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Liquid crystals derived from carbohydrates: Synthesis and properties of oxadecaline compounds

✍ Scribed by Vill, Volkmar ;Tunger, Hanns-Walter


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
455 KB
Volume
1995
Category
Article
ISSN
0947-3440

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✦ Synopsis


Abstract

Reaction of glucal 1 with alkoxybenzene leads after hydrogenation and deacetylation to β‐C glycosides 4, which can be used as chiral compounds in the synthesis of chiral calamitic liquid crystals. The combination with aliphatic aldehydes leads to liquid crystals 5 showing a monotropic S~A~ phase, with aromatic p‐alkoxy‐substituted aldehydes to compounds 6 with enantiotropic cholesteric and S~A~ phases. Reaction with p‐alkoxy‐substituted phenylboronic acids gives liquid crystals 7 forming S~A~ and ferroelectric S~C~* phases. They all exhibit a high twisting power and blue phases in contact preparation.


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Two poly(ester amides) containing three methoxy groups stereoregularly attached to the main chain have been prepared by using naturally occurring L-arabinose and D-xylose as the starting materials. The polymers were prepared by the active ester polycondensation method and characterized by elemental