The chemistry of liquid crystals

The nature of the liquid crystal phases formed by different compounds and the thermal and other physical characteristics of these phases are strongly affected by the stereochemistry and structure of the molecules. Precise structure-property correlations of an embracing nature cannot yet be quantified, but even a qualitative understanding of such relations is desirable from many standpoints, including that of the achievement of still better liquid crystal materials for the ever widening range of applications that is emerging for these ordered but fluid systems. By means of a range of selected examples, an attempt is made to illustrate not only those areas where generalizations seem possible, but also others wherein the properties of the materials are much more difficult to understand, to such an extent that doubt must be cast on at least some theoretical concepts of the liquid crystal state.

Author(s):  
H. N. W. Lekkerkerker ◽  
G. J. Vroege

A review is given of the field of mineral colloidal liquid crystals : liquid crystal phases formed by individual mineral particles within colloidal suspensions. Starting from their discovery in the 1920s, we discuss developments on the levels of both fundamentals and applications. We conclude by highlighting some promising results from recent years, which may point the way towards future developments.


1996 ◽  
Vol 425 ◽  
Author(s):  
X. Li ◽  
R. M. Hill ◽  
L. E. Scriven ◽  
H. T. Davis

AbstractPolyethylene trisiloxane surfactants M(D′En)M (n=6, 8, 10, 12) self assemble into sheet-like structure and form various lyotropic cubic, hexagonal and lamellar liquid crystal phases in ternary trisiloxane surfactant - silicone oil - water systems. Small angle X-ray scattering (SAXS) was used to identify and characterize the liquid crystal phases. Cyclic octamethylcyclotetrasiloxane (D4), decamethyl-cyclopentasiloxane(D5) and short linear decamethyltetrasiloxane (MD2M) silicone oils facilitate the formation of liquid crystals. The structures in liquid crystals (LC) progress from zero curvature lamellar liquid crystals to higher curvature cubic liquid crystals with increasing the surfactant hydrophilic head group size. The effects of surfactant and oil concentration on the lamellar bilayer thickness and molecular packing were studied with small angle X-ray scattering.


1994 ◽  
Vol 08 (11) ◽  
pp. 677-686 ◽  
Author(s):  
A. A. ISAYEV ◽  
M. Yu. KOVALEVSKY ◽  
S. V. PELETMINSKY

Dynamics of classical continuum and of some liquid crystal phases are considered in the Hamiltonian approach. Poisson brackets for variables of liquid crystals are obtained as subalgebras of the general algebra of continuum dynamic variables.


2013 ◽  
Vol 27 (15) ◽  
pp. 1362001 ◽  
Author(s):  
KUN YANG

Superfluidity in fermionic systems originates from pairing of fermions, and Bose condensation of these Cooper pairs. The Cooper pairs are usually made of fermions of different species; thus the most favorable situation for pairing and superfluidity is when the two species of fermions that form pairs have the same density. This paper studies the possible superfluid states when the two pairing species have different densities, and show that the resultant states have remarkable similarities to the phases of liquid crystals. This enables us to provide a unified description of the possible pairing phases and understand the phase transitions among them.


2011 ◽  
Vol 1 ◽  
pp. 25-31
Author(s):  
Krishna P. Sigdel

Liquid crystal is a delicate and beautiful phase of matter showing the order in between liquid and crystals. They have different phases and phase transitions. A powerful tool called AC calorimetry can be used to characterize the different phases and phase transitions. In this article, use of ac-calorimetry technique in liquid crystal phases and phase transitions is described.Key words: Liquid and crystals; AC calorimetryThe Himalayan Physics Vol.1, No.1, May, 2010Page: 25-31Uploaded Date: 28 July, 2011


1986 ◽  
Vol 41 (8) ◽  
pp. 1011-1014 ◽  
Author(s):  
W. Calaminus ◽  
F. Vögtle ◽  
R. Eidenschink

AbstractSeveral 3 .11-disubstituted dispiro[5.1.5.1]tetradecane-7,14-dions were prepared and the cis/trans-isomers were separated. The trans -stereoisomers were converted into the gem-dihalide ketones and mono- and dithioketones. The phase transfer temperatures were determined. Liquid crystal phases were observed.


2003 ◽  
Vol 297 (1) ◽  
pp. 91-105
Author(s):  
B. Żywucki ◽  
W. Kuczyński ◽  
J. Małecki

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