Selective Functionalization of Styrenes with Oxygen Using Different Electrode Materials: Olefin Cleavage and Synthesis of Tetrahydrofuran Derivatives

被引:67
作者
Imada, Yasushi [1 ]
Okada, Yohei [2 ]
Noguchi, Keiichi [3 ]
Chiba, Kazuhiro [1 ]
机构
[1] Tokyo Univ Agr & Technol, Dept Appl Biol Sci, 3-5-8 Saiwai Cho, Fuchu, Tokyo 1838509, Japan
[2] Tokyo Univ Agr & Technol, Dept Chem Engn, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
[3] Tokyo Univ Agr & Technol, Instrumentat Anal Ctr, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
关键词
electrochemistry; electrode material; olefin cleavage; styrenes; tetrahydrofurans synthesis; CATALYZED OXIDATIVE CLEAVAGE; GEM-DISUBSTITUTED ALKENES; C DOUBLE-BOND; CATIONIC-POLYMERIZATION; ALPHA-METHYLSTYRENE; MOLECULAR-OXYGEN; ANODIC-OXIDATION; SUPEROXIDE ION; METAL-FREE; PLATINUM;
D O I
10.1002/anie.201809454
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrode materials can have a significant impact on the course of an electrolysis reaction. Of particular interest is that different electrodes can generate different products from the same substrate. The electrode-material-selective transformations of styrene derivatives with molecular oxygen are reported. Platinum electrodes afford carbonyl products via cleavage of olefins, whereas tetrahydrofuran formation is achieved with carbon electrodes. A variety of different styrenes are available for both reactions. Electrolysis allows straightforward and mild chemical conversions that are metal- and oxidant-free. Electrochemical measurements illuminate the different effects of platinum and carbon electrodes on styrenes. The key to the differing reactions is probably that the oxidation potentials of the substrates are lower (higher HOMO energy) on carbon electrodes than on platinum electrodes. The adsorption of the substrates on carbon electrodes can also promote tetrahydrofuran formation.
引用
收藏
页码:125 / 129
页数:5
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