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https://hdl.handle.net/20.500.14094/0100477736
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0100477736 (fulltext)
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0100477736
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Singlet fission initiating triplet generations of BODIPY derivatives through π-stacking: a theoretical study
著者
著者ID
A2442
研究者ID
1000020312994
著者名
Tsuneda, Takao
常田, 貴夫
ツネダ, タカオ
所属機関名
科学技術イノベーション研究科
著者名
Taketsugu, Tetsuya
言語
English (英語)
収録物名
Scientific Reports
巻(号)
12(1)
ページ
19714
出版者
Nature Portfolio
刊行日
2022-11-16
公開日
2022-12-05
抄録
The role of singlet fission (SF) in the triplet-state generation mechanism of 1,3,5,7-tetramethyl-boron-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 π-stacking energies of these derivatives surprisingly show that the hierarchy of the solvation energies and π-stacking energies strongly correlates with the experimentally-suggested solvent dependence of the triplet-state 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 π-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 π-stacking also get a slow intersystem crossing active around the intersections of the lowest singlet excitations with the lowest triplet T1 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 π-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.
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科学技術イノベーション研究科
学術雑誌論文
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© The Author(s) 2022.
This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
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DOI
https://doi.org/10.1038/s41598-022-23370-y
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journal article
eISSN
2045-2322
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