Journal
CHEMISTRY LETTERS
Volume 38, Issue 2, Pages 140-141Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.2009.140
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Funding
- Ministry of Education, Culture, Sports, Science and Technology, Japan [19550040]
- Izumi Science and Technology Foundation [H18-J-93]
- Grants-in-Aid for Scientific Research [19550040] Funding Source: KAKEN
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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; lit showed excimeric fluorescence, whose emission maxima strongly depended on the angles and distances between carbazole rings.
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