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Ultrafast excited-state dynamics in photochromic N-salicylideneaniline studied by femtosecond time-resolved REMPI spectroscopy

https://hiroshima.repo.nii.ac.jp/records/2008926
https://hiroshima.repo.nii.ac.jp/records/2008926
1366ccfc-827a-4643-8007-d3d67d6ec01b
名前 / ファイル ライセンス アクション
JChemPhys_2004_121_9436.pdf JChemPhys_2004_121_9436.pdf (140.6 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 Ultrafast excited-state dynamics in photochromic N-salicylideneaniline studied by femtosecond time-resolved REMPI spectroscopy
言語 en
作成者 Okabe, Chie

× Okabe, Chie

en Okabe, Chie

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Nakabayashi, Takakazu

× Nakabayashi, Takakazu

en Nakabayashi, Takakazu

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Inokuchi, Yoshiya

× Inokuchi, Yoshiya

en Inokuchi, Yoshiya

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Nishi, Nobuyuki

× Nishi, Nobuyuki

en Nishi, Nobuyuki

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Sekiya, Hiroshi

× Sekiya, Hiroshi

en Sekiya, Hiroshi

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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) 2004 American Institute of Physics
主題
主題Scheme NDC
主題 430
内容記述
内容記述 Ultrafast processes in photoexcitedN-salicylideneaniline have been investigated with femtosecondtime-resolved resonance-enhanced multiphoton ionization spectroscopy. The ion signals via theS 1 (n,π * ) state of the enol form as well as the proton-transferred cis-keto form emerge within a few hundred femtoseconds after photoexcitation to the firstS 1 (π,π * ) state of the enol form. This reveals that two ultrafast processes,excited-state intramolecular proton transfer (ESIPT) reaction and an internal conversion (IC) to theS 1 (n,π * ) state, occur on a time scale less than a few hundred femtoseconds from theS 1 (π,π * ) state of the enol form. The rise time of the transient corresponding to the production of the proton-transferred cis-keto form is within 750 fs when near the red edge of the absorption is excited, indicating that the ESIPT reaction occurs within 750 fs. The decay time of theS 1 (π,π * ) state of the cis-keto form is 8.9 ps by exciting the enol form at 370 nm, but it dramatically decreases to be 1.5–1.6 ps for the excitation at 365–320 nm. The decrease in the decay time has been attributed to the opening of an efficient nonradiative channel; an IC fromS 1 (π,π * ) toS 1 (n,π * ) of the cis-keto form promotes the production of the trans-keto form as the final photochromic products. The two IC processes may provide opposite effect on the quantum yield of photochromic products: IC in the enol form may substantially reduce the quantum yield, but IC in the cis-keto form increase it.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported in part by Grant-in-Aid for Scientific Research No. 15350015 from the Ministry of Education, Sports and Culture in Japan, and by the Joint Studies Program (Grant No. 2002-2003) of Institute for Molecular Science.
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 10.1063/1.1801991
関連情報
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1063/1.1801991
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0021-9606
開始ページ
開始ページ 9436
書誌情報 The Journal of Chemical Physics
The Journal of Chemical Physics

巻 121, 号 19, p. 9436-9442, 発行日 2004-11-15
旧ID 37382
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