Synthesis of New Chiral Disubstituted Binaphthol Derivatives and their use as the Chiral Dopants

1996 ◽  
Vol 425 ◽  
Author(s):  
H.-J. Deussen ◽  
P. V. Shibaev ◽  
R. A. Vinokur ◽  
K. Schaumburg ◽  
T. Bjornholm ◽  
...  

AbstractA number of new chiral binaphthol (BN) derivatives with different substituents in the 6,6'-positions in open and bridged forms have been synthesized. Their possible liquid crystalline properties and their helical twisting power (B) of three different nematic liquid crystals (LCs) were investigated. Derivatives with spatially extended substituents in the 6,6'-positions (e.g. styryl or vinil) show unusual high helical twisting power (up to 120 μm–1). A direct correlation between the magnitude of β and the length of the substituents was found.From the different temperature dependence of β of the open and bridged BNs, a molecular model was developed relating the molecular conformation and twisting power

2013 ◽  
Vol 52 (19) ◽  
pp. 11042-11050 ◽  
Author(s):  
Jun Yoshida ◽  
Go Watanabe ◽  
Kaori Kakizawa ◽  
Yasuhiro Kawabata ◽  
Hidetaka Yuge

2019 ◽  
Vol 7 (8) ◽  
pp. 2225-2231 ◽  
Author(s):  
Daisuke Yoshizawa ◽  
Hiroki Higuchi ◽  
Yasushi Okumura ◽  
Hirotsugu Kikuchi

9,9′-biphenanthrene-type chiral dopants were newly synthesized for the development of functional liquid crystal (LC) materials with enhanced properties. A cholesteric LC (CLC) with a chiral dopant showed positive temperature dependence of helical twisting power and a CLC with temperature independence was developed by mixing two types of chiral dopants.


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