Choi H S, Suh S B, Cho S J, Kim K S
National Creative Research Initiative Center for Superfunctional Materials and Department of Chemistry, Pohang University of Science and Technology, San 31, Hyojadong, Namgu, Pohang 790-784, Korea.
Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12094-9. doi: 10.1073/pnas.95.21.12094.
Cation-pi interactions are important forces in molecular recognition by biological receptors, enzyme catalysis, and crystal engineering. We have harnessed these interactions in designing molecular systems with circular arrangement of benzene units that are capable of acting as ionophores and models for biological receptors. [n]Collarenes are promising candidates with high selectivity for a specific cation, depending on n, because of their structural rigidity and well-defined cavity size. The interaction energies of [n]collarenes with cations have been evaluated by using ab initio calculations. The selectivity of these [n]collarenes in aqueous solution was revealed by using statistical perturbation theory in conjunction with Monte Carlo and molecular dynamics simulations. It has been observed that in [n]collarenes the ratio of the interaction energies of a cation with it and the cation with the basic building unit (benzene) can be correlated to its ion selectivity. We find that collarenes are excellent and efficient ionophores that bind cations through cation-pi interactions. [6]Collarene is found to be a selective host for Li+ and Mg2+, [8]collarene for K+ and Sr2+, and [10]collarene for Cs+ and Ba2+. This finding indicates that [10]collarene and [8]collarene could be used for effective separation of highly radioactive isotopes, 137Cs and 90Sr, which are major constituents of nuclear wastes. More interestingly, collarenes of larger cavity size can be useful in capturing organic cations. [12]Collarene exhibits a pronounced affinity for tetramethylammonium cation and acetylcholine, which implies that it could serve as a model for acetylcholinestrase. Thus, collarenes can prove to be novel and effective ionophores/model-receptors capable of heralding a new direction in molecular recognition and host-guest chemistry.
阳离子-π相互作用是生物受体进行分子识别、酶催化以及晶体工程中的重要作用力。我们已利用这些相互作用来设计具有苯单元环状排列的分子体系,这些体系能够充当离子载体以及生物受体的模型。[n]环芳烃是有前景的候选物,由于其结构刚性和明确的空腔尺寸,根据n值的不同,对特定阳离子具有高选择性。通过从头算计算评估了[n]环芳烃与阳离子的相互作用能。结合蒙特卡罗和分子动力学模拟,利用统计微扰理论揭示了这些[n]环芳烃在水溶液中的选择性。据观察,在[n]环芳烃中,阳离子与其自身以及阳离子与基本构建单元(苯)的相互作用能之比与其离子选择性相关。我们发现环芳烃是优异且高效的离子载体,通过阳离子-π相互作用结合阳离子。已发现[6]环芳烃是Li⁺和Mg²⁺的选择性主体,[8]环芳烃是K⁺和Sr²⁺的选择性主体,[10]环芳烃是Cs⁺和Ba²⁺的选择性主体。这一发现表明,[10]环芳烃和[8]环芳烃可用于有效分离高放射性同位素¹³⁷Cs和⁹⁰Sr,它们是核废料的主要成分。更有趣的是,较大空腔尺寸的环芳烃可用于捕获有机阳离子。[12]环芳烃对四甲基铵阳离子和乙酰胆碱表现出明显的亲和力,这意味着它可以作为乙酰胆碱酯酶的模型。因此,环芳烃可以证明是新型且有效的离子载体/模型受体,能够在分子识别和主客体化学领域开创一个新方向。