Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2099
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dc.contributor.authorPal, S.K.-
dc.date.accessioned2020-11-24T05:15:34Z-
dc.date.available2020-11-24T05:15:34Z-
dc.date.issued2019-
dc.identifier.citationACS Omega, 4(4),pp. 7711-7722.en_US
dc.identifier.otherhttps://doi.org/10.1021/acsomega.9b00425-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsomega.9b00425-
dc.identifier.urihttp://hdl.handle.net/123456789/2099-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractWe report here the synthesis and thermotropic properties of novel short-core hockey stick-shaped liquid crystalline molecules based on the 1,3,4-thiadiazole core. Polar switching behavior is observed in the cybotactic nematic and smectic mesophases for the bent-core thiadiazole derivatives. The presence of the lateral methoxy moiety in the outer phenyl ring of the four-ring molecules facilitates the formation of spontaneous ordering in the nematic phase observed via X-ray diffraction measurements. Anomalous temperature dependence of spontaneous polarization on cooling is explained by the possible antiferroelectric packing of the molecules that require higher electric field for switching. The compounds exhibited a strong absorption band at ∼356 nm and a blue emission band at ∼445 nm with a good quantum yield of φf ∼0.39. The mega Stokes shift is observed and depends on the nature of the solvent.en_US
dc.language.isoenen_US
dc.publisherACS Publicationsen_US
dc.subjectThermotropic propertiesen_US
dc.subjectNovel short-coreen_US
dc.subjectCrystalline moleculesen_US
dc.titlePolar Switching and Cybotactic Nematic Ordering in 1,3,4-Thiadiazole-Based Short-Core Hockey Stick-Shaped Fluorescent Liquid Crystalsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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