Exploiting parameter space in MOFs: a 20-fold enhancement of phosphate-ester hydrolysis with UiO-66-NH2
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| Authors: | Michael J Katz Su-Young Moon Joseph E Mondloch M Hassan Beyzavi Casey J Stephenson Joseph T Hupp Omar K Farha |
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| Affiliation: | a Department of Chemistry , Northwestern University , 2145 Sheridan Road , Evanston , Illinois 60208 , USA . Email: ; Email: ; b Chemical Science and Engineering Division , Argonne National Laboratory , 9700 S. Cass Avenue , Argonne , Illinois 60439 , USA ; c Department of Chemistry , Faculty of Science , King Abdulaziz University , Jeddah , Saudi Arabia |
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| Abstract: | The hydrolysis of nerve agents is of primary concern due to the severe toxicity of these agents. Using a MOF-based catalyst (UiO-66), we have previously demonstrated that the hydrolysis can occur with relatively fast half-lives of 50 minutes. However, these rates are still prohibitively slow to be efficiently utilized for some practical applications (e.g., decontamination wipes used to clean exposed clothing/skin/vehicles). We thus turned our attention to derivatives of UiO-66 in order to probe the importance of functional groups on the hydrolysis rate. Three UiO-66 derivatives were explored; UiO-66-NO2 and UiO-66-(OH)2 showed little to no change in hydrolysis rate. However, UiO-66-NH2 showed a 20 fold increase in hydrolysis rate over the parent UiO-66 MOF. Half-lives of 1 minute were observed with this MOF. In order to probe the role of the amino moiety, we turned our attention to UiO-67, UiO-67-NMe2 and UiO-67-NH2. In these MOFs, the amino moiety is in close proximity to the zirconium node. We observed that UiO-67-NH2 is a faster catalyst than UiO-67 and UiO-67-NMe2. We conclude that the role of the amino moiety is to act as a proton-transfer agent during the catalytic cycle and not to hydrogen bond or to form a phosphorane intermediate. |
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