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Efficient Synthesis of a Novel, Twisted and Stable, Electroluminescent “Twistacene”

Authors :
Duong, H. M.
Bendikov, M.
Steiger, D.
Zhang, Q.
Sonmez, G.
Yamada, J.
Wudl, F.
Source :
Organic Letters; November 2003, Vol. 5 Issue: 23 p4433-4436, 4p
Publication Year :
2003

Abstract

<UFIGR ID="ol035751vn00001">A twistacene, 6,8,15,17-tetraphenyl-1.18,4.5,9.10,13.14-tetrabenzoheptacene (<BO>3</BO>), was synthesized using a mild and novel bisbenzyne precursor. It was characterized by X-ray crystallography, NMR, UV−vis, and IR spectroscopies, as well as cyclic voltammetry and DFT calculations. The heptacene derivative possesses a nonpropeller twist topology and is unusually stable for a highly conjugated oligoacene. In addition, it is fluorescent, with a quantum efficiency of 15%. Distortion from planarity, mostly due to the phenyl substituents, causes only marginal changes in electronic properties and is beneficial for redox reversibility, which is required for efficient OLED devices.

Details

Language :
English
ISSN :
15237060 and 15237052
Volume :
5
Issue :
23
Database :
Supplemental Index
Journal :
Organic Letters
Publication Type :
Periodical
Accession number :
ejs5414589