Porous MII/Pyrimidine‐4,6‐Dicarboxylato Neutral Frameworks: Synthetic Influence on the Adsorption Capacity and Evaluation of CO2‐Adsorbent Interactions |
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| Authors: | Dr Javier Cepeda Dr Sonia Pérez‐Yáñez Dr Garikoitz Beobide Dr Oscar Castillo Dr Michael Fischer Prof Antonio Luque Prof Paul A Wright |
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| Affiliation: | 1. Departmento de Química Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco (UPV/EHU), B° Sarriena, s/n, Apdo. 644, 48080 Bilbao (Spain), Fax: (+34)?94‐601‐35‐00;2. Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ (UK);3. EaStCHEM School of Chemistry, University of St. Andrews, Purdie Building, North Haugh, St. Andrews, Fife, KY16 9ST (UK) |
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| Abstract: | The understanding of the factors that affect the real pore‐network structure for a given bulk material due to different synthetic procedures is essential to develop the material with the best adsorption properties. In this work, we have deeply studied the influence of the crystallinity degree over the adsorption capacity on three new isostructural MOFs with the formula {CdM(μ4‐pmdc)2(H2O)2] ? solv}n (in which, pmdc=pyrimidine‐4,6‐dicarboxylate; solv=corresponding solvent; MII=Cd ( 1 ), Mn ( 2 ), Zn ( 3 )). Compared with other methods, the solvent‐free synthesis stands as the most effective route because, apart from enabling the preparation of the heterometallic compounds 2 and 3 , it also renders the adsorbents with the highest performance, which is indeed close to the expected one derived from Grand Canonical Monte Carlo (GCMC) calculations. The structural analysis of the as‐synthesised and evacuated frameworks reveals the existence of a metal atom exposed to the pore. The accessibility of this site is limited due to its atomic environment, which is why it is considered as a pseudo‐open‐metal site. The chemical and physical characterisation confirms that this site can be modified as the metal atom is replaced in compounds 2 and 3 . To assess the effect of the metal replacement on the adsorption behaviour, an exhaustive study of CO2 experimental isotherms has been performed. The affinity of the pseudo‐open metal sites towards CO2 and the distribution of the preferred adsorption sites are discussed on the basis of DFT and GCMC calculations. |
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| Keywords: | adsorption density functional calculations metal– organic frameworks open‐metal site synthetic methods |
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