A. Jacobi et W. Weissflog, LATERALLY 4-NITROBENZYLOXYCARBONYL SUBSTITUTED PHENYL BENZOATES - THEFIRST 2-RING MESOGENS WITH A LATERAL BRANCH CONTAINING A PHENYL RING, Liquid crystals, 22(2), 1997, pp. 107-111
The synthesis and properties of laterally 4-nitrobenzyloxycarbonyl sub
stituted phenyl benzoates are described; these compounds represent the
first two-ring mesogens having a phenyl ring in the lateral branch. T
he lengths of the terminal chains of the core carrying the branch have
a great influence, as shown by the phase behaviour of two homologous
series. Compounds having long alkyloxy groups exhibit enantiotropic sm
ectic A phases. It should be emphasized that the mesophase thermal sta
bility of these strongly branched derivatives can be higher than that
of the laterally unsubstituted parent compound. Connecting two of the
new mesogens by means of an aliphatic spacer results in a novel type o
f twin molecule.