Isolation of functionalized phenolic monomers through selective oxidation and C-O bond cleavage of the β-O-4 linkages in lignin

Angew Chem Int Ed Engl. 2015 Jan 2;54(1):258-62. doi: 10.1002/anie.201409408. Epub 2014 Nov 5.

Abstract

Functionalized phenolic monomers have been generated and isolated from an organosolv lignin through a two-step depolymerization process. Chemoselective catalytic oxidation of β-O-4 linkages promoted by the DDQ/tBuONO/O2 system was achieved in model compounds, including polymeric models and in real lignin. The oxidized β-O-4 linkages were then cleaved on reaction with zinc. Compared to many existing methods, this protocol, which can be achieved in one pot, is highly selective, giving rise to a simple mixture of products that can be readily purified to give pure compounds. The functionality present in these products makes them potentially valuable building blocks.

Keywords: biomass; depolymerization; lignin; oxidation; renewable chemicals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzoquinones / chemistry
  • Lignin / chemistry*
  • Oxidants / chemistry
  • Oxidation-Reduction
  • Phenols / chemistry*
  • Phenols / isolation & purification
  • Polymerization

Substances

  • Benzoquinones
  • Oxidants
  • Phenols
  • dichlorodicyanobenzoquinone
  • Lignin