The hole transport properties of ester substituted hexaalkyloxytriphenylene
s are investigated and compared with the materials without ester substituen
ts. The high hole mobilities of the recently investigated discotic liquid c
rystals of the hexaalkyloxytriphenylene-type are restricted to the very sma
ll temperature range of their mesophase. It is extended substantially by su
bstitution of one ester group, as this hinders crystallization and results
in glass formation. It is found that the substitution of an ester group alt
ers the temperature and field dependence of the mobility completely. In the
ester substituted compounds the mobility mu is not independent of temperat
ure but follows a ln mu proportional to 1/T-2 law. We attribute this to the
dipole moment of the ester group which causes random fluctuations in the l
ocal electric held and leads to disorder dominated charge carrier hopping a
s the prevailing transport mechanism.