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  Direct Synthesis of Formamide from CO2 and H2O with Nickel–Iron Nitride Heterostructures under Mild Hydrothermal Conditions

Beyazay, T., Martin, W. F., & Tüysüz, H. (2023). Direct Synthesis of Formamide from CO2 and H2O with Nickel–Iron Nitride Heterostructures under Mild Hydrothermal Conditions. Journal of the American Chemical Society, 145(36), 19768-19779. doi:10.1021/jacs.3c05412.

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 Creators:
Beyazay, Tuğçe1, Author           
Martin, William F.2, Author
Tüysüz, Harun1, Author           
Affiliations:
1Research Group Tüysüz, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1950290              
2Institute of Molecular Evolution, University of Düsseldorf, 40225 Düsseldorf, Germany, ou_persistent22              

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 Abstract: Formamide can serve as a key building block for the synthesis of organic molecules relevant to premetabolic processes. Natural pathways for its synthesis from CO2 under early earth conditions are lacking. Here, we report the thermocatalytic conversion of CO2 and H2O to formate and formamide over Ni–Fe nitride heterostructures in the absence of synthetic H2 and N2 under mild hydrothermal conditions. While water molecules act as both a solvent and hydrogen source, metal nitrides serve as nitrogen sources to produce formamide in the temperature range of 25–100 °C under 5–50 bar. Longer reaction times promote the C–C bond coupling and formation of acetate and acetamide as additional products. Besides liquid products, methane and ethane are also produced as gas-phase products. Postreaction characterization of Ni–Fe nitride particles reveals structural alteration and provides insights into the potential reaction mechanism. The findings indicate that gaseous CO2 can serve as a carbon source for the formation of C–N bonds in formamide and acetamide over the Ni–Fe nitride heterostructure under simulated hydrothermal vent conditions.

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Language(s): eng - English
 Dates: 2023-05-242023-08-292023-09-13
 Publication Status: Issued
 Pages: 12
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/jacs.3c05412
 Degree: -

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Title: Journal of the American Chemical Society
  Other : JACS
  Abbreviation : J. Am. Chem. Soc.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 145 (36) Sequence Number: - Start / End Page: 19768 - 19779 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870