Synthesis and red electroluminescence of a dimesityl-functionalized bistetracene |
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Authors: | Guixia Zhai Changting Wei Shulian Chen Xiaomeng Yin Jinchong Xiao Wenming Su |
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Affiliation: | 1. College of Chemistry and Environmental Science, Key Laboratory of Chemical Biology of Hebei Province, Hebei University, Baoding 071002, China;2. Printalbe Electronics Research Centre, Suzhou Institute of Nanotech and Nano-bionics, Chinese Academy of Sciences, Suzhou 215123, China;3. 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 |
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Abstract: | 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). |
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Keywords: | Synthesis Polycyclic aromatic hydrocarbons Single crystal Photophysical property Electroluminescence |
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