Laccase‐catalyzed polymerization of lignocatechol and affinity on proteins of resulting polymers

Takashi Yoshida, Rong Lü, Shuqin Han, Kazuyuki Hattori, Takahiro Katsuta, Kei‐ichi Takeda, Kazutoshi Sugimoto, Masamitsu Funaoka

Journal of Polymer Science Part A Polymer Chemistry · 2008 · 43 citations · 20 references

Concepts

Abstract

Abstract For the synthesis of a new biologically functional polymer from a natural resource by an environment‐friendly method, the laccase‐catalyzed polymerization of a lignin‐based macromonomer, lignocatechol, was carried out for the first time in ethanol–phosphate buffer solvent system to give crosslinked polymers in good yields. Lignocatechol was prepared by the phase separation system of lignin and catechol in aqueous sulfuric acid. The copolymerization was also performed with urushiol to afford the corresponding copolymers in high yields. The polymerization mechanism was estimated by the IR and pyrolysis GC‐MS measurements, suggesting that the polymerization proceeded mainly at the catechol ring through a quinone radical intermediate. The thermal properties were measured by the DSC, TG, and TMA analyses, indicating that the polymers had high thermal stabilities because of the crosslinked structures. In addition, it was found that the resulting polymers had the affinity of bovine serum albumin (BSA) and glucoamylase. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 824–832, 2009

References

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