Issue 4, 2017

Understanding gas capacity, guest selectivity, and diffusion in porous liquids

Abstract

Porous liquids are a new class of material that could have applications in areas such as gas separation and homogeneous catalysis. Here we use a combination of measurement techniques, molecular simulations, and control experiments to advance the quantitative understanding of these liquids. In particular, we show that the cage cavities remain unoccupied in the absence of a suitable guest, and that the liquids can adsorb large quantities of gas, with gas occupancy in the cages as high as 72% and 74% for Xe and SF6, respectively. Gases can be reversibly loaded and released by using non-chemical triggers such as sonication, suggesting potential for gas separation schemes. Diffusion NMR experiments show that gases are in dynamic equilibrium between a bound and unbound state in the cage cavities, in agreement with recent simulations for related porous liquids. Comparison with gas adsorption in porous organic cage solids suggests that porous liquids have similar gas binding affinities, and that the physical properties of the cage molecule are translated into the liquid state. By contrast, some physical properties are different: for example, solid homochiral porous cages show enantioselectivity for chiral aromatic alcohols, whereas the equivalent homochiral porous liquids do not. This can be attributed to a loss of supramolecular organisation in the isotropic porous liquid.

Graphical abstract: Understanding gas capacity, guest selectivity, and diffusion in porous liquids

Supplementary files

Article information

Article type
Edge Article
Submitted
25 Nov 2016
Accepted
12 Jan 2017
First published
31 Jan 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2017,8, 2640-2651

Understanding gas capacity, guest selectivity, and diffusion in porous liquids

R. L. Greenaway, D. Holden, E. G. B. Eden, A. Stephenson, C. W. Yong, M. J. Bennison, T. Hasell, M. E. Briggs, S. L. James and A. I. Cooper, Chem. Sci., 2017, 8, 2640 DOI: 10.1039/C6SC05196K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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