Evidence map›Paper›PMID 27812045›Full record

ArticleScientific reports2016

Fluorescence microscopy reveals molecular localisation at line defects in nematic liquid crystals.

Takuya Ohzono, Kaoru Katoh, Jun-Ichi Fukuda

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Volumetric imaging of the 3D orientation of cellular structures with a polarized fluorescence light-sheet microscope.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Article
  4. Scaling and spontaneous symmetry restoring of topological defect dynamics in liquid crystal.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Article
  6. 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

3 authors.

Takuya OhzonoResearch Institute for Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8565, Japan.
Kaoru KatohBiomedical Research Institute, AIST, 1-1-1 Higashi, Tsukuba 305-8566, Japan.
Jun-Ichi FukudaResearch Institute for Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8565, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Topological defects easily form in liquid crystals (LCs) as a result of frustrations in spatially dependent anisotropic molecular ordering, and have been regarded as promising tools for facilitating manipulation of relatively large non-LC materials such as colloids. However, it remains unclear whether low-molecular-weight (LMW) impurities that do not aggregate or self-assemble in bulk LCs because of the dominance of entropy can localise at LC defects. Here, by fluorescence microscopy, we directly show the localisation of LMW molecules at the topological line defects of a nematic LC. It is theoretically explained that excess free energy density of nematic ordering at the defect core allows LMW solutes to accumulate at a non-negligible level overcoming the entropy leading to their uniform distributions. Our results demonstrate the usefulness of LC defects as a bottom-up field that enables micromanipulation of LMW molecules and realisation of transformable three-dimensional micro-architectures composed of versatile small functional molecules.

Identifiers

PMID27812045
PMCPMC5095605

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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.