Molecular Design and Synthetic Approaches for the Realization of Multichannel Radiative Decay Pathways in Gold(III) Complexes and Their Applications in Organic Light-Emitting Devices

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ming-Yi Leung, Man-Chung Tang, Shun-Cheung Cheng, Ziyong Chen, Shiu-Lun Lai, Wai Kit Tang, Mei-Yee Chan, Chi-Chiu Ko* and Vivian Wing-Wah Yam*, 
{"title":"Molecular Design and Synthetic Approaches for the Realization of Multichannel Radiative Decay Pathways in Gold(III) Complexes and Their Applications in Organic Light-Emitting Devices","authors":"Ming-Yi Leung,&nbsp;Man-Chung Tang,&nbsp;Shun-Cheung Cheng,&nbsp;Ziyong Chen,&nbsp;Shiu-Lun Lai,&nbsp;Wai Kit Tang,&nbsp;Mei-Yee Chan,&nbsp;Chi-Chiu Ko* and Vivian Wing-Wah Yam*,&nbsp;","doi":"10.1021/jacs.4c0920710.1021/jacs.4c09207","DOIUrl":null,"url":null,"abstract":"<p >A unique class of tridentate diaryltriazine ligand-containing gold(III) complexes with thermally activated delayed fluorescence (TADF) and/or thermally stimulated delayed phosphorescence (TSDP) properties has been designed and synthesized. With a simple structural modification on the coordination of carbazole moiety in the monodentate ligand, a large spectral shift of ∼160 nm (ca. 4900 cm<sup>–1</sup>) spanning from sky blue to red emissions has been demonstrated in solid-state thin films. Three-state or four-state models have been employed in fitting the emission lifetimes of the gold(III) complexes at various temperatures. The findings clearly indicate the presence of three emitting states, S<sub>1</sub>, T<sub>1</sub>, and T<sub>1</sub>′, suggesting the coexistence of TADF, phosphorescence, and TSDP. Notably, a minor structural change in the donor moiety between phenylcarbazolyl and diphenylaminoaryl has been demonstrated to turn on/off the TSDP, resulting in TADF-TSDP-phosphorescence or TADF-phosphorescence emitters. The TADF and/or TSDP properties have also been supported by temperature-dependent ultrafast transient absorption studies, with the direct observation of reverse intersystem crossing (RISC) and reverse internal conversion (RIC) and the determination of the activation parameters and excited state dynamics. Solution-processed and vacuum-deposited organic light-emitting devices (OLEDs) have been prepared, in which sky blue emitting devices based on <b>5</b> exhibit an operational lifetime LT<sub>70</sub> ∼ 5 times longer than the previously reported sky blue emitting analogue that shows only TSDP property. These results have provided valuable insights into the manipulation of the excited states via rational molecular design toward the realization of gold(III)-based TSDP and/or TADF materials with multiple radiative decay pathways that show enhanced radiative decay rate constants (<i>k</i><sub>r</sub>) for practical OLED applications.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"146 45","pages":"30901–30912 30901–30912"},"PeriodicalIF":14.4000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.4c09207","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

A unique class of tridentate diaryltriazine ligand-containing gold(III) complexes with thermally activated delayed fluorescence (TADF) and/or thermally stimulated delayed phosphorescence (TSDP) properties has been designed and synthesized. With a simple structural modification on the coordination of carbazole moiety in the monodentate ligand, a large spectral shift of ∼160 nm (ca. 4900 cm–1) spanning from sky blue to red emissions has been demonstrated in solid-state thin films. Three-state or four-state models have been employed in fitting the emission lifetimes of the gold(III) complexes at various temperatures. The findings clearly indicate the presence of three emitting states, S1, T1, and T1′, suggesting the coexistence of TADF, phosphorescence, and TSDP. Notably, a minor structural change in the donor moiety between phenylcarbazolyl and diphenylaminoaryl has been demonstrated to turn on/off the TSDP, resulting in TADF-TSDP-phosphorescence or TADF-phosphorescence emitters. The TADF and/or TSDP properties have also been supported by temperature-dependent ultrafast transient absorption studies, with the direct observation of reverse intersystem crossing (RISC) and reverse internal conversion (RIC) and the determination of the activation parameters and excited state dynamics. Solution-processed and vacuum-deposited organic light-emitting devices (OLEDs) have been prepared, in which sky blue emitting devices based on 5 exhibit an operational lifetime LT70 ∼ 5 times longer than the previously reported sky blue emitting analogue that shows only TSDP property. These results have provided valuable insights into the manipulation of the excited states via rational molecular design toward the realization of gold(III)-based TSDP and/or TADF materials with multiple radiative decay pathways that show enhanced radiative decay rate constants (kr) for practical OLED applications.

Abstract Image

实现金(III)配合物多通道辐射衰变途径的分子设计和合成方法及其在有机发光器件中的应用
我们设计并合成了一类独特的具有热激活延迟荧光(TADF)和/或热刺激延迟磷光(TSDP)特性的三叉二元三嗪配体含金(III)配合物。通过对单齿配体中的咔唑配位进行简单的结构修改,在固态薄膜中实现了 ∼160 nm(约 4900 cm-1)的巨大光谱位移,从天蓝色发射到红色发射。在拟合金(III)配合物在不同温度下的发射寿命时,采用了三态或四态模型。研究结果清楚地表明存在三种发射状态:S1、T1 和 T1′,这表明 TADF、磷光和 TSDP 是共存的。值得注意的是,供体分子在苯基咔唑基和二苯基氨基芳基之间的微小结构变化已被证明可以开启/关闭 TSDP,从而产生 TADF-TSDP-磷光或 TADF-磷光发射体。温度依赖性超快瞬态吸收研究也支持了 TADF 和/或 TSDP 特性,直接观察到了反向系统间交叉(RISC)和反向内部转换(RIC),并确定了活化参数和激发态动力学。制备了溶液处理和真空沉积有机发光器件(OLED),其中基于 5 的天蓝色发光器件的工作寿命 LT70 ∼ 5 倍于之前报道的仅显示 TSDP 特性的天蓝色发光类似物。这些结果为通过合理的分子设计操纵激发态提供了宝贵的见解,有助于实现具有多种辐射衰变途径的金(III)基 TSDP 和/或 TADF 材料,从而提高辐射衰变速率常数 (kr),实现 OLED 的实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信