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Courses/Engineering/Chemical Engineering

Learning about Lewis Acid Catalysts using Epoxides

Exploring Catalyst Design, Selectivity, and Industrial Applications.

Created byAIChE
BeginnerUpdated Feb 17, 2025
Learning about Lewis Acid Catalysts using Epoxides

What You'll Learn

check_circleExplain the role of Lewis acid catalysts in epoxide synthesis and reactions.
check_circleDescribe methods for producing structurally-uniform supported oxide catalysts.
check_circleAnalyze the impact of support geometry and solvents on catalytic activity and selectivity.
check_circleDiscuss the regioselectivity of epoxide ring-opening using fluorinated arylborane catalysts.

About This Course

Over nearly 20 years, my research group and I have frequently returned to epoxides as a touchstone, especially for work on supported and homogeneous Lewis acid catalysts. This work has been enabled by many collaborations that will be mentioned throughout, but an especially important one has been a partnership with Dow Chemical Company researchers for more than a decade.

Lewis acidic oxides are used industrially as catalysts for epoxide synthesis from olefins and hydroperoxides. Supported oxides like titania-silica are relatively facile to produce but can be heterogeneous in structure. Over many years, we have developed ways to probe and control this heterogeneity to produce structurally-uniform M-SiO2 materials from bulky precursor molecules. These can give high selectivity and activity, and they serve as a platform for systematic scientific studies. For example, we have recently addressed the role of the support geometry and the solvent in setting activity and selectivity, and we have then designed new materials to tune these interactions.

In the above work, Lewis acid sites efficiently activate hydroperoxides, but they also open the resulting epoxide under a wide range of conditions. In a second set of studies, we have examined the regioselectivity of epoxide alcoholysis using strongly Lewis-acidic fluorinated arylborane catalysts. Presented with the interesting (and useful!) observation that B(C6F5)3 ring-opens terminal epoxides to give the primary alcohol ethers, we developed a microkinetic model that captured the unusually complex behavior of this seemingly-simple catalyst. This model then gave us the insight needed to develop new reaction conditions to further tune the activity of these catalysts.

Your Instructors

AIChE
AIChE

The Global Home of Chemical Engineers

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Justin  Notestein
Justin Notestein

Professor of Chemical and Biological Engineering at Northwestern University

Prof. Justin Notestein received his BSE at Princeton University in 2001 and his PhD at the University of California Berkeley in 2006, both in Chemical Engineering. He is a professor in the department of Chemical and Biological Engineering at Northwestern University, and he is the director-elect of the Center for Catalysis and Surface Science. Research in Prof. Notestein’s group focuses on the development of new hybrid, oxide, and nanostructured catalysts and adsorbents for transformations relevant to sustainable energy, selective oxidation, and improving industrial chemical processes. Special attention is on developing full synthesis-structure-function relationships for improving the process of new catalyst development. Prof. Notestein frequently collaborates with researchers in industry, and he is a member of the Inorganometallic Catalyst Design Center, a DOE EFRC, and the Center for Innovative and Strategic Transformation of Alkane Resources, a NSF ERC. He is the lead PI for the Institute for Catalysis and Energy Processes, a DOE BES catalysis center housed at Northwestern University.

Credit Information

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