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Updated: Jan 18, 2026
Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
How Does the Structural Organization of a Cyclic Ammonium Ionic Liquid Differ from That of Acyclic Branched Ammonium
Debashis Majhi1, Nayana Nupur Das1, Sunandan Sarkar1
1Department of Chemistry, National Institute of Technology, Tiruchirappalli 620015, India.
Abstract:
This study explored the structural organization of cyclic and acyclic ammonium-based ionic liquids (ILs). For this purpose, we selected one cyclic IL, N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (BMPyr-NTf2), and two acyclic ILs, methyl-tributylammonium (TBMA-NTf2) and methyl-trioctylammonium (TOMA-NTf2) bis(trifluoromethanesulfonyl)imide. Thermophysical properties, such as viscosity and density, were measured to evaluate the physicochemical behavior of the ILs. We complemented these measurements with time-resolved fluorescence anisotropy (TRFA), density functional theory (DFT) calculations, and fluorescence correlation spectroscopy (FCS). Viscosity and density data revealed notable differences between the cyclic IL (BMPyr-NTf2) and its acyclic counter IL (TBMA-NTf2), suggesting that anion-cation interactions play a key role in governing physicochemical properties. DFT results displayed that the binding energy of the cyclic IL is more than that of structurally analogous acyclic ILs, with a corresponding increase in anion-cation distance in the acyclic IL. TRFA measurements indicated that the cyclic IL exhibited significantly higher rotational correlation times (τr) than its acyclic counter IL under iso-viscous conditions. This resulted in a smaller hydrodynamic radius for acyclic ILs, likely due to weaker anion-cation interactions and reduced ion aggregation. FCS measurements supported these observations. Overall, our findings demonstrate that the structural organization of cyclic ammonium-based IL differs markedly from their acyclic counter ILs.
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