Abstract

Photocatalytic selective transform native lignin into valuable chemicals is an attractive but challenging task. Herein, we report a mesoporous sulfur-doped carbon nitride (MSCN-0.5) which is prepared by a facile one-step thermal condensation strategy. It is highly active and selective for the cleavage Cα−Cβ bond in β−O−4 lignin model compound under visible light radiation at room temperature, achieving 99% substrate conversion and 98% Cα−Cβ bond cleavage selectivity. Mechanistic studies revealed that the Cβ−H bond of lignin model compounds activated by holes and generate key Cβ radical intermediates, further induced the Cα−Cβ bond cleavage by superoxide anion radicals (•O2−) to produce aromatic oxygenates. Waste Camellia oleifera shell (WCOS) was taken as a representative to further understand the reaction mechanisms on native lignin. 33.2 mg of monophenolic compounds (Vanillin accounted for 22% and Syringaldehyde for 34%) can be obtained by each gram of WCOS lignin, which is 2.5 times as that of the pristine carbon nitride. The present work offers useful guidance for designing metal-free heterogeneous photocatalysts for Cα−Cβ bond cleavage to harvest monophenolic compounds.

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