Evidence map›Paper›PMID 41073404›Full record

ArticleNature communications2025

Reversible shape memory two-dimensional covalent organic frameworks.

Mingchao Shao, Jinyang Chen, Wenqiang Gao, Qingsong Zhang, Xiaofang Wei, Junhua Kuang, Guocai Liu, Yang Sun, Yangshuang Bian, Chengyu Wang and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Mingchao Shao *Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.ORCID http://orcid.org/0009-0004-7963-7596
Jinyang Chen *Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Wenqiang GaoBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Qingsong ZhangBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Xiaofang WeiBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.ORCID http://orcid.org/0000-0003-1588-8797
Junhua KuangBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Guocai LiuBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.ORCID http://orcid.org/0009-0002-7664-5318
Yang SunBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Yangshuang BianBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Chengyu WangBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Mingcong QinBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.
Xueli YangBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.ORCID http://orcid.org/0009-0001-4333-6714
Jichen DongBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China. dongjichen@iccas.ac.cn.ORCID http://orcid.org/0000-0003-1512-4711
Yunqi LiuBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China.ORCID http://orcid.org/0000-0001-5521-2316
Yunlong GuoBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, PR China. guoyunlong@iccas.ac.cn.ORCID http://orcid.org/0000-0003-1602-769X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two-dimensional covalent organic frameworks are a unique type of organic crystals with both weak layer-layer interaction and regular one-dimensional nanochannels. Therefore, it is possible to synthesize two-dimensional covalent organic frameworks with reversible stacking phases and thus pore sizes, which hold great potential applications in future nanoelectronics, nanoreactors, intelligent response, gas separation and storage. However, such a goal remains challenging up to now, because the slipped AA-stacking is the most thermodynamically stable phase. Here, we report the realization of shape memory two-dimensional covalent organic frameworks with reversible interlayer stacking sequences, of which AA and inclined phases are induced by the formation of hot ice and the strongly adsorbed organic molecules like Tetrahydrofuran inside the two-dimensional covalent organic frameworks confined nanochannels, respectively. Based on the reversible pore sizes and pore environments, we demonstrate the feasibility of the shape memory two-dimensional covalent organic frameworks in dynamically tunable permeability and intelligent response.

Identifiers

PMID41073404
PMCPMC12514173

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