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アイテム
シクロデキストリン共存下におけるピセンの2光子イオン化
https://doi.org/10.57375/00001519
https://doi.org/10.57375/00001519eea7b887-37a3-492a-bdbe-2a58fe75e896
名前 / ファイル | ライセンス | アクション |
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Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
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公開日 | 2017-07-11 | |||||
タイトル | ||||||
タイトル | シクロデキストリン共存下におけるピセンの2光子イオン化 | |||||
タイトル | ||||||
タイトル | Two-Photon Ionization of Picene in the Presence of Cyclodextrin | |||||
言語 | en | |||||
言語 | ||||||
言語 | jpn | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Picene, Cyclodextrin | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Two-Photon Ionization | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Laser Flash Photolysis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Inclusion Complex | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | departmental bulletin paper | |||||
ID登録 | ||||||
ID登録 | 10.57375/00001519 | |||||
ID登録タイプ | JaLC | |||||
著者 |
竹下, 達哉
× 竹下, 達哉× 久保, 葉月× 箕﨑, 知香× 矢野, 篤× 原, 道寛× Takeshita, Tatsuya× Kubo, Hazuki× Minosaki, Chika× Yano, Atsushi× Hara, Michihiro |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Two-photon ionization (TPI) of picene (Pi) in the presence of cyclodextrin (CD) was investigated by using 266-nm laser pulse excitation. TPI of Pi was compared with TPI of phenanthrene (PH) and chrysene (Ch) from view point of the number of benzene rings. The formation of incorporation complex of Pi with CD (Pi/CD) was confirmed by 1H NMR measurement. The transient absorption of hydrated electrons released by Pi/CD was observed at 720 nm after a 5 ns laser flash at 266 nm. The ionization quantum yield (Φion) of Pi in the presence of α-, β-, and γ-CD (1.0 × 10-2 M) was calculated to be 3.4 ± 0.1%, 1.9 ± 0.1%, and 1.7 ± 0.1%, respectively, and it was attributed to the stabilization energy arising from solvation, which was affected by the area of Pi protruding from the cavity of the CD. When the concentration of CD was lowered to 1.0 × 10-3 M, Φion of Pi was increased by the stabilization energy arising from solvation. Additionally, we found that Φion of Pi with five benzene rings was much higher than PH and Ch with three and four benzene rings, respectively, which is because its structure is relatively susceptible to the stabilization of solvation. Overall, we concluded that the stabilization energy of solvation is important for the TPI of Pi/CD. | |||||
書誌情報 |
福井工業大学研究紀要 号 47, p. 145-152, 発行日 2017-07-11 |
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出版者 | ||||||
出版者 | 福井工業大学 | |||||
書誌レコードID | ||||||
識別子タイプ | NCID | |||||
関連識別子 | TF00010400 | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 |