Abstract
In order to investigate the influence of the central linking group and the effect of flexibility on mesomorphism, we have synthesised a newly homologous series 3-(3-butoxyphenyl)-1-(4-n-alkoxy phenyl) prop-2-en-1-one (series-l) consisting of 13 homologues C1–C8, C10, C12, C14, C16 and C18. In the present series, mesophase commences from the C6 homologue. C1–C5 homologues did not exhibit liquid crystalline (LC) property, while C6–C12 homologues exhibited an enantiotropic nematic phase and the rest of the homologues C14–C18 displayed monotropic SmC and nematic mesophase. The transition temperatures of the synthesised compounds were determined by an optical polarising microscopy equipped with a heating stage. All newly synthesised compounds were confirmed by 1H-NMR, 13C-NMR, IR and elemental analysis.
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CITATION STYLE
Sharma, V. S., Vekariya, R. H., Sharma, A. S., & Patel, R. B. (2017). Mesomorphic properties of liquid crystalline compounds with chalconyl central linkage in two phenyl rings. Liquid Crystals Today, 26(3), 46–54. https://doi.org/10.1080/1358314X.2017.1359401
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