In
this report, we synthesized two series of deep-blue-emitting
homoleptic iridium(III) phosphors bearing 1,2,4-triazol-3-ylidene
and 5-(trifluoromethyl)-1,2,4-triazol-3-ylidene cyclometalate. Compared
with reported synthetic routes using Ag2O as the promoter,
herein, we adopted a different strategy to furnish these complexes
in high yields. Also, the meridional to facial isomerization was executed
in the presence of trifluoroacetic acid. These phosphors were examined
using NMR spectroscopies, single-crystal X-ray diffraction studies,
and photophysical methods. The results revealed that electron-withdrawing
trifluoromethyl substitution on the N-heterocyclic carbene fragment
only gave a minor variation of photoluminescence peak wavelengths
and a decrease in radiative lifetime but notable reduction in thermal
stabilities. The parent 1,2,4-triazol-3-ylidene complexes have been
demonstrated to be suitable for use as deep-blue phosphors, with structured
emission with the peak max. located at ∼420 nm and with photoluminescence
quantum yields in a range of 34.8–42.5% in degassed THF solution
at RT. Fabrication of both the phosphorescent organic light-emitting
diodes (OLEDs) and phosphor-sensitized OLEDs (or hyperphosphorescence)
was successfully conducted, from which the OLED device based on
m-tz1 showed a max. external quantum efficiency
(EQE) of 10% with CIE
x,y
coordinates of 0.15, 0.06, while the corresponding hyperphosphorescent
OLED using
m-tz2 as a sensitizer and t-DABNA as a terminal emitter afforded a significantly improved
max. EQE of 19.7%, EL λmax of 468 nm, and FWHM of
31 nm with CIE
x,y
coordinates
of 0.12, 0.13.