Miscibility Studies Indicating a Low Temperature Smectic A Phase in Biaromatic Liquid Crystals with Re-entrant Behaviour

1981 ◽  
Vol 36 (11) ◽  
pp. 1201-1204
Author(s):  
A. Göbl-Wunsch ◽  
G. Heppke ◽  
R. Hopf

Recent reports [1] have shown that compounds of the homologous series of the 4(4-n-alkyloxy- benzoyloxy)-4′-cyanoazobenzenes (Cn; n = 1 - 12), all have a low temperature smectic A phase (SA″). The homologues with alkyl chain length n≧9 exhibit in addition a high temperature smectic A phase (SA′), separated from the first one by a re-entrant nematic phase (N(re)). Homol­ogues of this series were used for miscibility studies with some compounds of the biaromatic liquid crystal series of the 4-cyano-4′-n-alkyloxybiphenyls (n̄ CBP) and of the 4-cyanobenzylidene- 4′-n-alkyloxyanilines (CN · n̄). The phase diagrams studied show that the smectic A phases of biaromatic liquid crystalline nitrile compounds correspond to the high temperature smectic SA′ type and are not miscible with the low temperature SA″ phase. Moreover, the shapes of the transition temperature curves to the SA″ phase indicate a low temperature smectic A phase (SA″) for the biaromatic compounds. This suggests that for biaromatic compounds with re-entrant behaviour, the dependence of liquid crystalline phase sequences on the alkyl chain length is very similar to that of triaromatic compounds.

1980 ◽  
Vol 35 (11) ◽  
pp. 1384-1388 ◽  
Author(s):  
Gerd Heppke ◽  
Reinhard Hopf ◽  
Bernd Kohne ◽  
Klaus Praefcke

The synthesis and the phase transition temperatures of homologous liquid crystalline 4(4-alkyloxybenzoyloxy)-4'-cyanoazobenzenes with alkyl chain length n = 1-12 and n = 16 are reported. All compounds exhibit smectic A phases; the SA phase region being interrupted by a "re-entrant" nematic phase for alkyl chain lengath n ≥ 9.


1976 ◽  
Vol 31 (12) ◽  
pp. 1700-1706 ◽  
Author(s):  
G. Heppke ◽  
F. Schneider ◽  
A. Sterzl

Abstract Investigation The electrical conductivity of the first eight homologous N-(4-n-alkoxybenzylidene)-4'-n-butylanilines is investigated in the isotropic, nematic and smectic phases using the electrolyte tetra-butylammonium picrate. The anisotropy ratio of the electrical conductivity shows pretransition behaviour in the nematic phases close to the transition to the smectic phases. This behaviour be-comes more distinct with increasing alkyl chain length of the liquid crystals. In the nematic phase of 40·4 an anisotropy ratio of V = 0.55 is determined at the lowest electrolyte concentration. Values of about V=0.05 were found in the smectic phases of several homologues. In the nematic phase, an increase of the electrolyte concentration effects an increase of the anisotropy ratio. This effect is systematically enhanced with increasing alkyl chain length.


1975 ◽  
Vol 30 (3) ◽  
pp. 316-322 ◽  
Author(s):  
G. Heppke ◽  
F. Schneider

The effect of temperature and concentration of the added electrolyte tetrabutylammoniumpicrate on the electric conductivity of homologous 4,4′-di-n-alkoxyazoxybenzenes (C1 to C8) in their nematic phase is investigated. In general an increase of the alkyl chain length results in a decrease of the ratio of anisotropy x∥/x⊥. At the lowest temperature of the nematic phase values between 1,6 (C2) and 0,45 (C8) are obtained. This behaviour can be explained by the formation of cybotactic groups with a smectic structure. Increasing the electrolyte concentration reduces the ratio of anisotropy for short alkyl chains, whereas for long chains the ratio rapidly increases.


1981 ◽  
Vol 10 (2) ◽  
pp. 269-272 ◽  
Author(s):  
Mitsuhiro Koden ◽  
Tadao Yagyu ◽  
Shunsuke Takenaka ◽  
Hikaru Terauchi ◽  
Shigekazu Kusabayashi

2014 ◽  
Vol 699 ◽  
pp. 233-238 ◽  
Author(s):  
Kok Leei Foo ◽  
Sie Tiong Ha

A series of new rod-shaped liquid crystal, 6-methoxy-2-(4-alkyloxybenzylidenamino) benzothiazoles possessingeven numbers of carbon atoms at the alkyloxy chain (CnH2n+1O-, n = 10, 12, 14, 16, 18) are prepared and characterized. The phase behaviour of these new compounds was studied by differential scanning calorimetry and polarising optical microscopy. All members exhibited mesophase. Influence of alkyl chain length on the mesomorphic properties was studied. Enantiotropic nematic phase was identified in all the members except for n = 18. Lower member (n = 10) exhibited monotropic (metastable) smectic A phase. The enantiotropic smectic A phase was observed fromn-dodecyloxy derivatives onward to the last homologous synthesized.


1998 ◽  
Vol 10 (1) ◽  
pp. 147-153 ◽  
Author(s):  
M Tanaka ◽  
M Konda ◽  
M Miyamoto ◽  
Y Kimura ◽  
A Yamaguchi

Anomalous solid structures formed by a thermotropic liquid crystalline polyimide (PI-LC) were investigated by thermal analysis, polarized light microscopy and x-ray analysis. It was revealed that PI-LC should undergo a phase transition from the crystalline to the isotropic phase through the smectic or nematic phase in the temperature range 277–300 °C. The PI-LC filament extruded at 280 °C, at which temperature the polymer was in liquid crystalline phase, was formed to have a structure similar to the smectic C phase, while that extruded and melt-drawn at 310 °C, at which temperature the polymer was in the isotropic phase, had a structure similar to the smectic A phase.


1994 ◽  
Vol 49 (4-5) ◽  
pp. 552-558 ◽  
Author(s):  
S. Urban ◽  
T. Brückert ◽  
A. Würflinger

Abstract Dielectric relaxation studies of 4-n-octyl-4'-cyanobiphenyl (8 CB) were performed in the pressure range 0.1 -120 MPa, the frequency range 1 kHz -13 MHz and the temperature range 295-331 K. The dielectric behaviour of 8C B in the nematic phase is similar to that of 5 CB, 6 CB and 7 CB. In particular, the activation enthalpy decreases with increasing pressure and the activation volume decreases with increasing temperature in the nematic phase. In the smectic A phase of 8 CB both these parameters are markedly lower and show opposite pressure and temperature dependencies. We tentatively interpret these effects as a result of breaking of the dipole-dipole correlations which manifests itself differently in these liquid crystalline phases.


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