Year: 2025
Type: article
Abstract: We report on the preparation and characterization of a new family of hydrogen-bonded nematogenic liquid crystalline dimers. The dimers are supramolecular complexes that consist of a benzoic acid derivative, acting as the proton donor, featuring a spacer with seven methylene groups and a terminal decyloxy chain, paired with an azopyridine derivative as the proton acceptor. The latter was either fluorinated or nonfluorinated with variable alkoxy chain length. The formation of a hydrogen bond between the individual components was confirmed using FTIR and 1H NMR spectroscopy. All supramolecules were investigated for their liquid crystalline behaviour via a polarized optical microscope (POM) and differential scanning calorimetry (DSC). All materials exhibit enantiotropic nematic phases as confirmed by X-ray diffraction (XRD) and POM investigations. The nematic phase range depends strongly on the degree and position of fluorine atoms. Additionally, the supramolecules demonstrated a rapid and reversible transition between the liquid crystal phase and the isotropic liquid state because of trans-cis photoisomerization upon light irradiation. Therefore, this study presents a straightforward approach to design photo-responsive nematic materials, which could be of interest for nonlinear optics applications.
Source: Crystals
Authors: Christian Anders, Muhammad Abu Bakar, Tejal Nirgude, Mohamed Alaasar
Institution: Martin Luther University Halle-Wittenberg
Language: English
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $2,534
Funder: Deutsche Forschungsgemeinschaft
OpenAlex ID: W4411421434