Kerckhoffs Jessica M C A, ten Cate Mattijs G J, Mateos-Timoneda Miguel A, van Leeuwen Fijs W B, Snellink-Ruël Bianca, Spek Anthony L, Kooijman Huub, Crego-Calama Mercedes, Reinhoudt David N
Laboratory of Supramolecular Chemistry and Technology, MESA Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.
J Am Chem Soc. 2005 Sep 14;127(36):12697-708. doi: 10.1021/ja0536973.
This article describes the synthesis and binding properties of highly selective noncovalent molecular receptors 1(3).(DEB)6 and 3(3).(DEB)6 for different hydroxyl functionalized anthraquinones 2. These receptors are formed by the self-assembly of three calix[4]arene dimelamine derivative molecules (1 or 3) and six diethylbarbiturate (DEB) molecules to give 1(3).(DEB)6 or 3(3).(DEB)6. Encapsulation of 2 occurs in a highly organized manner; that is, a noncovalent hydrogen-bonded trimer of 2 is formed within the hydrogen-bonded receptors 1(3).(DEB)6 and 3(3).(DEB)6. Both receptors 1(3).(DEB)6 and 3(3).(DEB)6 change conformation from staggered to eclipsed upon complexation to afford a better fit for the 2(3) trimer. The receptor selectivity toward different anthraquinone derivatives 2 has been studied using 1H NMR spectroscopy, X-ray crystallography, UV spectroscopy, and isothermal microcalorimetry (ITC). The pi-pi stacking between the electron-deficient center ring of the anthraquinone derivatives 2a-c and 2e-g and the relatively electron-poor melamine units of the receptor is the driving force for the encapsulation of the guest molecules. The selectivity of the hydrogen-bonded host for the anthraquinone derivatives is the result of steric interactions between the guest molecules and the calix[4]arene aromatic rings of the host.
本文描述了用于不同羟基官能化蒽醌2的高选择性非共价分子受体1(3).(DEB)6和3(3).(DEB)6的合成及结合特性。这些受体由三个杯[4]芳烃二三聚氰胺衍生物分子(1或3)和六个二乙基巴比妥酸盐(DEB)分子自组装形成1(3).(DEB)6或3(3).(DEB)6。2的包封以高度有序的方式发生;也就是说,在氢键受体1(3).(DEB)6和3(3).(DEB)6内形成了2的非共价氢键三聚体。受体1(3).(DEB)6和3(3).(DEB)6在络合时均从交错构象转变为重叠构象,以更好地契合2(3)三聚体。使用1H核磁共振光谱、X射线晶体学、紫外光谱和等温滴定量热法(ITC)研究了受体对不同蒽醌衍生物2的选择性。蒽醌衍生物2a - c和2e - g的缺电子中心环与受体相对贫电子的三聚氰胺单元之间的π-π堆积是客体分子包封的驱动力。氢键主体对蒽醌衍生物的选择性是客体分子与主体杯[4]芳烃芳环之间空间相互作用的结果。