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首页> 外文期刊>Chemistry: A European journal >Self-Assembly of Calix[6]arene-Diazapyrenium Pseudorotaxanes: Interplay of Molecular Recognition and Ion-Pairing Effects
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Self-Assembly of Calix[6]arene-Diazapyrenium Pseudorotaxanes: Interplay of Molecular Recognition and Ion-Pairing Effects

机译:杯[6]芳烃-重氮py假轮烷的自组装:分子识别和离子配对效应的相互作用。

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摘要

The calix[6]arene wheel CX forms pseudorotaxane species with the diazapyrenium-based axle 1 center dot 2PF(6) in CH2Cl2 solution. The macrocyclic component is a heteroditopic receptor, which can complex the electron-acceptor moiety of the axle inside its cavity and the counterions with the ureidic groups on the upper rim. The self-assembled supramolecular species is a complex structure, which involves three components-the wheel, the axle and its counterions-that can mutually interact and affect. The stoichiometry of the resulting supramolecular complex depends on the nature and concentration of the counterions. Namely, it is observed that in dilute solution and with low-coordinating anions the axle takes two wheels, whereas with highly coordinating anions or in concentrated solutions the complex has a 1:1 stoichiometry.
机译:杯[6]芳烃轮CX与二氮杂re基轴1的中心点2PF(6)在CH2Cl2溶液中形成假轮烷物种。大环成分是异位受体,可以使轴腔内的轴的电子受体部分和抗衡离子与上缘的尿素基团复合。自组装的超分子物种是一个复杂的结构,涉及三个组成部分-轮,轴和其抗衡离子-可以相互影响和相互作用。所得超分子复合物的化学计量取决于抗衡离子的性质和浓度。即,观察到在稀溶液中和低配位阴离子的情况下,轴需要两个轮子,而在高配位阴离子或浓溶液中,复合物的化学计量比为1:1。

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