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Heterogeneous photoredox flow chemistry for the scalable organosynthesis of fine chemicals

Author

Listed:
  • Can Yang

    (Fuzhou University)

  • Run Li

    (Max Planck Institute for Polymer Research)

  • Kai A. I. Zhang

    (Max Planck Institute for Polymer Research)

  • Wei Lin

    (Fuzhou University)

  • Katharina Landfester

    (Max Planck Institute for Polymer Research)

  • Xinchen Wang

    (Fuzhou University)

Abstract

Large-scale photochemical synthesis of high value chemicals under mild conditions is an ideal method of green chemical production. However, a scalable photocatalytic process has been barely reported due to the costly preparation, low stability of photosensitizers and critical reaction conditions required for classical photocatalysts. Here, we report the merging of flow chemistry with heterogeneous photoredox catalysis for the facile production of high value compounds in a continuous flow reactor with visible light at room temperature in air. In the flow reactor system, polymeric carbon nitrides, which are cheap, sustainable and stable heterogeneous photocatalysts, are immobilized onto glass beads and fibers, demonstrating a highly flexible construction possibility for devices of the photocatalytic materials. As an example of the production of high value chemicals, important chemical structures such as cyclobutanes, which are basic building blocks for many pharmaceutical compounds, like magnosalin, are synthesized in flow with high catalytic efficiency and stability.

Suggested Citation

  • Can Yang & Run Li & Kai A. I. Zhang & Wei Lin & Katharina Landfester & Xinchen Wang, 2020. "Heterogeneous photoredox flow chemistry for the scalable organosynthesis of fine chemicals," Nature Communications, Nature, vol. 11(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14983-w
    DOI: 10.1038/s41467-020-14983-w
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    Cited by:

    1. Lirong Guo & Rongchen Chu & Xinyu Hao & Yu Lei & Haibin Li & Dongge Ma & Guo Wang & Chen-Ho Tung & Yifeng Wang, 2024. "Ag3PO4 enables the generation of long-lived radical cations for visible light-driven [2 + 2] and [4 + 2] pericyclic reactions," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

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