Gelişmiş Arama

Basit öğe kaydını göster

dc.contributor.authorTahaoǧlu, Duygu
dc.contributor.authorUsta, Hakan
dc.contributor.authorAlkan, Fahri
dc.date.accessioned2022-07-21T06:44:30Z
dc.date.available2022-07-21T06:44:30Z
dc.date.issued2022en_US
dc.identifier.issn10895639
dc.identifier.urihttps://doi.org/10.1021/acs.jpca.2c02435?urlappend=%3Fref%3DPDF&jav=VoR&rel=cite-as
dc.identifier.urihttps://hdl.handle.net/20.500.12573/1321
dc.description.abstractIn this study, we performed a detailed investigation of the S1 potential energy surface (PES) of o-carborane-anthracene (o-CB-Ant) with respect to the C-C bond length on o-CB and the dihedral angle between o-CB and Ant moieties. The effects of different substituents (F, Cl, CN, and OH) on carbon- or boron-substituted o-CB, along with a π-extended acene-based fluorophore, pentacene, on the nature and energetics of S1 → S0 transitions are evaluated. Our results show the presence of a non-emissive S1 state with an almost pure charge transfer (CT) character for all systems as a result of significant C-C bond elongation (C-C = 2.50-2.56 Å) on o-CB. In the case of unsubstituted o-CB-Ant, the adiabatic energy of this CT state corresponds to the global minimum on the S1 PES, which suggests that the CT state could be involved in emission quenching. Despite large deformations on the o-CB geometry, predicted energy barriers are quite reasonable (0.3-0.4 eV), and the C-C bond elongation can even occur without a noticeable energy penalty for certain conformations. With substitution, it is shown that the dark CT state becomes even more energetically favorable when the substituent shows -M effects (e.g., -CN), whereas substituents showing +M effects (e.g., -OH) can result in an energy increase for the CT state, especially for partially stretched C-C bond lengths. It is also shown that the relative energy of the CT state on the PES depends strongly on the LUMO level of the fluorophore as this state is found to be energetically less favorable compared to other conformations when anthracene is replaced with π-extended pentacene. To our knowledge, this study shows a unique example of a detailed theoretical analysis on the PES of the S1 state in o-CB-fluorophore systems with respect to substituents or fluorophore energy levels. Our findings could guide future experimental work in emissive o-CB-fluorophore systems and their sensing/optoelectronic applications.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionof10.1021/acs.jpca.2c02435en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBond lengthen_US
dc.subjectCharge transferen_US
dc.subjectChlorine compoundsen_US
dc.subjectDihedral angleen_US
dc.subjectFluorophoresen_US
dc.subjectPotential energyen_US
dc.subjectQuantum chemistryen_US
dc.titleRevisiting the Role of Charge Transfer in the Emission Properties of Carborane-Fluorophore Systems: A TDDFT Investigationen_US
dc.typearticleen_US
dc.contributor.departmentAGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümüen_US
dc.contributor.authorID0000-0002-0618-1979en_US
dc.contributor.authorID0000-0002-5009-5197
dc.contributor.institutionauthorTahaoğlu, Duygu
dc.contributor.institutionauthorUsta, Hakan
dc.contributor.institutionauthorAlkan, Fahri
dc.identifier.volume126en_US
dc.identifier.issue26en_US
dc.identifier.startpage4199en_US
dc.identifier.endpage4210en_US
dc.relation.journalAmerican Chemical Societyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Bu öğenin dosyaları:

Thumbnail

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster