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Fractionation and DOSY NMR as analytical tools : from model polymers to a technical lignin
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dc.contributor.author | Montgomery, James | |
dc.contributor.author | Lancefield, Christopher Stuart | |
dc.contributor.author | Miles-Barrett, Daniel | |
dc.contributor.author | Ackermann, Katrin | |
dc.contributor.author | Bode, Bela Ernest | |
dc.contributor.author | Westwood, Nicholas James | |
dc.contributor.author | Lebl, Tomas | |
dc.date.accessioned | 2017-12-01T15:30:07Z | |
dc.date.available | 2017-12-01T15:30:07Z | |
dc.date.issued | 2017-11-30 | |
dc.identifier.citation | Montgomery , J , Lancefield , C S , Miles-Barrett , D , Ackermann , K , Bode , B E , Westwood , N J & Lebl , T 2017 , ' Fractionation and DOSY NMR as analytical tools : from model polymers to a technical lignin ' , ACS Omega , vol. 2 , no. 11 , pp. 8466-8474 . https://doi.org/10.1021/acsomega.7b01287 | en |
dc.identifier.issn | 2470-1343 | |
dc.identifier.other | PURE: 251516439 | |
dc.identifier.other | PURE UUID: 8763b273-dc0e-43e1-80b3-6387b6f89602 | |
dc.identifier.other | ORCID: /0000-0002-0269-3221/work/48131723 | |
dc.identifier.other | ORCID: /0000-0002-3384-271X/work/39245049 | |
dc.identifier.other | ORCID: /0000-0003-0630-0138/work/56424209 | |
dc.identifier.other | Scopus: 85051082983 | |
dc.identifier.other | WOS: 000418744100109 | |
dc.identifier.uri | https://hdl.handle.net/10023/12221 | |
dc.description | This work was supported by EPSRC Ph.D. studentships (EP/ 1518175 (DMB) and EP/1654168 (JRDM)), the Industrial Biotechnology Innovation Centre (Ph.D. studentship to DMB), and an EPSRC Doctoral Prize Fellowship (CSL). | en |
dc.description.abstract | 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. | |
dc.language.iso | eng | |
dc.relation.ispartof | ACS Omega | en |
dc.rights | © 2017 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. | en |
dc.subject | QD Chemistry | en |
dc.subject | DAS | en |
dc.subject.lcc | QD | en |
dc.title | Fractionation and DOSY NMR as analytical tools : from model polymers to a technical lignin | en |
dc.type | Journal article | en |
dc.description.version | Publisher PDF | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.contributor.institution | University of St Andrews. Biomedical Sciences Research Complex | en |
dc.contributor.institution | University of St Andrews. Centre of Magnetic Resonance | en |
dc.identifier.doi | https://doi.org/10.1021/acsomega.7b01287 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | http://pubs.acs.org/doi/suppl/10.1021/acsomega.7b01287 | en |
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