Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Structural Chemistry of Unstable and Stable, Species, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, P. R. China.
Chemistry. 2018 Sep 18;24(52):13734-13739. doi: 10.1002/chem.201803638. Epub 2018 Sep 6.
Host-guest interactions are widely employed in constructing responsive materials, although less is known to manipulate the chiral property of materials using such host-guest dynamics. With the supramolecular self-assembly based on β-cyclodextrin (β-CD) and alkyl amines (CH(CH)NH), we report that faster host-guest dynamics induces a dipole located above the cavity of β-CD, whereas slower dynamics create in-cavity dipole. These two scenarios correspond to negative and positive chiral signals, respectively. Considering that a larger fraction of amines facilitates faster exchange between the threaded and unthreaded amines, the chiral signal for the right-handed helical ribbons can be manipulated simply by alternatively increasing the fraction of amines and β-CD. Excitingly, enzyme responsive supramolecular chirality is obtained as a result of shifting the molar ratio by enzyme triggered hydrolysis of β-CD. We expect that this strategy may open up an area of rationally designed chiral supramolecular materials based on host-guest chemistry.
主体-客体相互作用广泛应用于构建响应性材料,尽管利用这种主体-客体动力学来操纵材料的手性性质知之甚少。基于超分子自组装的β-环糊精(β-CD)和烷基胺(CH(CH)NH),我们报告说,更快的主体-客体动力学诱导位于β-CD 空腔上方的偶极子,而较慢的动力学则在腔内产生偶极子。这两种情况分别对应于负和正手性信号。考虑到更多的胺有利于穿入和未穿入的胺之间更快的交换,通过交替增加胺和β-CD 的分数,可以简单地操纵右手螺旋带的手性信号。令人兴奋的是,由于β-CD 的酶触发水解导致摩尔比的变化,获得了酶响应的超分子手性。我们期望这种策略可以开辟一个基于主体-客体化学的合理设计的手性超分子材料的领域。