Luo Wenzhi, Mao Chong, Ji Pengju, Wu Jun-Yan, Yang Jin-Dong, Cheng Jin-Pei
Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University Beijing 100084 China
State Key Laboratory of Elemento-organic Chemistry, College of Chemistry, Nankai University Tianjin 300071 China.
Chem Sci. 2020 Mar 3;11(12):3365-3370. doi: 10.1039/c9sc06341b.
How would acidic bond dissociation be affected by adding a small quantity of a weakly polar ionic liquid IL (the "apparent" or "measured" dielectric constant of the IL is around 10-15) into a strongly polar molecular solvent (, of DMSO: 46.5), or ? The answer is blurred, because no previous investigation was reported in this regard. Toward this, we, taking various IL/DMSO mixtures as representatives, have thoroughly investigated the effects of the respective solvent in ionic-molecular binary systems on self-dissociation of C-H acid phenylmalononitrile PhCH(CN) p determination. As disclosed, in this category of binary media, (1) no linear correspondence exists between p and molar fractions of the respective solvent components; (2) only ∼1-2 mol% of weakly polar ILs in strongly polar DMSO make C-H bonds even dissociative than in neat DMSO; (3) a small fraction of DMSO in ILs (<10 mol%) can dramatically ease acidic C-H-dissociation; and (4) while the DMSO fraction further increases, its acidifying effect becomes much attenuated. These findings, though maybe counterintuitive, have been rationalized on the basis of the precise p measurement of this work in relation to the respective roles of each solvent component in solvation.
向强极性分子溶剂(如二甲基亚砜(DMSO),其介电常数为46.5)中加入少量弱极性离子液体IL(IL的“表观”或“测量”介电常数约为10 - 15),酸性键离解会受到怎样的影响呢?答案并不明确,因为此前尚无这方面的研究报道。为此,我们以各种IL/DMSO混合物为代表,深入研究了离子 - 分子二元体系中各溶剂对C - H酸苯基丙二腈PhCH(CN)₂自离解的影响。结果表明,在这类二元介质中,(1)pKa与各溶剂组分的摩尔分数之间不存在线性对应关系;(2)在强极性DMSO中仅加入约1 - 2 mol%的弱极性IL,就能使C - H键比在纯DMSO中更易离解;(3)在IL中加入少量DMSO(<10 mol%)能显著促进酸性C - H离解;(4)当DMSO的比例进一步增加时,其酸化作用会大大减弱。这些发现虽然可能有悖直觉,但已根据本研究中精确的pKa测量结果,结合各溶剂组分在溶剂化中的作用得到了合理的解释。