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Anion-binding behavior of hybrid calixpyrroles

机译:杂合杯吡咯的阴离子结合行为

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Hybrid calixpyrrole systems are calixpyrrole-like macrocycles that are based on more than one type of small molecule building block. Structurally, these "mixed-breed" macrocycles differ from calixpyrroles in that some pyrrolic units in the latter are replaced by other hetereocyclic units such as furan, thiophene, bipyrrole, and bithiophene. Although several such systems have been reported in recent years, only a few have been studied as possible anion receptors. In this paper, the results of detailed anion binding studies involving several prototypic systems are reported. Taken in concert, these results highlight the fact that some hybrid systems, including compounds 2-5, display anion affinities that are considerably weaker than those of the parent system 1. On the other hand, they also show that compounds 6-8 are good receptors for "Y-shaped" anions, such as carboxylates, and that they bind these species with high affinity. These findings are strongly supported by solid-state structural studies, which reveal an interesting "cross binding mode" for the binding of carboxylate anions by the bis-thiophene, bis-pyrrole system 7.
机译:杂合杯状吡咯系统是类似杯状吡咯的大环,其基于一种以上的小分子构件。从结构上讲,这些“混合品种”大环与杯吡咯的区别在于后者中的一些吡咯单元被其他杂环单元如呋喃,噻吩,联吡咯和联噻吩所取代。尽管近年来已经报道了几种这样的系统,但是仅研究了少数几种可能的阴离子受体。在本文中,报告了涉及几个原型系统的详细阴离子结合研究的结果。综上所述,这些结果突出了这样一个事实,即某些混合系统(包括化合物2-5)显示出的阴离子亲和力比母体系统1的阴离子亲和力弱得多。另一方面,它们还表明化合物6-8是好的“ Y形”阴离子(例如羧酸根)的受体,并且它们以高亲和力结合这些物质。这些发现得到了固态结构研究的有力支持,该研究揭示了一种有趣的“交叉结合模式”,可通过双噻吩双吡咯系统7结合羧酸根阴离子。

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