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Highly selective oxidation of benzene to phenol with air at room temperature promoted by water

Author

Listed:
  • Jijia Xie

    (University College London
    Sinopec Group)

  • Xiyi Li

    (University College London)

  • Jian Guo

    (University College London
    Sichuan University)

  • Lei Luo

    (Northwest University
    Chinese Academy of Sciences)

  • Juan J. Delgado

    (Universidad de Cádiz
    IMEYMAT, Instituto de Microscopía Electrónica y Materiales)

  • Natalia Martsinovich

    (University of Sheffield)

  • Junwang Tang

    (University College London
    Tsinghua University)

Abstract

Phenol is one of the most important fine chemical intermediates in the synthesis of plastics and drugs with a market size of ca. $30b1 and the commercial production is via a two-step selective oxidation of benzene, requiring high energy input (high temperature and high pressure) in the presence of a corrosive acidic medium, and causing serious environmental issues2–5. Here we present a four-phase interface strategy with well-designed Pd@Cu nanoarchitecture decorated TiO2 as a catalyst in a suspension system. The optimised catalyst leads to a turnover number of 16,000–100,000 for phenol generation with respect to the active sites and an excellent selectivity of ca. 93%. Such unprecedented results are attributed to the efficient activation of benzene by the atomically Cu coated Pd nanoarchitecture, enhanced charge separation, and an oxidant-lean environment. The rational design of catalyst and reaction system provides a green pathway for the selective conversion of symmetric organic molecules.

Suggested Citation

  • Jijia Xie & Xiyi Li & Jian Guo & Lei Luo & Juan J. Delgado & Natalia Martsinovich & Junwang Tang, 2023. "Highly selective oxidation of benzene to phenol with air at room temperature promoted by water," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40160-w
    DOI: 10.1038/s41467-023-40160-w
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