Molecular shape and volume effects on the orientational ordering of simple liquid crystals

1977 ◽  
Vol 67 (12) ◽  
pp. 5795-5801 ◽  
Author(s):  
Barbara A. Baron ◽  
William M. Gelbart
1990 ◽  
Vol 8 (5) ◽  
pp. 687-699 ◽  
Author(s):  
Wolfgang Richter ◽  
Dirk Reimer ◽  
B. M. Fung ◽  
R. J. Twieg ◽  
K. Betterton

1999 ◽  
Vol 60 (5) ◽  
pp. 5584-5590 ◽  
Author(s):  
Jianling Xu ◽  
Robin L. B. Selinger ◽  
Jonathan V. Selinger ◽  
B. R. Ratna ◽  
R. Shashidhar

1991 ◽  
Vol 94 (4) ◽  
pp. 2758-2772 ◽  
Author(s):  
Demetri J. Photinos ◽  
Edward T. Samulski ◽  
Hirokazu Toriumi

2014 ◽  
Vol 18 (10n11) ◽  
pp. 856-868 ◽  
Author(s):  
Miho Yoshioka ◽  
Kazuchika Ohta ◽  
Yohei Miwa ◽  
Shoichi Kutsumizu ◽  
Mikio Yasutake

We have synthesized a novel type of donor–acceptor liquid crystalline material, phthalocyanine-fullerene ( Pc - C 60) dyad, [m,p,m′-( C 14 O )3 PhO ]6 PcCu - C 60 (7), and the Pc precursors, [m,p,m′-( C 14 O )3 PhO ]6 PcCu - OFBA (6) and [m,p,m′-( C 14 O )3 PhO ]6 PcCu - OH (5), and established their mesomorphism by using a polarizing optical microscope, a differential scanning calorimeter and a small angle X-ray diffractometer. Very interestingly, their corresponding previous parent Pc derivative, [m,p,m′-( C 14 O )3 PhO ]8 PcCu (4), shows a very wide temperature region ca. 90°C of a bicontinuous Cub(Pn3m) mesophase, whereas the present children Pc precursors (5 and 6) and Pc- C 60 dyad 7 show not the Cub mesophase but a Colho mesophase. It is also noteworthy that the staking distance in the Colho mesophase of the Pc- C 60 dyad 7was a very big value of ca. 9.1 Å, which is the biggest in discotic liquid crystals to our best knowledge. It may be originated from the biggest excluded volume caused by thermal fluctuation of peripheral long alkoxy chains at m, m′-positions. The excluded volume caused by thermal fluctuation of the peripheral long chains is so big that the molecular shape of the Pc derivative 4 and the Pc- C 60 dyad 7 very resembles a flat pumpkin.


1990 ◽  
Vol 68 (6) ◽  
pp. 875-880 ◽  
Author(s):  
C. T. Yim ◽  
D. F. R. Gllson

The orientational order parameters of benzonitrile and o-, m-, and p-dicyanobenzene, monobromo- and p-dibromobenzene, and p-benzoquinone, dissolved in two nematic solvents, 1132 and EBBA, have been measured as functions of temperature, and used to determine the potential energy parameters for each solute–solvent pair. These parameters have been correlated with a short-range interaction based upon a shape and size function of the solute molecule and a long-range contribution due to the interaction between the solute molecular quadrupole moment and the average electric field gradient. Keywords: nematic liquid crystals, orientational ordering of solutes.


1982 ◽  
Vol 46 (3) ◽  
pp. 659-664 ◽  
Author(s):  
J.W. Emsley ◽  
G.R. Luckhurst ◽  
B.A. Timimi

1992 ◽  
Vol 76 (4) ◽  
pp. 951-977 ◽  
Author(s):  
R.W. Date ◽  
I.W. Hamley ◽  
G.R. Luckhurst ◽  
J.M. Seddon ◽  
R.M. Richardson

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