479020 Design of Highly Efficient Bifunctional Metal-Organic Framework Catalysts for Tandem Catalysis By Shortening the Reaction Pathway

Monday, November 14, 2016
Grand Ballroom B (Hilton San Francisco Union Square)
Benjamin Yeh, Chemical & Petroleum Engineering, University of Pittsburgh, Pittsburgh, PA, Zhigang Hu, National University of Singapore, Singapore, Singapore and Dan Zhao, Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, Singapore

Tandem reactions are important in the scientific community because they reduce time and money to carry out a reaction as well as chemical waste. However, most tandem reactions require two consecutive steps with different catalysts. Metal-organic frameworks have the capability to catalyze reactions; more specifically, the UiO-66 can be functionalized with two different moieties, making them a good candidate for tandem deacetalization−Knoevenagel reaction. In this study, it is shown that the UiO-66-type MOF, synthesized using the MHT synthesis method, can be functionalized with both an acidic and basic site at varying amounts. To analyze these affects, a kinetic study using 1H NMR was used to calculate the conversion of benzaldehyde dimethyl acetal (BADA) to benzalmalonitrile.

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