Evidence map›Paper›PMID 41306882›Full record

ReviewRSC advances2025

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

Veronika D Badazhkova, Risto Savela, Reko Leino

Abstract readReview
In one paragraph

Review in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Veronika D BadazhkovaJohan Gadolin Process Chemistry Centre, Laboratory of Molecular Science and Engineering, Organic Chemistry Research Group, Åbo Akademi University FI-20500 Turku Finland reko.leino@abo.fi.ORCID https://orcid.org/0000-0002-6949-2731
Risto SavelaTurku PET Centre, University of Turku and Turku University Hospital FI-20520 Turku Finland.ORCID https://orcid.org/0000-0002-4815-5189
Reko LeinoJohan Gadolin Process Chemistry Centre, Laboratory of Molecular Science and Engineering, Organic Chemistry Research Group, Åbo Akademi University FI-20500 Turku Finland reko.leino@abo.fi.ORCID https://orcid.org/0000-0002-1111-9125

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Identifiers

PMID41306882
PMCPMC12645374

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.