Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/7526
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dc.contributor.authorMohammad, AbdulKarim-Talaq-
dc.contributor.authorMohammed, Hameed Madlool-
dc.contributor.authorSrinivasa, H.T.-
dc.contributor.authorAhmed Ameen, Wissam-
dc.date.accessioned2020-09-11T06:00:36Z-
dc.date.available2020-09-11T06:00:36Z-
dc.date.issued2020-09-
dc.identifier.citationJournal of Molecular Liquids, 2020, Vol.314, p113782en_US
dc.identifier.issn0167-7322-
dc.identifier.urihttp://hdl.handle.net/2289/7526-
dc.descriptionRestricted Access.en_US
dc.description.abstractThe 2, 6-diaminopyridine was symmetrically substituted with coumarins from a lateral side of the molecules. All the molecules characterized by standard spectroscopic methods such as infrared spectroscopy, and nuclear magnetic resonance spectroscopy techniques. Mesomorphic properties are evaluated by the differential scanning calorimetry and the polarized optical microscope. The measurements show that the lower members did not favour liquid crystal formation, while higher members are exhibiting liquid crystalline, namely Nematic mesophase. The DFT computations manifest the nature of liquid crystal geometrical aspects.en_US
dc.language.isoenen_US
dc.publisherElsevier B.Ven_US
dc.relation.urihttps://doi.org/10.1016/j.molliq.2020.113782en_US
dc.rights2020 Elsevier B.V.en_US
dc.subject2,6-diaminopyridineen_US
dc.subjectCoumarinen_US
dc.subjectHeterocyclesen_US
dc.subjectAzomethaneen_US
dc.subjectLiquid crystalsen_US
dc.subjectNematic mesophaseen_US
dc.titleCoumarin substituted symmetric diaminopyridine molecules: Synthesis, mesomorphic characterizations and DFT studiesen_US
dc.typeArticleen_US
dc.additionalSupplementary Information Availableen_US
Appears in Collections:Research Papers (SCM)

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