Partial oxidation of cyclohexene over histidine-modified Cu-UiO-66 under aerobic conditions

New publication in the Journal of Catalysis by Ning Cao, PhD student at the Hylleraas Centre. 

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Portratit of Ning Cao at Hylleraas Centre.

Authors: Ning Cao, Ainara Nova et. al. Ning Cao is a PhD-student, working in research team 5 (RT5) at Hylleraas Centre. 

Catalytic testing

Enzyme-inspired catalysis is an attractive approach for developing selective hydrocarbon partial oxidation processes. Here, histidine was introduced into defective UiO-66 metal–organic framework by ligand exchange, followed by Cu(II) ion insertion. Density functional theory modeling combined with X-ray Absorption spectroscopy revealed that Cu(II) has a higher affinity for open Zr-O node sites than for histidine, leading to a series of materials where Cu(II) ions are predominantly anchored to the Zr6O4(OH)4 nodes, while only minority fractions of Cu(II) are anchored to histidine. 

Catalytic testing for aerobic cyclohexene oxidation with tert-butyl hydroperoxide (t-BuOOH) in trifluorotoluene solution at 25 °C showed activity for cyclohexene oxidation to cyclohexenol and cyclohexenone, with high selectivity. Benchmark tests revealed that Cu and t-BuOOH are both essential for the reaction, yet t-BuOOH consumption was far inferior to product formation rates, suggesting a radical reaction pathway involving O2. 

Publication: August, 22 nd 2024.  https://doi.org/10.1016/j.jcat.2024.115722 

Funding by:

  • European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement No 856446 (CUBE)).
  • Research Council of Norway through the Centre of Excellence (No. 262695) and Sigma2 for computational resources (No. nn4654k).
Tags: Hylleraas Centre, RT5, MOF, Cyclohexene oxidation, hydrocarbon, aerobic cyclohexene oxidation
Published Oct. 2, 2024 12:12 PM - Last modified Oct. 3, 2024 9:18 AM