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Effects of donor substituents on the conformational heterogeneity, photophysical, mechanochromic and electroluminescent properties of the donor-substituted fluorine-containing triphenylpyrimidines.

Authors :
Starykov, Hryhorii
Bezvikonnyi, Oleksandr
Sych, Galyna
Simokaitiene, Jurate
Volyniuk, Dmytro
Lazauskas, Algirdas
Grazulevicius, Juozas Vidas
Source :
Spectrochimica Acta Part A: Molecular & Biomolecular Spectroscopy. Nov2024, Vol. 321, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

[Display omitted] • New triphenylpyrimidines with different donors synthesized. • Experimental signs of SSLE, TADF, RTP and TTA detected for one compound. • Mechanochromism predetermined by conformational heterogeneity. • Efficient OLED and oxygen sensor application operating utilizing triplet states. Three derivatives of fluorinated triphenylpyrimidine with the attached carbazole, phenothiazine, or acridan donor moieties are synthesized by Buchwald-Hartwig reactions. The impact of the donor units on emissive and other properties of the compounds is reported. The compounds exhibit excellent thermal stability, competitive photophysical phenomena such as room temperature phosphorescence (RTP) appearing when compounds are molecularly dispersed in the rigid polymer matrix and thermally activated delayed fluorescence (TADF). The compounds with carbazole and phenothiazine donor moieties show the manifestation of triplet–triplet annihilation in the electroluminescence when used as emitters in organic light-emitting diodes (OLEDs). The phenothiazine-containing compound exhibit dual photoluminescence with the blue-shifted peak corresponding to the quasi-axial conformer and a red-shifted peak to the quasi-equatorial conformer. This derivative shows reversible shifts of emission spectra exceeding 100 nm due to the stable (at least 4 cycles) mechanochromic luminescence under the application of external stimuli. After grinding the emission intensity maximum is observed at 555 nm, after fuming at. ca 448 nm and after melting at 555 nm. The photoluminescence shifts and ON/OFF delayed fluorescence of the phenothiazine-based emitter occur due to the alteration between the crystalline and amorphous states. Optimization of the device structure allows to control the charge balance resulting in external quantum efficiency of up to 5.7 % observed for the OLED based on the phenothiazine-based emitter. This compound also shows the biggest response to the presence of oxygen acting as the quencher of triplet excited energy. The film of the compound doped in rigid Zeonex shows an 8.4-fold increase in emission intensity after evacuation. The optical sensor fabricated using the derivative of fluorinated triphenylpyrimidine and phenothiazine is characterized by the Stern-Volmer constant 1.37 × 10-4 ppm−1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13861425
Volume :
321
Database :
Academic Search Index
Journal :
Spectrochimica Acta Part A: Molecular & Biomolecular Spectroscopy
Publication Type :
Academic Journal
Accession number :
178909081
Full Text :
https://doi.org/10.1016/j.saa.2024.124668