Highly Efficient and Robust Blue Phosphorescent Pt(II) Compounds with a Phenyl‐1,2,3‐triazolyl and a Pyridyl‐1,2,4‐triazolyl Chelate Core
Source abstract
Abstract
A new class of brightly phosphorescent Pt(II) compounds that contain an N∧C‐chelate phenyl‐1,2,3‐triazolyl ligand (ptrz) and an N∧C‐chelate pyridyl‐1,2,4‐triazolyl ligand (pytrz) in the central core is achieved. The impact of various substituent groups on phosphorescence of this class of molecules is examined. Crystal structural analyses revealed that this class of compounds has a great tendency to form stacked dimers—one of which is persistent even in the gas phase—leading to excimer emission. The introduction of bulky substituents, such as diphenyl amino (NPh2) or trityl (CPh3), is found to greatly diminish the excimer emission. Using this approach, several highly efficient blue and green phosphorescent Pt(II) compounds with λem at ≈450–460 nm and Φp ≈ 0.70 to 1.00 are obtained. These molecules are highly robust with exceptionally high thermal stability. Bright bluish‐green electrophosphorescent devices with external quantum efficiencies as high as 16.7% are fabricated.
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Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Catalytic Cross-Coupling Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry Queen's University Kingston Ontario K7L 3N6 Canada
Department of Materials Science and Engineering University of Toronto Toronto Ontario M5S 3E4 Canada
Department of Chemistry University of Toronto 80 St George St. Toronto Ontario M5S 3H6 Canada
References (55)
Show source-provided references
1. 10.1016/S1369-7021(11)70211-510.1016/S1369-7021(11)70211-5 ↗
2. 10.1117/1.352941210.1117/1.3529412 ↗
3. 10.1002/adma.20120062710.1002/adma.201200627 ↗
4. 10.1039/c3nj00170a10.1039/c3nj00170a ↗
5. 10.1021/ic050324u10.1021/ic050324u ↗
6. 10.1021/ic048599h10.1021/ic048599h ↗
7. 10.1021/cm061173b10.1021/cm061173b ↗
8. 10.1021/ic701110p10.1021/ic701110p ↗
9. 10.1002/anie.20080074810.1002/anie.200800748 ↗
10. 10.1021/am800122n10.1021/am800122n ↗
11. 10.1039/B812281D10.1039/B812281D ↗
12. 10.1039/c0cc04684a10.1039/c0cc04684a ↗
13. 10.1039/C2TC00270A10.1039/C2TC00270A ↗
14. 10.1039/c2jm32717a10.1039/c2jm32717a ↗
15. 10.1002/adma.20130109110.1002/adma.201301091 ↗
16. 10.1021/ja406518810.1021/ja4065188 ↗
17. 10.1002/adfm.20130407210.1002/adfm.201304072 ↗
18. 10.1002/adfm.20130378510.1002/adfm.201303785 ↗
19. 10.1021/ic025550810.1021/ic0255508 ↗
20. 10.1016/j.ccr.2006.02.00710.1016/j.ccr.2006.02.007 ↗
21. 10.1021/ic801415710.1021/ic8014157 ↗
22. 10.1016/j.ccr.2008.03.01410.1016/j.ccr.2008.03.014 ↗
23. 10.1063/1.326843410.1063/1.3268434 ↗
24. 10.1016/j.ccr.2011.01.04910.1016/j.ccr.2011.01.049 ↗
25. 10.1595/147106713X65901910.1595/147106713X659019 ↗
26. 10.1002/adma.20070294010.1002/adma.200702940 ↗
27. 10.1039/c2cc31330h10.1039/c2cc31330h ↗
28. 10.1002/anie.20130254110.1002/anie.201302541 ↗
29. Schläfer H. L. · 1969
30. 10.1016/S0301-0104(02)00921-710.1016/S0301-0104(02)00921-7 ↗
31. 10.1021/ic051049e10.1021/ic051049e ↗
32. 10.1002/adfm.20060016710.1002/adfm.200600167 ↗
33. 10.1021/cm070726v10.1021/cm070726v ↗
34. 10.1002/adfm.20100090410.1002/adfm.201000904 ↗
35. 10.1002/adfm.20110016510.1002/adfm.201100165 ↗
36. 10.1002/adfm.20040013110.1002/adfm.200400131 ↗
37. 10.1039/c0jm01159b10.1039/c0jm01159b ↗
38. 10.1039/C0CC04014B10.1039/C0CC04014B ↗
39. 10.1063/1.359349510.1063/1.3593495 ↗
40. 10.1021/ja304865610.1021/ja3048656 ↗
41. 10.1002/chem.20120125510.1002/chem.201201255 ↗
42. 10.1002/adfm.20130287110.1002/adfm.201302871 ↗
43. 10.1039/c3nj00468f10.1039/c3nj00468f ↗
44. Park H. J. · J. Org. Chem. · 2013 · 78 · 805
45. 10.1021/ol300242f10.1021/ol300242f ↗
46. 10.1021/ja061422x10.1021/ja061422x ↗
47. 10.1021/ja047955s10.1021/ja047955s ↗
48. Frisch M. J. · 2009
49. 10.1002/adma.20100312810.1002/adma.201003128 ↗
50. 10.1021/cm403755510.1021/cm4037555 ↗
51. 10.1021/ja903317w10.1021/ja903317w ↗
52. Q.Wang H. Z.Sibnoi X.Wang S.Wang H.Aziz unpublished work.
53. 10.1002/adma.20030215110.1002/adma.200302151 ↗
54. SHELXTL Version 6.14 Bruker Analytical X‐ray Systems copyright 2000–2003.
55. These data can be obtained free of charge from The Cambridge Crystallographic Data Center viawww.ccdc.cam.ac.uk/data_request/cif.