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Bloch ED, Hudson MR, Mason JA, et al. Reversible CO binding enables tunable CO/H₂ and CO/N₂ separations in metal-organic frameworks with exposed divalent metal cations. J Am Chem Soc. 2014;136(30):10752-61doi: 10.1021/ja505318p.
Bloch, E. D., Hudson, M. R., Mason, J. A., Chavan, S., Crocellà, V., Howe, J. D., Lee, K., Dzubak, A. L., Queen, W. L., Zadrozny, J. M., Geier, S. J., Lin, L. C., Gagliardi, L., Smit, B., Neaton, J. B., Bordiga, S., Brown, C. M., & Long, J. R. (2014). Reversible CO binding enables tunable CO/H₂ and CO/N₂ separations in metal-organic frameworks with exposed divalent metal cations. Journal of the American Chemical Society, 136(30), 10752-61. https://doi.org/10.1021/ja505318p
Bloch, Eric D, et al. "Reversible CO binding enables tunable CO/H₂ and CO/N₂ separations in metal-organic frameworks with exposed divalent metal cations." Journal of the American Chemical Society vol. 136,30 (2014): 10752-61. doi: https://doi.org/10.1021/ja505318p
Bloch ED, Hudson MR, Mason JA, Chavan S, Crocellà V, Howe JD, Lee K, Dzubak AL, Queen WL, Zadrozny JM, Geier SJ, Lin LC, Gagliardi L, Smit B, Neaton JB, Bordiga S, Brown CM, Long JR. Reversible CO binding enables tunable CO/H₂ and CO/N₂ separations in metal-organic frameworks with exposed divalent metal cations. J Am Chem Soc. 2014 Jul 30;136(30):10752-61. doi: 10.1021/ja505318p. Epub 2014 Jul 18. PMID: 24999916.
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