Molecular Shells and Range of Interactions in Ionic Liquids as a Function of Temperature

Room-temperature ionic liquids (RTILs) represent a versatile class of chemical systems composed entirely of oppositely charged species whose bulk properties can be fine-tuned by adjusting molecular structures and, consequently, intermolecular interactions. Understanding the intricate dynamics between ionic species can aid in the rational design of RTILs for specific applications in a range of fields, including catalysis and electrochemistry. Here, we investigate the temperature dependence of intermolecular interactions through magnetization transfer by means of 1H–19F heteronuclear Overhauser effect spectroscopy (HOESY) for two ionic liquids, namely, [BMIM][BF4] and [BMIM][PF6]. We find that the cross-relaxation rates vary significantly over a rather small temperature range, even changing sign. Molecular dynamics (MD) simulations on neat RTIL systems replicate this behavior well and further show that the dynamic properties rather than coordination changes of RTILs account for the observed temperature behavior. Furthermore, the investigation of different coordination shells highlights the change of interaction range with temperature even to the point where inner and outer coordination shells could be in distinct motional regimes with cross-relaxation rates of opposite sign. Since temperature changes lead primarily to dynamic changes rather than structural ones, these findings underscore the versatility and high thermal stability of ionic liquids.