Evidence map›Paper›PMID 31075868›Full record

ArticleMolecules (Basel, Switzerland)2019

Lignin Modification Supported by DFT-Based Theoretical Study as a Way to Produce Competitive Natural Antioxidants.

Liga Lauberte, Gabin Fabre, Jevgenija Ponomarenko, Tatiana Dizhbite, Dmitry V Evtuguin, Galina Telysheva, Patrick Trouillas

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

10 citing papers in PubMed, 42 citations in OpenAlex.

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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

7 authors at 3 institutions in 4 countries.

Liga LauberteLatvian State Institute of Wood Chemistry, Dzerbenes Str. 27, LV-1006 Riga, Latvia. roze@edi.lv.
Gabin FabreINSERM UMR 1248, Université de Limoges, Faculté de Pharmacie, 2 rue du Docteur Marcland, 87025 Limoges Cedex, France. gabin.fabre@gmail.com.ORCID 0000-0002-9272-1918
Jevgenija PonomarenkoLatvian State Institute of Wood Chemistry, Dzerbenes Str. 27, LV-1006 Riga, Latvia. jevgenijaponomarenko@inbox.lv.
Tatiana DizhbiteLatvian State Institute of Wood Chemistry, Dzerbenes Str. 27, LV-1006 Riga, Latvia. lcl@edi.lv.
Dmitry V EvtuguinCICECO/University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal. dmitrye@ua.pt.ORCID 0000-0002-6304-5105
Galina TelyshevaLatvian State Institute of Wood Chemistry, Dzerbenes Str. 27, LV-1006 Riga, Latvia. ligno@edi.lv.
Patrick TrouillasINSERM UMR 1248, Université de Limoges, Faculté de Pharmacie, 2 rue du Docteur Marcland, 87025 Limoges Cedex, France. patrick.trouillas@unilim.fr.
Latvian State Institute of Wood Chemistry · LVInserm · FRUniversity of Aveiro · PT

Funding

Czech Science Foundation P208/12/G016The CICECO-Aveiro Institute of Materials, POCI-01-0145-FEDER-007679, financed by national funds through the FCT/MEC and when appropriate co-financed by FEDER under the PT2020 Partnership Agreement FCT Ref. UID/CTM/50011/2013The Latvian-France collaboration programme "OSMOZE" OSMOZEThe Latvian State Institute of Wood Chemistry Bioeconomy grant "LigProBK" LigProBKThe Ministry of Education, Youth and Sports of the Czech Republic Project LO1305The student project IGA_PrF_2017_028 of Palacky University IGA_PrF_2017_028
6 · The paper itself

Abstract

The valorization of lignins as renewable aromatic feedstock is of utmost importance in terms of the use of sustainable resources. This study provides a deductive approach towards market-oriented lignin-derived antioxidants by ascertaining the direct effect of different structural features of lignin on the reactivity of its phenolic OH groups in the radical scavenging reactions. The antioxidant activity of a series of compounds, modeling lignin structural units, was experimentally characterized and rationalized, using thermodynamic descriptors. The calculated O-H bond dissociation enthalpies (BDE) of characteristic lignin subunits were used to predict the modification pathways of technical lignins. The last ones were isolated by soda delignification from different biomass sources and their oligomeric fractions were studied as a raw material for modification and production of optimized antioxidants. These were characterized in terms of chemical structure, molecular weight distribution, content of the functional groups, and the antioxidant activity. The developed approach for the targeted modification of lignins allowed the products competitive with two commercial synthetic phenolic antioxidants in both free radical scavenging and stabilization of thermooxidative destruction of polyurethane films.

Indexed as

Density Functional TheoryModels, TheoreticalAntioxidantsDimerizationElectronsHydrogenKineticsLigninPolyphenolsPolyurethanesProton Magnetic Resonance SpectroscopySpectroscopy, Fourier Transform InfraredTemperatureAntioxidantsHydrogenLigninPolyphenolsPolyurethanesantioxidant activityligninsmodificationmolecular rationalizationstabilizers for polymers

Identifiers

PMID31075868
PMCPMC6539611
OpenAlexW2943876589

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.