Darbost Ulrich, Rager Marie-Noëlle, Petit Samuel, Jabin Ivan, Reinaud Olivia
URCOM, Université du Havre, Faculté des Sciences et Techniques, 25 rue Philippe Lebon, BP 540, 76058 Le Havre Cedex, France.
J Am Chem Soc. 2005 Jun 15;127(23):8517-25. doi: 10.1021/ja051299u.
The host-guest properties of calix[6]tren 1 have been evaluated. The receptor is based on a calix[6]arene that is covalently capped at the narrow rim by a tren unit. As a result, the system presents a concave hydrophobic cavity with, at its bottom, a grid-like nitrogenous core. Despite its well-defined cavity and opening to the outside at the large rim, 1 did not behave as a good receptor for neutral molecules in chloroform. However, it exhibited efficient endo-complexation of ammonium guests. By contrast, the per-protonated host, 1.4H(+), behaved as a remarkable receptor for small organic molecules. The complexation is driven by a strong charge-dipole interaction and hydrogen bonds between the polar guest and the tetracationic cap of the calixarene. Finally, coordination of Zn(2+) to the tren core led to the asymmetrization of calixarene cavity and to the strong but selective endo-binding of neutral ligands. This study emphasizes the efficiency of a receptor presenting a concave hydrophobic cavity that is polarized at its bottom. The resulting combination of charge-dipole, hydrogen bonding, CH-pi, and van der Waals interactions highly stabilizes the supramolecular architectures. Also, importantly, the tren cap allows the tuning of the polarization, offering either a basic (1), a highly charged and acidic (1.4H(+)), or a coordination (1.Zn(2+)) site. As a result, the system proved to be highly versatile, tunable, and interconvertible in solution by simple addition of protons, bases, or metal ions.
杯[6]三乙烯四胺1的主客体性质已得到评估。该受体基于一个杯[6]芳烃,其窄口端通过一个三乙烯四胺单元共价封端。因此,该体系呈现出一个凹形疏水腔,在其底部有一个网格状含氮核心。尽管其腔结构明确且大口端向外开放,但1在氯仿中对中性分子并非良好的受体。然而,它对铵客体表现出高效的内络合作用。相比之下,全质子化的主体1·4H⁺对小分子有机化合物表现出显著的受体行为。这种络合作用是由极性客体与杯芳烃四价阳离子帽之间强烈的电荷 - 偶极相互作用和氢键驱动的。最后,Zn²⁺与三乙烯四胺核心的配位导致杯芳烃腔不对称化,并导致中性配体强烈但选择性的内结合。这项研究强调了具有底部极化的凹形疏水腔的受体的效率。由此产生的电荷 - 偶极、氢键、CH - π和范德华相互作用的组合高度稳定了超分子结构。同样重要的是,三乙烯四胺帽允许调节极化,提供一个碱性位点(1)、一个高电荷和酸性位点(1·4H⁺)或一个配位位点(1·Zn²⁺)。结果,通过简单添加质子、碱或金属离子,该体系在溶液中被证明具有高度的通用性、可调节性和可相互转化性。