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How Far Can We Push the Rigid Oligomers/Polymers toward Ferroelectric Nematic Liquid Crystals?

Authors :
Li J
Xia R
Xu H
Yang J
Zhang X
Kougo J
Lei H
Dai S
Huang H
Zhang G
Cen F
Jiang Y
Aya S
Huang M
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2021 Oct 27; Vol. 143 (42), pp. 17857-17861. Date of Electronic Publication: 2021 Oct 17.
Publication Year :
2021

Abstract

The emerging ferroelectric nematic ( N <subscript> F </subscript> ) liquid crystal is a novel 3D-ordered liquid exhibiting macroscopic electric polarization. The combination of the ultrahigh dielectric constant, strong nonlinear optical signal, and high sensitivity to the electric field makes N <subscript> F </subscript> materials promising for the development of advanced liquid crystal electroopic devices. Previously, all studies focused on the rod-shaped small molecules with limited length ( l ) range and dipole moment (μ) values. Here, through the precision synthesis, we extend the aromatic rod-shaped mesogen to oligomer/polymer (repeat unit up to 12 with monodisperse molecular-weight dispersion) and increase the μ value over 30 Debye (D). The N <subscript> F </subscript> phase has a widespread existence far beyond our expectation and could be observed in all the oligomer/polymer length range. Notably, the N <subscript> F </subscript> phase experiences a nontrivial evolution pathway with the traditional apolar nematic phase completely suppressed, i.e., the N <subscript> F </subscript> phase nucleates directly from the isotropic liquid phase. The discovery of thte ferroelectric packing of oligomer/polymer rods not only offers the concept of extending the N <subscript> F </subscript> state to oligomers/polymers but also provides some previously overlooked insights in oxybenzoate-based liquid crystal polymer materials.

Details

Language :
English
ISSN :
1520-5126
Volume :
143
Issue :
42
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
34657433
Full Text :
https://doi.org/10.1021/jacs.1c09594