木质素
解聚
化学
有机化学
反应性(心理学)
乙二醇
催化作用
脱碳
单体
产量(工程)
醛
缩醛
材料科学
聚合物
医学
替代医学
病理
冶金
作者
Peter J. Deuss,Ciaran W. Lahive,Christopher S. Lancefield,Nicholas J. Westwood,Paul C. J. Kamer,Katalin Barta,Johannes G. de Vries
出处
期刊:Chemsuschem
[Wiley]
日期:2016-09-21
卷期号:9 (20): 2974-2981
被引量:88
标识
DOI:10.1002/cssc.201600831
摘要
Abstract The depolymerization of lignin into valuable aromatic chemicals is one of the key goals towards establishing economically viable biorefineries. In this contribution we present a simple approach for converting lignin to aromatic monomers in high yields under mild reaction conditions. The methodology relies on the use of catalytic amounts of easy‐to‐handle metal triflates (M(OTf) x ). Initially, we evaluated the reactivity of a broad range of metal triflates using simple lignin model compounds. More advanced lignin model compounds were also used to study the reactivity of different lignin linkages. The product aromatic monomers were either phenolic C2‐acetals obtained by stabilization of the aldehyde cleavage products by reaction with ethylene glycol or methyl aromatics obtained by catalytic decarbonylation. Notably, when the method was ultimately tested on lignin, especially Fe(OTf) 3 proved very effective and the phenolic C2‐acetal products were obtained in an excellent, 19.3±3.2 wt % yield.
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