K. Radley et N. Mclay, TRANS AND CIS ROTAMERIZATION IN AMPHIPHILIC CHOLESTERIC LIQUID-CRYSTALS WHERE THE CHIRAL DOPANT IS THE HYDROCHLORIDE OF DECYL-L-PROLINE, Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 287, 1996, pp. 305-308
Data from a previous study, where a reversal in the sense of the helic
al twist in an amphiphilic cholesteric liquid crystal (ACLC) is induce
d by the chiral dopant the hydrochloride of decyl-L-proline, is taken
and its interpretation extended. The interpretation involves trans and
cis conformers resulting from hindered rotation. The C-13 NMR data is
used to determine the rotamer populations, which facilitates the calc
ulation of the twisting powers for the individual rotamers. The twisti
ng powers of the trans and cis rotamers are found to be 3900 +/- 900 c
m(-1) and -650 +/- 150 cm(-1) respectively.