Li Tian-Ren, Das Chintu, Cornu Ivan, Prescimone Alessandro, Piccini GiovanniMaria, Tiefenbacher Konrad
Department of Chemistry, University of Basel, Mattenstrasse 24a, 4058 Basel, Switzerland.
Institute of Technical and Macromolecular Chemistry RWTH Aachen University, Worringerweg 2, 52074 Aachen, Germany.
JACS Au. 2024 May 3;4(5):1901-1910. doi: 10.1021/jacsau.4c00097. eCollection 2024 May 27.
The hexameric resorcin[4]arene capsule has been utilized as one of the most versatile supramolecular capsule catalysts. Enlarging its size would enable expansion of the substrate size scope. However, no larger catalytically active versions have been reported. Herein, we introduce a novel class of macrocycles, named window[1]resorcin[3]arene (wRS), that assemble to a cage-like hexameric host. The new host was studied by NMR, encapsulation experiments, and molecular dynamics simulations. The cage is able to bind tetraalkylammonium ions that are too large for encapsulation inside the hexameric resorcin[4]arene capsule. Most importantly, it retained its catalytic activity, and the accelerated conversion of a large substrate that does not fit the closed hexameric resorcin[4]arene capsule was observed. Thus, it will help to expand the limited substrate size scope of the closed hexameric resorcin[4]arene capsule.
六聚间苯二酚[4]芳烃胶囊已被用作最通用的超分子胶囊催化剂之一。扩大其尺寸将能够扩大底物尺寸范围。然而,尚未报道过更大的具有催化活性的变体。在此,我们介绍了一类新型大环化合物,称为窗[1]间苯二酚[3]芳烃(wRS),它能组装成笼状六聚主体。通过核磁共振、包封实验和分子动力学模拟对这种新主体进行了研究。该笼能够结合对于六聚间苯二酚[4]芳烃胶囊来说太大而无法包封在其内部的四烷基铵离子。最重要的是,它保留了其催化活性,并且观察到一种不适合封闭的六聚间苯二酚[4]芳烃胶囊的大底物的加速转化。因此,它将有助于扩大封闭的六聚间苯二酚[4]芳烃胶囊有限的底物尺寸范围。