TRANS AND CIS ROTAMERIZATION IN AMPHIPHILIC CHOLESTERIC LIQUID-CRYSTALS WHERE THE CHIRAL DOPANT IS THE HYDROCHLORIDE OF DECYL-L-PROLINE

Authors
Citation
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
Citations number
13
Categorie Soggetti
Crystallography
ISSN journal
1058725X
Volume
287
Year of publication
1996
Pages
305 - 308
Database
ISI
SICI code
1058-725X(1996)287:<305:TACRIA>2.0.ZU;2-Y
Abstract
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.