Each year, the pulp and paper industry produces approximately 50 million metric tons of lignin as waste, 95% of which is combusted or abandoned. Here, we report the use of lignin as a photocatalyst that forms H2O2 by O2 reduction and H2O oxidation under visible light. We investigated the photophysical and electronic properties of two lignin models, lignosulfonate and kraft lignin, by spectroscopic and photoelectrochemical analyses, and demonstrated the photoredox chemistry of lignin using these and other lignin models (for example, native-like cellulolytic enzyme lignin, artificial lignin dehydrogenation polymer and phenolic β-aryl ether-type lignin dimer). Furthermore, the integration of lignin and H2O2-dependent unspecific peroxygenases (UPOs) enabled the highly enantioselective oxyfunctionalization of various C–H bonds. The use of lignin photocatalysts solves a number of the challenges relating to the sustainable activation of UPOs, notably, eliminating the need for artificial electron donors and suppressing the HO·-mediated inactivation of UPOs. Thus, the lignin–UPO hybrid catalyst achieved a total turnover number of UPO of 81,000 for solar-powered biocatalytic oxyfunctionalization in photochemical platforms.
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This work was supported by the National Research Foundation (NRF; grant nos. NRF-2015R1A3A2066191 (C.B.P. and J.K.) and 2017M1A2A2087630 (Y.H.K.)) and the Global Ph.D. Fellowship Program (grant no. NRF-2019H1A2A1075810 (J.K.)), Republic of Korea. The authors thank G. Jung from B. Shin’s group (Korea Advanced Institute of Science and Technology) for permitting us to use a micro gas chromatograph.
The authors declare no competing interests.
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Kim, J., Nguyen, T.V.T., Kim, Y.H. et al. Lignin as a multifunctional photocatalyst for solar-powered biocatalytic oxyfunctionalization of C–H bonds. Nat Synth 1, 217–226 (2022). https://doi.org/10.1038/s44160-022-00035-2
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