论文标题

超低质子活性的离子液体

Ionic liquids of ultralow proton activity

论文作者

Angell, C. Austen

论文摘要

最近的工作已经描述了通过质子从分子超级酸转移到弱分子碱等弱分子碱基到超酸性离子液体的途径。在这里,我们考虑通过类似的过程制作超碱性离子液体的过程,并遇到找到足够碱性的分子碱基的问题,以接受弱酸中的质子以形成具有高碱度和高标志性的离子液体。结果是,尚未制成质子碱基限量以外的质子活性的离子液体。通过考虑六种可能类型的质子转移过程来解决该问题,从而选择从弱分子酸到非常碱性的离子阴离子的转移过程 - 与碱金属阳离子合作,然后通过测定替换碱金属阳离子,替换碱金属阳离子。在许多情况下,靶阴离子的碱金属盐是商业上可用的,并且仅需要元理解反应才能获得碱性离子液体。描述了对水尺度评估碱性水平的热力学途径,即相对于H3O+/H2O供体/受体水平,并在纯H2SO4的情况下进行了验证。然后将其应用于如何通过约25个数量级扩展可能的质子活性范围,以达到40顺序的PKA值,而原则上可能更高的值。

The route to super acidic ionic liquids by proton transfer from molecular super acids to weak molecular bases like pentafluoropyridine, has been described in recent work. Here we consider the process of making super basic ionic liquids by a similar procedure, and encounter the problem of finding molecular bases of high enough basicity to accept protons from weak acids to form ionic liquids of both high basicity and high iconicity. The consequence is that no ionic liquid with proton activity outside the aqueous base limit of pH =14, has yet been made. The problem is resolved by considering the six possible types of proton transfer processes, selecting the process of transfer from weak molecular acids to very basic ionic anions - partnered with alkali metal cations, and then replacing the alkali metals cations with reduction-resistant organic cations by metathesis. In many cases the alkali metal salts of target anions are commercially available, and only the metathesis reaction is needed to obtain the basic ionic liquid. A thermodynamic route to the assessment of basicity levels on the water scale, i.e. relative to the H3O+/H2O donor/acceptor level, is described, and is verified for the case of pure H2SO4. It is then applied to show how to extend the possible proton activity range down, by some 25 orders of magnitude, to reach pKa values of order 40, with even higher values possible in principle.

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