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
Liquid crystals derived from carbohydrates: Synthesis and properties of oxadecaline compounds
β 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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β¦ Synopsis
Abstract
Reaction of glucal 1 with alkoxybenzene leads after hydrogenation and deacetylation to Ξ²βC 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 pβalkoxyβsubstituted aldehydes to compounds 6 with enantiotropic cholesteric and S~A~ phases. Reaction with pβalkoxyβsubstituted 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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