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Water-Soluble Anthraquinone Photocatalysts Enable Methanol-Driven Enzymatic Halogenation and Hydroxylation Reactions

  • Bo Yuan
  • , Durga Mahor
  • , Qiang Fei
  • , Ron Wever
  • , Miguel Alcalde
  • , Wuyuan Zhang
  • , Frank Hollmann
  • Xi'an Jiaotong University
  • University of Amsterdam
  • CSIC - Instituto de Catálisis y Petroleoquímica (ICP)
  • Delft University of Technology

科研成果: 期刊稿件文章同行评审

63 引用 (Scopus)

摘要

Peroxyzymes simply use H2O2 as a cosubstrate to oxidize a broad range of inert C-H bonds. The lability of many peroxyzymes against H2O2 can be addressed by a controlled supply of H2O2, ideally in situ. Here, we report a simple, robust, and water-soluble anthraquinone sulfonate (SAS) as a promising organophotocatalyst to drive both haloperoxidase-catalyzed halogenation and peroxygenase-catalyzed oxyfunctionalization reactions. Simple alcohols, methanol in particular, can be used both as a cosolvent and an electron donor for H2O2 generation. Very promising turnover numbers for the biocatalysts of up to 318 »000 have been achieved.

源语言英语
页(从-至)8277-8284
页数8
期刊ACS Catalysis
10
15
DOI
出版状态已出版 - 7 8月 2020

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