Study on a nonclassical radical cation using time-resolved absorption spectroscopy and DFT calculations
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- Ikeda Hiroshi
- Grad. Sch. of Sci., Tohoku Univ.
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- Namai Hayato
- Grad. Sch. of Sci., Tohoku Univ.
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- Ueda Minoru
- Grad. Sch. of Sci., Tohoku Univ.
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- Hirano Takashi
- Dept. of Applied Physics, The Univ. of Electro-Communications
Bibliographic Information
- Other Title
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- 時間分解吸収スペクトル及び DFT 計算による非古典的ラジカルカチオンの評価
Abstract
We previously reported the photoinduced electron-transfer (PET) degenerate methylenecyclopropane (MCP) rearrangement of diarylmethylenecyclopropane (1). The reaction proceeds via two different types of intermediates, a trimethylenemethane (TMM) radical cation (2 radical cation), and TMM biradical (2-biradical). The MCP rearrangement of 1 was also triggered by g-ray irradiation in a low temperature glassy matrix. The most characteristic feature is that the intense thermoluminescence (TL) was observed on the annealing of the sample matrix. Spectroscopic studies and energetic analyses suggest that the TL is originated from the excited state of TMM, (2-biradical)*, which is generated by electron-transfer (ET) reaction of 1 followed by bond cleavage and charge recombination. A potential application of the ET reaction of 1 toward organic electroluminescence will be also discussed.
Journal
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- Abstracts of Symposium on Physical Organic Chemistry
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Abstracts of Symposium on Physical Organic Chemistry 55 (0), 30-30, 2005
The Society of Physical Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390001205553917952
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- NII Article ID
- 130004646363
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed