Abstract
A new noncatenated metal-organic framework containing pendant alcohol functionalities was synthesized. The alcohols were then post-synthetically converted to either lithium or magnesium alkoxides, with the incorporated metals anchored far from nodes or carboxylate functionalities. The metal alkoxide sites can be obtained stoichiometrically while maintaining the permanent porosity and large surface area of the parent hydroxylated material. The incorporated metal ions are found to induce an unusual pattern of binding energetics for H 2: isosteric heats of adsorption increase, rather than decrease, with increasing H 2 loading. Additionally, at 1 atm and 77 K, uptake (at least with low Li + loading) is increased by two hydrogen molecules per Li +.
Original language | English (US) |
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Pages (from-to) | 3866-3868 |
Number of pages | 3 |
Journal | Journal of the American Chemical Society |
Volume | 131 |
Issue number | 11 |
DOIs | |
State | Published - Mar 25 2009 |
ASJC Scopus subject areas
- General Chemistry
- Biochemistry
- Catalysis
- Colloid and Surface Chemistry
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CCDC 733333: Experimental Crystal Structure Determination
Mulfort, K. L. (Creator), Farha, O. K. (Creator), Stern, C. L. (Creator), Sarjeant, A. A. (Creator) & Hupp, J. T. (Creator), Cambridge Crystallographic Data Centre, 2009
DOI: 10.5517/ccsm2xc, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccsm2xc&sid=DataCite
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