解聚
木质素
硫化物
催化作用
键裂
乙醚
单体
冷凝
化学
产量(工程)
劈理(地质)
有机化学
药物化学
高分子化学
聚合物
材料科学
复合材料
冶金
物理
热力学
断裂(地质)
作者
Chaofeng Zhang,Hongji Li,Jianmin Lü,Xiaochen Zhang,Katherine E. MacArthur,Marc Heggen,Feng Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-04-06
卷期号:7 (5): 3419-3429
被引量:204
标识
DOI:10.1021/acscatal.7b00148
摘要
For lignin valorization, simultaneously achieving the efficient cleavage of ether bonds and restraining the condensation of the formed fragments represents a challenge thus far. Herein, we report a two-step oxidation–hydrogenation strategy to achieve this goal. In the oxidation step, the O2/NaNO2/DDQ/NHPI system selectively oxidizes CαH–OH to Cα═O within the β-O-4 structure. In the subsequent hydrogenation step, the α-O-4 and the preoxidized β-O-4 structures are further hydrogenated over a NiMo sulfide catalyst, leading to the cleavage of Cβ–OPh and Cα–OPh bonds. Besides the transformation of lignin model compounds, the yield of phenolic monomers from birch wood is up to 32% by using this two-step strategy. The preoxidation of CαH–OH to Cα═O not only weakens the Cβ–OPh ether bond but also avoids the condensation reactions caused by the presence of Cα+ from dehydroxylation of CαH–OH. Furthermore, the NiMo sulfide prefers to catalyze the hydrogenative cleavage of the Cβ–OPh bond connecting with a Cα═O rather than catalyze the hydrogenation of Cα═O back to the original CαH–OH, which further ensures and utilizes the advantages of preoxidation.
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