Evidence map›Paper›PMID 41117559›Full record

ArticleAngewandte Chemie (International ed. in English)2025

[3]CycloBODIPY: A Highly Strained Cyclic BODIPY Trimer with Effective Macrocyclic Conjugation.

Masaki Sugino, Yoshitaka Tsuchido, Rento Maeda, Ichiro Hisaki, Hideaki Takano, Hiroshi Shinokubo

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Naphthalimide-fused BODIPYsChemical science · 2026
    Article
  2. A Highly Strained All-BODIPY-Based Nanohoop.Angewandte Chemie (International ed. in English) · 2026
    Article
  3. Article
  4. 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

6 authors.

Masaki SuginoDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya, 464-8603, Japan.
Yoshitaka TsuchidoDepartment of Chemistry, Faculty of Science, Tokyo University of Science, Shinjuku-ku, Tokyo, 162-8601, Japan.ORCID https://orcid.org/0000-0001-8860-0745
Rento MaedaDivision of Chemistry, Graduate School of Engineering Science, The University of Osaka, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.
Ichiro HisakiDivision of Chemistry, Graduate School of Engineering Science, The University of Osaka, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.ORCID https://orcid.org/0000-0002-8170-5605
Hideaki TakanoDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya, 464-8603, Japan.ORCID https://orcid.org/0000-0003-0744-9292
Hiroshi ShinokuboDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya, 464-8603, Japan.ORCID https://orcid.org/0000-0002-5321-2205

Funding

Japan Society for the Promotion of Science JP20H05862Japan Society for the Promotion of Science JP20H05863Japan Society for the Promotion of Science JP22H04974Japan Society for the Promotion of Science JP24K01468Japan Society for the Promotion of Science JP24K17675Leading Initiative for Excellent Young Researchers JPMXS0320220200MEXT (Japan)
6 · The paper itself

Abstract

Cyclic oligomers containing porphyrinic chromophores have attracted significant attention in broad areas of science as artificial models for photosynthetic light-harvesting antennae due to their structural and functional resemblance to natural chlorophyll arrays. Here, the synthesis of a macrocyclic [3]cycloBODIPY derivative, which consists of only boron-dipyrromethene (BODIPY) units, via an Au-mediated macrocyclization protocol is reported. While this [3]cycloBODIPY derivative exhibits a high total strain energy of 86.4 kcal mol

Indexed as

Au complexBODIPYDeformationMacrocyclic compoundsπ‐Conjugated compounds

Identifiers

PMID41117559
PMCPMC12624325

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.