Evidence map›Paper›PMID 42338909›Full record

ArticleChemical science2026

Electron-injection-induced global aromaticity enables stable open-shell nanopillars with intense mid-infrared magnetic circular dichroism.

Kongchuan Wu, Shicheng Dong, Qiqi Chen, Yuanfeng Pan, Jun Zhu, Jianbin Lin, Hui-Jun Zhang

Abstract read
In one paragraph

Article in Chemical science, 2026. 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
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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

7 authors.

Kongchuan WuDepartment of Chemistry, Fujian Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University Xiamen 361005 Fujian China meghjzhang@xmu.edu.cn.
Shicheng DongGuangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University Nanning Guangxi 530004 China.
Qiqi ChenDepartment of Chemistry, Fujian Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University Xiamen 361005 Fujian China meghjzhang@xmu.edu.cn.
Yuanfeng PanDepartment of Chemistry, Fujian Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University Xiamen 361005 Fujian China meghjzhang@xmu.edu.cn.
Jun ZhuGuangdong Basic Research Center of Excellence for Aggregate Science, School of Science and Engineering, The Chinese University of Hong Kong (Shenzhen) Longgang Shenzhen Guangdong 518172 China jun.zhu@cuhk.edu.cn.ORCID https://orcid.org/0000-0002-2099-3156
Jianbin LinDepartment of Chemistry, Fujian Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University Xiamen 361005 Fujian China meghjzhang@xmu.edu.cn.ORCID https://orcid.org/0000-0002-0064-3079
Hui-Jun ZhangDepartment of Chemistry, Fujian Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University Xiamen 361005 Fujian China meghjzhang@xmu.edu.cn.ORCID https://orcid.org/0000-0001-9567-3010

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Open-shell species are central to spintronics and infrared optoelectronics, but remain challenging to stabilize in discrete molecular systems. Herein, we report that electron injection into pillar-shaped, radially π-conjugated [4]cyclonaphthodithiophene diimides ([4]C-NDTIs) triggers global aromaticity, yielding radical species with notable stability and optical properties. These globally aromatic radicals exhibit record-high mid-infrared (MIR) absorption (

Identifiers

PMID42338909
PMCPMC13286027

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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.