issn>2208-3502</issn><eissn>2208-3510</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/jera.v9i2.9879</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Electrochemically Driven Nickel-Catalyzed Phenol Synthesis via Sustainable Oxygen Atom Transfer from Nitrous Oxide</title><url>https://artdesignp.com/journal/JERA/9/2/10.26689/jera.v9i2.9879</url><author>ZhangQiyu,XieWenbin,MohamedYasser M. A.,El NazerHossam A.,ElnazerAhmed A.,HanYinghui</author><pub-date pub-type="publication-year"><year>2025</year></pub-date><volume>9</volume><issue>2</issue><history><date date-type="pub"><published-time>2025-03-21</published-time></date></history><abstract>The valorization of nitrous oxide (N2O) as an oxygen atom donor presents an attractive opportunity for green chemistry applications, leveraging both its industrial abundance and thermodynamically favorable oxidation potential. However, practical implementation has been constrained by the inherent kinetic inertness and poor coordinating ability of N2O. While prior studies achieved N2O-mediated conversion of aryl halides to phenols, such transformations necessitated stoichiometric chemical reductants and elevated pressure (2 atm), posing challenges in operational safety and process scalability. This study focuses on an electrochemical strategy that enables efficient oxygen atom transfer under ambient pressure through controlled current application. This methodology facilitates the selective transformation of aryl iodides to phenols without external reducing agents, establishing an environmentally benign synthetic pathway. By replacing traditional chemical reductants with electrons as the sole reducing equivalent, our approach addresses critical sustainability challenges in aromatic oxygenation chemistry while maintaining operational simplicity under mild conditions.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>William BT, 2010, Binding and Activation of N2O at Transition-Metal Centers: Recent Mechanistic Insights. Angew Chem Int Ed, 49: 1018-1024. http://doi.org/10.1002/anie.200905364.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Vaillant FL, Calbet AM, Gonzalez-Pelayo S, et al., 2022. Catalytic Synthesis of Phenols with Nitrous Oxide. Nature, 604: 677-683. http://doi.org/10.1038/s41586-022-04516-4.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B3" content-type="article"><label>3</label><element-citation publication-type="journal"><p>Ni SY, Cornella J, 2023, Catalytic Hydroxylation of Arylthianthrenium Salts with Nitrous Oxide. Tetrahedron, 145: 133602. http://doi.org/10.1016/j.tet.2023.133602.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B4" content-type="article"><label>4</label><element-citation publication-type="journal"><p>Zhang HH, Rodrigalvarez J, and Martin R, 2023, C(sp2)-H hydroxylation via catalytic 1,4-Ni migration with N2O. J Am Chem Soc, 145: 17564-17569. http://doi.org10.1021/jacs.3c07018.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B5" content-type="article"><label>5</label><element-citation publication-type="journal"><p>Jiao KJ, Li ZM, Xu XT, et al., 2018, Palladium-Catalyzed Reductive Electrocarboxylation of Allyl Esters with Carbon Dioxide. Org Chem Front, 5: 2244-2248. http://doi.org10.1039/c8qo00507a.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B6" content-type="article"><label>6</label><element-citation publication-type="journal"><p>Baldinelli L, Belanzoni P, Bistoni G, et al., 2024, Mechanism of Nitrous Oxide Activation in C(sp2)-O Bond Formation Reactions Catalyzed by Nickel Complexes. J Am Chem Soc, 146: 6016-6024. http://doi.org/10.1021/jacs.3c12922.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
