Introduction of amino groups into lignin and lignin model compounds: recent advances

dc.contributor.authorBadazhkova, Veronika D.
dc.contributor.authorSavela, Risto
dc.contributor.authorLeino, Reko
dc.contributor.organizationfi=PET-keskus|en=Turku PET Centre|
dc.contributor.organizationfi=kemian laitos|en=Department of Chemistry|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.14646305228
dc.converis.publication-id505633208
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/505633208
dc.date.accessioned2026-01-21T14:42:55Z
dc.date.available2026-01-21T14:42:55Z
dc.description.abstract<p>Research on lignin valorization has attracted considerable attention in recent decades. Lignin, a natural aromatic polymer, is a renewable and readily available source for producing new biobased chemicals and materials. For successful lignin valorization towards value-added products, development of efficient procedures allowing the introduction of new functionalities to its structure becomes essential. One of the approaches for chemical modification of lignin involves the introduction of amino groups. Lignin amination methodologies potentially provide aromatic amines that could be used as building blocks for the synthesis of different compounds, including pharmaceuticals and precursors for bio-based polymeric materials. Due to the complex structure of lignin, however, model compounds are commonly used for studying the reactivity and for developing lignin modification procedures. In several studies, it has been demonstrated that lignin model compounds imitating the most abundant lignin β-O-4 linkage can be converted to nitrogen containing aromatic compounds with various potential applications. However, it has also been observed in several cases that the developed amination procedures only have functioned on the model compounds but not on extracted lignin polymer. Overall, in recent years, several procedures have been developed for amination of lignin model compounds and lignin, allowing materials containing primary, secondary and tertiary amines to be obtained, for example the Mannich reaction, silylation and epoxy functionalization. The chemical modification and analysis of lignin are nevertheless hampered by its complex and inconsistent structure, varying significantly depending on the source and method of isolation. While the bulk of currently available lignin is present mainly in the form of Kraft lignin with condensed structure and low solubility, new efficient methods could facilitate switching to lignin-first approaches, preserving its original structure and improving the processing towards value-added products.<br></p>
dc.format.pagerange46413
dc.format.pagerange46424
dc.identifier.eissn2046-2069
dc.identifier.olddbid213605
dc.identifier.oldhandle10024/196623
dc.identifier.urihttps://www.utupub.fi/handle/11111/55634
dc.identifier.urlhttps://doi.org/10.1039/d5ra05735c
dc.identifier.urnURN:NBN:fi-fe202601216809
dc.language.isoen
dc.okm.affiliatedauthorSavela, Risto
dc.okm.affiliatedauthorDataimport, Kemian laitoksen yhteiset
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherRoyal Society of Chemistry (RSC)
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1039/d5ra05735c
dc.relation.ispartofjournalRSC Advances
dc.relation.volume15
dc.source.identifierhttps://www.utupub.fi/handle/10024/196623
dc.titleIntroduction of amino groups into lignin and lignin model compounds: recent advances
dc.year.issued2025

Tiedostot

Näytetään 1 - 1 / 1
Ladataan...
Name:
d5ra05735c.pdf
Size:
1.62 MB
Format:
Adobe Portable Document Format