Counterintuitive Isomerization of TFSI^– and TFSI^––Cation Correlated Isomerization: Insights into the Low Melting Points of TFSI^–-Based Ionic Liquids

Ionic liquids (ILs), particularly bis(trifluoromethane)sulfonamide (TFSI^-)-based ILs, have attracted substantial attention in electrochemical energy storage, ionic gating for superconductivity, and iontronic sensing. However, underestimating TFSI^- isomerization and overlooking TFSI^--cation correlation make the origin of their most characteristic property, low melting points (<i>T</i>_m), ambiguous. Traditional static electronic structure calculations assume that <i>C</i>₂-symmetric <i>trans</i> enantiomers of TFSI^- easily isomerize into <i>cis</i> enantiomers through four symmetrically equivalent pathways over a barrier of 7.1 kJ mol^-1. Herein, ab initio molecular dynamics (AIMD) simulations combined with metadynamics reveal that the unusual oscillation of the central nitrogen atom promotes TFSI^- to undergo complex isomerization. Specifically, asymmetric <i>trans</i>-to-<i>cis</i> diastereomers of TFSI^- experience restricted interconversion (20-52 kJ mol^-1) through four distinct asymmetric pathways. The adaptive oscillation and hybridization of chiral nitrogen boost n_N → σ*_S-C negative hyperconjugation for stabilizing conformational structures and enlarging energy barriers. The orientational distortion of oxygen atoms' lone pairs enhances conjugation but breaks the <i>C</i>₂-symmetry. The coexistence of both helicity and chiral nitrogen breaks the enantiomeric relationship. Furthermore, Raman characterization and AIMD simulations confirm the positive correlation between the relative stability of <i>cis</i>-TFSI^- and its countercation's polarity. TFSI^- and countercations make a mutual conformational selection instead of free isomerization. Surprisingly, <i>T</i>_m increases with the cation-dependent conformational rigidity of TFSI^-, offering new fundamental insights into the low <i>T</i>_m of ILs. This descriptor encoding the dependence of thermal property on cation-anion correlated isomerization provides material design guidelines and property prediction capability.