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dc.contributor.authorGarcía-Frutos, Eva M.-
dc.contributor.authorOmenat, Ana-
dc.contributor.authorBarberá, Joaquín-
dc.contributor.authorSerrano, José Luis-
dc.contributor.authorGómez-Lor, Berta-
dc.date.accessioned2012-07-05T07:31:46Z-
dc.date.available2012-07-05T07:31:46Z-
dc.date.issued2011-
dc.identifierdoi: 10.1039/C0JM04395H-
dc.identifierissn: 0959-9428-
dc.identifiere-issn: 1364-5501-
dc.identifier.citationJournal of Materials Chemistry 21(19): 6831-6836 (2011)-
dc.identifier.urihttp://hdl.handle.net/10261/52812-
dc.description.abstractNew π-extended discotic liquid crystals based on heptacyclic triindole have been synthesized and their mesomorphic behaviour investigated. The synthesis of π-extended compounds was carried out by oxidative cyclodehydrogenation of differently substituted star-shaped hexaaryltriindoles to afford the planar derivatives with an extended core. Extending the conjugation in these materials results in a significant increase in the order and range of the mesophases. The influence of the peripherally attached groups in the mesomorphic and electronic properties offers a great opportunity to further tune the properties of these compounds intended to their incorporation in devices. © 2011 The Royal Society of Chemistry.-
dc.description.sponsorshipFinancial support from the MEC CTQ 2009-09030, CTQ2010- 18813 and the CAM (Project S2009/MAT-1756/CAM), is gratefully acknowledged.-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry (UK)-
dc.rightsclosedAccess-
dc.titleHighly ordered π-extended discotic liquid-crystalline triindoles-
dc.typeartículo-
dc.identifier.doi10.1039/C0JM04395H-
dc.date.updated2012-07-05T07:31:46Z-
dc.description.versionPeer Reviewed-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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