Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/6989
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dc.contributor.authorVadivel, Marichandran-
dc.contributor.authorSiva Kumar, Irla-
dc.contributor.authorSwamynathan, K.-
dc.contributor.authorRaghunathan, V.A.-
dc.contributor.authorKumar, Sandeep-
dc.date.accessioned2018-08-22T13:40:19Z-
dc.date.available2018-08-22T13:40:19Z-
dc.date.issued2018-08-18-
dc.identifier.citationChemistry Select, 2018, Vol.3, p8763-8769en_US
dc.identifier.issn2365-6549 (Online)-
dc.identifier.urihttp://hdl.handle.net/2289/6989-
dc.descriptionOpen Accessen_US
dc.description.abstractTriphenylenes have been frontrunner in discotic liquid crystalline materials since their discovery. They possess great richness of mesomorphism in them. Chemists have been exploring this potential quite often by some substitutions in the core or periphery of the triphenylene molecule. In this current report, we extended the triphenylene ring system by fusing with nitrogen and studied their mesomorphic and optical properties. Four new compounds are prepared using Pictet‐Spengler cyclization of hexaalkoxytriphenylene‐1‐amine with various aldehydes. All the new compounds are well characterized using spectral and elemental analysis. Their mesomorphic properties are evaluated using polarizing optical microscopy, differential scanning calorimetry and X‐ray diffractometry. These derivatives showed columnar hexagonal phase with great promise for further studies.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.urihttps://doi.org/10.1002/slct.201801738en_US
dc.rights2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.titleNovel Annulated Triphenylene Discotic Liquid CrystalsGenerated by Pictet-Spengler Cyclizationen_US
dc.typeArticleen_US
dc.additionalSupporting information for this article is availableen_US
Appears in Collections:Research Papers (SCM)

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