2017
DOI: 10.1021/acs.jpcc.7b08034
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Impact of Donor Substitution Pattern on the TADF Properties in the Carbazolyl-Substituted Triazine Derivatives

Abstract: In this work, we report on the synthesis and photophysical investigation of a new star-shaped triazine-carbazole derivative 2,4,6-tris­(3-(3,6-di-tert-butyl-9H-carbazol-9-yl)­phenyl)-1,3,5-triazine. Comparative study of the photophysical properties of the newly synthesized emitter along with its para-substituted isomer 2,4,6-tris­(4-(3,6-di-tert-butyl-9H-carbazol-9-yl)­phenyl)-1,3,5-triazine was performed. While para-linkage caused higher oscillator strength of the lowest energy absorption band and high fluore… Show more

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Cited by 55 publications
(28 citation statements)
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“…This low‐energy absorption could be ascribed to the intramolecular charge transfer (ICT) transition from nido ‐carborane donor (HOMO) to the PhBMes 2 acceptor (LUMO) moiety (see the TD‐DFT results below). Nido ‐ p1 – p4 also exhibited similar absorption patterns, but had low‐energy absorptions much more intense than those of the meta compounds, indicating substantial HOMO–LUMO overlap (Supporting Information, Figure S11) . Electrochemical measurements of nido ‐ m1 – m4 display typical features for the triarylborane‐centered, reversible reduction (LUMO) and the nido ‐carborane‐centered, irreversible oxidation (HOMO; Supporting Information, Figure S10) .…”
Section: Methodscontrasting
confidence: 56%
“…This low‐energy absorption could be ascribed to the intramolecular charge transfer (ICT) transition from nido ‐carborane donor (HOMO) to the PhBMes 2 acceptor (LUMO) moiety (see the TD‐DFT results below). Nido ‐ p1 – p4 also exhibited similar absorption patterns, but had low‐energy absorptions much more intense than those of the meta compounds, indicating substantial HOMO–LUMO overlap (Supporting Information, Figure S11) . Electrochemical measurements of nido ‐ m1 – m4 display typical features for the triarylborane‐centered, reversible reduction (LUMO) and the nido ‐carborane‐centered, irreversible oxidation (HOMO; Supporting Information, Figure S10) .…”
Section: Methodscontrasting
confidence: 56%
“…The FL spectra of SFI nx Tz in dilute toluene solution showed CT‐featured structure‐less broad blue emissions peaked from 430 to 460 nm. It is noteworthy that compared to their meta‐analogs the emissions of SFI n pTz are hypochromatically shifted by ≈10 nm, revealing their weaker ICT states and reduced nonradiation energy loss . And the emissions from SFI n pTzs are remarkably brighter, consistent with their higher radiative transition probabilities as indicated by more overlap of HOMO and LUMO .…”
Section: Resultsmentioning
confidence: 91%
“…It is obvious that the absorption band at the range of 350–425 nm belongs to the CT transition between the ACRPh unit and the TRZ unit since the similar absorption band was observed for TRZ‐ p ‐ACR and TRZ‐ m ‐ACR. Since the TRZ based materials with meta‐position configuration usually have stronger CT states than their isomers with para‐position configuration, TRZ‐ p ‐ACRSA is expected to have higher PLQY due to its higher oscillator strength ( f ) of transition between S 0 and S 1 , which has positive correlation with ε. Meanwhile, as shown in Figure S7 in the Supporting Information, PL spectra of the ACRSA based materials show obvious blueshift compared with the ACRPh based materials due to the weaker electron‐donating ability of the ACRSA moiety, which are in accord with the results of the TDDFT calculation.…”
Section: Resultsmentioning
confidence: 99%