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- 森崎 泰弘
- 関西学院大学生命環境学部
書誌事項
- タイトル別名
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- Photochemistry Opened up by [2.2]Paracyclophane
- [2.2]パラシクロフアンが拓く光化学
- [2.2]パラシクロフアン ガ ヒラク コウカガク
- 公開日
- 2025-04-28
- 資源種別
- journal article
- DOI
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- 10.60391/koukagaku.56.1_2
- 公開者
- 光化学協会
この論文をさがす
説明
<p>Since the first synthesis of [2.2]paracyclophanes in 1949, a wide variety of the derivatives have been synthesized, and their physical properties have been extensively investigated. However, there have not been many cases in which [2.2]paracyclophanes have been applied beyond the field of organic chemistry and organometallic chemistry. In the first half of this paper, the through-space conjugation and photoluminescence properties of π-stacked molecules (polymers and oligomers) consisting of [2.2]paracyclophane as a key unit are introduced. One of the characteristics of the [2.2]paracyclophane skeleton is planar chirality without chiral center(s). Due to the suppressed rotational motion of benzene rings in [2.2]paracyclophane, it exhibits planar chirality depending on the substitution position(s). In the latter half, circularly polarized luminescence (CPL) profiles of some optically active π-stacked molecules based on the planar chiral [2.2]paracyclophane moiety are introduced.</p>
収録刊行物
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- 光化学
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光化学 56 (1), 2-7, 2025-04-28
光化学協会
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詳細情報 詳細情報について
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- CRID
- 1390022487765933568
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- NII書誌ID
- AN10131680
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- ISSN
- 27590836
- 09134689
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- NDL書誌ID
- 034144569
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- 本文言語コード
- ja
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- 資料種別
- journal article
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- データソース種別
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- JaLC
- NDLサーチ
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可
