Evidence map›Paper›PMID 39758639›Full record

ArticleACS omega2024

Synthesis of 2,7-Dihydrooxepine-spirodithiophene Derivatives via an Intramolecular Ring Closure Reaction.

Xiaochen Liu, Tian Gao, Ruiyao Wang, Jianan Liu, Hua-Jun Shawn Fan, Jin Fang, Chang-Qi Ma, Yi Lin

Abstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xiaochen LiuDepartment of Chemistry and Materials Science, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215000, P. R. China.
Tian GaoDepartment of Chemistry and Materials Science, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215000, P. R. China.
Ruiyao WangWisdom Lake Academy of Pharmacy, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215000, P. R. China.
Jianan LiuDepartment of Chemical Engineering, Sichuan University of Science & Technology, Zigong, Sichuan 643000, P. R. China.
Hua-Jun Shawn FanDepartment of Chemical Engineering, Sichuan University of Science & Technology, Zigong, Sichuan 643000, P. R. China.
Jin Fangi-Lab & Printable Electronics Research Center, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, P. R. China.
Chang-Qi Mai-Lab & Printable Electronics Research Center, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, P. R. China.ORCID https://orcid.org/0000-0002-9293-5027
Yi LinDepartment of Chemistry and Materials Science, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215000, P. R. China.ORCID https://orcid.org/0000-0001-9478-152X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spiro architectures with π-conjugation have improved thermal stability and stronger photosensitivity, making them potentially useful for organic optoelectronic devices. Our recent work has demonstrated the synthetic chemistry of a novel thiophene oligomer combining 2,7-dihydrooxepine and dispiro structure and derived it into A-D-A-type compounds. The optical spectroscopy and electrochemical characteristics were investigated. The results show that the presence of the alkyl side chains enhances the nucleophilicity of aromatic anions but induces strong steric hindrance so that the selectivity toward a dispiro[cyclopenta[2,1-b:3,4-b']dithiophene-4,4'-dithieno[3,2-c:2',3'-

Identifiers

PMID39758639
PMCPMC11696398

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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.