Naranjo Teresa, Álvarez-Asencio Rubén, Pedraz Patricia, Nieto-Ortega Belén, Silva Sara Moreno-Da, Burzurí Enrique, Rutland Mark W, Pérez Emilio M
IMDEA Nanociencia, Faraday 9, Campus UAM, 28049, Madrid, Spain.
RISE Research Institutes of Sweden, Bioscience and Materials, 114 28, Stockholm, Sweden.
Sci Rep. 2020 Sep 22;10(1):15414. doi: 10.1038/s41598-020-71803-3.
We show that H-bonded host-guest systems associate in ionic liquids (ILs), pure salts with melting point below room temperature, in which dipole-dipole electrostatic interactions should be negligible in comparison with dipole-charge interactions. Binding constants (K) obtained from titrations of four H-bonded host-guest systems in two organic solvents and two ionic liquids yield smaller yet comparable K values in ionic liquids than in organic solvents. We also detect the association event using force spectroscopy, which confirms that the binding is not solely due to (de)solvation processes. Our results indicate that classic H-bonded host-guest supramolecular chemistry takes place in ILs. This implies that strong H-bonds are only moderately affected by surroundings composed entirely of charges, which can be interpreted as an indication that the balance of Coulombic to covalent forces in strong H-bonds is not tipped towards the former.
我们证明,氢键连接的主客体体系能在离子液体(ILs)中缔合,离子液体是熔点低于室温的纯盐,与偶极 - 电荷相互作用相比,其中的偶极 - 偶极静电相互作用应可忽略不计。通过在两种有机溶剂和两种离子液体中对四种氢键连接的主客体体系进行滴定得到的结合常数(K)表明,离子液体中的K值比有机溶剂中的小,但具有可比性。我们还使用力谱法检测到缔合事件,这证实了结合并非仅仅归因于(去)溶剂化过程。我们的结果表明,经典的氢键连接主客体超分子化学在离子液体中发生。这意味着强氢键仅受到完全由电荷组成的环境的适度影响,这可解释为表明强氢键中库仑力与共价力的平衡并未偏向前者。