Evidence map›Paper›PMID 38116244›Full record

ArticleBeilstein journal of organic chemistry2023

Aromatic systems with two and three pyridine-2,6-dicarbazolyl-3,5-dicarbonitrile fragments as electron-transporting organic semiconductors exhibiting long-lived emissions.

Karolis Leitonas, Brigita Vigante, Dmytro Volyniuk, Audrius Bucinskas, Pavels Dimitrijevs, Sindija Lapcinska, Pavel Arsenyan, Juozas Vidas Grazulevicius

Abstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Organic electron transport materials.Beilstein journal of organic chemistry · 2024
    Article
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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

8 authors.

Karolis LeitonasDepartment of Polymer Chemistry and Technology, Kaunas University of Technology, Radvilenu pl. 19, LT-50254, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-8070-0792
Brigita ViganteLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006, Riga, Latvia.
Dmytro VolyniukDepartment of Polymer Chemistry and Technology, Kaunas University of Technology, Radvilenu pl. 19, LT-50254, Kaunas, Lithuania.ORCID https://orcid.org/0000-0003-3526-2679
Audrius BucinskasDepartment of Polymer Chemistry and Technology, Kaunas University of Technology, Radvilenu pl. 19, LT-50254, Kaunas, Lithuania.
Pavels DimitrijevsLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006, Riga, Latvia.ORCID https://orcid.org/0000-0002-6332-2395
Sindija LapcinskaLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006, Riga, Latvia.ORCID https://orcid.org/0000-0001-7745-8392
Pavel ArsenyanLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006, Riga, Latvia.ORCID https://orcid.org/0000-0001-5875-2799
Juozas Vidas GrazuleviciusDepartment of Polymer Chemistry and Technology, Kaunas University of Technology, Radvilenu pl. 19, LT-50254, Kaunas, Lithuania.ORCID https://orcid.org/0000-0002-4408-9727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pyridine-3,5-dicarbonitrile moiety has gained significant attention in the field of materials chemistry, particularly in the development of heavy-metal-free pure organic light-emitting diodes (OLEDs). Extensive research on organic compounds exhibiting thermally activated delayed fluorescence (TADF) has led to numerous patents and research articles. This study focuses on the synthesis and investigation of the semiconducting properties of polyaromatic π-systems containing two and three fragments of pyridine-2,6-dicarbazolyl-3,5-dicarbonitrile. The compounds are synthesized by Sonogashira coupling reactions and characterized by steady-state and time-resolved luminescence spectroscopy. The compounds show efficient intramolecular charge transfer (ICT) from the donor to the acceptor. The photoluminescence (PL) spectra of the solutions of the compounds showed non-structured emission peaks in the visible region, which are attributed to ICT emission. The PL intensities of the solutions of the compounds are enhanced after deoxygenation, which is indicative of TADF. The photoluminescence quantum yields and TADF properties of the compounds are sensitive to the medium. Cyclic voltammetry measurements indicate good hole-blocking and electron-injecting properties due to their high ionization potentials. Photoelectron spectroscopy and time-of-flight measurements reveal good electron-transporting properties for one of the compounds. In general, polyaromatic π-systems with pyridine-3,5-dicarbonitrile fragments demonstrate promising potential for use in organic electronic devices, such as OLEDs.

Indexed as

charge transportintramolecular charge transferphotophysical propertiespyridine-3,5-dicarbonitrile

Identifiers

PMID38116244
PMCPMC10729123

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