Pyrene-Based Triphenylamine Light-Harvesting Materials with Related Structure–Property Relationships DOI

Shaoling Li,

Jie Lin, Xiaoxue Chen

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Май 11, 2025

In this study, a series of novel pyrene-based triphenylamine (TPA) and its derivatives (4,4'-dimethoxytriphenylamine, TPA-OMe) were synthesized from newly developed chemical intermediate, bromopyrene. This approach provides unique opportunity to systematically investigate the effects substituent number position on their photophysical properties. The results demonstrate that molar absorption coefficients fluorescence quantum yields these pyrene significantly increase with TPA or TPA-OMe units, exhibiting excellent light-harvesting antenna characteristics. introduction units at 1,6-positions induces blue shift in while having minimal impact bands solution. Single-crystal X-ray diffraction analysis solid-state spectroscopy reveal steric hindrance effect groups suppresses complex intramolecular interactions, thereby preserving properties derivatives. Furthermore, concentration-dependent time-resolved spectra provide insights into molecular aggregation behavior energy transfer processes. findings study offer new strategy for designing efficient artificial systems lay theoretical foundation applications conversion.

Язык: Английский

Pyrene‐Based Blue Aggregation‐Induced Emission Luminogens: The Synergistic Effect of Through‐Space Conjugation for High Exciton Utilization Efficiency and Narrow‐Band and Blue OLEDs DOI
Wei Liu, Siwei Zhang, Tao Jiang

и другие.

Advanced Optical Materials, Год журнала: 2025, Номер unknown

Опубликована: Апрель 26, 2025

Abstract Achieving outstanding narrow‐band emission and improving the triplet exciton utilization efficiency is crucial for high organic light‐emitting diodes (OLEDs) electroluminescence (EL) efficiency. Herein, novel 1,3‐asymmetrical substituted pyrene‐based blue “hot exciton” materials with aggregation‐induced (AIE) characteristics are synthesized, utilizing pyrene ring's staggered energy levels high‐performance OLEDs. The triphenylamine‐decorated emitters exhibited narrow full width at half maxima (FWHM) < 60 nm, while tetraphenylethylene‐decorated compounds displayed a higher fluorescence quantum yield but broader FWHM in film state. These AIE luminogens (AIEgens) show good EL (>35.6%) nondoped OLED devices. Meanwhile, both pyrenes further utilized as an emitter layer thermally activated delayed (TADF)‐sensitized OLEDs great performance. Moreover, TPE‐decorated TPE‐ m 2Ph demonstrated maximum brightness, current efficiency, power external of 35230 cd −2 , 42 A −1 48 lm W 14.9%, respectively.

Язык: Английский

Процитировано

0

Pyrene-Based Triphenylamine Light-Harvesting Materials with Related Structure–Property Relationships DOI

Shaoling Li,

Jie Lin, Xiaoxue Chen

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Май 11, 2025

In this study, a series of novel pyrene-based triphenylamine (TPA) and its derivatives (4,4'-dimethoxytriphenylamine, TPA-OMe) were synthesized from newly developed chemical intermediate, bromopyrene. This approach provides unique opportunity to systematically investigate the effects substituent number position on their photophysical properties. The results demonstrate that molar absorption coefficients fluorescence quantum yields these pyrene significantly increase with TPA or TPA-OMe units, exhibiting excellent light-harvesting antenna characteristics. introduction units at 1,6-positions induces blue shift in while having minimal impact bands solution. Single-crystal X-ray diffraction analysis solid-state spectroscopy reveal steric hindrance effect groups suppresses complex intramolecular interactions, thereby preserving properties derivatives. Furthermore, concentration-dependent time-resolved spectra provide insights into molecular aggregation behavior energy transfer processes. findings study offer new strategy for designing efficient artificial systems lay theoretical foundation applications conversion.

Язык: Английский

Процитировано

0