Selective Electrochemical Synthesis of the <i>para,para</i> C–C Dimer from Diphenylphenol and Its Conversion into Dibenzofuran

carbon-carbon dimer tetraphenyl dibenzoquinone from diphenylphenol is reported under electrochemical conditions and variable potential. The dibenzoquinone dimer was converted into its reduced state and dibenzofurans, at room temperature, a process that was controlled by electricity and light.

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Publication Details

Journal
Organic Letters
Published
2026-03-31
DOI
https://doi.org/10.1021/acs.orglett.5c05196
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Selective Electrochemical Synthesis of the para,para C–C Dimer from Diphenylphenol and Its Conversion into Dibenzofuran

Theresa M. McCormick, Avik Bhattacharjee, Sanela Martić, Abigail Boon et al.
Organic Letters
Radical Photochemical Reactions
article

Selective Electrochemical Synthesis of the para,para C–C Dimer from Diphenylphenol and Its Conversion into Dibenzofuran

Theresa M. McCormick, Avik Bhattacharjee, Sanela Martić, Abigail Boon, Christopher B. Caputo, Stephanie Gao, Tyra Lewis, MacKenna Mourre
article en

Abstract

carbon-carbon dimer tetraphenyl dibenzoquinone from diphenylphenol is reported under electrochemical conditions and variable potential. The dibenzoquinone dimer was converted into its reduced state and dibenzofurans, at room temperature, a process that was controlled by electricity and light.

Organic LettersVol. 28(14)
Portland State University (US), York University (CA), Trent University (CA)
Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 32%
Radical Photochemical Reactions
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Selective Electrochemical Synthesis of the <i>para,para</i> C–C Dimer from Diphenylphenol and Its Conversion into Dibenzofuran — Theresa M. McCormick, Avik Bhattacharjee, et al. · Organic Letters (2026) | TGRS Research Map | TGRS