English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Zendy Open

Presents the pdf analysis as premium feature

PDF Analysis

Insights

Presents the summarisation as premium feature

Summarisation

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the zaia usage as premium feature

ZAIA

Zendy Tools

Zendy Plus

Presents the access of premium content as premium feature

Premium Content

Horseradish peroxidase (HRP)-catalyzed dehydrogenative copolymerization of guaiacyl (G)-type monolignol glycoside (isoconiferin, coniferyl alcohol γ- O -β- d -glucopyranoside, iso-G) and syringyl (S)-type monolignol glycoside (isosyringin, sinapyl alcohol γ- O -β- d -glucopyranoside, iso-S) were performed in continuous dehydrogenation mode (end-wise polymerization) to result in the formation of water-soluble lignin-like copolymers (iso-G/S-DHPs) in a homogeneous phase. The yield of iso-G/S-DHP increased with increasing iso-G content in the mixture of monomers from 23% (iso-G/iso-S 0:100) to 81% (iso-G/iso-S 50:50). The degree of polymerization (DP) of the resulting iso-G/S-DHP also increased proportionally from 7 (iso-G/iso-S 0:100) to 27 (iso-G/iso-S 50:50) as the iso-G content increased. It is obvious that iso-G plays an important role in the polymerization of iso-S. A similar tendency was also observed in conventional copolymerization of coniferyl alcohol (G-alc) and sinapyl alcohol (S-alc). The highest DP for DHP obtained in the conventional system was only ∼10 due to the heterogeneous reaction system. As the HRP-catalyzed monomer consumption rate of iso-S was greatly enhanced by addition of iso-G as a co-monomer, radical transfer from iso-G to iso-S seems to be plausible. Conventional copolymerization of G-alc and S-alc also supports this view. Spectroscopic studies and alkaline nitrobenzene oxidation analyses indicated that iso-G/S-DHPs had typical lignin structures composed of both G and S units. It was confirmed that the copolymerization behavior of the glycosides iso-G and iso-S in a homogeneous phase are well reflected by that of the monolignols G-alc and S-alc in a heterogeneous phase. Results also indicated that the presence of G-type co-monomers sensitively affects the polymerization of S-type monomers.

holzforschung

Studies on the dehydrogenative polymerizations (DHPs) of monolignol β-glycosides: Part 4. Horseradish peroxidase-catalyzed copolymerization of isoconiferin and isosyringin