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dc.contributor.authorCasado-Cordon, Juan 
dc.date.accessioned2017-07-05T07:45:25Z
dc.date.available2017-07-05T07:45:25Z
dc.date.created2017
dc.date.issued2017-07-05
dc.identifier.urihttp://hdl.handle.net/10630/14106
dc.description.abstractOligothiophenes are π-conjugated compounds made by concatenation of thiophenes. [1] Due to the low aromaticity of thiophene, inter-ring π-electron delocalization is favored which has strong implication in their electro-optical properties and in their applications in organic electronic devices. [2] In despite of the plenty of oligothiophenes reported so far, new derivatives are welcome which would enhance these properties in regard of their exploitation in new devices. [3] In this presentation, we will show our latest development of oligothiophenes based on the thieno[3,4-c]pyrrole-4,6-dione (TPD, See Figure 1) units, and with different size, from a dimer to a hexamer. In particular, thieno[3,4-c]pyrrole-4,6-dione (TPD) motifs are of great interest due to their high power conversion efficiency (PCE) and its moderate short-circuit current (Jsc) in organic photovoltaic (OPV) devices, [4] when implemented in donor-acceptor polymers, making them excellent candidates for their application in polymer solar cells.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.subjectTiofenoes_ES
dc.subjectEspectroscopía Ramanes_ES
dc.subject.otherOligotiofenoses_ES
dc.titleOligomers of thieno[3,4-c]pyrrole-4,6-dione: Raman spectraes_ES
dc.typeinfo:eu-repo/semantics/conferenceObjectes_ES
dc.centroFacultad de Cienciases_ES
dc.relation.eventtitleBienal de Químicaes_ES
dc.relation.eventplaceSitges, Barcelonaes_ES
dc.relation.eventdate25 de junio de 2017es_ES
dc.cclicenseby-nc-ndes_ES


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