Evidence map›Paper›PMID 39254816›Full record

ArticleJournal of fluorescence2025

Constructing ESIPT-Capable α-Cyanostilbene Luminogens: Influence of Different Aromatic Substitutions Tethered to H-Acceptor (CH = N) on Photophysical Properties, Cu

Meihui Chen, Yulin Zhou, Yi Li, Donghong Xie, Yuanbin Wu, Huihua Gong, Zhenye Wang, Yue Yu, Jianqiang Chen, Mingguang Zhu

Abstract read
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In one paragraph

Article in Journal of fluorescence, 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. 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

10 authors.

Meihui ChenCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Yulin ZhouCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Yi LiCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Donghong XieCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Yuanbin WuCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Huihua GongCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Zhenye WangCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Yue YuCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China. yuy190@nenu.edu.cn.
Jianqiang ChenCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China.
Mingguang ZhuCollege of Chemistry and Chemical Engineering, Neijiang Normal University, Neijiang, 641100, P. R. China. zhumg91_njun@126.com.

Funding

Fundamental Research Program of Neijiang City NJJH202314Fundamental Research Program of Neijiang City NJJH202323
6 · The paper itself

Abstract

Herein, two excited-state intramolecular proton transfer (ESIPT)-capable α-cyanostilbene luminogens were synthesized by Schiff base reaction of salicylaldehyde-like α-cyanostilbene candidate with 1-naphthylamine and 3-biphenylamine, respectively. We systematically analyzed their photophysical properties compared with their analogue, and demonstrated that their fluorescence behaviors could be elaborately modulated by different aromatic substitutions tethered to H-acceptor (CH = N). In virtue of the outstanding solid fluorescence, the 3-biphenylamine-decorated fluorophore was applied for monitoring Cu

Indexed as

Aggregation-induced emissionDual-sensing probeExcited-state intramolecular proton transferMonitoring Cu2+/Fe3+Α-cyanostilbene

Identifiers

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Registered trials

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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.