Acidity Scale in a Quaternary Phosphonium Ionic Liquid and Its Implication on Carbon Dioxide Absorption

离子液体 二氧化碳 吸收(声学) 第四纪 化学 无机化学 比例(比率) 离子键合 材料科学 有机化学 离子 地质学 物理 催化作用 古生物学 复合材料 量子力学
作者
Zhen Wang,Qian-Hang Niu,Wei Liu,Yongjun Zheng,Pengju Ji
出处
期刊:Journal of Organic Chemistry [American Chemical Society]
卷期号:90 (34): 12088-12098
标识
DOI:10.1021/acs.joc.5c00925
摘要

In this work, an acidity scale that comprises 23 organic Brønsted acids of different structural and electronic features was established in a representative quaternary phosphonium ionic liquid (QPIL), i.e., [P4,4,4,16][OTf] (with water content of 100 ppm), by the UV–vis spectroscopic method. The established acidity scale ranges from 5.4 to 22.2, covers about 17 pK units. We found that [P4,4,4,16][OTf] has fairly good stability toward some very strong bases. Acidity comparisons and regression analyses among various solvents show that the counteranion of [P4,4,4,16][OTf] is freer than those of imidazolium-based counterparts, which governs the solvation behavior of the QPIL. With the established acidity scale, we also studied CO2 absorptions in QPILs. To investigate the CO2 absorption in QPILs, a series of anion-functionalized QPILs, i.e., [P4,4,4,16][X] were synthesized, and their absorption capacities and kinetics were measured. The results show that the maximum absorption capacity of [P4,4,4,16][X] is much greater than that of other types of ILs, and a more basic QPIL leads to a faster absorption rate and a higher absorption capacity. The kinetic profiles and correlation analysis suggest that the capacity and mechanism of CO2 absorption in [P4,4,4,16][X] are closely associated with the basicities of anions of these QPILs.
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