Evidence map›Paper›PMID 34368088›Full record

ArticleFrontiers in chemistry2021

Bis(Triphenylamine)Benzodifuran Chromophores: Synthesis, Electronic Properties and Application in Organic Light-Emitting Diodes.

Hui Li, Ryutaro Komatsu, Jihane Hankache, Hisahiro Sasabe, Latevi Max Lawson Daku, Bilal Özen, Songjie Chen, Jürg Hauser, Andreas Hauser, Silvio Decurtins and 2 more

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In one paragraph

Article in Frontiers in chemistry, 2021. 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

12 authors.

Hui LiDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.
Ryutaro KomatsuDepartment of Organic Device Engineering Research Center for Organic Electronics, Yamagata University, Yamagata, Japan.
Jihane HankacheDepartment of Physical Chemistry, University of Geneva, Geneva, Switzerland.
Hisahiro SasabeDepartment of Organic Device Engineering Research Center for Organic Electronics, Yamagata University, Yamagata, Japan.
Latevi Max Lawson DakuDepartment of Physical Chemistry, University of Geneva, Geneva, Switzerland.
Bilal ÖzenDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.
Songjie ChenDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.
Jürg HauserDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.
Andreas HauserDepartment of Physical Chemistry, University of Geneva, Geneva, Switzerland.
Silvio DecurtinsDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.
Junji KidoDepartment of Organic Device Engineering Research Center for Organic Electronics, Yamagata University, Yamagata, Japan.
Shi-Xia LiuDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of bis(triphenylamine)benzodifuran chromophores have been synthesized and fully characterised. Starting from suitably functionalized benzodifuran (BDF) precursors, two triphenylamine (TPA) moieties are symmetrically coupled to a central BDF unit either at 4,8-positions through double bonds (

Indexed as

benzodifuranoptical spectroscopyorganic light-emitting diodespectroelectrochemistrytriphenylamine

Identifiers

PMID34368088
PMCPMC8333860

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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.