Understanding the structure of technical lignins resulting from acid-catalysed treatment of lignocellulosic biomass is important for their future applications. Here we report an investigation into the fate of lignin under acidic aqueous organosolv conditions. In particular we examine in detail the formation and reactivity of non-native Hibbert ketone structures found in isolated organosolv lignins from both Douglas fir and beech woods. Through the use of model compounds combined with HSQC, HMBC and HSQC-TOCSY NMR experiments we demonstrate that, depending on the lignin source, both S and G lignin-bound Hibbert ketone units can be present. We also show that these units can serve as a source of novel mono-aromatic compounds following an additional lignin depolymerisation reaction.

One key challenge hindering the valorization of lignin is its structural complexity. Artificial lignin-like materials provide a stepping stone between the simplicity of model compounds and the complexity of lignin. Here, we report an optimized synthesis of an all-G β-O-4 polymer 1 designed to model softwood lignin. After acetylation, the polymer Ac-1(V) was fractionated using a protocol that involved only volatile organic solvents, which left no insoluble residue. Using diffusion ordered spectroscopy NMR in combination with gel permeation chromatography, it was revealed that this fractionated material behaved like a flexible linear polymer in solution (average α > 0.5). Acetylated kraft lignin was subsequently processed using the same fractionation protocol. By comparison with the model polymer, we propose that the acetylated kraft lignin is composed of two classes of materials that exhibit contrasting physical properties. One is comparable to the acetylated all-G β-O-4 polymer Ac-1 , and the second has a significantly different macromolecular structure.

A new method has been developed to enable the modification of the organosolv technical lignin. Using a walnut shell butanol alkoxasolv lignin as a source of high β-O-4 content material, the β-O-4 γ-position has been selectively modified via tosylation, azidation and coppercatalyzed azide-alkyne triazole formation . In addition, extensive model studies were used to aid the detailed characterization of the modified lignin structure. The copper catalyzed click reaction was used to attach modified PEG chains and the resulting lignin-based co-polymer displayed improved thermal stability. This protocol was also used to incorporate a novel BODIPY-type

With lignin-first biorefineries likely to become a reality, controlled depolymerization of high-quality lignin streams to high-value products has become a priority. Using bisulfite chemistry, access to a high-β-O-4 content water-soluble lignosulfonate has been achieved, allowing follow-up procedures in water to be conducted. We show that phenolic β-O-4 units preferentially react under acidic bisulfite conditions, while nonphenolic β-O-4 units react much more slowly. Exploiting this improved chemical understanding and inherent selectivity, we have prepared a softwood lignosulfonate in which phenolic β-O-4 α-sulfonation has occurred, leaving significant native β-O-4 content. Use of an O-benzoylation protocol with lignin coupled with advanced two-dimensional nuclear magnetic resonance methods has allowed detailed analysis of this and other commercial and industrial lignosulfonates. Conversion of the native β-O-4 to benzylic, oxidized β-O-4 units was followed by a selective reductive cleavage to give a premium aromatic monomer in pure form.

Recent reports demonstrate that applications of the biopolymer lignin can be helped by the use of a fraction of the lignin which has an optimal molecular weight range. Unfortunately, the current methods used to determine lignin's molecular weight are inconsistent or not widely accessible. Here, an approach that relies on 2D DOSY NMR analysis is described that provides a measure of lignin's molecular weight. Consistent results were obtained using this well‐established NMR technique across a range of lignins.