Macroscopic chirality of twist-bend nematic phase in bent dimers confirmed by circular dichroism
Many achiral bent molecules and some polymers with such repeat units exhibit a liquid crystal phase transition between a conventional nematic (N), and a second nematic (N x ) with periodically modulated orientation. Theory predicts several possible structures for the N x phase, some of which are chi...
Gespeichert in:
Veröffentlicht in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2020, Vol.8 (3), p.141-147 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Many achiral bent molecules and some polymers with such repeat units exhibit a liquid crystal phase transition between a conventional nematic (N), and a second nematic (N
x
) with periodically modulated orientation. Theory predicts several possible structures for the N
x
phase, some of which are chiral (helical), and others achiral (
e.g.
zigzag). Experimentally distinguishing which modulation type is present is non-trivial and the structure is often assumed to be helical despite the other possibilities. Here we use circular dichroism (CD) spectroscopy to directly and unambiguously identify chirality in the N
x
phase of two different dimer series, "DTC5C
n
" and "CBC
n
CB", which vary in (CH
2
)
n
spacer length (
n
= 5, 7, 9). In doing so we have determined that the modulation type is helical in all samples. The temperature dependence of the CD signal was also investigated, suggesting that the helical structure progressively unwinds on approach to the high temperature N phase.
Long-range global chirality is confirmed in the twist-bend nematic phase of bent dimers using circular dichroism spectroscopy. The phase absorbs left and right circularly polarized light differently, confirming its helical rather than wavy character. |
---|---|
ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/c9tc05061b |