催化作用
环加成
环氧化物
化学
合理设计
可再生能源
有机化学
功能群
密度泛函理论
氢
固碳
碳纤维
化学工程
组合化学
化学稳定性
反应条件
碘化物
氢键
绿色化学
材料科学
二氧化碳
傅里叶变换红外光谱
海泡石
化学过程
羰基化
氢甲酰化
作者
Yan Chen,Qingmei Ge,Hang Cong,Jiang Zhao,Wenfeng Zhao
标识
DOI:10.1021/acsapm.5c04455
摘要
The chemical fixation of carbon dioxide (CO 2 ) into value-added chemicals is a pivotal research direction toward achieving carbon neutrality and sustainable chemistry. Herein, a biomass-derived poly(ionic liquid) (BPIL) was designed from renewable chitin and low-cost pyridinium. The as-prepared catalyst exhibits excellent performance in the cycloaddition of CO 2 with various epoxides under mild/solvent-free/cocatalyst-free conditions. Furthermore, the catalyst demonstrates remarkable stability and recyclability with no significant loss of activity over five consecutive cycles. More importantly, a combination of in situ FTIR experimental studies and density functional theory (DFT) calculations reveals a crucial synergistic effect between the hydroxyl groups on the biomass support, acting as hydrogen bond donors (HBDs), and the iodide anions. This synergy effectively activates the epoxide and significantly lowers the energy barrier of the rate-determining step. This work not only provides an efficient and green catalytic system for CO 2 valorization but also offers a strategy for the rational design of multifunctional catalysts from renewable biomass.
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