1997
DOI: 10.1080/026782997207704
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Lateral substitution in nematic systems

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Cited by 34 publications
(16 citation statements)
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“…The methyl lateral group on the imine linkage decreases the S C phase stability and this also affects the stability of nematic phase, which results in a reduced N-I range compared to series-B [47].…”
Section: -{4-[(24-dihydroxybenzylidene) Amino] Phenyl}-3-(4-alkoxypmentioning
confidence: 96%
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“…The methyl lateral group on the imine linkage decreases the S C phase stability and this also affects the stability of nematic phase, which results in a reduced N-I range compared to series-B [47].…”
Section: -{4-[(24-dihydroxybenzylidene) Amino] Phenyl}-3-(4-alkoxypmentioning
confidence: 96%
“…In addition, terminal and lateral subtituents also play a vital role in imparting liquid crystallinity to potentially mesogenic compounds [15][16][17][18][19]. The correlation between chemical structure and mesomorphic properties is one of the most important problems in liquid crystals science [20].…”
Section: Introductionmentioning
confidence: 99%
“…[30][31][32][33] (B) Lateral substituted p-terphenyls, p-quaterphenyls and p-quinquephenyls (10-17), which, as our investigations have shown [34][35][36][37], are easily formed in a one-stage procedure from the corresponding 3,6-disubstituted cyclohex-2-enones (I.3) (Scheme 7).…”
Section: Synthesis Of Liquid-crystalline and Anisotropic Compoundsmentioning
confidence: 94%
“…In this case, we can say that the axial NCS or CONCS substitutions work as the lateral ones, which usually reduce the intermolecular interactions and consequently, the clearing points [87]. The position of the axial substituent NCS in the molecular core of liquid crystals plays an important role in their mesomorphic properties: the axial substituent A in the middle of the core gives more significant reduction of the melting and clearing points in comparison with those of the axial substituent B at the terminal position of the core (compounds 10-1, 10-2).…”
Section: Axial Substitutionmentioning
confidence: 99%
“…It can be explained by the largest size of the NCS group among lateral substituents under consideration [4]. Such a large substituent would reduce the intermolecular interactions and destroy the liquid crystal packing in the most significant way [87].…”
Section: Lateral Substitutionmentioning
confidence: 99%