Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/7827
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dc.contributor.authorBhat, Vanishree S.-
dc.contributor.authorRaghunathan, V.A.-
dc.contributor.authorKumar, Sandeep-
dc.date.accessioned2021-10-08T06:29:38Z-
dc.date.available2021-10-08T06:29:38Z-
dc.date.issued2021-10-
dc.identifier.citationJournal of Molecular Liquids, 2021, Vol. 340, Article Number 117219en_US
dc.identifier.issn0167-7322-
dc.identifier.urihttp://hdl.handle.net/2289/7827-
dc.descriptionRestricted Access.en_US
dc.description.abstractThe steroidal derivatives are found to be extremely good mesogens since their inception. Because of their inherent chirality, they have the potential to induce a wide variety of liquid crystalline phases, including frustrated phases depending upon the structure of the steroidal skeleton and the substituents attached. In this report, a series of novel monoalkoxy and dialkoxy benzoate derivatives of ergosterol and a few monoalkoxy derivatives of stigmasterol have been synthesized and their mesomorphic property has been investigated. The derivatives exhibited various mesophases including SmA, SmC*, N*, TGB and blue phases. Also, the gelation ability of some of these derivatives with various organic solvents has been examined. Furthermore, the mesomorphism of these derivatives has been compared with the analogous cholesteryl counterparts.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.urihttps://doi.org/10.1016/j.molliq.2021.117219en_US
dc.rights2021 Elsevier B.V.en_US
dc.titleSynthesis and mesomorphic characterization of some novel steroidal mesogens: A structure-property correlationen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (SCM)

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