S. Hvilsted et al., NOVEL SIDE-CHAIN LIQUID-CRYSTALLINE POLYESTER ARCHITECTURE FOR REVERSIBLE OPTICAL STORAGE, Macromolecules, 28(7), 1995, pp. 2172-2183
New side-chain liquid crystalline polyesters have been prepared by mel
t transesterification of diphenyl tetradecanedioate and a series of me
sogenic 2-[omega-[4-[(4-cyanophenyl)azo]phenoxyl] alkyl]-1,3-propanedi
ols, where the alkyl spacer is hexa-, octa-, and decamethylene in turn
. The polyesters have molecular masses in the range 5000-89 000. Solut
ion C-13 NMR spectroscopy has been employed to identify carbons of pol
yester repeat units and of both types of end groups. Polyester phases
and phase transitions have been investigated in detail by polarizing o
ptical microscopy and differential scanning calorimetry for the hexame
thylene spacer architecture with different molecular masses. Using FTI
R polarization spectroscopy, the segmental orientation in unoriented p
olyester films induced by argon ion laser irradiation has been followe
d and an irradiation-dependent order parameter for the cyanoazobenzene
mesogens calculated. FTIR is also utilized to follow the temperature-
dependent erasure of the induced orientation. Optical storage properti
es of thin unoriented polyester films are examined through measurement
s of polarization anisotropy and holography. A resolution of over 5000
lines/mm and diffraction efficiencies of about 40% have been achieved
. Lifetimes greater than 30 months for information stored have been ob
tained, even though the glass transition temperatures are about 20 deg
rees C. Complete erasure of the information can be obtained by heating
the films to about 80 degrees C, and the films can be reused many tim
es without fatigue.