Darbost Ulrich, Sénèque Olivier, Li Yun, Bertho Gildas, Marrot Jérôme, Rager Marie-Noëlle, Reinaud Olivia, Jabin Ivan
Unité de Recherche en Chimie Organique et Macromoléculaire, Université du Havre, 25 rue Philippe Lebon, 76058 Le Havre cedex, France.
Chemistry. 2007;13(7):2078-88. doi: 10.1002/chem.200601040.
Molecular recognition by calix[6]arene-based receptors bearing three primary alkylamino side chain arms (1) is described. Complexation of Zn(II) ion provides the dinuclear mu-hydroxo complex 2G(OH), XRD characterization of which, together with solution studies, provided evidence of its hosting of neutral polar organic guests G. Treatment of this complex with a carboxylic acid or a sulfonamide (XH) results in the formation of mononuclear species 3G(X), one of which (X = Cl) has been characterized by XRD. A dicationic complex 3G(RNH2) is obtained upon treatment of 2G(OH) with a mixture of an alkylamine and a strong acid. Each of these Zn(II) complexes features a tetrahedral metal ion bound to the three amino arms of ligand 1 and to an exogenous ligand (either HO-, X-, or RNH2) sitting outside of the cavity. As a result, the metal ion structures the calixarene core, constraining it in a cone conformation suitable for guest hosting. The receptor properties of these compounds have been explored in detail and are compared with those of the trisammonium receptor 1G(3H+), based on the same calixarene core, as well as those of the trisimidazole-based dicationic Zn funnel complexes. This study reveals very different host properties, in spite of the common hydrophobic, pi-basic, and hydrogen-bonding acceptor properties of the calixarene cores. A harder external ligand produces a less polarized receptor that is consequently particularly sensitive to the hydrogen-bonding ability of its guest. The less electron-rich the apical ligand, and a fortiori the trisammonium host, the more sensitive the receptor to the dipole moment of the guest. All this stands in contrast with the funnel Zn complexes, in which the coordination link plays a dominant role. It is also shown that the asymmetry of an exo-coordinated enantiopure amino ligand is sensed by the guest. This supramolecular system nicely illustrates how the receptor properties of a hydrophobic cavity can be allosterically tuned by the environment.
本文描述了带有三个伯烷基氨基侧链臂的杯[6]芳烃受体(1)的分子识别。锌(II)离子的络合作用生成了双核μ-羟基络合物2G(OH),通过X射线衍射(XRD)对其进行表征,并结合溶液研究,证明了其对中性极性有机客体G的容纳。用羧酸或磺酰胺(XH)处理该络合物会生成单核物种3G(X),其中之一(X = Cl)已通过XRD进行了表征。用烷基胺和强酸的混合物处理2G(OH)可得到二价阳离子络合物3G(RNH2)。这些锌(II)络合物中的每一个都具有一个四面体金属离子,该金属离子与配体1的三个氨基臂以及位于空腔外部的外源配体(HO-、X-或RNH2)相连。结果,金属离子使杯芳烃核心形成特定结构,将其限制在适合客体容纳的锥状构象中。已详细研究了这些化合物的受体性质,并将其与基于相同杯芳烃核心的三铵受体1G(3H+)以及基于三咪唑的二价阳离子锌漏斗络合物的受体性质进行了比较。尽管杯芳烃核心具有共同的疏水、π碱性和氢键受体性质,但这项研究揭示了截然不同的主体性质。一个更强硬的外部配体会产生极化程度更低的受体,因此该受体对客体的氢键能力特别敏感。顶端配体的富电子程度越低,更不用说三铵主体了,受体对客体偶极矩就越敏感。所有这些都与漏斗状锌络合物形成对比,在漏斗状锌络合物中配位键起主导作用。研究还表明,客体能够感知外配位对映体纯氨基配体的不对称性。这个超分子体系很好地说明了疏水空腔的受体性质是如何通过环境进行变构调节的。