Distinct Ir(III) complexes containing unsymmetric ligands with fluorene-oxadiazole groups and their performance of organic light-emitting diodes. (June 2022)
- Record Type:
- Journal Article
- Title:
- Distinct Ir(III) complexes containing unsymmetric ligands with fluorene-oxadiazole groups and their performance of organic light-emitting diodes. (June 2022)
- Main Title:
- Distinct Ir(III) complexes containing unsymmetric ligands with fluorene-oxadiazole groups and their performance of organic light-emitting diodes
- Authors:
- Liu, Jia-Wei
Zhou, Han-Chen
Wang, Zi-Kun
Tang, Xiong
Wu, Hua-Yu
Wang, Shi
Lai, Wen-Yong
Li, Yong-Hua - Abstract:
- Abstract: 1, 3, 4-Oxadiazole was modified with phenyl and fluorenyl groups at the 2- and 5- positions, respectively, which can be used as a new cyclometalating ligand to synthesize a series of novel Ir(III) complexes. In the preparation of picolinate iridium(III) complexes [Ir(N^C)2(pic)] (N^C = cyclometalating ligand, pic = picolinate), two isomeric products were isolated unexpectedly, among which, the iridium(III) center in one product was cyclometalated at the phenyl site of two cyclometalating ligands. In the other, the cyclometalations occurred at the fluorenyl site and phenyl site from the two ligands respectively. Another possible isomer completely coordinated by two fluorenyl groups was not obtained owing to the very low product yield. The obtained two isomers were characterized by 1 H NMR and MALDI-TOF. Single-crystal X-ray structural analysis of their methyl-substituted analogues confirmed the different coordination modes. Electrochemical and photophysical investigation revealed that the excited-state properties of the two isomers were closely related to their coordination modes, and thus a facile strategy was provided that is to regulate luminescent and electrochemical properties by easily changing coordination sites. Both isomers were used to fabricate high performance electroluminescence devices using spin-coating techniques. The unsymmetric coordination complex FP-DP exhibited the highest performance among all the devices, achieving a maximum current efficiencyAbstract: 1, 3, 4-Oxadiazole was modified with phenyl and fluorenyl groups at the 2- and 5- positions, respectively, which can be used as a new cyclometalating ligand to synthesize a series of novel Ir(III) complexes. In the preparation of picolinate iridium(III) complexes [Ir(N^C)2(pic)] (N^C = cyclometalating ligand, pic = picolinate), two isomeric products were isolated unexpectedly, among which, the iridium(III) center in one product was cyclometalated at the phenyl site of two cyclometalating ligands. In the other, the cyclometalations occurred at the fluorenyl site and phenyl site from the two ligands respectively. Another possible isomer completely coordinated by two fluorenyl groups was not obtained owing to the very low product yield. The obtained two isomers were characterized by 1 H NMR and MALDI-TOF. Single-crystal X-ray structural analysis of their methyl-substituted analogues confirmed the different coordination modes. Electrochemical and photophysical investigation revealed that the excited-state properties of the two isomers were closely related to their coordination modes, and thus a facile strategy was provided that is to regulate luminescent and electrochemical properties by easily changing coordination sites. Both isomers were used to fabricate high performance electroluminescence devices using spin-coating techniques. The unsymmetric coordination complex FP-DP exhibited the highest performance among all the devices, achieving a maximum current efficiency of 12.16 cd/A and luminance of 7037.69 cd/m 2 . Highlights: We provide a facile method to synthesize unsymmetric Ir-complexes based on 1, 3, 4-oxadiazole. The FP-type complexes have better optical properties by photophysical and electrochemical analysis. The FP-type complexes are more suitable as doped emitters to fabricate monochromatic OLEDs. … (more)
- Is Part Of:
- Dyes and pigments. Volume 202(2022)
- Journal:
- Dyes and pigments
- Issue:
- Volume 202(2022)
- Issue Display:
- Volume 202, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 202
- Issue:
- 2022
- Issue Sort Value:
- 2022-0202-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-06
- Subjects:
- Iridium complexes -- OLED -- Electroluminescence -- AIPE
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2022.110252 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
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