Li Tian-Ren, Das Chintu, Piccini GiovanniMaria, Tiefenbacher Konrad
Department of Chemistry, University of Basel, Mattenstrasse 22, Basel 4058, Switzerland.
Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, Aachen 52074, Germany.
J Am Chem Soc. 2025 Apr 2;147(13):11108-11116. doi: 10.1021/jacs.4c17029. Epub 2025 Feb 5.
This study presents the development and catalytic applications of the tetrafluororesorcin[4]arene hexameric capsule (capsule II) as a novel supramolecular catalyst. It demonstrates unprecedented catalytic activity, enabling the β-selective glycosylation of glycals to 2-deoxy glycosides─a transformation that has not been achieved before in molecular and supramolecular catalysis. Mechanistic investigations, including experimental and computational studies, revealed that the high β-selectivity arises from a proton wire mechanism along the capsule's surface, coupling glycal protonation with nucleophile deprotonation. Control experiments confirmed the unique reactivity of capsule II compared to its nonfluorinated predecessor, capsule I, showcasing its potential to expand the boundaries of supramolecular catalysis.
本研究介绍了作为新型超分子催化剂的四氟间苯二酚[4]芳烃六聚体胶囊(胶囊II)的开发及其催化应用。它展示了前所未有的催化活性,能够实现糖烯向2-脱氧糖苷的β-选择性糖基化反应——这是分子催化和超分子催化之前均未实现的转化反应。包括实验和计算研究在内的机理研究表明,高β-选择性源于沿胶囊表面的质子线机制,该机制将糖烯质子化与亲核试剂去质子化相耦合。对照实验证实了胶囊II与其未氟化的前身胶囊I相比具有独特的反应活性,展示了其扩展超分子催化边界的潜力。