| Literature DB >> 18236415 |
Bjart F Lutnaes1, Bernt O Myrvold, Rolf A Lauten, Molla M Endeshaw.
Abstract
Although there has been a major progress in the analysis of native lignin using NMR in the recent years, not much attention has been paid to lignosulfonates. Lignosulfonates are more difficult to analyse because of solubility issues and a more complex structure owing to chemical modification during the pulping process. A large database of NMR data is available for the building blocks of native lignin, but no data are available for the corresponding sulfonated compounds. We have prepared 15 monomeric and seven dimeric sulfonated model compounds characterised by NMR. These include models for end groups, as well as beta-beta, beta-5, 5-5 and beta-O-5 linkages in lignosulfonates, and will be important for further structural investigation on lignosulfonate. Copyright (c) 2008 John Wiley & Sons, Ltd.Entities:
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Year: 2008 PMID: 18236415 DOI: 10.1002/mrc.2184
Source DB: PubMed Journal: Magn Reson Chem ISSN: 0749-1581 Impact factor: 2.447