Year: 2026
Type: article
Abstract: ABSTRACT Type II porous ionic liquids could be prepared at room temperature by dissolving up to 5 wt.% of anti ‐cryptophane‐A derivatives functionalized with alkyl or fluorinated alkyl chains in phosphonium‐ and pyrrolidinium‐based ionic liquids. In this study, we provide the first direct experimental evidence that these molecular cages retain their internal free volume when dissolved in ionic liquids. At 303 K and 1 bar, the porous ionic liquids prepared as solutions of anti ‐cryptophane‐A grafted with a ten‐carbon alkyl chain in the ionic liquids [] (1:36), [ (1:52) and [] (1:50) absorb 3.0, 3.5 and 11 times more methane than the pure ionic liquid, respectively. The solution of anti ‐cryptophane‐A grafted with a fluorinated alkyl chain in [] (1:73) absorbs in turn 1.8 times more methane than the pure ionic liquid. We show that 97(2)% of the cryptophane dissolved in [] can encapsulate one molecule of methane, whereas only 60(1)% of the cavities in solid cryptophane are available for gas encapsulation. The presence of permanent porosity in the liquid solution is further supported by controlled atmosphere NMR spectroscopy that allows to distinguish between free and caged methane, thus providing molecular‐level evidence that the gas is encapsulated in the free cryptophane cavities.
Source: Advanced Materials Interfaces
Institutions: École Normale Supérieure de Lyon, Centre National de la Recherche Scientifique, Université du littoral côte d'opale, Laboratoire de Chimie, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Université Paris-Saclay, CEA Paris-Saclay - Etablissement de Saclay, CEA Paris-Saclay, UiT The Arctic University of Norway
Language: English
Subfield: Catalysis
Field: Chemical Engineering
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $3,100
Awards: G1754313052, Biocompatible Porous Liquids based on Cyclodextrin-MOFs and eutectic solvents, G2908540654, Institut for Multiscale Science and Technology : from Fundamental Physics and Chemistry to Engineering in New Material and Processes and Ecotechnologies, Direct (photo)electrochemical conversion of atmospheric N2 to ammonia, G7240651115
OpenAlex ID: W7130401279
