化学
键裂
木质素
劈理(地质)
酮
光化学
电子顺磁共振
有机化学
催化作用
可见光谱
绿色化学
腈
乙醇
选择性
吸收光谱法
共轭体系
组合化学
还原消去
共价键
还原剂
光催化
作者
Ayesha Khan,Logan W. Evans,David B. C. Martin
标识
DOI:10.1021/acssuschemeng.5c03068
摘要
The selective cleavage of the β-O-4 bond in lignin model compounds is a crucial step in realizing the full potential of transforming lignin to value-added aromatic compounds. Herein, we report an additive-free, visible-light-driven ligand-to-metal charge transfer (LMCT)-mediated strategy for the reductive cleavage of β-O-4 lignin model ketones in ethanol, utilizing TiO2 as the photocatalyst. We found that ethanol can act as a sensitizer and forms an LMCT complex on the surface of titania, which enables the reductive cleavage of the β-O-4 ketone under blue light (440 nm). The LMCT-sensitized titania showed moderate conversion (58%) for the reductive cleavage of β-O-4 ketone. Additionally, we observed that nitrogen doping of titania further enhances the visible light absorption and improves the conversion of the β-O-4 ketone up to 91%. EPR studies indicate the in situ generation of Ti3+ under blue light irradiation, which likely enables the reductive cleavage of β-O-4 ketone. Our work demonstrates a promising potential for the reductive cleavage of β-O-4 lignin model ketone to form value-added aromatic compounds under mild conditions without the use of an additional reductant by using ethanol (reaction solvent).
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