Tokuda Hiroyuki, Tsuzuki Seiji, Susan Md Abu Bin Hasan, Hayamizu Kikuko, Watanabe Masayoshi
Department of Chemistry and Biotechnology, Yokohama National University, and CREST-JST, 79-5 Tokiwadai, Yokohama 240-8501, Japan.
J Phys Chem B. 2006 Oct 5;110(39):19593-600. doi: 10.1021/jp064159v.
Room-temperature ionic liquids (RTILs) are liquids consisting entirely of ions, and their important properties, e.g., negligible vapor pressure, are considered to result from the ionic nature. However, we do not know how ionic the RTILs are. The ionic nature of the RTILs is defined in this study as the molar conductivity ratio (Lambda(imp)/Lambda(NMR)), calculated from the molar conductivity measured by the electrochemical impedance method (Lambda(imp)) and that estimated by use of pulse-field-gradient spin-echo NMR ionic self-diffusion coefficients and the Nernst-Einstein relation (Lambda(NMR)). This ratio is compared with solvatochromic polarity scales: anionic donor ability (Lewis basicity), E(T)(30), hydrogen bond donor acidity (alpha), and dipolarity/polarizability (pi), as well as NMR chemical shifts. The Lambda(imp)/Lambda(NMR) well illustrates the degree of cation-anion aggregation in the RTILs at equilibrium, which can be explained by the effects of anionic donor and cationic acceptor abilities for the RTILs having different anionic and cationic backbone structures with fixed counterparts, and by the inductive and dispersive forces for the various alkyl chain lengths in the cations. As a measure of the electrostatic interaction of the RTILs, the effective ionic concentration (C(eff)), which is a dominant parameter for the electrostatic forces of the RTILs, was introduced as the product of Lambda(imp)/Lambda(NMR) and the molar concentration and was compared with some physical properties, such as reported normal boiling points and distillation rates, glass transition temperature, and viscosity. A decrease in C(eff) of the RTILs is well correlated with the normal boiling point and distillation rate, whereas the liquid-state dynamics is controlled by a subtle balance between the electrostatic and other intermolecular forces.
室温离子液体(RTILs)是完全由离子组成的液体,其重要性质,如可忽略不计的蒸气压,被认为是由离子性质导致的。然而,我们并不清楚RTILs的离子性究竟如何。在本研究中,RTILs的离子性定义为摩尔电导率比(Λ(imp)/Λ(NMR)),它是通过电化学阻抗法测得的摩尔电导率(Λ(imp))与利用脉冲场梯度自旋回波NMR离子自扩散系数和能斯特 - 爱因斯坦关系估算出的摩尔电导率(Λ(NMR))计算得出的。该比率与溶剂化显色极性标度进行了比较:阴离子给体能力(路易斯碱性)、E(T)(30)、氢键给体酸度(α)和偶极/极化率(π),以及NMR化学位移。Λ(imp)/Λ(NMR)很好地说明了RTILs在平衡时阳离子 - 阴离子聚集的程度,这可以通过具有固定对应物的不同阴离子和阳离子主链结构的RTILs的阴离子给体和阳离子受体能力的影响,以及阳离子中各种烷基链长度的诱导力和色散力来解释。作为RTILs静电相互作用的一种度量,有效离子浓度(C(eff))作为Λ(imp)/Λ(NMR)与摩尔浓度的乘积被引入,它是RTILs静电力的一个主要参数,并与一些物理性质进行了比较,如报道的正常沸点和蒸馏速率、玻璃化转变温度以及粘度。RTILs的C(eff)降低与正常沸点和蒸馏速率密切相关,而液态动力学则由静电和其他分子间力之间的微妙平衡所控制。