Induced Aggregation of AIE‐Active Mono‐Cyclometalated Ir(III) Complex into Supramolecular Branched Wires for Light‐Emitting Diodes
Source abstract
Abstract
Aggregation‐induced emission (AIE) is commonly observed in irregular bulk form. Herein, unique aggregation properties of an AIE‐active complex into branched supramolecular wires are reported for the first time. Mono‐cyclometalated Ir(III) complex shows in‐plane J‐aggregation at the air–water interface owing to the restriction of intramolecular vibration of bidentate phenylpyridinato and intramolecular rotations of monodentate triphenylphosphine ligands at air–water interface. As a consequence, a large enhancement of luminescence comparable to the solid state is obtained from the monolayers of supramolecular wires. This unique feature is utilized for the fabrication of light‐emitting diodes with low threshold voltage using supramolecular wires as active layer. This study opens up the need of ordered assembly of AIE complexes to achieve optimal luminescence characteristics.
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Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Centre for Advanced Materials (CAM) Indian Association for the Cultivation of Science Jadavpur Kolkata 700032 India
Department of Chemistry Birla Institute of Technology and Science (BITS) Pilani Rajasthan 333031 India
Department of Physical Chemistry Indian Association for the Cultivation of Science Jadavpur Kolkata 700032 India
Funding
Science and Engineering Research Board · Department of Science and Technology, Ministry of Science and Technology · Department of Biotechnology , Ministry of Science and Technology
References (34)
Show source-provided references
1. 10.1021/cr030204910.1021/cr0302049 ↗
2. 10.1002/ange.20130289410.1002/ange.201302894 ↗
3. 10.1039/b502436f10.1039/b502436f ↗
4. 10.1002/adma.20130117410.1002/adma.201301174 ↗
5. 10.1016/j.mattod.2015.03.00410.1016/j.mattod.2015.03.004 ↗
6. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
7. Pope M. · 1982
8. 10.1021/cr050133910.1021/cr0501339 ↗
9. 10.1039/b105159h10.1039/b105159h ↗
10. 10.1039/b904665h10.1039/b904665h ↗
11. 10.1021/cm021715z10.1021/cm021715z ↗
12. 10.1002/adma.20140135610.1002/adma.201401356 ↗
13. 10.1039/C4CS00325J10.1039/C4CS00325J ↗
14. 10.1039/c1cs15113d10.1039/c1cs15113d ↗
15. 10.1002/chem.20100338210.1002/chem.201003382 ↗
16. 10.1021/jp046659z10.1021/jp046659z ↗
17. 10.1039/C4RA08363F10.1039/C4RA08363F ↗
18. 10.1039/c1cc12025e10.1039/c1cc12025e ↗
19. 10.1021/cm401999f10.1021/cm401999f ↗
20. 10.1002/adma.20130228310.1002/adma.201302283 ↗
21. 10.1038/pj.2016.810.1038/pj.2016.8 ↗
22. 10.1021/ic800376e10.1021/ic800376e ↗
23. 10.1039/C4TC00466C10.1039/C4TC00466C ↗
24. 10.1039/c2dt30771e10.1039/c2dt30771e ↗
25. 10.1002/adma.20040028410.1002/adma.200400284 ↗
26. 10.1039/B712416C10.1039/B712416C ↗
27. 10.1021/ja504014k10.1021/ja504014k ↗
28. 10.1021/ic800376e10.1021/ic800376e ↗
29. 10.1039/C3SC52495G10.1039/C3SC52495G ↗
30. 10.1021/ja017768j10.1021/ja017768j ↗
31. 10.1039/C6CC03493D10.1039/C6CC03493D ↗
32. 10.1021/la00042a02110.1021/la00042a021 ↗
33. 10.1021/la970272o10.1021/la970272o ↗
34. 10.1021/ac200030310.1021/ac2000303 ↗