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基于三芴衍生大环和百草枯衍生物形成的 1:2 主客体配合物:PF6(-)和联吡啶环在固态中的阴离子-π 相互作用。

Formation of 1:2 host-guest complexes based on triptycene-derived macrotricycle and paraquat derivatives: anion-π interactions between PF6(-) and bipyridinium rings in the solid state.

机构信息

Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Org Lett. 2011 Oct 21;13(20):5688-91. doi: 10.1021/ol2024168. Epub 2011 Sep 30.

DOI:10.1021/ol2024168
PMID:21962056
Abstract

A triptycene-derived macrotricyclic host containing two dibenzo-[30]-crown-10 moieties forms stable 1:2 host-guest complexes with paraquat derivatives in both solution and the solid state, in which anion-π interactions between PF(6)(-) and the bipyridinium rings play an important role. Moreover, it was found that binding and release of the guest molecules in the complexes could be easily controlled by the addition and removal of potassium ions.

摘要

一种基于三联苯的大环主体,其中包含两个二苯并[30]冠-10 部分,在溶液和固态中均与对醌衍生物形成稳定的 1:2 主客体配合物,其中 PF(6)(-)与双吡啶环之间的阴离子-π 相互作用起着重要作用。此外,还发现配合物中客体分子的结合和释放可以通过添加和去除钾离子来轻松控制。

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