Next Article in Journal
High-Resolution Lipidomics of the Early Life Stages of the Red Seaweed Porphyra dioica
Next Article in Special Issue
AIEgen-Based Fluorescent Nanomaterials: Fabrication and Biological Applications
Previous Article in Journal
Lewis Pair Catalysts in the Polymerization of Lactide and Related Cyclic Esters
Previous Article in Special Issue
Construction of Luminogen Exhibiting Multicolored Emission Switching through Combination of Twisted Conjugation Core and Donor-Acceptor Units
Open AccessFeature PaperArticle

Preparation of Cyano-Substituted Tetraphenylethylene Derivatives and Their Applications in Solution-Processable OLEDs

1
State Key Laboratory of Supramolecular Structure and Materials, Jilin University, 2699 Qianjin Avenue, Changchun 130012, China
2
State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China
*
Author to whom correspondence should be addressed.
Molecules 2018, 23(1), 190; https://doi.org/10.3390/molecules23010190
Received: 29 December 2017 / Revised: 14 January 2018 / Accepted: 14 January 2018 / Published: 17 January 2018
Creation of organic luminescent materials with high solid-state efficiency is of vital importance for their applications in optoelectronic fields. Here, a series of AIE luminogens (AIE gens), (Z)-2,3-bis(4-(9,9-bis(6-(9H-carbazol-9-yl)hexyl)-9H-fluoren-2-yl)phenyl)-3-phenylacrylonitrile (SFC), and 2,3-bis(4-(9,9-bis(6-(9H-carbazol-9-yl)hexyl)-9H-fluoren-2-yl)phenyl)fumaronitrile (DFC), utilizing 2,3,3-triphenylacrylonitrile and 2,3-diphenylfumaronitrile as respective centers, are designed and synthesized by Suzuki coupling reactions with high yields. The cis- and trans-isomers of DFC are also successfully obtained. All of them are thermally stable and show good solubility in common organic solvents. They all emit weakly in solution, but become strong emitters when fabricated into solid films. It is found introduction of one additional cyano group in DFC induced a big red-shift in solid-state emission, owing to its high electron-withdrawing ability. The cis- and trans-DFC show similar photophysical and Cyclic voltammogram (CV) behaviors. Non-doped solution-processed organic light-emitting diodes (OLEDs) using the three compounds as light-emitting layers are fabricated. SFC gives the best device performance with a maximum luminance of 5201 cd m−2, a maximum current efficiency of 3.67 cd A−1 and a maximum external quantum efficiencies (EQE) of 1.37%. Red-shifted EL spectra are observed for cis- and trans-DFC-based device, and the OLED using trans-DFC as active layer exhibits better performance, which might derive from their different conformation in film state. View Full-Text
Keywords: diphenylfumaronitrile; fluorene; AIE; solution-processability; OLED diphenylfumaronitrile; fluorene; AIE; solution-processability; OLED
Show Figures

Figure 1

MDPI and ACS Style

Sun, X.; Zhao, L.; Han, X.; Liu, H.; Gao, Y.; Tao, Y.; Zhang, H.; Yang, B.; Lu, P. Preparation of Cyano-Substituted Tetraphenylethylene Derivatives and Their Applications in Solution-Processable OLEDs. Molecules 2018, 23, 190.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Search more from Scilit
 
Search
Back to TopTop