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Proceedings Paper

New synthetic possibilities for the preparation of liquid crystalline dicyclohexyl derivatives
Author(s): Genadz Sasnouski; Vladimir Bezborodov; Roman S. Dabrowski; Jerzy Dziaduszek
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Paper Abstract

A new synthetic approach for the preparation of two- and three ring liquid crystalline compounds possessing trans,trans-dicyclohexyl moiety is proposed and realized. Recently discovered reaction of Grignard reagents with esters leading to 1-substituted cyclopropanoles in the presence of tetraisopropoxytitanium was used as a key stage. Starting from ethyl trans-4-alkylcyclohexancarboxylates the corresponding 6-(4-alkylcyclohexyl)-3-alkyl (or aryl) cyclohex-2-en-1-ones have been prepared. Their catalytic hydrogenation in the base media gave mainly saturated trans, trans-ketones which are liquid crystalline and have been used also as a promising intermediate products for the preparation of different kinds of other LC compounds.

Paper Details

Date Published: 12 May 2000
PDF: 6 pages
Proc. SPIE 4147, Liquid Crystals: Chemistry, Physics, and Applications, (12 May 2000); doi: 10.1117/12.385719
Show Author Affiliations
Genadz Sasnouski, Belarusian State Univ. (Belarus)
Vladimir Bezborodov, Belarusian State Univ. (Belarus)
Roman S. Dabrowski, Military Univ. of Technology (Poland)
Jerzy Dziaduszek, Military Univ. of Technology (Poland)


Published in SPIE Proceedings Vol. 4147:
Liquid Crystals: Chemistry, Physics, and Applications
Stanislaw J. Klosowicz; Jolanta Rutkowska; Jerzy Zielinski; Jozef Zmija, Editor(s)

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