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 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.
| Original language | English |
|---|---|
| Pages (from-to) | 8277-8284 |
| Journal | ACS Catalysis |
| Volume | 10 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 2020 |
Keywords
- HOgeneration
- halogenation
- hydroxylation
- peroxyzymes
- photobiocatalysis
Fingerprint
Dive into the research topics of 'Water-Soluble Anthraquinone Photocatalysts Enable Methanol-Driven Enzymatic Halogenation and Hydroxylation Reactions'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver