NMR INVESTIGATION OF THE OXYETHYLENE UNIT ORDERING IN SOME RELATED DIALKOXY LATERALLY SUBSTITUTED NEMATOGENS

Citation
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
Citations number
27
Categorie Soggetti
Crystallography
Journal title
ISSN journal
02678292
Volume
25
Issue
3
Year of publication
1998
Pages
427 - 436
Database
ISI
SICI code
0267-8292(1998)25:3<427:NIOTOU>2.0.ZU;2-R
Abstract
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 .