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

Open Access
Authors
  • M. Alcalde
  • W. Zhang
  • F. Hollmann
Publication date 07-08-2020
Journal ACS Catalysis
Volume | Issue number 10 | 15
Pages (from-to) 8277-8284
Number of pages 8
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract
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 organo-photocatalyst 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.
Document type Article
Note With supplementary file
Language English
Published at https://doi.org/10.1021/acscatal.0c01958
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acscatal.0c01958 (Final published version)
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