Evidence map›Paper›PMID 40052769›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Hydrogen-Bond-Directed Supramolecular Organic Semiconductor Thin Films Realized via Thermal Precursor Approach.

So Ueno, Mitsuaki Yamauchi, Nobutaka Shioya, Hiroshi Matsuda, Takeshi Hasegawa, Keitaro Yamamoto, Yoshiyuki Mizuhata, Hiroko Yamada

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. 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. Nanoarchitectonics in Materials Science, Second Edition.Materials (Basel, Switzerland) · 2026
    Article
  2. 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

8 authors.

So UenoInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Mitsuaki YamauchiInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Nobutaka ShioyaInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Hiroshi MatsudaInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Takeshi HasegawaInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Keitaro YamamotoInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Yoshiyuki MizuhataInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Hiroko YamadaInstitute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.

Funding

Institute for Chemical ResearchJapan Science and Technology Agency JPMJFS2123Japan Society for the Promotion of Science JP 20H05833Japan Society for the Promotion of Science JP 22H02106Japan Society for the Promotion of Science JP 22K14556Japan Society for the Promotion of Science JP 24H01714Japan Society for the Promotion of Science JP 24K01496Japan Society for the Promotion of Science JP 24K17738
6 · The paper itself

Abstract

Flexible organic semiconductors are regarded as an important class of functional materials, enabling their fabrication via a solution-processed method. However, supramolecularly designed organic thin-film transistor (OTFT) devices using hydrogen bonds have not been sufficiently developed. This is because of the reduced solubility caused by introducing hydrogen bond sites and the difficulty in controlling molecular orientations and packing structures. Herein, we report a reasonable strategy for the formation of hydrogen-bonded semiconductor thin films of a tetrabenzoporphyrin derivative with amide groups using the thermal precursor approach. The thin films are successfully fabricated by thermal conversion of the corresponding precursor in the film state. Assembly structure with a hydrogen-bond network is revealed by the combination of X-ray diffraction and infrared p-polarized multiple-angle incidence resolution spectrometry. The OTFT devices exhibit high hole mobility of 0.25 cm

Indexed as

Hydrogen bondOrganic thin‐film transistorSupramolecular chemistryTetrabenzoporphyrinThermal precursor approach

Identifiers

PMID40052769
PMCPMC12304868

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.