Frontiers in Chemistry (Feb 2020)
How Molecular Chiralities of Bis(mandelato)borate Anions Affect Their Binding Structures With Alkali Metal Ions and Microstructural Properties in Tetraalkylphosphonium Ionic Liquids
Abstract
Spiroborate anion-based inorganic electrolytes and ionic liquids (ILs) have fascinating electrochemical and tribological properties and have received widespread attention in industrial applications. The molecular chiralities of spiroborate anions have a significant effect on the microstructures and macroscopic functionalities of these ionic materials in application and thus deserve fundamental consideration. In the current work, we performed quantum chemistry calculations to address the binding strength and coordination structures of chiral bis(mandelato)borate ([BMB]) anions with representative alkali metal ions, as well as the electronic properties of alkali metal ion-[BMB] ion pair complexes. The optimized [BMB] conformers are categorized into V-shaped, bent, and twisted structures with varied electrostatic potential contours and conformational energies and distinct alkali metal ion-[BMB] binding structures. Alkali metal ions have additional associations with phenyl groups in V-shaped [BMB] conformers owing to preferential cation-π interactions. Furthermore, the effects of the molecular chiralities of [BMB] anions on the thermodynamics and microstructural properties of tetraalkylphosphonium [BMB] ILs were studied by performing extensive atomistic interactions. Oxygen atoms in [BMB] anions have competitive hydrogen bonding interactions with hydrogen atoms in cations depending on the molecular chiralities and steric hindrance effects of [BMB] anions. However, the molecular chiralities of [BMB] anions have a negligible effect on the liquid densities of tetraalkylphosphonium [BMB] ILs and the spatial distributions of boron atoms in anions around phosphorous atoms in cations. Enlarging tetraalkylphosphonium cation sizes leads to enhanced cation-anion intermolecular hydrogen bonding and Coulombic interactions due to enhanced segregation of polar groups in apolar networks in heterogeneous IL matrices, as verified by scattering structural functions.
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