A Relay-Type Solid-State Macrocyclic Host-Guest System for Selective Isomer Adsorption, Controlled Release, and Turn-On Colorimetric Sensing of 1-/2-Bromoalkanes

© 2025 Wiley‐VCH GmbH.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2025) vom: 19. Mai, Seite e2504417
Auteur principal: Ren, Susu (Auteur)
Autres auteurs: Sun, Yu-Xiang, Liu, Yuan-Zheng, Wang, Haitao, Wu, Jia-Rui
Format: Article en ligne
Langue:English
Publié: 2025
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article charge‐transfer cocrystals host–guest systems macrocycles nonporous adaptive crystals
Description
Résumé:© 2025 Wiley‐VCH GmbH.
Macrocycle-based adaptive crystals have gained significant attention for their precise adsorption and separation capabilities. However, achieving controlled analyte release under nonthermal stimuli remains a major challenge. Here, a relay-type solid-state host-guest system based on a fluorinated pillararene derivative, EtFLP6, is presented, which enables selective adsorption of 1-/2-bromoalkane isomers, room-temperature-controlled desorption, and turn-on colorimetric sensing. Activated EtFLP6 crystals selectively adsorb 1-bromoalkanes from mixtures of 1-/2-positional isomers and release them at room temperature upon introduction of electron-deficient aromatic acceptors (4-nitrobenzonitrile and 1,5-difluoro-2,4-dinitrobenzene), triggering a distinct color change from colorless to orange. Single-crystal structures incorporating X-ray powder diffraction and spectral analyses reveal that the desorption and color change result from the disassembly of solid-state host-guest complexes, driven by competitive binding with acceptors. This process is governed by the dynamic intermolecular interactions and selective molecular recognition of EtFLP6 in the solid state. This work bridges traditional macrocyclic adsorbents with functional organic cocrystals, offering a novel strategy for designing intelligent supramolecular materials
Description:Date Revised 19.05.2025
published: Print-Electronic
Citation Status Publisher
ISSN:1521-4095
DOI:10.1002/adma.202504417