4.8 Article

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

Journal

ACS CATALYSIS
Volume 10, Issue 15, Pages 8277-8284

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c01958

Keywords

photobiocatalysis; peroxyzymes; halogenation; hydroxylation; H2O2 generation

Funding

  1. Young Talent Support Plan of Xi'an Jiaotong University [7121191208]
  2. National Natural Science Foundation of China [21706205]
  3. China Postdoctoral Science Foundation [2018M633518]
  4. Natural Science Foundation of Shaanxi Province [2018JQ2062]
  5. European Research Commission (ERC) [648026]
  6. Netherlands Organisation for Scientific Research (VICI grant) [724.014.003]
  7. Spanish Government Project [BIO2016-79106-R-Lignolution]
  8. Comunidad de Madrid Synergy CAM project [Y2018/BIO-4738-EVOCHIMERA-CM]

Ask authors/readers for more resources

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.

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