Activation of light alkanes at room temperature and ambient pressure
Abstract
Light alkane activation under mild conditions remains a substantial challenge. Here we report an aqueous reaction system capable of selectively converting light alkanes into corresponding olefins and oxygenates at room temperature and ambient pressure using Cu powder as the catalyst and O₂ as the oxidant. In ethane activation, we achieved a combined production of ethylene and acetic acid at a rate of 2.27 mmol g_(Cu)⁻¹ h⁻¹, with a combined selectivity up to 97%. Propane is converted to propylene with a selectivity up to 94% and a production rate up to 1.83 mmol g_(Cu)⁻¹ h⁻¹, while methane is converted mainly to carbon dioxide, methanol and acetic acid. On the basis of catalytic experiments, isotopic labelling experiments, spectroscopic insights and density functional theory calculations, we put forward mechanistic understandings in which the C–H bond is activated by the surface oxide species generated during the oxidation process, forming alkyl groups as key reaction intermediates.
Additional Information
© The Author(s), under exclusive licence to Springer Nature Limited 2023. H.Z., C.L., W.L. and Q.L. acknowledge the financial support from the State Key Laboratory of Chemical Engineering (no. SKL-ChE-23T02) and the Tsinghua University Initiative Scientific Research Program (20211080099). B.X. acknowledges the financial support from Beijing National Laboratory for Molecular Sciences. M.-J.C. acknowledges financial support from the Ministry of Science and Technology of the Republic of China under grant no. MOST 109-2113-M-006-009. W.A.G. acknowledges National Science Foundation (CBET-2005250). All NMR experiments were carried out at the BioNMR Facility, Tsinghua University Branch of China National Center for Protein Sciences (Beijing). We thank N. Xu for the assistance in the NMR data collection. We thank K. Zhao for the insightful discussion on the reaction mechanism. We thank J. Zhang for editing the paper. Data availability: The data supporting the findings of this study are available within the paper and its supplementary information files. All data are available from the corresponding authors upon reasonable request. Source data are provided with this paper. These authors contributed equally: Haochen Zhang, Chunsong Li. Contributions: H.Z., B.X. and Q.L. designed the project and wrote the paper. H.Z., W.L. and C.L. performed alkane activation experiments and physical characterizations. C.L. and H.Z. conducted the in situ SERS experiments. H.Z. and M.-J.C. performed DFT calculations and MD simulations. W.A.G. and G.L. contributed to data analysis and discussion. Q.L. supervised the entire project. Competing interests: A patent application (2022100080937) on the alkane activation system based on these results has been filed by Tsinghua University and Peking University with Q.L., H.C., C.L., G.L. and B.X. as inventors.Attached Files
Supplemental Material - 41929_2023_990_MOESM1_ESM.pdf
Supplemental Material - 41929_2023_990_MOESM2_ESM.txt
Supplemental Material - 41929_2023_990_MOESM3_ESM.txt
Supplemental Material - 41929_2023_990_MOESM4_ESM.xlsx
Supplemental Material - 41929_2023_990_MOESM5_ESM.xlsx
Supplemental Material - 41929_2023_990_MOESM6_ESM.xlsx
Supplemental Material - 41929_2023_990_MOESM7_ESM.xlsx
Supplemental Material - 41929_2023_990_MOESM8_ESM.xlsx
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Additional details
- Eprint ID
- 122421
- Resolver ID
- CaltechAUTHORS:20230725-48998000.5
- State Key Laboratory of Chemical Engineering
- SKL-ChE-23T02
- Tsinghua University Initiative Scientific Research Program
- 20211080099
- Beijing National Laboratory for Molecular Sciences
- Ministry of Science and Technology (Taipei)
- MOST 109-2113-M-006-009
- NSF
- CBET-2005250
- Created
-
2023-08-14Created from EPrint's datestamp field
- Updated
-
2023-08-14Created from EPrint's last_modified field