Evidence map›Paper›PMID 42657098›Full record

ArticleChemical science2026

Naphthalimide-fused BODIPYs

Heng Li, Qi Zhang, Rui Gan, Fan Ni, Qinghua Wu, Huiquan Zuo, Hua Wang, Erhong Hao, Lijuan Jiao

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.

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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

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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

9 authors.

Heng LiKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.
Qi ZhangKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.
Rui GanKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.
Fan NiSchool of Instrument Science and Optoelectronic Engineering, Hefei University of Technology Hefei Anhui 230009 P. R. China.ORCID https://orcid.org/0000-0002-0467-1974
Qinghua WuSchool of Pharmacy, Anhui University of Chinese Medicine Hefei 230012 China.
Huiquan ZuoKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.
Hua WangKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.
Erhong HaoKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.ORCID https://orcid.org/0000-0001-7234-4994
Lijuan JiaoKey Laboratory of Functional Molecular Solids of Ministry of Education, College of Chemistry and Materials Science, School of Physics and Electronic Information, Anhui Normal University Wuhu 241002 China jiao421@ahnu.edu.cn haoehong@ahnu.edu.cn.ORCID https://orcid.org/0000-0002-3895-9642

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Near-infrared (NIR) n-type organic semiconductors with low-lying LUMO levels are essential building blocks for advanced optoelectronics, yet their development is hindered by laborious multi-step synthesis, insufficient electron affinity and limited stability. Herein, we report the precise synthesis and optoelectronic properties of a series of naphthalimide (NMI)-fused BODIPY derivatives as near-infrared absorbing n-type organic semiconductors, accessed through a palladium-catalyzed one-pot quadruple C-H activation strategy that constructs the fused conjugated framework in a single step. This annulation extends the large π-conjugated system and enables a favorable face-to-face molecular stacking in the crystalline state. The resulting dyes exhibit efficient NIR emission (

Identifiers

PMID42657098
PMCPMC13509142

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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.