{Reference Type}: Journal Article
{Title}: Selective lignin arylation for biomass fractionation and benign bisphenols.
{Author}: Li N;Yan K;Rukkijakan T;Liang J;Liu Y;Wang Z;Nie H;Muangmeesri S;Castiella-Ona G;Pan X;Zhou Q;Jiang G;Zhou G;Ralph J;Samec JSM;Wang F;
{Journal}: Nature
{Volume}: 630
{Issue}: 8016
{Year}: 2024 Jun 29
{Factor}: 69.504
{DOI}: 10.1038/s41586-024-07446-5
{Abstract}: Lignocellulose is mainly composed of hydrophobic lignin and hydrophilic polysaccharide polymers, contributing to an indispensable carbon resource for green biorefineries1,2. When chemically treated, lignin is compromised owing to detrimental intra- and intermolecular crosslinking that hampers downstream process3,4. The current valorization paradigms aim to avoid the formation of new C-C bonds, referred to as condensation, by blocking or stabilizing the vulnerable moieties of lignin5-7. Although there have been efforts to enhance biomass utilization through the incorporation of phenolic additives8,9, exploiting lignin's proclivity towards condensation remains unproven for valorizing both lignin and carbohydrates to high-value products. Here we leverage the proclivity by directing the C-C bond formation in a catalytic arylation pathway using lignin-derived phenols with high nucleophilicity. The selectively condensed lignin, isolated in near-quantitative yields while preserving its prominent cleavable β-ether units, can be unlocked in a tandem catalytic process involving aryl migration and transfer hydrogenation. Lignin in wood is thereby converted to benign bisphenols (34-48 wt%) that represent performance-advantaged replacements for their fossil-based counterparts. Delignified pulp from cellulose and xylose from xylan are co-produced for textile fibres and renewable chemicals. This condensation-driven strategy represents a key advancement complementary to other promising monophenol-oriented approaches targeting valuable platform chemicals and materials, thereby contributing to holistic biomass valorization.