Abstract
A polymer of ring-labeled [14C]o-methoxyphenol ([14C]guaiacol) was prepared by peroxidase-H2O2-catalyzed oxidation of the 14C-labeled monomeric compound. The ring-labeled [14C]polyguaiacol contained 67.71% carbon, 5.09% hydrogen, 27.49% oxygen, 25.44% methoxyl, and 8.60% phenolic hydroxyl. The polymer had an average molecular weight of between 5,000 and 15,000, as determined by gel chromatography. A schematic representation of the polymer, similar to previously published structures of polyguaiacols, was devised to meet these and other analytical parameters. The polymer is primarily composed of o-o and p-p-linked guaiacol moieties, with an occasional o-p-biphenyl link and some p-diphenoquinone structures. An approximate molecular formula is [C49O14H31]n, where n ⋝ 5.8. Its C6 formula is C6H2.3O0.3carbonyl (OH)0.7(OCH3)1.0. Polyguaiacol has many of the characteristics of a synthetic lignin. It is easier and less expensive to prepare than standard synthetic lignins (dehydrogenation polymers of coniferyl alcohol). It is degraded ([14C]polyguaiacol → 14CO2) by the lignolytic system of the white-rot fungus Phanaerochaete chrysosporium. It is suggested that [14C]polyguaiacol may be of value as a substrate for lignin biodegradation research.
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Selected References
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