Evidence map›Paper›PMID 41454056›Full record

ArticleCommunications chemistry2025

Synergistic 3D π-π networks enforce persistent foldamer configuration with tunable full-color circularly polarized luminescence.

Hao Hu, Qiangsheng Zhang, Ziyan Wu, Hongtao Liu, Jialin Xie, Zhenchang Wen, Weijie Chi, Jianwei Li, Chunman Jia

Abstract read
In one paragraph

Article in Communications chemistry, 2025. 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

9 authors.

Hao Hu *Hainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China.
Qiangsheng Zhang *Hainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China.
Ziyan WuHainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China.
Hongtao LiuHainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China.
Jialin XieHainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China.
Zhenchang WenAnalytical & Testing Center (Center for Advanced Studies in Precision Instruments), Hainan University, Haikou, China.
Weijie ChiHainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China.ORCID http://orcid.org/0000-0003-1776-0025
Jianwei LiMediCity Research Laboratory, University of Turku, Turku, Finland. lijianwei@must.edu.mo.ORCID http://orcid.org/0000-0002-3682-6934
Chunman JiaHainan Provincial Key Lab of Fine Chem, School of Chemistry and Chemical Engineering, Hainan University, Haikou, China. jiachunman@hainanu.edu.cn.ORCID http://orcid.org/0000-0002-8075-8772

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22161017, 22161016, 22401064, 22403022
6 · The paper itself

Abstract

Achieving molecular chirality with enantiostability in purely π-conjugated foldamers remains a substantial challenge due to inherently weak π-π stacking interactions and facile racemization. Herein, we introduce a novel design strategy employing synergistic intramolecular 3D π-π stacking networks within a 1,8-diarylnaphthalene framework, enabling foldamers to exhibit extraordinary configurational stability. A systematic series of quinoxaline- and phenazine-based foldamers incorporating carbazole (CZ) and diphenylamine (DPA) donors were synthesized, with chiral configurations stabilized through complementary face-to-face and laterally offset π-π stacking interactions. Single-crystal X-ray analyses and computational studies confirmed the formation of complex intramolecular π-networks, providing exceptional racemization barriers (ΔG

Identifiers

PMID41454056
PMCPMC12848006

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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.