Evidence map›Paper›PMID 42022949›Full record

ArticleRSC advances2026

One-pot mechanochemical access to quinoline-linked covalent organic frameworks.

Yizhou Zhan, Yuxuan Yang, Wei Zhao, Xi Wang, Jiarong Qiu, Zhaonan Tang, Jiao He, Chenglong Deng, Heshen Xiao, Yiying Pang and 1 more

Abstract read
In one paragraph

Article in RSC advances, 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
–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

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

11 authors.

Yizhou ZhanSchool of Materials Science and Engineering, Dongguan University of Technology Dongguan 523808 P.R. China zhanyizhou@dgut.edu.cn.ORCID https://orcid.org/0009-0002-8366-2343
Yuxuan YangSchool of Materials Science and Engineering, Dongguan University of Technology Dongguan 523808 P.R. China zhanyizhou@dgut.edu.cn.
Wei ZhaoSchool of Materials Science and Engineering, Dongguan University of Technology Dongguan 523808 P.R. China zhanyizhou@dgut.edu.cn.
Xi WangSchool of Materials Science and Engineering, Dongguan University of Technology Dongguan 523808 P.R. China zhanyizhou@dgut.edu.cn.
Jiarong QiuSchool of Materials Science and Engineering, Dongguan University of Technology Dongguan 523808 P.R. China zhanyizhou@dgut.edu.cn.
Zhaonan TangSchool of Life and Health Technology, Dongguan University of Technology Dongguan 523808 P.R. China.
Jiao HeCollege of Chemistry and Environmental Engineering, Key Laboratory of Green Catalysis of Higher Education Institutes of Sichuan, Sichuan University of Science and Engineering Zigong 643000 P. R. China.
Chenglong DengCollege of Chemistry and Environmental Engineering, Key Laboratory of Green Catalysis of Higher Education Institutes of Sichuan, Sichuan University of Science and Engineering Zigong 643000 P. R. China.
Heshen XiaoAnalytical and Testing Center, Dongguan University of Technology Dongguan 523808 P.R. China.
Yiying PangSchool of Chemical Engineering and Energy Technology, Dongguan University of Technology Dongguan 523808 P.R. China wangxj@dgut.edu.cn pangyiying@dgut.edu.cn.
Xiaoji WangSchool of Chemical Engineering and Energy Technology, Dongguan University of Technology Dongguan 523808 P.R. China wangxj@dgut.edu.cn pangyiying@dgut.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quinoline-linked COFs are formed by transforming reversible imine bonds into irreversible, π-extended quinoline linkages, thereby enhancing framework robustness and structural stability. Most reported syntheses, however, still rely on solvothermal methods that require high temperatures, multi-day reactions, and hazardous solvents. While mechanochemical synthesis has emerged as a solid-state and scalable alternative for COF construction, existing studies have predominantly focused on reversible linkages, such as imine and β-ketoenamine bonds, leaving the direct formation of irreversible quinoline-linked frameworks largely unexplored. Herein, we report a one-pot mechanochemical Povarov cascade that enables the

Identifiers

PMID42022949
PMCPMC13097302

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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.