TY - JOUR
T1 - Active site engineering in UiO-66 type metal--organic frameworks by intentional creation of defects: a theoretical rationalization
T2 - A theoretical rationalization
AU - Vandichel, Matthias
AU - Hajek, Julianna
AU - Vermoortele, Frederik
AU - Waroquier, Michel
AU - De Vos, Dirk E.
AU - Van Speybroeck, Veronique
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2015/1/14
Y1 - 2015/1/14
N2 - The catalytic activity of the Zr-benzenedicarboxylate (Zr-BDC) UiO-66 can be drastically increased if some BDC linkers are missing, as this removes the full coordination of the framework metal ions. As a result, metal centers become more accessible and thus more active for Lewis acid catalysed reactions. Addition of modulators (MDL) to the synthesis mixture can create more linker deficiencies (Vermoortele et al., J. Am. Chem. Soc., 2013, 135, 11465) and leads to a significant increase in the catalytic activity due to the creation of a larger number of open sites. In this paper, we rationalize the function of the modulators under real synthesis conditions by the construction of free energy diagrams. The UiO-66 type materials form a very appropriate test case as the effect of addition of modulators hydrochloric acid (HCl) and trifluoroacetate (TFA) has been intensively investigated experimentally for the synthesis process and post-synthetic thermal activation. Under synthesis conditions, direct removal of BDC linkers requires a high free energy, but replacement of such linker by one or more TFA species might occur especially at high TFA:BDC ratios in the reaction mixture. Post-synthesis activation procedures at higher temperatures lead to substantial removal of the species coordinated to the Zr bricks, creating open metal sites. A mechanistic pathway is presented for the dehydroxylation process of the hexanuclear Zr cluster. For the citronellal cyclization, we show that the presence of some residual TFA in the structure may lead to faster reactions in complete agreement with the experiment. Hirshfeld-e partial charges for the Zr ions have been computed to investigate their sensitivity to substituent effects; a strong correlation with the experimental Hammett parameters and with the rates of the citronellal cyclization is found. The theoretical rationalization may serve as a basis for detailed active site engineering studies.
AB - The catalytic activity of the Zr-benzenedicarboxylate (Zr-BDC) UiO-66 can be drastically increased if some BDC linkers are missing, as this removes the full coordination of the framework metal ions. As a result, metal centers become more accessible and thus more active for Lewis acid catalysed reactions. Addition of modulators (MDL) to the synthesis mixture can create more linker deficiencies (Vermoortele et al., J. Am. Chem. Soc., 2013, 135, 11465) and leads to a significant increase in the catalytic activity due to the creation of a larger number of open sites. In this paper, we rationalize the function of the modulators under real synthesis conditions by the construction of free energy diagrams. The UiO-66 type materials form a very appropriate test case as the effect of addition of modulators hydrochloric acid (HCl) and trifluoroacetate (TFA) has been intensively investigated experimentally for the synthesis process and post-synthetic thermal activation. Under synthesis conditions, direct removal of BDC linkers requires a high free energy, but replacement of such linker by one or more TFA species might occur especially at high TFA:BDC ratios in the reaction mixture. Post-synthesis activation procedures at higher temperatures lead to substantial removal of the species coordinated to the Zr bricks, creating open metal sites. A mechanistic pathway is presented for the dehydroxylation process of the hexanuclear Zr cluster. For the citronellal cyclization, we show that the presence of some residual TFA in the structure may lead to faster reactions in complete agreement with the experiment. Hirshfeld-e partial charges for the Zr ions have been computed to investigate their sensitivity to substituent effects; a strong correlation with the experimental Hammett parameters and with the rates of the citronellal cyclization is found. The theoretical rationalization may serve as a basis for detailed active site engineering studies.
UR - http://www.scopus.com/inward/record.url?scp=84915820530&partnerID=8YFLogxK
U2 - 10.1039/c4ce01672f
DO - 10.1039/c4ce01672f
M3 - Article
AN - SCOPUS:84915820530
SN - 1466-8033
VL - 17
SP - 395
EP - 406
JO - CrystEngComm
JF - CrystEngComm
IS - 2
ER -