Chen Hong-Jie, Hsu I-Jui, Tseng Mei-Chun, Shyu Shin-Guang
Institute of Chemistry, Academia Sinica, Taipei 115, Taiwan, Republic of China.
Dalton Trans. 2014 Aug 7;43(29):11410-7. doi: 10.1039/c4dt00582a. Epub 2014 Jun 17.
The C-O coupling reaction between 2,4-dimethylphenol and 4-bromotoluene catalyzed by the CuI/K2CO3/phen system can be inhibited by the radical scavenger cumene. Complexes Cu(i)(phen)(1-(2,4-dimethylphenoxy)-4-methylbenzene) (denoted as A), {H[Cu(i)(phen)(2,4-dimethylphenoxy)]}(+) and Cu(i)(2,4-dimethylphenoxy)2 (denoted as B) were observed by in situ electrospray ionization mass spectrometry (ESI-MS) analysis of the copper(i)-catalyzed C-O coupling reaction under the catalytic reaction conditions indicating that they could be intermediates in the reaction. The in situ EPR study of the reaction solution detected the Cu(ii) species with a fitted g value of 2.188. A catalytic cycle with a single electron transfer (SET) step was proposed based on these observations.
由CuI/K2CO3/邻菲罗啉体系催化的2,4-二甲基苯酚与4-溴甲苯之间的C-O偶联反应可被自由基清除剂异丙苯抑制。通过在催化反应条件下对铜(I)催化的C-O偶联反应进行原位电喷雾电离质谱(ESI-MS)分析,观察到配合物Cu(i)(phen)(1-(2,4-二甲基苯氧基)-4-甲基苯)(记为A)、{H[Cu(i)(phen)(2,4-二甲基苯氧基)]}(+)和Cu(i)(2,4-二甲基苯氧基)2(记为B),这表明它们可能是反应的中间体。对反应溶液的原位电子顺磁共振研究检测到g值拟合为2.188的Cu(II)物种。基于这些观察结果,提出了一个具有单电子转移(SET)步骤的催化循环。