Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 55, 2014
Previous Article Next Article

Insights into an intriguing gas sorption mechanism in a polar metal–organic framework with open-metal sites and narrow channels

Author affiliations

Abstract

Simulations of H2 and CO2 sorption were performed in the metal–organic framework (MOF), [Cu(Me-4py-trz-ia)]. This MOF was recently shown experimentally to exhibit high uptake for H2 and CO2 sorption and this was reproduced and elucidated through the simulations performed herein. Consistent with experiment, the theoretical isosteric heat of adsorption, Qst, values were nearly constant across all loadings for both sorbates. The simulations revealed that sorption directly onto the open-metal sites was not observed in this MOF, ostensibly a consequence of the low partial positive charges of the Cu2+ ions as determined through electronic structure calculations. Sorption was primarily observed between adjacent carboxylate oxygen atoms (site 1) and between nearby methyl groups (site 2) of the organic linkers. In addition, saturation of the most energetically favorable sites (site 1) is possible only after filling a nearby site (site 2) first due to the MOF topology. This suggests that the lack of dependence on loading for the Qst is due to the concurrent filling of sites 1 and 2, leading to an observed average Qst value.

Graphical abstract: Insights into an intriguing gas sorption mechanism in a polar metal–organic framework with open-metal sites and narrow channels

Back to tab navigation

Supplementary files

Article information


Submitted
25 Apr 2014
Accepted
19 May 2014
First published
20 May 2014

Chem. Commun., 2014,50, 7283-7286
Article type
Communication
Author version available

Insights into an intriguing gas sorption mechanism in a polar metal–organic framework with open-metal sites and narrow channels

K. A. Forrest, T. Pham, K. McLaughlin, A. Hogan and B. Space, Chem. Commun., 2014, 50, 7283
DOI: 10.1039/C4CC03070B

Social activity

Search articles by author

Spotlight

Advertisements