1446317-69-6

Basic information

• Product Name: 2-(4-trifluoromethylphenyl)-5-(pentafluorophenyl)-1,3,4-oxadiazole
• Synonyms: 2-(4-trifluoromethylphenyl)-5-(pentafluorophenyl)-1,3,4-oxadiazole
• CAS NO: 1446317-69-6
• Molecular Weight: 380.197
• Mol File: 1446317-69-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(4-trifluoromethylphenyl)-5-(pentafluorophenyl)-1,3,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-trifluoromethylphenyl)-5-(pentafluorophenyl)-1,3,4-oxadiazole(1446317-69-6)
• EPA Substance Registry System: 2-(4-trifluoromethylphenyl)-5-(pentafluorophenyl)-1,3,4-oxadiazole(1446317-69-6)

Safety Data

• Hazardous Substances Data: 1446317-69-6(Hazardous Substances Data)

Upstream product

• 477886-85-4 5-(4-(trifluoromethyl)phenyl)-1,3,4-oxadiazole 
• 363-72-4 Pentafluorobenzene 
• 583-02-8 ethyl 4-(trifluoromethyl)benzoate 
• 339-59-3 4-(trifluoromethyl)benzoic acid hydrazide 
• 2251-50-5 pentafluorobenzoylchloride 
• 602-94-8 Pentafluorobenzoic acid 

Relevant articles and documents

Manipulating peripheral non-conjugated substituents in carbazole/oxadiazole hybrid TADF emitters towards high-efficiency OLEDs

The chemical modification of existing thermally activated delayed fluorescence (TADF) materials is a simple strategy to increase the luminescence efficiency and is also favorable for a deeper understanding of the structure-property relationship. In this work, based on a previous multi-functional carbazole/oxadiazole hybrid light-blue TADF emitter 2-(2,3,4,5,6-penta(9H-carbazol-9-yl)phenyl)-5-phenyl-1,3,4-oxadiazole (5CzOXD), a series of 5CzOXD derivatives have been designed by rationally introducing non-conjugated electron-donatingtert-butyl (t-Bu) units at the 3- and 6-positions of carbazole and/or electron-withdrawing trifluoromethyl (CF3) units at thepara- ormeta-positions of the terminal phenyl ring in the diphenyl-1,3,4-oxadiazole group. The TADF emission colors were slightly affected by non-conjugated peripheral substituents, while a singlet-triplet band gap (ΔEST) value could be easily tuned from 0.24 to ～0 eV. It is interesting that through step-by-step chemical modification, progressively increased photoluminescence (22-88%) and electroluminescence (2.3-13.7%) quantum efficiencies could be achieved for the TADF emitters in doped films of theo-CzOXD host matrix. Similar trends were also obtained for 26DCzPPy-hosted TADF OLEDs. For example, bare 5CzOXD showed a maximum external quantum efficiency (EQE) of 8.7%, the value oft-Bu-modified 5tCzOXD was increased to 14.2%, and even higher EQE values in the range of 20-22% were obtained fort-Bu and single CF3-substitutedmCF35tCzOXD andpCF35tCzOXD. The best EQE value of 23.3% was achieved for dCF35tCzOXD by synergisticalt-Bu and double CF3-substitution due to its ～0 eV of ΔESTfor a significantly increased reverse intersystem crossing rate and a decreased triplet non-radiative decay rate. This work provides an effective strategy for achieving high-efficiency TADF OLEDs through the modification of currently less efficient TADF emitters.