Evidence map›Paper›PMID 40341386›Full record

ArticleNature communications2025

Diverse redox-mediated transformations to realize the para-quinoid, σ-bond, and ortho-diphenoquinoid forms.

Takashi Harimoto, Moto Kikuchi, Takanori Suzuki, Yusuke Ishigaki

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. 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

4 authors.

Takashi HarimotoDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan. t-harimoto@ims.ac.jp.ORCID http://orcid.org/0000-0002-0405-5506
Moto KikuchiDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.
Takanori SuzukiDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.ORCID http://orcid.org/0000-0002-1230-2044
Yusuke IshigakiDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan. yishigaki@sci.hokudai.ac.jp.ORCID http://orcid.org/0000-0001-7961-3595

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP23H04011MEXT | Japan Society for the Promotion of Science (JSPS) JP24K23093MEXT | Japan Society for the Promotion of Science (JSPS) JP25H00873MEXT | Japan Society for the Promotion of Science (JSPS) JP25K08604MEXT | Japan Society for the Promotion of Science (JSPS) JP25K18023MEXT | JST | Precursory Research for Embryonic Science and Technology (PRESTO) JPMJPR23Q1
6 · The paper itself

Abstract

π-Electron systems with multiple redox-active units have attracted attention in various fields due to their potential applications. However, the design strategy remains elusive to selectively synthesize the diverse molecular structures of redox-convertible species. In this study, covalently linked quinodimethane derivatives with a sulfur bridge [(Ar

Identifiers

PMID40341386
PMCPMC12062416

What OpenQuestion holds

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Registered trials

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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.