The liquid crystal molecule 3-fluoro-4-(3,4,5-trifluorophenyl)phenyl
2,6-difluoro-4-(trans-5-n-propyl-1,3-dioxane-2-yl)benzoate
(DIO) has attracted considerable interest owing to its unique ferroelectric
nematic phase and extraordinarily high dielectric constant. To expand
the DIO series, novel analogs with 1,3-dioxane units converted to
ester units (EST analogs) were synthesized, and their physical properties
were characterized. The EST analogs exhibited ferroelectric phases
similar to those of the corresponding DIO analogs. Interestingly,
an EST analogue featuring a defluorinated benzoate unit exhibited
a ferroelectric smectic A phase, despite its smaller longitudinal
dipole moment of 6.9 D. This result diverges from the common knowledge
that the formation of large longitudinal dipoles is traditionally
effective in the emergence of ferroelectric phases. Unlike the DIO
series, the EST analogs can be readily obtained without the formation
of undesired geometric isomers, which is advantageous for practical
applications. The results of this study provide valuable insights
into the design of liquid-crystalline materials expressing ferroelectric
phases