Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/6594
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dc.contributor.authorMohammad, AbdulKarim-Talaq-
dc.contributor.authorSrinivasa, H.T.-
dc.contributor.authorHariprasad, S.-
dc.contributor.authorYeap, Guan-Yeow-
dc.date.accessioned2017-01-16T11:16:01Z-
dc.date.available2017-01-16T11:16:01Z-
dc.date.issued2016-04-
dc.identifier.citationLiquid Crystals, 2016, Vol.43, p 1174-1183en_US
dc.identifier.issn0267-8292-
dc.identifier.issn1366-5855 (Online)-
dc.identifier.urihttp://hdl.handle.net/2289/6594-
dc.descriptionRestricted Access.en_US
dc.description.abstractNew substituted derivatives of 5-vinyl-1,3-dimethylbarbituric acid were synthesised and evaluated for liquid crystal properties. Two sets of molecules were prepared. One end of all the molecules possesses the 1,3-dimethylbarbituric core. The first set comprises biphenyl ethers, 4a–n and the second set biphenyl esters, 5a–g. Liquid crystalline properties were investigated by POM and DSC techniques. All the compounds exhibited enantiotropic smectic A and nematic mesophases. The LC properties were found to depend on the spacer and terminal alkoxy- chain and alkoxy- ester moiety of the molecules. Smaller alkyl chain members showed a smectic phase, while higher alkyl chain members showed a nematic phase.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.relation.urihttp://dx.doi.org/10.1080/02678292.2016.1162857en_US
dc.rights2016 Taylor & Francisen_US
dc.titleNew mesogenic compounds possessing a biphenyl ester and ether moiety comprising 1,3-dimethylbarbituric acid: synthesis, characterisation and mesomorphic studiesen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (SCM)

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