Synthesis and photoluminescent properties of new aza-indenofluorene derivatives

Su Jin Jung; Won Sam Kim; Byung Sun Park; Jae Kyun Lee; Jung Hwan Park; Kihang Choi; So Ha Lee

doi:10.1002/hc.21058

Synthesis and photoluminescent properties of new aza-indenofluorene derivatives

Su Jin Jung, Won Sam Kim, Byung Sun Park, Jae Kyun Lee, Jung Hwan Park, Kihang Choi, So Ha Lee

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

6 Citations (Scopus)

Abstract

The carbazole derivatives 5a-h 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 × 10^-5 M CH₂Cl₂. Also, the X-ray structure of the carbazole derivative 6 was elucidated by an X-ray diffractometer.

Original language	English
Pages (from-to)	18-24
Number of pages	7
Journal	Heteroatom Chemistry
Volume	24
Issue number	1
DOIs	https://doi.org/10.1002/hc.21058
Publication status	Published - 2013 Jan

ASJC Scopus subject areas

Chemistry(all)

Access to Document

10.1002/hc.21058

Cite this

@article{9477c0a087d54e5b8cfdc20e909b2cef,

title = "Synthesis and photoluminescent properties of new aza-indenofluorene derivatives",

abstract = "The carbazole derivatives 5a-h 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 × 10-5 M CH2Cl2. Also, the X-ray structure of the carbazole derivative 6 was elucidated by an X-ray diffractometer.",

author = "Jung, {Su Jin} and Kim, {Won Sam} and Park, {Byung Sun} and Lee, {Jae Kyun} and Park, {Jung Hwan} and Kihang Choi and Lee, {So Ha}",

year = "2013",

month = jan,

doi = "10.1002/hc.21058",

language = "English",

volume = "24",

pages = "18--24",

journal = "Heteroatom Chemistry",

issn = "1042-7163",

publisher = "Wiley-Blackwell",

number = "1",

}

TY - JOUR

T1 - Synthesis and photoluminescent properties of new aza-indenofluorene derivatives

AU - Jung, Su Jin

AU - Kim, Won Sam

AU - Park, Byung Sun

AU - Lee, Jae Kyun

AU - Park, Jung Hwan

AU - Choi, Kihang

AU - Lee, So Ha

PY - 2013/1

Y1 - 2013/1

N2 - The carbazole derivatives 5a-h 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 × 10-5 M CH2Cl2. Also, the X-ray structure of the carbazole derivative 6 was elucidated by an X-ray diffractometer.

AB - The carbazole derivatives 5a-h 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 × 10-5 M CH2Cl2. Also, the X-ray structure of the carbazole derivative 6 was elucidated by an X-ray diffractometer.

UR - http://www.scopus.com/inward/record.url?scp=84872265610&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84872265610&partnerID=8YFLogxK

U2 - 10.1002/hc.21058

DO - 10.1002/hc.21058

M3 - Article

AN - SCOPUS:84872265610

SN - 1042-7163

VL - 24

SP - 18

EP - 24

JO - Heteroatom Chemistry

JF - Heteroatom Chemistry

IS - 1

ER -

Synthesis and photoluminescent properties of new aza-indenofluorene derivatives

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this