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Synthesis and Photoluminescent Properties of New Aza-Indenofluorene Derivatives

Authors
Jung, Su JinKim, Won SamPark, Byung SunLee, Jae KyunPark, Jung HwanChoi, KihangLee, So Ha
Issue Date
2013
Publisher
WILEY-BLACKWELL
Citation
HETEROATOM CHEMISTRY, v.24, no.1, pp.18 - 24
Indexed
SCIE
SCOPUS
Journal Title
HETEROATOM CHEMISTRY
Volume
24
Number
1
Start Page
18
End Page
24
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/106516
DOI
10.1002/hc.21058
ISSN
1042-7163
Abstract
The carbazole derivatives 5ah were synthesized by four steps involving Suzuki coupling of boronic acid 1 with 1-bromo-2-nitrobenzene, followed with the Cadogan ring closure reaction. Their UV and photoluminescence properties are also reported, and the compounds showed medium-to-strong photoluminescence between 370 and 446 nm at the concentration of 1 x 10-5 M CH2Cl2. Also, the X-ray structure of the carbazole derivative 6 was elucidated by an X-ray diffractometer. (c) 2012 Wiley Periodicals, Inc. Heteroatom Chem 24:1824, 2013; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.21058
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