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dc.contributor.authorBruchlos, Kirsten
dc.contributor.authorMalacrida, Claudia
dc.contributor.authorArnaboldi, serena
dc.contributor.authorRomana Mussini, Patrizia
dc.contributor.authorPanigati, Monica
dc.contributor.authorLópez Navarrete, Juan T.
dc.contributor.authorRuiz Delgado, M. Carmen
dc.contributor.authorAppoloni, Giulio
dc.contributor.authorLudwigs, Sabine
dc.contributor.authorGámez-Valenzuela, Sergio
dc.contributor.authorBenincori, Tiziana
dc.contributor.authorGoll, Miriam
dc.date.accessioned2018-12-18T11:48:49Z
dc.date.available2018-12-18T11:48:49Z
dc.date.created2018
dc.date.issued2018-12-18
dc.identifier.urihttps://hdl.handle.net/10630/17085
dc.description.abstractIn the last years, conjugated oligothiophene macrocycles have attracted increasing scientific interest due to some peculiar properties related to their cyclic structure [1-3]. T. Benincori et al. synthesized the 2,2′-bis(2,2′-bithiophene-5-yl)-3,3′-bithianaphthene nicknamed BT2T4 (Figure 1) that represents the first member of a new class of chiral oligothiophenes in which chirality results from a tailored torsion produced in the polyconjugated backbone and not from the presence of stereogenic centres, external to it. Interestingly, the FeCl3 oxidation of the enantiopure BT2T4 produce a mixture of chiral macrocycles, like dimers and trimers. [4] Recently, also thanks to DFT and TD-DFT calculations, we have studied the new monomer BT2E4 in order to investigate the role of the insertion of 3,4-ethylenedioxythiophene (EDOT) units on the electronic and molecular properties of neutral and charged monomer and oligomer species. Furthermore, the electroactive films were evaluated by cyclic voltammetry (CV), UV/vis spectroelectrochemistry and CV coupled with in-situ conductance measurements. [5]en_US
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Techen_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMatemáticasen_US
dc.subject.otherConjugated materialsen_US
dc.subject.otherChiral oligothiophenesen_US
dc.subject.otherDft calculationsen_US
dc.titleTheoretical insights into the Electronic and Structural Properties of New, Low-band Gap Inherently Chiral Ethylendioxythiophene-based Oligothiopheneen_US
dc.typeinfo:eu-repo/semantics/conferenceObjecten_US
dc.centroFacultad de Cienciasen_US
dc.relation.eventtitlepi-Figuration Japan-Spain Symposiumen_US
dc.relation.eventplaceMadriden_US
dc.relation.eventdate23-25 Noviembre 2018en_US
dc.rights.ccAttribution-NonCommercial-NoDerivatives 4.0 Internacional*


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