Issue 12, 2024

Visible-light-mediated metal-free regioselective oxidative C–C bond cleavage of lignin dimers to aromatic acids

Abstract

The upgrading of lignin is a sustainable and promising pathway for fossil-based aromatic compounds but always faces low selectivity. Herein, a metal-free photocatalyst, 2,4,6-triphenylpyrylium tetrafluoroborate (TPP), was illustrated to remarkably facilitate the regioselective oxidative Cα–Cβ bond cleavage of β-1 and β-O-4 lignin alcohol/ketone models into aromatic acids (92–99% yields) under visible-light irradiation at room temperature without any additive/co-catalyst, which was enabled by the synergistic effect of Cβ–H⋯C(TPP) interaction and·˙O2/1O2 species. The synergy of the catalyst–substrate interaction and active species offers a reference for the enhancive and selective transformation of polymeric biomass and complex molecules.

Graphical abstract: Visible-light-mediated metal-free regioselective oxidative C–C bond cleavage of lignin dimers to aromatic acids

Supplementary files

Article information

Article type
Communication
Submitted
06 Dec 2023
Accepted
09 Jan 2024
First published
10 Jan 2024

Chem. Commun., 2024,60, 1642-1645

Visible-light-mediated metal-free regioselective oxidative C–C bond cleavage of lignin dimers to aromatic acids

Y. Meng, J. Li, H. Liu, H. Wu and H. Li, Chem. Commun., 2024, 60, 1642 DOI: 10.1039/D3CC05958H

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