高效的芘基蓝色发射器,利用优化的侧基团

IF 3.9 3区 工程技术 Q2 CHEMISTRY, APPLIED Dyes and Pigments Pub Date : 2025-04-01 Epub Date: 2024-12-12 DOI:10.1016/j.dyepig.2024.112596
Saeyoung Oh , Hyocheol Jung , Sangwook Park , Suhyeon Jeong , Kiho Lee , Young Il Park , Hayoon Lee , Jongwook Park
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引用次数: 0

摘要

基于芘核发色团,通过引入二苯并呋喃和二苯并噻吩侧基,设计合成了3,8-二异丙基-N1, n6 -二苯基-N1, n6 -双(8-苯基二苯并[b,d]呋喃-2-基)芘-1,6-二胺(DBF-DIP)和N1-(二苯并[b,d]噻吩-2-基)-3,8-二异丙基-N1, n6 -二苯基- n6 -(8-苯基二苯并[b,d]噻吩-2-基)芘-1,6-二胺(DBT-DIP)两个蓝色荧光掺杂剂。合成的DBF-DIP和DBT-DIP化合物的分解温度(Td)分别为496℃和505℃,玻璃化转变温度(Tg)分别为170℃和174℃,表明它们具有良好的热稳定性。当DBF-DIP和DBT-DIP作为掺杂剂用于OLED器件时,均表现出优异的电致发光(EL)器件性能,电流效率(CE)均超过10 cd/A。特别是DBT-DIP器件在10 mA/cm2下的最大外量子效率为8.25%,CE为11.2 cd/ a。
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Highly efficient pyrene-based blue emitters utilizing optimized side groups
We designed and synthesized two blue fluorescent dopants, 3,8-diisopropyl-N1, N6-diphenyl-N1,N6-bis(8-phenyldibenzo [b,d]furan-2-yl)pyrene-1,6-diamine (DBF-DIP) and N1-(dibenzo [b,d]thiophen-2-yl)-3,8-diisopropyl-N1,N6-diphenyl-N6-(8-phenyldibenzo [b,d]thiophen-2-yl)pyrene-1,6-diamine (DBT-DIP), by introducing dibenzofuran and dibenzothiophene side groups, based on pyrene core chromophore. The synthesized two compounds, DBF-DIP and DBT-DIP, exhibited decomposition temperatures (Td) of 496 °C and 505 °C, respectively, along with glass transition temperatures (Tg) of 170 °C and 174 °C, indicating their excellent thermal stability. When used as dopants in OLED devices, both DBF-DIP and DBT-DIP exhibited an excellent electroluminescent (EL) device performances with current efficiencies (CE) of over 10 cd/A. Especially, the DBT-DIP device demonstrated a maximum external quantum efficiency of 8.25 % and CE of 11.2 cd/A at 10 mA/cm2.
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来源期刊
Dyes and Pigments
Dyes and Pigments 工程技术-材料科学:纺织
CiteScore
8.20
自引率
13.30%
发文量
933
审稿时长
33 days
期刊介绍: Dyes and Pigments covers the scientific and technical aspects of the chemistry and physics of dyes, pigments and their intermediates. Emphasis is placed on the properties of the colouring matters themselves rather than on their applications or the system in which they may be applied. Thus the journal accepts research and review papers on the synthesis of dyes, pigments and intermediates, their physical or chemical properties, e.g. spectroscopic, surface, solution or solid state characteristics, the physical aspects of their preparation, e.g. precipitation, nucleation and growth, crystal formation, liquid crystalline characteristics, their photochemical, ecological or biological properties and the relationship between colour and chemical constitution. However, papers are considered which deal with the more fundamental aspects of colourant application and of the interactions of colourants with substrates or media. The journal will interest a wide variety of workers in a range of disciplines whose work involves dyes, pigments and their intermediates, and provides a platform for investigators with common interests but diverse fields of activity such as cosmetics, reprographics, dye and pigment synthesis, medical research, polymers, etc.
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