Helical Twisting Power of New Chiral Dopants Having a Trifluoromethyl Group at the Chiral Center for Nematic Liquid Crystals

2003 ◽  
Vol 398 (1) ◽  
pp. 189-193 ◽  
Author(s):  
Yoshio Aoki ◽  
Kentarou Matsushima ◽  
Tetsu Taroura ◽  
Takuji Hirose ◽  
Hiroyuki Nohira
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

1994 ◽  
Vol 23 (5) ◽  
pp. 839-842 ◽  
Author(s):  
Keizou Itoh ◽  
Mitsunori Takeda ◽  
Masaaki Namekawa ◽  
Shinichi Nayuki ◽  
Yoshinobu Murayama ◽  
...  

2005 ◽  
Vol 11 (11) ◽  
pp. 3405-3412 ◽  
Author(s):  
Manfred Braun ◽  
Antje Hahn ◽  
Marco Engelmann ◽  
Ralf Fleischer ◽  
Walter Frank ◽  
...  

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