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Pore with Gate: Enhancement of the Isosteric Heat of Adsorption of Dihydrogen via Postsynthetic Cation Exchange in Metal−Organic Frameworks

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journal contribution
posted on 03.10.2011, 00:00 by Sihai Yang, Gregory S. B. Martin, Jeremy J. Titman, Alexander J. Blake, David R. Allan, Neil R. Champness, Martin Schröder
Three isostructural anionic frameworks {[(Hdma)(H3O)][In2(L1)2]·4DMF·5H2O} (NOTT-206-solv), {[H2ppz][In2(L2)2]·3.5DMF·5H2O} (NOTT-200-solv), and {[H2ppz][In2(L3)2]·4DMF·5.5H2O} (NOTT-208-solv) (dma = dimethylamine; ppz = piperazine) each featuring organic countercations that selectively block the channels and act as pore gates have been prepared. The organic cations within the as-synthesized frameworks can be replaced by Li+ ions to yield the corresponding Li+-containing frameworks {Li1.2(H3O)0.8[In2(L1)2]·14H2O} (NOTT-207-solv), {Li1.5(H3O)0.5[In2(L2)2]·11H2O} (NOTT-201-solv), and {Li1.4(H3O)0.6[In2(L3)2]·4acetone·11H2O} (NOTT-209-solv) in which the pores are now unblocked. The desolvated framework materials NOTT-200a, NOTT-206a, and NOTT-208a display nonporous, hysteretic and reversible N2 uptakes, respectively, while NOTT-206a and NOTT-200a provide a strong kinetic trap showing adsorption/desorption hysteresis with H2. Single crystal X-ray analysis confirms that the Li+ ions are either tetrahedrally (in NOTT-201-solv and NOTT-209-solv) or octahedrally (in NOTT-207-solv) coordinated by carboxylate oxygen atoms and/or water molecules. This is supported by 7Li solid-state NMR spectroscopy. NOTT-209a, compared with NOTT-208a, shows a 31% enhancement in H2 storage capacity coupled to a 38% increase in the isosteric heat of adsorption to 12 kJ/mol at zero coverage. Thus, by modulating the pore environment via postsynthetic cation exchange, the gas adsorption properties of the resultant MOF can be fine-tuned. This affords a methodology for the development of high capacity storage materials that may operate at more ambient temperatures.

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