Oxidation, Oligomerization, Isomerization of Hydrocarbons Using Metal–Organic Frameworks
The selective conversion of hydrocarbons into higher-value fuels and feedstocks is essential to the global energy and chemistry landscape. While porous inorganic materials have enabled significant progress in these transformations, achieving high activity, selectivity, and stability under industrially relevant conditions remains challenging. Metal–organic frameworks (MOFs) are a promising platform to precisely control active-site environments and interrogate structure–function relationships due to their crystallinity, tunability, and porosity. This review highlights relevant hydrocarbon transformations and outlines the general mechanisms for oxidation, oligomerization, and isomerization. Metal node acidity, confinement effects, and active site dispersion are analyzed for their impact on reactivity and selectivity across the three reactions. Finally, we discuss current limitations in catalyst stability and offer a perspective on integrating reticular chemistry with high-throughput experimentation and machine learning to accelerate the discovery and design of robust, next-generation MOF catalysts.
Authors
- Seryeong Lee (ORCID: https://orcid.org/0000-0003-0621-6024)
- Omar K. Farha (ORCID: https://orcid.org/0000-0002-9904-9845)
- Haomiao Xie (ORCID: https://orcid.org/0000-0001-7688-6571)
- Justin Notestein
- Milad Ahmadi Khoshooei
- Massimiliano Delferro
- Dawson A. Grimes
Institutions
- Argonne National Laboratory (US)
- University of Chicago (US)
- Institute for Sustainability (GB)
Publication Details
- Journal
- ACS Energy Letters
- Published
- 2026-01-29
- DOI
- https://doi.org/10.1021/acsenergylett.5c03748
- Primary Topic
- Metal-Organic Frameworks: Synthesis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00