V. Rayssac et al., NMR INVESTIGATION OF THE OXYETHYLENE UNIT ORDERING IN SOME RELATED DIALKOXY LATERALLY SUBSTITUTED NEMATOGENS, Liquid crystals, 25(3), 1998, pp. 427-436
Laterally dialkylated nematogens containing a short terminal polyoxyet
hylene chain present a wide nematic range starting from room temperatu
re. The ordering of the oxyethylene (OE) unit has been studied by C-13
NMR in the liquid crystalline phase. The values of the order paramete
rs were derived from the transient oscillations observed during variab
le contact-time cross-polarization experiments. Along the oxyethylene
chain, the order parameters decrease monotonically. These order parame
ter values do not present the usual odd-even effect and are noticeably
smaller than those found for terminal alkoxy chains. Entering the nem
atic phase, the C-13 thermal evolution of the field-induced chemical s
hift in the OE unit is far smaller than the one usually observed for t
erminal alkyl or alkoxy chains, regardless of their non-negligible ord
er parameters. In addition, no linear correlation between the order pa
rameter and the field-induced chemical shift is observed for the carbo
ns in the OE unit. This is an indication that the proportion between g
auche- and trans-conformations in the OE unit is temperature dependent
.