Mg Electrodes Coiled with Cu Wires Promoted Formation of Diphenylacetylene from Tetrachloroethylene and Bromobenzene: One-step Electrochemical Synthesis without Pd Catalyst

It was found that diphenylacetylene was synthesized by using electrochemical reduction with Mg electrodes, coiled with Cu wires. The electrochemical reaction of tetrachloroethylene and bromobenzene in LiClO4/THF afforded diphenylacetylene in up to 38 % yield. The reaction took place in the absence of Pd catalyst. The scope and limitations, and investigation of reaction mechanism were also studied.

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Publication Details

Journal
Electrochemistry
Published
2024-08-21
DOI
https://doi.org/10.5796/electrochemistry.24-00079
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Mg Electrodes Coiled with Cu Wires Promoted Formation of Diphenylacetylene from Tetrachloroethylene and Bromobenzene: One-step Electrochemical Synthesis without Pd Catalyst

Kengo Hamasaki, Pengyu Xu, Kouichi Matsumoto, Ryoichi TOMIYAMA et al.
1 citations
Electrochemistry
Radical Photochemical Reactions
0.25
article

Mg Electrodes Coiled with Cu Wires Promoted Formation of Diphenylacetylene from Tetrachloroethylene and Bromobenzene: One-step Electrochemical Synthesis without Pd Catalyst

Kengo Hamasaki, Pengyu Xu, Kouichi Matsumoto, Ryoichi TOMIYAMA, Shin YONEYAMA
article en
1 citations

Abstract

It was found that diphenylacetylene was synthesized by using electrochemical reduction with Mg electrodes, coiled with Cu wires. The electrochemical reaction of tetrachloroethylene and bromobenzene in LiClO4/THF afforded diphenylacetylene in up to 38 % yield. The reaction took place in the absence of Pd catalyst. The scope and limitations, and investigation of reaction mechanism were also studied.

ElectrochemistryVol. 92(10)
Synlab Czech (Czechia) (CZ), Kindai University (JP)
Kindai University, Kanazawa University, Japan Society for the Promotion of Science
Openalex Percentile: Top 49%
Radical Photochemical Reactions
0.25
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