Cyclohexanone oxime is an important precursor for Nylon-6 and is typically synthesized via the nucleophilic addition-elimination of hydroxylamine with cyclohexanone. Current technologies for hydroxylamine production are, however, not environment-friendly due to the requirement of harsh reaction conditions. Here, we report an electrochemical method for the one-pot synthesis of cyclohexanone oxime under ambient conditions with aqueous nitrate as the nitrogen source. A series of Zn-Cu alloy catalysts are developed to drive the electrochemical reduction of nitrate, where the hydroxylamine intermediate formed in the electroreduction process can undergo a chemical reaction with the cyclohexanone present in the electrolyte to produce the corresponding oxime. The best performance is achieved on a ZnCu electrocatalyst with a 97% yield and a 27% Faradaic efficiency for cyclohexanone oxime at 100 mA/cm. By analyzing the catalytic activities/selectivities of the different Zn-Cu alloys and conducting in-depth mechanistic studies via Raman spectroscopy and theoretical calculations, we demonstrate that the adsorption of nitrogen species plays a central role in catalytic performance. Overall, this work provides an attractive strategy to build the C-N bond in oxime and drive organic synthesis through electrochemical nitrate reduction, while highlighting the importance of controlling surface adsorption for product selectivity in electrosynthesis.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10913030 | PMC |
http://dx.doi.org/10.1021/acscatal.3c05388 | DOI Listing |
Adv Sci (Weinh)
December 2024
Soochow Institute for Energy and Materials InnovationS (SIEMIS), Soochow University, Suzhou, 215006, China.
Hydrogen peroxide (HO) is an important chemical in synthetic chemistry with huge demands. Photocatalytic synthesis of HO via oxygen reduction and water oxidation reactions (ORR and WOR) is considered as a promising and desirable solution for on-site applications. However, the efficiency of such a process is low due to the poor solubility of molecular oxygen and the rapid reverse reaction of hydroxyl radicals (OH) with hydrogen atoms (H).
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Key Laboratory of Materials Physics, Centre for Environmental and Energy Nanomaterials, Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, HFIPS, Chinese Academy of Sciences, Hefei, 230031, China.
Cyclohexanone oxime, a critical precursor for nylon-6 production, is traditionally synthesized via the hydroxylamine method under industrial harsh conditions. Here is present a one-step electrochemical integrated approach for the efficient production of cyclohexanone oxime under ambient conditions. This approach employed the coupling of in situ electro-synthesized HO over a cobalt (Co)-based electrocatalyst with the titanium silicate-1 (TS-1) heterogeneous catalyst to achieve the cyclohexanone ammoximation process.
View Article and Find Full Text PDFNat Commun
November 2024
Department of Materials Science and Engineering, Southern University of Science and Technology, Shenzhen, 518055, China.
The electrocatalytic reduction of nitrogenous waste offers a sustainable approach to producing nitrogen-containing chemicals. The selective synthesis of high-value hydroxylamine (NHOH) is challenging due to the instability of NHOH as an intermediate. Here, we present a rational electrocatalyst design strategy for promoting NHOH electrosynthesis by suppressing the competing pathways of further reduction.
View Article and Find Full Text PDFChem Asian J
January 2025
College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310027, China.
Pure silica ITH zeolite is normally synthesized under neutral or acidic conditions in the presence of HF, but it is challenging for synthesis of this zeolite under alkaline conditions. In this work, it is successful for alkaline synthesis of pure silica ITH in the absence of HF using a designed organic template containing F species, showing that the sample obtained has high crystallinity associated with ITH structure, nanosheet morphology, and rich silanol nests. Very importantly, this ITH zeolite exhibited better performance in vapor phase Beckmann rearrangement of cyclohexanone oxime than that of Silicalite-1 zeolite, one of the best catalysts for this reaction.
View Article and Find Full Text PDFJ Am Chem Soc
October 2024
Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Coupling with the nitrate electroreduction reaction (NitRR), the electrosynthesis of cyclohexanone oxime (CHO, the vital feedstock in the nylon-6 industry) from cyclohexanone provides a promising alternative to the traditional energy consumption process. However, it still suffers from low efficiency because selective production of *NHOH intermediate from NitRR under large current densities is challenging. We here report a CuMoO/nitrogen-doped carbon (NC) electrocatalyst with high-density Cu-Mo dual sites for NitRR to selectively produce and stabilize *NHOH, with the subsequent cyclohexanone oximation achieving the highest CHO Faradaic efficiency of 94.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!