Role of Spacer Effects in Acyl Moiety on Unimolecular Dissociation for <I>N</I>-(3-Phenylpropanoyl)-1-azacycloalkan-2-ones and Their Analogues
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- Kawaguchi Miwa
- Osaka Prefecture Univ.
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- Okada Kyoko
- Osaka Prefecture Univ.
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- Hirakawa Nahoko
- Osaka Women's Univ.
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- Isa Kimio
- Univ. of Fukui
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- Maekawa Tetsuya
- Univ. of Fukui
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- Yamaoka Hiroshi
- Osaka Prefecture Univ. Osaka Women's Univ.
Bibliographic Information
- Other Title
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- <I>N</I>－（3－フェニルプロピオニル）ラクタム類縁体の気相単分子イオン分解 ―アシル鎖長のスペーサとしての役割―
Abstract
Metastable ion spectra for electron ionized molecular ions for titled N-(3-Phenylpropanoyl)-1-azacycloalkan-2-ones derivatives gave double hydrogen transferred ion and unusual product ions whose mass is M-57 during 3rd field free region by a four sector tandem mass spectrometer. These data reveal the origin for unusual gas phase unimolecular dissociation based on role of spacer effects in acyl moiety.
Journal
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- Abstracts of Symposium on Physical Organic Chemistry
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Abstracts of Symposium on Physical Organic Chemistry 2008 (0), 59-59, 2008
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
- 1390001205556799744
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- NII Article ID
- 130004645544
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed