Increased intermolecular interactions and cluster formation at the onset of the twist-bend nematic phase in thioether cyanobiphenyl-based liquid crystal dimers

TL;DR

This study combines infrared spectroscopy and quantum chemistry to reveal increased intermolecular interactions and specific molecular arrangements at the transition from nematic to twist-bend nematic phases in thioether cyanobiphenyl-based liquid crystal dimers.

Contribution

It provides new insights into molecular interactions and structural changes during phase transition using combined IR spectroscopy and DFT calculations.

Findings

Increased intermolecular interactions at the N to NTB phase transition.

Decrease in IR absorbance for longitudinal dipoles during transition.

Correlation of dipoles increases significantly in the NTB phase.

Abstract

Infrared spectroscopy (IR) and quantum chemistry calculations, based on density functional theory (DFT) were used to study the structure and the molecular interactions in the nematic (N) and twist-bend (NTB) phases of thioether-linked dimers. Infrared absorbance measurements were conducted in a polarized beam for homogeneously aligned samples to measure and understand the orientation of the vibrational transition dipole moments in the liquid crystal states. Revealing temperature-dependent changes in the mean IR absorbance in the twist-bend nematic phase were observed. In the transition from the N to the NTB phase, is was found to be associated with a decrease in absorbance for the longitudinal dipoles. This is a result of the antiparallel axial interactions of the dipoles, while the absorbance of the transverse dipoles remained unchanged up to 340 K and then increased and the dipoles correlated in parallel. In order to account for the molecular arrangement in the nematic phase, DFT calculations were conducted for the system nearest to the lateral neighborhoods. Changes in the square of transition dipoles were found to be quite similar to the mean absorbance that was observed in the IR spectra. Interactions of molecules that were dominated by pair formation was observed as well as a shift of the long axes of the molecules relative to each other. The most important observation from the spectroscopic measurements was the sudden increase in the intermolecular interactions as the temperature decreased from the N to the NTB phase. This was evidenced by a significant increase in the correlation of the dipoles that were induced in the dimer cores.