Ether chain-modified Alkanolguanidine for CO2 capture and subsequent conversion

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Abstract

Capturing CO2 and converting it into valuable chemicals has attracted considerable attention in recent years. Herein, a kind of ether chain-modified alkanolguanidines (ECMAs) was designed and synthesized as a dual functional reagent for carbon dioxide capture and conversion. Due to the presence of basic sites and CO2-philic ether chains, these ECMAs demonstrated almost equimolar CO2 capture at room temperature and atmospheric pressure through the synergy of physical and chemical absorption. Even for diluted CO2 (15 % CO2), 0.7 mol CO2 per mole capture reagent can still be achieved, showing their potential application in post-combustion capture. The synthesized ECMAs can also serve as catalyst in the cycloaddition reaction of CO2 with various epoxides, affording 75–99 % yield of corresponding cyclic carbonates under 3 MPa CO2 with tetrabutylammonium iodide (TBAI) as co-catalyst. Moreover, these ECMAs can be applied to the integrated CO2 capture and conversion, in which the ECMAs can react with CO2, forming the alkyl carbonate zwitterion as active CO2 species in the capture step. And in the subsequent cycloaddition reaction with propylene oxide, 52 % yield of propylene carbonate was obtained.

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用于二氧化碳捕获和后续转化的醚链改性烷醇胍
近年来,捕集二氧化碳并将其转化为有价值的化学品已引起了广泛关注。本文设计并合成了一种醚链修饰的烷醇胍(ECMAs),作为二氧化碳捕集和转化的双功能试剂。由于存在碱性位点和亲二氧化碳的醚链,这些 ECMAs 通过物理和化学吸收的协同作用,在室温和大气压力下几乎等摩尔捕获二氧化碳。即使是稀释的 CO2(15% CO2),每摩尔捕集试剂仍可捕集 0.7 摩尔 CO2,显示了它们在燃烧后捕集方面的应用潜力。合成的 ECMAs 还可在二氧化碳与各种环氧化物的环加成反应中用作催化剂,在 3 兆帕二氧化碳条件下,以碘化四丁基铵(TBAI)为助催化剂,可生成 75-99% 的相应环碳酸盐。此外,这些 ECMAs 还可应用于二氧化碳的捕获和转化,在捕获步骤中,ECMAs 可与二氧化碳发生反应,形成碳酸烷基齐聚物作为活性二氧化碳物种。在随后与环氧丙烷的环化反应中,碳酸丙烯酯的收率为 52%。
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