## Abstract Attachment of triarylamino‐functional groups at the 9‐position of 2,7‐linked carbazole polymers results in blue‐emitting materials with two independent redox processes that were attributed to the triarylamino groups and the polymer backbone, respectively. This new class of blue‐emitting
Synthesis of Poly(N-aryl-2,7-carbazole)s for Efficient Blue Electroluminescence Materials
✍ Scribed by Ryohei Koguchi; Norifumi Kobayashi; Toshinobu Shinnai; Kazuma Oikawa; Kazuhiko Tsuchiya; Masashi Kijima
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 239 KB
- Volume
- 209
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Several poly(N‐phenyl‐2,7‐carbazole)s that have dialkoxy groups at the m‐ and p‐positions (P__mp__CzDC, P__mp__PhDC, P__mp__CBiDC, P__mp__EHC), a silyl group at the p‐position (P__p__PhDSiC), and a diphenylamino group (P__m__PhDAC, P__m__EHAC) at the m‐position of the N‐phenyl portion are synthesized, and their optical properties are characterized. These polymers have been used as emitting layer materials of organic light‐emitting diode (OLED) devices that have a configuration of ITO/PEDOT(PSS)/polymer/CsF/Al. The OLED devices embedded with P__mp__CzDC, P__mp__PhDC, and P__mp__EHC show intense luminance of about 15 000 cd · m^−2^ with efficiencies of about 1 cd · A^−1^, while the devices embedded with P__p__PhDSiC, P__m__PhDAC, and P__m__EHAC show less luminance but retain the color purity of blue emission under a wide range of applied voltages.
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📜 SIMILAR VOLUMES
## Abstract The effects of __N__‐methyl‐2‐pyrrolidinone (NMP) as solvent on the polymerization reactions of 1,3‐bis(4‐chlorobenzoyl)benzene (1,3‐CBB) and 1,3‐bis(4‐fluorobenzoyl)benzene (1,3‐FBB) with 4,4′‐isopropylidenediphenol (bisphenol‐A) were examined. The failure of these reactions to produce