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IR laser manipulation of cis ↔ trans isomerization of 2-naphthol and its hydrogen-bonded clusters

https://hiroshima.repo.nii.ac.jp/records/2007273
https://hiroshima.repo.nii.ac.jp/records/2007273
f55926a5-6d18-48b0-8e03-d5d08d05b6b2
名前 / ファイル ライセンス アクション
JCP_124_054315.pdf JCP_124_054315.pdf (698.4 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル IR laser manipulation of cis ↔ trans isomerization of 2-naphthol and its hydrogen-bonded clusters
言語 en
作成者 Kouyama, Kyouko

× Kouyama, Kyouko

en Kouyama, Kyouko

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Miyazaki, Mitsuhiko

× Miyazaki, Mitsuhiko

en Miyazaki, Mitsuhiko

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Mikami, Naohiko

× Mikami, Naohiko

en Mikami, Naohiko

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Ebata, Takayuki

× Ebata, Takayuki

en Ebata, Takayuki

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 Copyright (c) 2006 American Institute of Physics.
内容記述
内容記述 The cis↔trans isomerization reaction has been carried out for 2-naphthol and its hydrogen (H) bonded clusters by infrared (IR) laser in the electronic excited state (S1) in supersonic jets. A specific isomer in the jet was pumped to the X-H stretching vibration in the S1 state, where X refers to C, O, or N atom, by using a stepwise UV-IR excitation, and the dispersed emission spectra of the excited species or generated fragments were observed. It was found that the isomerization occurs only in the H-bonded clusters but a bare molecule does not exhibit the isomerization in the examined energy region of Ev ≤3610 cm-1, indicating a reduction of the isomerization barrier height upon the H bonding. The relative yield of the isomerization was observed as a function of internal energy. The isomerization yield was found to be very high at the low IR frequency excitation, and was rapidly reduced with the IR frequency due to the competition of the dissociation of the H bond within the isomer. Density-functional theory (DFT) and time-dependent DFT calculations were performed for estimating the barrier height of the isomerization for bare 2-naphthol and its cluster for electronic ground and excited states. The calculation showed that the isomerization barrier height is highly dependent on the electronic states. However, the reduction of the height upon the hydrogen bonding was not suggested at the level of our calculation.
言語 en
出版者
出版者 American Institute of Physics
言語
言語 eng
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 journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ DOI
関連識別子 10.1063/1.2162164
関連情報
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1063/1.2162164
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0021-9606
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00694991
書誌情報 Journal of Chemical Physics
Journal of Chemical Physics

巻 124, 号 5, 発行日 2006-02-07
旧ID 18622
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