Cargando…

Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin

[Image: see text] 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...

Descripción completa

Detalles Bibliográficos
Autores principales: Montgomery, James R. D., Lancefield, Christopher S., Miles-Barrett, Daniel M., Ackermann, Katrin, Bode, Bela E., Westwood, Nicholas J., Lebl, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645228/
https://www.ncbi.nlm.nih.gov/pubmed/31457383
http://dx.doi.org/10.1021/acsomega.7b01287
_version_ 1783437417660809216
author Montgomery, James R. D.
Lancefield, Christopher S.
Miles-Barrett, Daniel M.
Ackermann, Katrin
Bode, Bela E.
Westwood, Nicholas J.
Lebl, Tomas
author_facet Montgomery, James R. D.
Lancefield, Christopher S.
Miles-Barrett, Daniel M.
Ackermann, Katrin
Bode, Bela E.
Westwood, Nicholas J.
Lebl, Tomas
author_sort Montgomery, James R. D.
collection PubMed
description [Image: see text] 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.
format Online
Article
Text
id pubmed-6645228
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-66452282019-08-27 Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin Montgomery, James R. D. Lancefield, Christopher S. Miles-Barrett, Daniel M. Ackermann, Katrin Bode, Bela E. Westwood, Nicholas J. Lebl, Tomas ACS Omega [Image: see text] 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. American Chemical Society 2017-11-30 /pmc/articles/PMC6645228/ /pubmed/31457383 http://dx.doi.org/10.1021/acsomega.7b01287 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Montgomery, James R. D.
Lancefield, Christopher S.
Miles-Barrett, Daniel M.
Ackermann, Katrin
Bode, Bela E.
Westwood, Nicholas J.
Lebl, Tomas
Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin
title Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin
title_full Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin
title_fullStr Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin
title_full_unstemmed Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin
title_short Fractionation and DOSY NMR as Analytical Tools: From Model Polymers to a Technical Lignin
title_sort fractionation and dosy nmr as analytical tools: from model polymers to a technical lignin
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645228/
https://www.ncbi.nlm.nih.gov/pubmed/31457383
http://dx.doi.org/10.1021/acsomega.7b01287
work_keys_str_mv AT montgomeryjamesrd fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin
AT lancefieldchristophers fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin
AT milesbarrettdanielm fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin
AT ackermannkatrin fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin
AT bodebelae fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin
AT westwoodnicholasj fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin
AT lebltomas fractionationanddosynmrasanalyticaltoolsfrommodelpolymerstoatechnicallignin