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Singlet fission initiating triplet generations of BODIPY derivatives through π-stacking : a theoretical study

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Title: Singlet fission initiating triplet generations of BODIPY derivatives through π-stacking : a theoretical study
Authors: Tsuneda, Takao Browse this author
Taketsugu, Tetsuya Browse this author →KAKEN DB
Issue Date: 16-Nov-2022
Publisher: Nature Portfolio
Journal Title: Scientific reports
Volume: 12
Issue: 1
Start Page: 19714
Publisher DOI: 10.1038/s41598-022-23370-y
Abstract: The role of singlet fission (SF) in the triplet-state generation mechanism of 1,3,5,7-tetramethylboron-dipyrromethene derivatives is revealed by exploring the cause for the solvent dependence of the generation rate. Comparing the adsorption energy calculations of solvent molecules, i.e., cyclohexane, chloroform and acetonitrile molecules, to the derivatives with the pi-stacking energies of these derivatives surprisingly show that the hierarchy of the solvation energies and pi-stacking energies strongly correlates with the experimentally-suggested solvent dependence of the tripletstate generation of these derivatives for five and more adsorbing solvent molecules. Following this finding, the excitation spectra of these derivatives in acetonitrile solvent are explored using the proprietary spin-flip long-range corrected time-dependent density functional theory. It is, consequently, confirmed that the pi-stacking activates the second lowest singlet excitation to trigger the spin-allowed transition to the singlet doubly-excited tetraradical (TT)(1) state, which generates the long-lived quintet (TT)(1) state causing the SF. However, it is also found that the pi-stacking also get a slow intersystem crossing active around the intersections of the lowest singlet excitations with the lowest triplet T-1 excitations in parallel with the SF due to the charge transfer characters of the lowest singlet excitations. These results suggest that SF initiates the triplet-state generations through near-degenerate low-lying singlet and (TT) excitations with a considerable singlet-triplet energy gap after the pi-stacking of chromophores stronger than but not far from the solvation. Since these derivatives are organic photosensitizers, this study proposes that SF should be taken into consideration in developing novel heavy atom-free organic photosensitizers, which will contribute to a variety of research fields such as medical care, photobiology, energy science, and synthetic chemistry.
Type: article
URI: http://hdl.handle.net/2115/87519
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

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