超强碱
共晶体系
催化作用
固定(群体遗传学)
化学
材料科学
有机化学
化学工程
工程类
生物化学
基因
合金
作者
Sara García-Argüelles,M. Luisa Ferrer,M. Iglesias,Francisco del Monte,Marı́a C. Gutiérrez
出处
期刊:Materials
[Multidisciplinary Digital Publishing Institute]
日期:2017-07-07
卷期号:10 (7): 759-759
被引量:33
摘要
Superbases have shown high performance as catalysts in the chemical fixation of CO₂ to epoxides. The proposed reaction mechanism typically assumes the formation of a superbase, the CO₂ adduct as the intermediate, most likely because of the well-known affinity between superbases and CO₂, i.e., superbases have actually proven quite effective for CO₂ absorption. In this latter use, concerns about the chemical stability upon successive absorption-desorption cycles also merits attention when using superbases as catalysts. In this work, ¹H NMR spectroscopy was used to get further insights about (1) whether a superbase, the CO₂ adduct, is formed as an intermediate and (2) the chemical stability of the catalyst after reaction. For this purpose, we proposed as a model system the chemical fixation of CO₂ to epichlorohydrin (EP) using a deep eutectic solvent (DES) composed of a superbase, e.g., 2,3,4,6,7,8-hexahydro-1
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