ReviewChemPlusChem2026
Soft Ferroelectrics in One Dimension: Ferroelectric Columnar Liquid Crystals.
Review in ChemPlusChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ferroelectric columnar liquid crystals (FCLCs) are attractive candidates for ultra-high-density organic memories because bistable information can be encoded within individual polar columns. However, most "switching" columnar LCs relax into paraelectric or antiferroelectric states once the electric field is removed, which severely limits their practical utility. In this concept article, we summarize the limited number of FCLC systems reported to date and present a materials-design perspective that integrates molecular design with supramolecular locking/structural stabilization strategies to achieve long-lived axial polarization. Central to this framework is suppressing rotation-driven depolarization by "locking" polar motifs through directional hydrogen-bonding and steric confinement, which is often realized as well-defined intracolumnar helical order. In particular, we discuss how representative polar building blocks-amide, thioamide, benzene-1,3,5-tricarboxamide (BTA), urea, and the recently emerging aromatic 1,2,3-triazole unit-govern polar switching and polarization stabilization. Finally, we propose actionable molecular and device-level strategies to further enhance FCLC performance and accelerate their translation toward memory applications.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.