Evidence map›Paper›PMID 36741537›Full record

ArticleChemical science2023

Diazazethrene bisimide: a strongly electron-accepting π-system synthesized

Keita Tajima, Kyohei Matsuo, Hiroko Yamada, Norihito Fukui, Hiroshi Shinokubo

Abstract read
In one paragraph

Article in Chemical science, 2023. 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

5 authors.

Keita TajimaDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya Aichi 464-8603 Japan fukui@chembio.nagoya-u.ac.jp hshino@chembio.nagoya-u.ac.jp.
Kyohei MatsuoDivision of Material Science, Graduate of School of Science and Technology, Nara Institute of Science and Technology 8916-5 Takayama-cho, Ikoma Nara 630-0912 Japan hyamada@ms.naist.jp.ORCID https://orcid.org/0000-0002-2472-9459
Hiroko YamadaDivision of Material Science, Graduate of School of Science and Technology, Nara Institute of Science and Technology 8916-5 Takayama-cho, Ikoma Nara 630-0912 Japan hyamada@ms.naist.jp.ORCID https://orcid.org/0000-0002-2138-5902
Norihito FukuiDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya Aichi 464-8603 Japan fukui@chembio.nagoya-u.ac.jp hshino@chembio.nagoya-u.ac.jp.ORCID https://orcid.org/0000-0002-0466-0116
Hiroshi ShinokuboDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya Aichi 464-8603 Japan fukui@chembio.nagoya-u.ac.jp hshino@chembio.nagoya-u.ac.jp.ORCID https://orcid.org/0000-0002-5321-2205

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of highly electron-accepting π-systems is a fundamentally challenging issue despite their potential applications as high-performance n-type organic semiconductors, organic rechargeable batteries, and stable redox-active organocatalysts. Herein, we demonstrate that the incorporation of both imide substituents and imine-type nitrogen atoms into zethrene affords the strongly electron-accepting π-system diazazethrene bisimide (DAZBI). DAZBI has a low-lying LUMO (-4.3 eV

Identifiers

PMID36741537
PMCPMC9847653

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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.