Active Molybdenum-Based Anode for Dehydrogenative Coupling Reactions

被引:50
作者
Beil, Sebastian B. [1 ,2 ]
Mueller, Timo [1 ]
Sillart, Sydney B. [1 ]
Franzmann, Peter [1 ]
Bomm, Alexander [3 ]
Holtkamp, Michael [4 ]
Karst, Uwe [4 ]
Schade, Wolfgang [3 ]
Waldvogel, Siegfried R. [1 ,2 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Organ Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
[2] Grad Sch Excellence, Mat Sci Mainz MAINZ, Staudingerweg 9, D-55128 Mainz, Germany
[3] Fraunhofer Heinrich Hertz Inst, Abt Faseropt Sensorsyst, Stollen 19H, D-38640 Goslar, Germany
[4] Univ Munster, Inst Inorgan & Analyt Chem, Corrensstr 30, D-48149 Munster, Germany
关键词
anode; arene coupling; electrochemistry; molybdenum; oxidative coupling; SINGLE AROMATIC SUBSTRATE; N BOND FORMATION; DIARYLIODONIUM(III) SALTS; ORGANIC-COMPOUNDS; ALKALI SOLUTION; LIGNIN; ELECTRODES; REDUCTION; DEGRADATION; SELECTIVITY;
D O I
10.1002/anie.201712718
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new and powerful active anode system that can be operated in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) has been discovered. In HFIP the molybdenum anode forms a compact, conductive, and electroactive layer of higher-valent molybdenum species. This system can replace powerful but stoichiometrically required Mo-V reagents for the dehydrogenative coupling of aryls. This electrolytic reaction is more sustainable and allows the conversion of a broad scope of activated arenes.
引用
收藏
页码:2450 / 2454
页数:5
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