Abstract

Phenolic hydroxyl groups in three lignin model compounds, guaiacol, acetoguaiacone, and dehydrodiisoeugenol, and in organosolv lignin were blocked by etherification with polyethylene glycol (PEG). Polyethylene glycol modification, even at a low degree of substitution, greatly enhanced the hydrophilicity of the substrate, producing water-soluble substances. When etherified by reaction with PEG-mesylate, the lignin dimer model compound, dehydrodiisoeugenol, was stabilized considerably against light-induced yellowing.

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