Experimental and theoretical study on the excited-state dynamics of ortho-, meta-, and para-methoxy methylcinnamate
The Journal of Chemical Physics 141 巻
244313-1-244313-12 頁
2014-12-31 発行
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タイトル ( eng ) |
Experimental and theoretical study on the excited-state dynamics of ortho-, meta-, and para-methoxy methylcinnamate
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作成者 |
Miyazaki Yasunori
Yamamoto Kanji
Aoki Jun
Ehara Masahiro
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収録物名 |
The Journal of Chemical Physics
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巻 | 141 |
開始ページ | 244313-1 |
終了ページ | 244313-12 |
抄録 |
The S1 state dynamics of methoxy methylcinnamate (MMC) has been investigated under supersonic jet-cooled conditions. The vibrationally resolved S1-S0 absorption spectrum was recorded by laser induced fluorescence and mass-resolved resonant two-photon ionization spectroscopy and separated into conformers by UV-UV hole-burning (UV-UV HB) spectroscopy. The S1 lifetime measurements revealed different dynamics of para-methoxy methylcinnamate from ortho-methoxy methylcinnamate and meta-methoxy methylcinnamate (hereafter, abbreviated as p-, o-, and m-MMCs, respectively). The lifetimes of o-MMC and m-MMC are on the nanosecond time scale and exhibit little tendency of excess energy dependence. On the other hand, p-MMC decays much faster and its lifetime is conformer and excess energy dependent. In addition, the p-MMC-H2O complex was studied to explore the effect of hydration on the S1 state dynamics of p-MMC, and it was found that the hydration significantly accelerates the nonradiative decay. Quantum chemical calculation was employed to search the major decay route from S1(ππ*) for three MMCs and p-MMC-H2O in terms of (i) trans → cis isomerization and (ii) internal conversion to the 1nπ* state. In o-MMC and m-MMC, the large energy barrier is created for the nonradiative decay along (i) the double-bond twisting coordinate (~1000 cm-1) in S1 as well as (ii) the linear interpolating internal coordinate (~1000 cm-1) from S1 to 1nπ? states. The calculation on p-MMC decay dynamics suggests that both (i) and (ii) are available due to small energy barrier, i.e., 160 cm-1 by the double-bond twisting and 390 cm-1 by the potential energy crossing. The hydration of p-MMC raises the energy barrier of the IC route to the S1/1nπ* conical intersection, convincing that the direct isomerization is more likely to occur.
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NDC分類 |
化学 [ 430 ]
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言語 |
英語
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資源タイプ | 学術雑誌論文 |
出版者 |
American Institute of Physics
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発行日 | 2014-12-31 |
権利情報 |
Copyright (c) 2014 AIP Publishing LLC.
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出版タイプ | Version of Record(出版社版。早期公開を含む) |
アクセス権 | オープンアクセス |
収録物識別子 |
[ISSN] 0021-9606
[DOI] 10.1063/1.4904268
[DOI] http://dx.doi.org/10.1063/1.4904268
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