Evidence map›Paper›PMID 38341421›Full record

ArticleNature communications2024

Robust links in photoactive covalent organic frameworks enable effective photocatalytic reactions under harsh conditions.

Jia-Rui Wang, Kepeng Song, Tian-Xiang Luan, Ke Cheng, Qiurong Wang, Yue Wang, William W Yu, Pei-Zhou Li, Yanli Zhao

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Aqueous and Surfactant-Free Synthesis of Nanoscale Covalent Organic Frameworks.Angewandte Chemie (International ed. in English) · 2026
    Article
  9. Covalent Organic Frameworks on CuJournal of the American Chemical Society · 2026
    Article
  10. Article
  11. Covalent Organic Frameworks for Photocatalysis.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
  12. Review
  13. Micro-Environment Programmable Quinoline COFs for High-Performance Photocatalytic HAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Engineering Polyheptazine and Polytriazine Imides for Photocatalysis.Angewandte Chemie (International ed. in English) · 2024
    Review
  20. Photons, Excitons, and Electrons in Covalent Organic Frameworks.Journal of the American Chemical Society · 2024
    Review
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.

Jia-Rui WangSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.
Kepeng SongSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.ORCID http://orcid.org/0000-0003-3860-5761
Tian-Xiang LuanSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.
Ke ChengSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.
Qiurong WangSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.
Yue WangSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.
William W YuSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China.ORCID http://orcid.org/0000-0001-5354-6718
Pei-Zhou LiSchool of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Shandong University, No. 27 Shanda South Road, Ji'nan, 250100, PR China. pzli@sdu.edu.cn.ORCID http://orcid.org/0000-0002-3146-8410
Yanli ZhaoSchool of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, 21 Nanyang Link, 637371, Singapore, Singapore. zhaoyanli@ntu.edu.sg.ORCID http://orcid.org/0000-0002-9231-8360

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing heterogeneous photocatalysts for the applications in harsh conditions is of high importance but challenging. Herein, by converting the imine linkages into quinoline groups of triphenylamine incorporated covalent organic frameworks (COFs), two photosensitive COFs, namely TFPA-TAPT-COF-Q and TFPA-TPB-COF-Q, are successfully constructed. The obtained quinoline-linked COFs display improved stability and photocatalytic activity, making them suitable photocatalysts for photocatalytic reactions under harsh conditions, as verified by the recyclable photocatalytic reactions of organic acid involving oxidative decarboxylation and organic base involving benzylamine coupling. Under strong oxidative condition, the quinoline-linked COFs show a high efficiency up to 11831.6 μmol·g

Identifiers

PMID38341421
PMCPMC10858907

What OpenQuestion holds

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Registered trials

None linked

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.