4.6 Review

Recent Advances in Characterization of Lignin Polymer by Solution-State Nuclear Magnetic Resonance (NMR) Methodology

Journal

MATERIALS
Volume 6, Issue 1, Pages 359-391

Publisher

MDPI
DOI: 10.3390/ma6010359

Keywords

lignin; solution-state NMR; quantitative heteronuclear-single-quantum-coherence spectra (HSQC); in situ characterization

Funding

  1. Fundamental Research Funds for the Central Universities [BLYJ201313]
  2. National Natural Science Foundation of China [31110103902]
  3. Major State Basic Research Projects of China [973-2010CB732204]
  4. State Forestry Administration [201204803]

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The demand for efficient utilization of biomass induces a detailed analysis of the fundamental chemical structures of biomass, especially the complex structures of lignin polymers, which have long been recognized for their negative impact on biorefinery. Traditionally, it has been attempted to reveal the complicated and heterogeneous structure of lignin by a series of chemical analyses, such as thioacidolysis (TA), nitrobenzene oxidation (NBO), and derivatization followed by reductive cleavage (DFRC). Recent advances in nuclear magnetic resonance (NMR) technology undoubtedly have made solution-state NMR become the most widely used technique in structural characterization of lignin due to its versatility in illustrating structural features and structural transformations of lignin polymers. As one of the most promising diagnostic tools, NMR provides unambiguous evidence for specific structures as well as quantitative structural information. The recent advances in two-dimensional solution-state NMR techniques for structural analysis of lignin in isolated and whole cell wall states (in situ), as well as their applications are reviewed.

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