Synthesis and mesophase behavior of mesogens bearing omega,alpha,alpha-trihydroperfluoroalkoxy end tails

Authors
Citation
Bq. Chen et Jx. Wen, Synthesis and mesophase behavior of mesogens bearing omega,alpha,alpha-trihydroperfluoroalkoxy end tails, LIQ CRYST, 26(8), 1999, pp. 1135-1140
Citations number
28
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LIQUID CRYSTALS
ISSN journal
02678292 → ACNP
Volume
26
Issue
8
Year of publication
1999
Pages
1135 - 1140
Database
ISI
SICI code
0267-8292(199908)26:8<1135:SAMBOM>2.0.ZU;2-J
Abstract
One series of two-ring and two series of three-ring liquid crystal compound s, all containing omega,alpha,alpha-trihydroperfluoroalkoxy terminal tails, were prepared and characterized by IR, NMR, MS and elemental analysis. The ir phase transition behaviour was investigated by DSC and polarizing optica l microscopy. Biphenylene derivatives with the omega,alpha,alpha-trihydrope rfluoroalkoxy end group form a stable smectic A phase. In the three-ring sy stem, biphenylene ester compounds exhibit a smectic phase without a nematic phase. The compounds exhibit smectic A and smectic C phases when the termi nal groups are intermediate length alkyl and fluorinated alkyl chains. Meso gens with fluorinated tails have a broader smectic C phase than the non-flu orinated mesogens.