1653975-45-1Relevant articles and documents
Photoluminescence and electroluminescence of iridium(iii) complexes with 2′,6′-bis(trifluoromethyl)-2,4′-bipyridine and 1,3,4-oxadiazole/1,3,4-thiadiazole derivative ligands
Jing, Yi-Ming,Zhao, Yue,Zheng, You-Xuan
, p. 845 - 853 (2017)
Using 2′,6′-bis(trifluoromethyl)-2,4′-bipyridine as a monoanionic cyclometalated ligand, 2-(5-(4-(trifluoromethyl)phenyl)-1,3,4-oxadiazol-2-yl)phenol and 2-(5-(4-(trifluoromethyl) phenyl)-1,3,4-thiadiazol-2-yl)phenol as ancillary ligands, two new heteroleptic iridium(iii) complexes (Ir1 and Ir2) were prepared and investigated. The ancillary ligand variations affected their emissions greatly, and the complexes Ir1 and Ir2 emitted green (503 nm) and orange (579 nm) lights, respectively. Moreover, the electron mobility of the two complexes is as high as that of the electron transport material Alq3 (tris-(8-hydroxyquinoline)aluminium), which is useful for their performances in organic light-emitting diodes (OLEDs). The OLEDs with Ir1 as the emitter showed excellent performances with a maximum current efficiency of 74.8 cd A?1, a maximum external quantum efficiency of 27.0%, a maximum power efficiency of 33.4 lm W?1, and the efficiency roll-off is mild. These results suggest that complexes with 1,3,4-oxadiazole/1,3,4-thiadiazole derivatives have potential application as efficient emitters in OLEDs.
Versatile functionalization of trifluoromethyl based deep blue thermally activated delayed fluorescence materials for organic light emitting diodes
Liang, Xiao,Han, Hua-Bo,Yan, Zhi-Ping,Liu, Liang,Zheng, You-Xuan,Meng, Hong,Huang, Wei
, p. 4317 - 4323 (2018)
Thermally activated delayed fluorescence (TADF) materials have been thoroughly developed and have proven to be the most promising means to generate an efficient deep blue emission. In this work, we prepared a series of deep blue TADF emitters based on trifluoromethyl featuring phenyl and N-heterocyclic rings as electron-withdrawing units and carbazole as electron-donating moieties. Efficient organic light-emitting diodes (OLEDs) utilizing these emitters have a deep blue emission and a high external quantum efficiency of up to 20.4%. These blue emitters are among the bluest in the TADF based OLED category. They can also be implemented in OLED as hosts for green phosphorescent iridium(iii) complexes, exhibiting high brightness and a decent external quantum yield.
Efficient OLEDs with low efficiency roll-off using iridium complexes possessing good electron mobility
Xu, Qiu-Lei,Liang, Xiao,Zhang, Song,Jing, Yi-Ming,Liu, Xuan,Lu, Guang-Zhao,Zheng, You-Xuan,Zuo, Jing-Lin
, p. 3694 - 3701 (2015)
Two bis-cyclometalated iridium complexes (Ir1 and Ir2) with trifluoromethyl substituted bipyridine (2′,6′-bis(trifluoromethyl)-2,3′-bipyridine (L1) and 2′,6′-bis(trifluoromethyl)-2,4′-bipyridine (L2)) as the main ligands and tetraphenylimidodiphosphinate
High efficiency electroluminescence of orange-red iridium(III) complexes for OLEDs with an EQE over 30%
Li, Shuaibing,Qu, Junle,Song, Jun,Su, Ning,Yang, Kun,Zhou, Feifan,Zhou, Liang
, (2021/08/24)
In this study, three pyrazol-pyridine ligands, 2-(3-methyl-1H-pyrazol-5-yl)pyridine (mepzpy), 2-(3-(trifluoromethyl)-1H-pyrazol-5-yl)pyridine (cf3pzpy), and 2-(3-phenyl-1H-pyrazol-5-yl)pyridine (phpzpy) were successfully synthesized for three orange-red iridium (III) complexes Ir1, Ir2, and Ir3, respectively, in which (2,6-bis(trifluoromethyl)pyridin-4-yl)isoquinoline (BTPIQ) was applied as main ligand. Their single crystals were obtained by vacuum sublimation. They showed distinct photoluminescent emissions at 583 nm with a shoulder peak at 624 nm, with high phosphorescence quantum yields of up to 89%. Organic light-emitting devices (OLEDs) with these complexes as emitters exhibits good performances. Especially, the device with Ir3 complex achieves the best performance with a maximum luminance of 24,188 cd m?2, and a highest external quantum efficiency of 30.65%. This research proved that Ir(III) complexes show highly enhanced performance by the modification of electro-donating benzene ring group into ancillary ligands, which also offers us an efficient strategy to obtain high efficiency orange-red Ir(III) complexes for OLEDs.
Efficient green photoluminescence and electroluminescence of iridium complexes with high electron mobility
Han, Hua-Bo,Wu, Zheng-Guang,Yan, Zhi-Ping,Zhao, Yue,Zheng, You-Xuan
, p. 16543 - 16550 (2018/12/05)
Aiming to balance the injection and transport of electrons and holes, nitrogen heterocycle and 1,3,4-oxadiazole derivatives were introduced in iridium(iii) complexes to obtain organic light-emitting diodes (OLEDs) with high performances. Thus, two novel Ir(iii) complexes (Ir(tfmphpm)2(pop) and Ir(tfmppm)2(pop)) with green emissions using 2-(3,5-bis(trifluoromethyl)phenyl)pyrimidine (tfmphpm) and 2-(2,6-bis(trifluoromethyl)pyridin-4-yl)pyrimidine (tfmppm) as cyclometalating ligands, and 2-(5-phenyl-1,3,4-oxadiazol-2-yl)phenol (pop) as an ancillary ligand were synthesized. Both emitters show high photoluminescence efficiencies up to 94% and good electron mobility. The devices using two emitters with the structure of ITO (indium-tin-oxide)/MoO3 (molybdenum oxide, 5 nm)/TAPC (di-[4-(N,N-ditolyl-amino)-phenyl]cyclohexane, 30 nm)/mCP (1,3-bis(9H-carbazol-9-yl)benzene, 5 nm)/Ir(iii) complexes (6 wt%):PPO21 (3-(diphenylphosphoryl)-9-(4-(diphenylphosphoryl)phenyl)-9H-carbazole, 10 nm)/TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl) benzene, 40 nm)/LiF (1 nm)/Al (100 nm) display good electroluminescence performances with a maximum luminance of 48981 cd m2, a maximum current efficiency of 92.79 cd A1 and a maximum external quantum efficiency up to 31.8%, respectively, and the efficiency roll-off ratio is low, suggesting that they have potential application in OLEDs.
