Ogoshi T, Yamagishi T
Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192, Japan.
Chem Commun (Camb). 2014 May 14;50(37):4776-87. doi: 10.1039/c4cc00738g.
Pillar[n]arenes, which we first synthesized and named in 2008, are new pillar-shaped macrocyclic hosts. Pillar[n]arene homologues with n = 5-10 have already been synthesized, but the cyclic pentamers, i.e., pillar[5]arenes, and cyclic hexamers, i.e., pillar[6]arenes, have been most widely used because these can be obtained in good yields. To date, nearly all pillar[n]arene-based supramolecular assemblies have been constructed using pillar[5]- and pillar[6]arene scaffolds. In this feature article, we describe supramolecular assemblies built using host-guest interactions depending on the cavity sizes of pillar[5]- and pillar[6]arenes. We first discuss the effects of the type of substituents on the rims of pillar[5]- and pillar[6]arenes on their solubilities, functionalities and host-guest properties. We then discuss supramolecular assemblies based on their host-guest properties and pillar-shaped architectures.
柱芳烃是我们于2008年首次合成并命名的新型柱状大环主体。已合成出n = 5 - 10的柱[n]芳烃同系物,但环状五聚体即柱[5]芳烃和环状六聚体即柱[6]芳烃应用最为广泛,因为它们能以较高产率获得。迄今为止,几乎所有基于柱[n]芳烃的超分子组装体都是使用柱[5]芳烃和柱[6]芳烃骨架构建的。在这篇专题文章中,我们描述了利用基于柱[5]芳烃和柱[6]芳烃空腔大小的主客体相互作用构建的超分子组装体。我们首先讨论柱[5]芳烃和柱[6]芳烃边缘取代基类型对其溶解度、功能及主客体性质的影响。然后我们基于其主客体性质和柱状结构讨论超分子组装体。