Peroxidative Oxidation of Lignin and a Lignin Model Compound by a Manganese SALEN Derivative

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• 作者：Stephen D. Springer ; Jian He ; Megan Chui ; R. Daniel Little ; Marcus Foston ; Alison Butler
• 刊名：ACS Sustainable Chemistry & Engineering
• 出版年：2016
• 出版时间：June 6, 2016
• 年：2016
• 卷：4
• 期：6
• 页码：3212-3219
• 全文大小：374K
• 年卷期：0
• ISSN：2168-0485

文摘

The manganese catalyst, (1R,2R)-(−)-[1,2-cyclohexanediamino-N,N′-bis(3,5-di-t-butylsalicylidene)]manganese(III) chloride, was used to activate H₂O₂ to oxidize organosolv lignin and a lignin model compound. Oxidation of the β-O-4 lignin model substrate 1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-diol (320.3 m/z) and poplar organosolv lignin resulted in both fragmentation and polymerization processes, likely via phenoxy radical formation. Matrix-assisted laser desorption/ionization (MALDI) time-of-flight (TOF) mass spectrometry (MS) of the reaction products from the β-O-4 model substrate showed oligomers of the substrate with masses of 661.192, 979.355, and 1297.466 m/z that correspond to a dimer, trimer, and tetramer of the β-O-4 model substrate, respectively. Nuclear magnetic resonance (NMR) shows the formation of 5–5 diphenyl and 4-O-5 linkages in the β-O-4 model substrate oxidation products. Gel permeation chromatography (GPC) detected three peaks, corresponding to the β-O-4 model substrate and its oligomers. Products from the Mn-catalyzed oxidation of poplar organosolv lignin by H₂O₂ were analyzed by GPC, ³¹P NMR, and ¹³C NMR. GPC showed an increase by approximately four in the number-average molecular weight of organosolv lignin upon oxidation. NMR shows that polymerization occurs at positions consistent with phenoxy radical coupling, where the observed changes in guaiacyl subunit chemical shifts are most likely due to the formation of 5–5 biphenyl linkages.