SCI和EI收录∣中国化工学会会刊

中国化学工程学报 ›› 2022, Vol. 50 ›› Issue (10): 264-282.DOI: 10.1016/j.cjche.2022.09.003

• Catalysis, Kinetics and Reaction Engineering • 上一篇    下一篇

Direct carboxylation of thiophene with CO2 in the solvent-free carboxylate-carbonate molten medium: Experimental and mechanistic insights

Qingjun Zhang1, Pengyuan Shi1, Xigang Yuan1,2, Youguang Ma1,2, Aiwu Zeng1,2   

  1. 1 State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China;
    2 Chemical Engineering Research Center, Collaborative Innovative Center of Chemical Science and Engineering (Tianjin), Tianjin 300350, China
  • 收稿日期:2022-04-14 修回日期:2022-09-14 出版日期:2022-10-28 发布日期:2023-01-04
  • 通讯作者: Aiwu Zeng,E-mail:awzeng@tju.edu.cn

Direct carboxylation of thiophene with CO2 in the solvent-free carboxylate-carbonate molten medium: Experimental and mechanistic insights

Qingjun Zhang1, Pengyuan Shi1, Xigang Yuan1,2, Youguang Ma1,2, Aiwu Zeng1,2   

  1. 1 State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China;
    2 Chemical Engineering Research Center, Collaborative Innovative Center of Chemical Science and Engineering (Tianjin), Tianjin 300350, China
  • Received:2022-04-14 Revised:2022-09-14 Online:2022-10-28 Published:2023-01-04
  • Contact: Aiwu Zeng,E-mail:awzeng@tju.edu.cn

摘要: A feasible synthesis route is devised for realizing direct carboxylation of thiophene and CO2 in a relatively mild solvent-free carboxylate-assisted carbonate (semi) molten medium. The effects of reaction factors on product yield are investigated, and the phase behavior analysis of the reaction medium is detected through the thermal characterization techniques. Product yield varies with the alternative carboxylate co-salts, which is attributed to the difference in deprotonation capacity caused by the base effect within the system. Besides, the detailed mechanism of this carbonate-promoted carboxylation reaction is studied, including two consecutive steps of the formation of carbanion through breaking the C—H bond(s) via the carbonate and the nucleophile attacking the weak electrophile CO2 to form C—C bond(s). The activation energy barrier in C—H activation step is higher than the following CO2 insertion step whether for the formation of the mono- and/or di-carboxylate, which is in good agreement with that of kinetic isotope effect (KIE) experiments, indicating that the C—H deprotonation is slow and the forming presumed carbanion reacts rapidly with CO2. Both the activation energy barriers in deprotonation steps are the minimal for the cesium cluster system since there have the weak the cesium Cs-heteroatom S (thiophene) and Cs-the broken proton interactions compared to the K2CO3 system, which is likely to enhance the acidity of C—H bond, lowering the C—H activation barrier. Besides, these mechanistic insights are further assessed by investigating base and C—H substrate effects via replacing Cs2CO3 with K2CO3 and furoate (1a) with thiophene monocarboxylate (1b) or benzoate (1c).

关键词: Inert C—H bond, Carboxylation, Solvent-free medium, Base effect, Density functional theory (DFT) study

Abstract: A feasible synthesis route is devised for realizing direct carboxylation of thiophene and CO2 in a relatively mild solvent-free carboxylate-assisted carbonate (semi) molten medium. The effects of reaction factors on product yield are investigated, and the phase behavior analysis of the reaction medium is detected through the thermal characterization techniques. Product yield varies with the alternative carboxylate co-salts, which is attributed to the difference in deprotonation capacity caused by the base effect within the system. Besides, the detailed mechanism of this carbonate-promoted carboxylation reaction is studied, including two consecutive steps of the formation of carbanion through breaking the C—H bond(s) via the carbonate and the nucleophile attacking the weak electrophile CO2 to form C—C bond(s). The activation energy barrier in C—H activation step is higher than the following CO2 insertion step whether for the formation of the mono- and/or di-carboxylate, which is in good agreement with that of kinetic isotope effect (KIE) experiments, indicating that the C—H deprotonation is slow and the forming presumed carbanion reacts rapidly with CO2. Both the activation energy barriers in deprotonation steps are the minimal for the cesium cluster system since there have the weak the cesium Cs-heteroatom S (thiophene) and Cs-the broken proton interactions compared to the K2CO3 system, which is likely to enhance the acidity of C—H bond, lowering the C—H activation barrier. Besides, these mechanistic insights are further assessed by investigating base and C—H substrate effects via replacing Cs2CO3 with K2CO3 and furoate (1a) with thiophene monocarboxylate (1b) or benzoate (1c).

Key words: Inert C—H bond, Carboxylation, Solvent-free medium, Base effect, Density functional theory (DFT) study