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    Spectroscopic Evidence for Clusters of Like-Charged Ions in Ionic Liquids Stabilized by Cooperative Hydrogen Bonding
    (Weinheim : Wiley-VCH, 2016) Knorr, Anne; Stange, Peter; Fumino, Koichi; Weinhold, Frank; Ludwig, Ralf
    Infrared spectroscopy and density functional theory calculations provide strong evidence for the formation of clusters of like-charged ions in ionic liquids. With decreasing temperature, cooperative hydrogen bonding overcomes repulsive electrostatic interaction. The resulting cyclic tetramers nicely resemble well-known molecular clusters of alcohols.
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    Three in One: The Versatility of Hydrogen Bonding Interaction in Halide Salts with Hydroxy-Functionalized Pyridinium Cations
    (Weinheim : Wiley-VCH Verl., 2021) Al Sheakh, Loai; Niemann, Thomas; Villinger, Alexander; Stange, Peter; Zaitsau, Dzmitry H.; Strate, Anne; Ludwig, Ralf
    The paradigm of supramolecular chemistry relies on the delicate balance of noncovalent forces. Here we present a systematic approach for controlling the structural versatility of halide salts by the nature of hydrogen bonding interactions. We synthesized halide salts with hydroxy-functionalized pyridinium cations [HOCn Py]+ (n=2, 3, 4) and chloride, bromide and iodide anions, which are typically used as precursor material for synthesizing ionic liquids by anion metathesis reaction. The X-ray structures of these omnium halides show two types of hydrogen bonding: 'intra-ionic' H-bonds, wherein the anion interacts with the hydroxy group and the positively charged ring at the same cation, and 'inter-ionic' H-bonds, wherein the anion also interacts with the hydroxy group and the ring system but of different cations. We show that hydrogen bonding is controllable by the length of the hydroxyalkyl chain and the interaction strength of the anion. Some molten halide salts exhibit a third type of hydrogen bonding. IR spectra reveal elusive H-bonds between the OH groups of cations, showing interaction between ions of like charge. They are formed despite the repulsive interaction between the like-charged ions and compete with the favored cation-anion H-bonds. All types of H-bonding are analyzed by quantum chemical methods and the natural bond orbital approach, emphasizing the importance of charge transfer in these interactions. For simple omnium salts, we evidenced three distinct types of hydrogen bonds: Three in one!