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dc.contributor.authorGarcía-Frutos, Eva M.-
dc.contributor.authorCoya, Carmen-
dc.contributor.authorGutiérrez-Puebla, Enrique-
dc.contributor.authorMonge, M. Ángeles-
dc.contributor.authorAndrés, Alicia de-
dc.contributor.authorGómez-Lor, Berta-
dc.date.accessioned2013-11-12T10:03:01Z-
dc.date.available2013-11-12T10:03:01Z-
dc.date.issued2010-08-
dc.identifier.citationProceedings of SPIE 7778: 777806 (2010)es_ES
dc.identifier.issn1996-756X-
dc.identifier.urihttp://hdl.handle.net/10261/86322-
dc.descriptionTrabajo presentado como comunicación al "IX Organic Field-Effect Transistors" celebrado en San Diego (USA) en Agosto del 2010.es_ES
dc.description.abstractWe introduce a new family of stable high-mobility organic π-type semiconductors based on the electron-rich 10,15- dihydro-5H-diindolo[3,2-a:3',2'-c]carbazole (triindole) extended π-conjugated system. This platform tends to form columnar stacks of the aromatic cores maximizing π-orbital overlap between adjacent molecules, thus paving the way for the one-dimensional migration of charge carriers along the columns. In addition these compounds have two different types of positions that can be functionalized independently offering the possibility of tuning their electronic properties as well as their morphology through chemical functionalization. The integration of the optimized triindole derivatives into solution processed devices as active layer is explored in this work.es_ES
dc.description.sponsorshipFinancial support from the MEC (CTQ2007-65683/BQU and S2009/MAT-1756/CAM are gratefully acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherSociety of Photo-Optical Instrumentation Engineerses_ES
dc.relationS2009/MAT-1756 PHAMA-
dc.rightsopenAccesses_ES
dc.titleNew triindole-based organic semiconductors: structure-property relationshipses_ES
dc.typeArtículoes_ES
dc.identifier.doi10.1117/12.860553-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1117/12.860553es_ES
dc.identifier.e-issn0277-786X-
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