A pressure‐ and temperature‐controlled sample cell for the structural investigation of lyotropic liquid crystals using a small‐angle x‐ray diffraction line source

1996 ◽  
Vol 67 (12) ◽  
pp. 4228-4234 ◽  
Author(s):  
P. M. Duesing ◽  
R. H. Templer ◽  
J. M. Seddon
2012 ◽  
Vol 90 (12) ◽  
pp. 1056-1062 ◽  
Author(s):  
Joseph K.-H. Hui ◽  
Jian Jiang ◽  
Mark J. MacLachlan

Schiff-base macrocycles 1, which have a crown ether-like interior, form ionic nematic lyotropic liquid crystals in various organic solvents when functionalized with long alkoxy substituents and complexed to diverse ammonium and alkali metal salts. From X-ray diffraction and transmission electron microscopy studies, and by comparison with the organization of macrocycles functionalized with shorter chains, these macrocycles assemble into lyotropic liquid crystals where the macrocycles are stacked and the cation is included in their interiors.


1991 ◽  
Vol 113 (15) ◽  
pp. 5809-5816 ◽  
Author(s):  
Stefania Bonazzi ◽  
Massimo Capobianco ◽  
Monica Mirande De Morais ◽  
Anna Garbesi ◽  
Giovanni Gottarelli ◽  
...  

2018 ◽  
Vol 22 (08) ◽  
pp. 693-715 ◽  
Author(s):  
Kohei Ishikawa ◽  
Ayumi Watarai ◽  
Mikio Yasutake ◽  
Kazuchika Ohta

We have synthesized twelve novel discotic columnar liquid crystals based on a phenoxy-group-substituted phthalocyaninato copper(II) complex having the same alkoxy chain of C[Formula: see text]H[Formula: see text]O at different positions in the phenoxy group: the parent compounds {0a~0c-16}and the OH-substituted compounds {3a~3c-16}, the OFBA-substituted compounds {2a~2c-16}and the C[Formula: see text]-substituted dyads {1a~1c-16}. The letters of a, b and c mean substitution positions of C[Formula: see text]H[Formula: see text]O group at [Formula: see text], [Formula: see text] and [Formula: see text], respectively. We have investigated the influence of both substitution position of the alkoxy chains and the kind of terminal groups (OH, OFBA and C[Formula: see text] on the mesomorphism and the helical supramolecular structure, by using DSC, POM and temperature-variable small angle X-ray diffraction measurements. As a result, an additional big peak (Peak H) tends to appear at around 2[Formula: see text] = 1.1[Formula: see text] in the X-ray diffraction patterns only for the dyads {1a~1c-16}but not for the other compounds, {0a~0c-16}, {3a~3c-16}and {2a~2c-16}, regardless of the substitution positions of the alkoxy group. Moreover, we revealed that both the m-substituted derivative 1a-16 and the m,p-substituted derivative 1c-16 gave Peak H, but that only the p-substituted derivative 1b-16 did not give Peak H among these three dyads {1a~1c-16}. From the temperature-variable small angle X-ray diffraction measurements for the m,p-substituted derivative 1c-16 using two different sample preparation methods, we proved that the Peak H originates from a helical pitch of fullerenes. We also pointed out that the m-substituted long alkoxy chains are at least needed to form the helical supramolecular structure in the present (PhO)[Formula: see text]PcM-C[Formula: see text]-based dyads.


2012 ◽  
Vol 54 (10) ◽  
pp. 2073-2082 ◽  
Author(s):  
A. K. Samusev ◽  
I. S. Sinev ◽  
K. B. Samusev ◽  
M. V. Rybin ◽  
A. A. Mistonov ◽  
...  
Keyword(s):  

Polymer ◽  
2001 ◽  
Vol 42 (21) ◽  
pp. 8965-8973 ◽  
Author(s):  
Zhi-Gang Wang ◽  
Xuehui Wang ◽  
Benjamin S. Hsiao ◽  
Saša Andjelić ◽  
Dennis Jamiolkowski ◽  
...  

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