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Synthesis and Characterization of New 5‐Linked Pinoresinol Lignin Models
Authors:Dr. Fengxia Yue  Dr. Fachuang Lu  Prof. Dr. Runcang Sun  Prof. Dr. John Ralph
Affiliation:1. State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, 510640 (P.R. China), Fax: (+1)?608‐265‐2904;2. Dept. of Biochemistry, the Wisconsin Energy Institute and the DOE Great Lakes Bioenergy Research Center, University of Wisconsin‐Madison, Madison, WI 53726 (USA)
Abstract:Pinoresinol structures, featuring a β‐β′‐linkage between lignin monomer units, are important in softwood lignins and in dicots and monocots, particularly those that are downregulated in syringyl‐specific genes. Although readily detected by NMR spectroscopy, pinoresinol structures largely escaped detection by β‐ether‐cleaving degradation analyses presumably due to the presence of the linkages at the 5 positions, in 5‐5′‐ or 5‐O‐4′‐structures. In this study, which is aimed at helping better understand 5‐linked pinoresinol structures by providing the required data for NMR characterization, new lignin model compounds were synthesized through biomimetic peroxidase‐mediated oxidative coupling reactions between pre‐formed (free‐phenolic) coniferyl alcohol 5‐5′‐ or 5‐O‐4′‐linked dimers and a coniferyl alcohol monomer. It was found that such dimers containing free‐phenolic coniferyl alcohol moieties can cross‐couple with the coniferyl alcohol producing pinoresinol‐containing trimers (and higher oligomers) in addition to other homo‐ and cross‐coupled products. Eight new lignin model compounds were obtained and characterized by NMR spectroscopy, and one tentatively identified cross‐coupled β‐O‐4′‐product was formed from a coniferyl alcohol 5‐O‐4′‐linked dimer. It was demonstrated that the 5‐5′‐ and 5‐O‐4′‐linked pinoresinol structures could be readily differentiated by using heteronuclear multiple‐bond correlation (HMBC) NMR spectroscopy. With appropriate modification (etherification or acetylation) to the newly obtained model compounds, it would be possible to identify the 5‐5′‐ or 5‐O‐4′‐linked pinoresinol structures in softwood lignins by 2D HMBC NMR spectroscopic methods. Identification of the cross‐coupled dibenzodioxocin from a coniferyl alcohol 5‐5′‐linked moiety suggested that thioacidolysis or derivatization followed by reductive cleavage (DFRC) could be used to detect and identify whether the coniferyl alcohol itself undergoes 5‐5′‐cross‐linking during lignification.
Keywords:lignins  NMR spectroscopy  oxidation  radical reactions  synthetic methods
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