Synthesis, mesomorphic properties and potential applications of aryl esters of 4-n-alkylcyclohexene-1-carboxylic acids in electrooptic displays
- 1 February 1989
- journal article
- research article
- Published by Taylor & Francis in Liquid Crystals
- Vol. 4 (2) , 209-215
- https://doi.org/10.1080/02678298908029074
Abstract
The reaction of 4-substituted phenols with 4-n-alkylcyclohexene-1-carbonyl chlorides, which differ in the position of their double bond in the ring, has yielded the corresponding esters. Investigation of their mesophoric properties including the electrooptic parameters of mixtures containing these compounds show that aryl esters of acids containing the double bond in the second position of the cyclohexene fragment are the most promising for use as components of liquid crystal mixtures.Keywords
This publication has 6 references indexed in Scilit:
- Mesomorphic Properties of Cyanophenyl CyclohexenesMolecular Crystals and Liquid Crystals, 1982
- Liquid Crystal Compounds Incorporating the Trans-1,4-Substituted Cyclohexane Ring SystemMolecular Crystals and Liquid Crystals, 1979
- Kristallin‐flüssige trans‐4‐n‐Alkylcyclohexan‐carbonsäurephenylesterJournal für Praktische Chemie, 1978
- Kristallin‐flüssige trans‐4‐n‐Alkylcyclohexancarbonsäure‐[4‐cyanophenylester]Zeitschrift für Chemie, 1977
- Bicyclobutyl derivatives. IV. Bromination of fluorinated bicyclobutenyl derivativesThe Journal of Organic Chemistry, 1967
- The Preparation of 2-Alkylbutadienes1Journal of the American Chemical Society, 1948