Evidence map›Paper›PMID 42240104›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Ladderization: A Powerful Strategy for Controlling Supramolecular Helical Ordering, Amplifying Asymmetry, and Emerging and Enhancing Circularly Polarized Luminescence.

Tomoyuki Ikai, Koki Nishino, Nichito Kawabata, Kosuke Oki, Mitsuo Hara, Yukikazu Takeoka, Eiji Yashima

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 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

7 authors.

Tomoyuki IkaiDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.ORCID https://orcid.org/0000-0002-5211-2421
Koki NishinoDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Nichito KawabataDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Kosuke OkiDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Mitsuo HaraDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Yukikazu TakeokaDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Eiji YashimaDepartment of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Nagoya, Japan.ORCID https://orcid.org/0000-0001-6307-198X

Funding

Foundation of Public Interest of TatematsuJSPS KAKENHI 18H05209JSPS KAKENHI 24K01537JSPS KAKENHI 25H01407JSPS KAKENHI 25K22284JST PRESTO JPMJPR21A1Mitsubishi FoundationNagase Science and Technology Foundation
6 · The paper itself

Abstract

We report the synthesis of optically-active π-conjugated coplanar ladder polymers with enantiopure side groups that enable helical ordering-induced circular dichroism (CD) and circularly polarized luminescence (CPL) in a specific solvent mixture and in the film state, whereas the corresponding linear polymer precursor showed a negligible CD and CPL in any state, demonstrating the key role of the coplanar ladder framework in forming well-ordered supramolecular chiral aggregates. The CPL activities of the pristine films of the chiral ladder polymers were significantly enhanced after solvent vapor exposure, leading to a luminescence dissymmetry factor exceeding 0.1, which arises from the supramolecular helical aggregation through cholesteric ordering. This methodology for enhancing the CPL was versatile and highly effective in generating a comparably intense CPL even when the films contained up to 75 mol% of an achiral analogue of the chiral ladder polymer, demonstrating strong amplification of the asymmetry. Furthermore, the CPL color of the film could be readily tuned by Förster resonance energy transfer to an achiral ladder polymer with a backbone structure different from that of the chiral ladder polymer.

Indexed as

alkyne benzannulationsamplification of asymmetrycircularly polarized luminescenceladder polymersself‐assembly

Identifiers

PMID42240104
PMCPMC13410664

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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.