Revisiting the Role of Charge Transfer in the Emission Properties of Carborane-Fluorophore Systems: A TDDFT Investigation

dc.contributor.author Tahaoǧlu, Duygu
dc.contributor.author Usta, Hakan
dc.contributor.author Alkan, Fahri
dc.contributor.authorID 0000-0002-0618-1979 en_US
dc.contributor.authorID 0000-0002-5009-5197
dc.contributor.department AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü en_US
dc.contributor.institutionauthor Tahaoğlu, Duygu
dc.contributor.institutionauthor Usta, Hakan
dc.contributor.institutionauthor Alkan, Fahri
dc.date.accessioned 2022-07-21T06:44:30Z
dc.date.available 2022-07-21T06:44:30Z
dc.date.issued 2022 en_US
dc.description.abstract In 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.identifier.endpage 4210 en_US
dc.identifier.issn 10895639
dc.identifier.issue 26 en_US
dc.identifier.startpage 4199 en_US
dc.identifier.uri https://doi.org/10.1021/acs.jpca.2c02435?urlappend=%3Fref%3DPDF&jav=VoR&rel=cite-as
dc.identifier.uri https://hdl.handle.net/20.500.12573/1321
dc.identifier.volume 126 en_US
dc.language.iso eng en_US
dc.publisher American Chemical Society en_US
dc.relation.isversionof 10.1021/acs.jpca.2c02435 en_US
dc.relation.journal American Chemical Society en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Bond length en_US
dc.subject Charge transfer en_US
dc.subject Chlorine compounds en_US
dc.subject Dihedral angle en_US
dc.subject Fluorophores en_US
dc.subject Potential energy en_US
dc.subject Quantum chemistry en_US
dc.title Revisiting the Role of Charge Transfer in the Emission Properties of Carborane-Fluorophore Systems: A TDDFT Investigation en_US
dc.type article en_US

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