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Synthesis and Emission Behavior of Carbazolophanes Containing Imino Group in the Presence of Metal Ions.
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- Tani Keita
- Osaka Kyoiku University
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- Kaji Keiichi
- Osaka Kyoiku University
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- Nakagawa Sayuri
- Osaka Kyoiku University
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- Kubono Koji
- Osaka Kyoiku University
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- Hori Kazushige
- Osaka Kyoiku University
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- Tohda Yasuo
- Osaka Kyoiku University
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- Benten Hiroaki
- International Innovation Center
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- Ohkita Hideo
- Kyoto University
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- Ito Shinzaburo
- Kyoto University
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- Yamamoto Masahide
- Ritsumeikan University
Bibliographic Information
- Other Title
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- イミノ基を有するカルバゾロファンの合成と金属イオン存在下での発光挙動
Description
We have prepared crownocarbazolophanes, whose fluorescence was changed in the presence of metal ions. Here, we synthesized carbazole imine cyclophane (2n) and the emission behavior in the presence of metal ions was investigated. The structures of (2n) were identified by NMR, MS and elemental analysis. In the proton NMR spectrum of (2n), H1, H2, and H4 in carbazole ring shifted upfield compared with those of the reference, suggesting that two carbazole rings in (2n) are situated in partially overlapped geometry. Fluorescence spectra of (2n) were monomer-like emission. In the presence of metal ions, monomer-like emission was generally quenched, while in the presence of zinc and cadmium ions, new fluorescence shifted to longer wavelength appeared.
Journal
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- Abstracts of Symposium on Physical Organic Chemistry
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Abstracts of Symposium on Physical Organic Chemistry 37 (0), 122-122, 2007
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
- 1390282680532839296
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- NII Article ID
- 130004646105
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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