Department of Molecular Spectroscopy, Max Planck Institute for Polymer Research, 55128, Mainz, Germany.
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, 100190, China.
Chemphyschem. 2020 Sep 2;21(17):1957-1965. doi: 10.1002/cphc.202000507. Epub 2020 Aug 13.
Tritopic ion-pair receptors can bind bivalent salts in solution; yet, these salts have a tendency to form ion-pairs even in the absence of receptors. The extent to which such receptors can enhance ion pairing has however remained elusive. Here, we study ion pairing of M (Ba , Sr ) and X (I , ClO ) in acetonitrile with and without a dichlorooxacalix[2]arene[2]triazine-related receptor containing a pentaethylene-glycol moiety. We find marked ion association already in receptor-free solutions. When present, most of the MX ion-pairs are bound to the receptor and the overall degree of ion association is enhanced due to coordinative, hydrogen-bonding, and anion-π interactions. The receptor shows higher selectivity for iodides but also stabilizes perchlorates, despite the latter are often considered as weakly coordinating anions. Our results show that ion-pair binding is strongly correlated to ion pairing in these solutions, thereby highlighting the importance of taking ion association in organic solvents into account.
三齿离子对受体可以在溶液中结合二价盐;然而,这些盐即使在没有受体的情况下也有形成离子对的倾向。然而,这些受体增强离子配对的程度仍然难以捉摸。在这里,我们研究了含有五亚乙基二醇部分的二氯氧杂杯[2]芳烃[2]三嗪相关受体存在和不存在的情况下,M(Ba,Sr)和 X(I,ClO )在乙腈中的离子配对。我们发现即使在没有受体的溶液中也存在明显的离子缔合。当存在时,大多数 MX 离子对与受体结合,由于配位、氢键和阴离子-π 相互作用,整体离子缔合程度增强。该受体对碘化物表现出更高的选择性,但也稳定高氯酸盐,尽管后者通常被认为是弱配位阴离子。我们的结果表明,离子对结合与这些溶液中的离子配对密切相关,从而强调了在有机溶剂中考虑离子缔合的重要性。