Revisiting the Role of Charge Transfer in the Emission Properties of Carborane-Fluorophore Systems: A TDDFT Investigation
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Date
2022
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Amer Chemical Soc
Open Access Color
HYBRID
Green Open Access
Yes
OpenAIRE Downloads
70
OpenAIRE Views
126
Publicly Funded
No
Abstract
In this study, we performed a detailed investigation of the S-1 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 pi-extended acene-based fluorophore, pentacene, on the nature and energetics of S-1 -> S-0 transitions are evaluated. Our results show the presence of a non-emissive S-1 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 angstrom) 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 S-1 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 pi-extended pentacene. To our knowledge, this study shows a unique example of a detailed theoretical analysis on the PES of the S-1 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.
Description
Alkan, Fahri/0000-0002-4046-9044;
ORCID
Keywords
Charge transfer, Potential energy, Dihedral angle, Fluorophores, Bond length, Quantum chemistry, Chlorine compounds
Turkish CoHE Thesis Center URL
Fields of Science
01 natural sciences, 0104 chemical sciences
Citation
WoS Q
Q2
Scopus Q
Q2

OpenCitations Citation Count
13
Source
Journal of Physical Chemistry a
Volume
126
Issue
26
Start Page
4199
End Page
4210
PlumX Metrics
Citations
CrossRef : 1
Scopus : 26
PubMed : 4
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Mendeley Readers : 16
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