In this work, three series of ferroelectric side-chain
polysiloxanes containing oligooxyethylene spacers and (S)-2-methyl-1-butyl
(2S)-2-[6-(4-hydroxybiphenyl-4‘-carbonyloxy)-2‘-naphthyl]propionates, (R)-1-methylheptyl
(2S)-2-[6-(4-hydroxybiphenyl-4‘-carbonyloxy)-2‘-naphthyl]propionates, and
(2S,3S)-2-chloro-3-methylpentyl
(2S)-2-[6-(4-hydroxybiphenyl-4‘-carbonyloxy)-2‘-naphthyl]propionates mesogenic groups were
synthesized. The mesomorphic
behaviors of three series of ferroelectric side-chain
liquid-crystalline polysiloxanes were also
studied using differential scanning calorimetry, optical polarizing
microscopy, and high-resolution X-ray diffraction measurements. Some of these side-chain
polysiloxanes containing
four phenyl rings of ester cores (i.e., −Ph−Ph−COO−naphthyl−)
and chiral heptyl tail
present a smectic A (SA), and a chiral smectic C (Sc*)
phase (around 100 °C). Another two
series containing four phenyl rings of ester cores and chiral butyl and
pentyl chain tail reveal
a cholesteric (N*), an SA phase and an Sc* phase. The
polymer PS12NC derivative with
one unit of oxyethylene spacer (n = 1) of PSn2NC series
reveals a N* phase, a twist grain
boundary A (TGBA) phase, and a Sc* phase. X-ray
investigations reveal that the packing of
mesogenic groups for PS02NA, PS02NB, PS02NC with the shortest spacers
(n = 0) exhibit
a bilayer (two-layer) packing structures. Moreover, polymer
PS32NA, PS32NB, PS32NC
with the longest spacer chain (n = 3) reveal a monolayer
packing structure. However, these
two types of packing structure appear simultaneously in PS12NA
(n = 1), PS12NC (n = 1),
PS12NB (n = 1), and PS22NB (n = 2), depending
on the chiral tail length. Results obtained
in this study again demonstrate that the tendency toward chiral smectic
C mesomorphism
increases as the rigidity of phenyl ester mesogens increases via the
flexible oligooxyethylene
spacers system. Furthermore, the thermal stability of the chiral
smectic C mesophase is
determined by the flexibility of the chiral tail.