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dc.contributor.authorLópez Espejo, Guzmán
dc.date.accessioned2017-07-07T10:52:14Z
dc.date.available2017-07-07T10:52:14Z
dc.date.created2017
dc.date.issued2017-07-07
dc.identifier.urihttp://hdl.handle.net/10630/14154
dc.description.abstractA brand new series of thiophene bridged bis-naphthalimides has been obtained. These molecules can act as semiconductors and have an even or an odd number of thiophene rings, so that they vary their molecular dipole moments, which have some influence in their molecular packing. With theoretical calculations, the stability of their derivative -dimers (either parallel or antiparallel) has been elucidated. Results indicate a face-to-face parallel molecular packing for these semiconductors, regardless of their estimated molecular dipole moments. The results obtained are reasonable regarding the field-effect mobilities that have been measured in a bottom-gate topcontact transistor architecture; no direct correlation between performances and dipolar moments is shown. Ambipolar field-effect mobilities have been recorded for the systems of greatest length (2NDI-4T and 2NDI-5T).es_ES
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.es_ES
dc.language.isoenges_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectEspectroscopía Ramanes_ES
dc.subjectTiofenoes_ES
dc.subject.otherRaman spectroscopyes_ES
dc.subject.otherOligothiopheneses_ES
dc.titleThiophene-bridged bis-naphthalimidic structures (even and odd) with n-type and ambipolar ofets applicationses_ES
dc.typeinfo:eu-repo/semantics/conferenceObjectes_ES
dc.centroFacultad de Cienciases_ES
dc.relation.eventtitleBienal de Química de la RSEQes_ES
dc.relation.eventplaceSitges, Barcelonaes_ES
dc.relation.eventdate25 de junio de 2017es_ES
dc.cclicenseby-nc-ndes_ES


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