EFFECT OF THE POSITION OF LATERAL FLUORO SUBSTITUENTS ON THE PHASE-BEHAVIOR AND FERROELECTRIC PROPERTIES OF CHIRAL 1-METHYLHEPTYL ECYLOXPHENYL)PROPIOLOYLOXY]BIPHENYL-4-CARBOXYLATES OR CYLOXYPHENYL)PROPIOLOYLOXY]BIPHENYL-4-CARBOXYLATES
Cj. Booth et al., EFFECT OF THE POSITION OF LATERAL FLUORO SUBSTITUENTS ON THE PHASE-BEHAVIOR AND FERROELECTRIC PROPERTIES OF CHIRAL 1-METHYLHEPTYL ECYLOXPHENYL)PROPIOLOYLOXY]BIPHENYL-4-CARBOXYLATES OR CYLOXYPHENYL)PROPIOLOYLOXY]BIPHENYL-4-CARBOXYLATES, Journal of materials chemistry, 4(5), 1994, pp. 747-759
The syntheses of four chiral laterally fluoro-substituted propiolate e
sters are described, along with transition temperatures, ferroelectric
properties, phase diagrams and related data. The position of the fluo
ro-substituent was found to influence dramatically the formation of tw
ist grain boundary (TGB A and TGB C*) phases as well as the magnitude
s of spontaneous polarization and optical tilt angle in the ferroelect
ric smectic C mesophases. Differential scanning calorimetric studies
revealed the presence of a diffuse liquid-liquid transition above the
clearing point in both of the 3-fluoro enantiomers, but not in the rac
emate. Circular dichroism and optical rotation measurements, carried o
ut over a temperature range in which the diffuse peak occurs, appear t
o confirm the presence of a degree of chiral organization within the i
sotropic liquid. It is suggested that this phenomenon may be due to th
e presence of cybotactic groups or a network of entangled screw disloc
ations occurring close to the clearing point.