Evidence map›Paper›PMID 42498983›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Force-Induced Control of Circularly Polarized Luminescence With Rotaxane Architecture.

Keigo Nonaka, Takumi Kuroda, Kota Masuda, Toshiki Nishitani, Masaki Enokido, Makoto Tsurui, Yuichi Kitagawa, Yasuchika Hasegawa, Keiichi Noguchi, Koji Nakano and 1 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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.

Keigo NonakaDepartment of Materials Science and Engineering, Institute of Science Tokyo, Meguro-ku, Tokyo, Japan.
Takumi KurodaDepartment of Materials Science and Engineering, Institute of Science Tokyo, Meguro-ku, Tokyo, Japan.
Kota MasudaDepartment of Materials Science and Engineering, Institute of Science Tokyo, Meguro-ku, Tokyo, Japan.
Toshiki NishitaniDepartment of Materials Science and Engineering, Institute of Science Tokyo, Meguro-ku, Tokyo, Japan.
Masaki EnokidoGraduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo, Hokkaido, Japan.
Makoto TsuruiGraduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo, Hokkaido, Japan.
Yuichi KitagawaFaculty of Engineering, Hokkaido University, Sapporo, Hokkaido, Japan.ORCID https://orcid.org/0000-0003-1487-2531
Yasuchika HasegawaFaculty of Engineering, Hokkaido University, Sapporo, Hokkaido, Japan.ORCID https://orcid.org/0000-0002-6622-8011
Keiichi NoguchiInstrumentation Analysis Center, Tokyo University of Agriculture and Technology, Koganei, Tokyo, Japan.
Koji NakanoDepartment of Applied Chemistry, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4166-7074
Yoshimitsu SagaraDepartment of Materials Science and Engineering, Institute of Science Tokyo, Meguro-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2502-3041

Funding

Japan Science and Technology AgencyJapan Society for the Promotion of Science
6 · The paper itself

Abstract

The reversible molecular motions of mechanically interlocked molecules (MIMs) have played a crucial role in realizing stimuli-responsive functions. While the reversible switching of circularly polarized luminescence (CPL) properties has been achieved using MIMs through pH change and/or addition of chemicals, the mechanically controlled CPL utilizing the interlocked architecture has not yet been demonstrated. Here, we introduce a rotaxane-based mechanophore designed for force-induced CPL on/off switching. The mechanophore consists of a ring featuring a CPL-active helicene luminophore and an axle with a matching quencher. The rotaxane mechanophores covalently introduced at the cross-linking points of a double-network (DN) gel are reversibly activated and deactivated in response to changes in applied force transduced through the polymer chains during the macroscopic swelling and shrinking of the DN gel. The isotropic swelling of the DN gel effectively suppresses artifacts arising from macroscopic sample orientation, enabling accurate detection of reciprocal CPL derived from a single chiral emitter. This work establishes the first example of mechanical control of CPL at the single-molecule level and provides a robust measurement methodology for force-induced CPL switching in soft materials.

Indexed as

circularly polarized luminescencegelsmechanoresponsive luminescencerotaxanessupramolecular mechanophores

Identifiers

PMID42498983
PMCPMC13592300

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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.