Three series of dimer liquid crystals containing an aromatic and a choleste
ryl mesogenic unit were synthesized and investigated The compounds within t
he series differ in the length of the spacer connecting the mesogenic group
s. Two of the three series contain an aromatic mesogenic group that is conn
ected to the spacer at a meta-position instead of the para-position. Due to
the presence of this bent mesogenic group, the odd-even effect in the tran
sitional properties that is normally observed for dimer liquid crystals is
reversed as compared with that of the third series, which contains a para-s
ubstituted aromatic mesogenic group. The reversed odd-even effect is found
for the isotropization temperatures, the associated enthalpy changes and al
so for the optical properties.