Citation: Zhai Guixia, Wei Changting, Chen Shulian, Yin Xiaomeng, Xiao Jinchong, Su Wenming. Synthesis and red electroluminescence of a dimesityl-functionalized bistetracene[J]. Chinese Chemical Letters, ;2018, 29(2): 293-296. doi: 10.1016/j.cclet.2017.10.035 shu

Synthesis and red electroluminescence of a dimesityl-functionalized bistetracene

a.
College of Chemistry and Environmental Science, Key Laboratory of Chemical Biology of Hebei Province, Hebei University, Baoding 071002, China
b.
Printalbe Electronics Research Centre, Suzhou Institute of Nanotech and Nano-bionics, Chinese Academy of Sciences, Suzhou 215123, China
c.
MⅡT Key Laboratory of Advanced Display Materials and Devices, Institute of Optoelectronics & Nanomaterials, School of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094, China

Corresponding author: Xiao Jinchong, jcxiaoicas@163.com Su Wenming, wmsu2008@sinano.ac.cn
Received Date: 24 September 2017
Revised Date: 26 October 2017
Accepted Date: 26 October 2017
Available Online: 2 February 2017

Figures(4)

A novel dimesityl-decorated bistetracene derivative 8, 16-dimesityltetraceno[2, 1, 12, 11-opqra]tetracene (DMTA) has been synthesized and characterized. Its single crystal analysis demonstrates that the parent bistetracene backbone is almost in a plane without any intermolecular π-stacking interaction. DMTA exhibited the low-energy absorption at 560/607 nm and emission spectra at 617/663 nm, respectively. The fabricated device based on DMTA doping into 2, 6-bis(3-(9H-carbazol-9-yl)phenyl)pyridine (1%) as an emitter present a maximum brightness of 632 cd/m² at 14.7 V with the CIE coordinate of (0.623, 0.349).
- Synthesis,
- Polycyclic aromatic hydrocarbons,
- Single crystal,
- Photophysical property,
- Electroluminescence
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1.
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