D. Haarer et al., ELECTRONIC-PROPERTIES OF DISCOTIC LC-MATERIALS, Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 283, 1996, pp. 63-68
We have made extensive studies of the charge-carrier mobilities in the
discotic hexagonal mesophases of triphenylene-based discotic liquid c
rystals. Using the time-of-flight technique, transient photocurrents w
ere measured yielding charge-carrier mobilities for various electric f
ields and temperatures. Starting from promising results obtained with
the monomeric discotic liquid crystalline model compound hexapentyloxy
triphenylene (H5T), we synthesized a ''discotic twin'' with two triphe
nylene units linked together by a suitable spacer. Additionally, we sy
nthesized a discotic liquid crystalline oligomer consisting of four tr
iphenylene units which are bound to a flexible cyclosiloxane ring. In
the dimer and in the oligomer the discotic mesophase can be maintained
in a discotic glass. Our data show that in both H5T as well as in the
dimer and in the oligomer hole mobilities on the order of magnitude o
f 10(-3)cm(2)/Vs can be reached. Since the mobilities obtained in the
oligomeric compounds are comparable to those found in the monomeric mo
del compound, it becomes clear that the excellent charge-carrier trans
port properties in the discotic hexagonal mesophase can be preserved i
n easily processible and anisotropic organic thin films. Therefore, ou
r results are an important step towards the applicability of highly or
dered discotic liquid crystalline materials in the field of electronic
applications.