Abstract

Standard Sonogashira coupling afforded rod-like, phenylacetylene extended biphenyl mesogens substituted with different chiral alkoxy chains, starting from commercially available 4-(4′-bromophenyl)phenol. Depending on the position of the chiral center and the polar nature of the target molecules as determined by the electron withdrawing end-groups, different types of smectic liquid crystals are formed. The liquid crystal phases are fully characterized by polarized optical microscopy, differential scanning calorimetry, and X-ray diffraction. In two cases, the molecular chirality is transferred to the supramolecular assembly, which is proved by circular dichroism measurements in the chiral mesophase.

Keywords:
Liquid crystal Phenylacetylene Chirality (physics) Sonogashira coupling Circular dichroism Molecule Supramolecular chemistry Biphenyl Supramolecular chirality

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Topics

Liquid Crystal Research Advancements
Physical Sciences →  Materials Science →  Electronic, Optical and Magnetic Materials
Synthesis and Properties of Aromatic Compounds
Physical Sciences →  Chemistry →  Organic Chemistry
Molecular spectroscopy and chirality
Physical Sciences →  Chemistry →  Spectroscopy

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