Synthesis and Photophysical Properties of Tris-bridged [3.3.n](3,6,9)Carbazolophanes
Tris-bridged [3.3.n](3,6,9)carbazolophanes 1n (n=3–6), which are appropriate model compounds for fully overlapped excimer in carbazole chromophore, have been synthesized and characterized by NMR, X-ray, absorption and fluorescence spectra; 1n showed excimeric fluorescence, whose emission maxima stro...
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| Veröffentlicht in: | Chemistry letters 2009-02, Vol.38 (2), p.140-141 |
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| container_end_page | 141 |
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| container_title | Chemistry letters |
| container_volume | 38 |
| creator | Tani, Keita Sakumoto, Naoki Kubono, Koji Hori, Kazushige Tohda, Yasuo Benten, Hiroaki Ohkita, Hideo Ito, Shinzaburo Yamamoto, Masahide |
| description | Tris-bridged [3.3.n](3,6,9)carbazolophanes 1n (n=3–6), which are appropriate model compounds for fully overlapped excimer in carbazole chromophore, have been synthesized and characterized by NMR, X-ray, absorption and fluorescence spectra; 1n showed excimeric fluorescence, whose emission maxima strongly depended on the angles and distances between carbazole rings. |
| doi_str_mv | 10.1246/cl.2009.140 |
| format | Article |
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| identifier | ISSN: 0366-7022 |
| ispartof | Chemistry letters, 2009-02, Vol.38 (2), p.140-141 |
| issn | 0366-7022 1348-0715 |
| language | eng |
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| source | Oxford Academic Journals (OUP) |
| title | Synthesis and Photophysical Properties of Tris-bridged [3.3.n](3,6,9)Carbazolophanes |
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