DOI: 10.1016/j.jcou.2018.01.016
Scopus记录号: 2-s2.0-85041480514
论文题名: Organocatalyst system for disubstituted carbonates from cycloaddition between CO2 and internal epoxides
作者: Hirose T. ; Qu S. ; Kodama K. ; Wang X.
刊名: Journal of CO2 Utilization
ISSN: 22129820
出版年: 2018
卷: 24 起始页码: 261
结束页码: 265
语种: 英语
英文关键词: Carbon dioxide fixation
; Internal epoxides
; Mild conditions
; Organocatalyst system
Scopus关键词: Carbon
; Carbon dioxide
; Carbonates
; Catalysis
; Catalysts
; 1 ,8-diazabicyclo[5.4.0]undec-7-ene
; Alternative systems
; Carbon dioxide fixation
; Catalyst screening
; Internal epoxides
; Mild conditions
; Organocatalyst system
; Steric hindrances
; Chlorine compounds
英文摘要: An organocatalyst system, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and nBu4NCl, was developed for the conversion of CO2 and internal epoxides to the corresponding disubstituted cyclic carbonates under rather mild conditions (1–4 atm of CO2 and 100–120 °C). Catalyst screening revealed that small Cl− opens epoxide rings more effectively than larger Br− and I− do when used as the counter anion of nBu4N+, suggesting that the steric hindrance of the internal epoxides is a factor. A practical and economical alternative system, DBU and nBuCl, is also presented. © 2018 Elsevier Ltd
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资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/111966
Appears in Collections: 气候减缓与适应
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作者单位: Graduate School of Science and Engineering, Saitama University, 255 Shimo-Okubo, Sakura-ku, Saitama, 338-8570, Japan
Recommended Citation:
Hirose T.,Qu S.,Kodama K.,et al. Organocatalyst system for disubstituted carbonates from cycloaddition between CO2 and internal epoxides[J]. Journal of CO2 Utilization,2018-01-01,24