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Oxidative cleavage of C-C bonds in lignin
Stockholm University, Faculty of Science, Department of Organic Chemistry.ORCID iD: 0000-0003-4330-6387
Stockholm University, Faculty of Science, Department of Organic Chemistry.ORCID iD: 0000-0003-3020-631X
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).ORCID iD: 0000-0001-5704-5750
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Number of Authors: 62021 (English)In: Nature Chemistry, ISSN 1755-4330, E-ISSN 1755-4349, Vol. 13, p. 1118-1125Article in journal (Refereed) Published
Abstract [en]

Lignin is an aromatic polymer that constitutes up to 30 wt% of woody biomass and is considered the largest source of renewable aromatics. Valorization of the lignin stream is pivotal for making biorefining sustainable. Monomeric units in lignin are bound via C–O and C–C bonds. The majority of existing methods for the production of valuable compounds from lignin are based on the depolymerization of lignin via cleavage of relatively labile C–O bonds within lignin structure, which leads to yields of only 36–40 wt%. The remaining fraction (60 wt%) is a complex mixture of high-molecular-weight lignin, generally left unvalorized. Here we present a method to produce additional valuable monomers from the high-molecular-weight lignin fraction through oxidative C–C bond cleavage. This oxidation reaction proceeds with a high selectivity to give 2,6-dimethoxybenzoquinone (DMBQ) from high-molecular-weight lignin in 18 wt% yield, thus increasing the yield of monomers by 32%. This is an important step to make biorefining competitive with petroleum-based refineries.

Place, publisher, year, edition, pages
2021. Vol. 13, p. 1118-1125
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Chemical Sciences
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URN: urn:nbn:se:su:diva-198688DOI: 10.1038/s41557-021-00783-2ISI: 000698534700001PubMedID: 34556848OAI: oai:DiVA.org:su-198688DiVA, id: diva2:1611508
Available from: 2021-11-15 Created: 2021-11-15 Last updated: 2021-11-25Bibliographically approved

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Subbotina, ElenaRukkijakan, ThanyaYu, XiaowenJohnsson, MatsSamec, Joseph S. M.

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