全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

螺芴咪唑–咔唑位点异构体的光物理性质及发光效率差异研究
Photophysical Properties and Luminescence Efficiency Differences of Spirofluorene-Imidazole/Carbazole Positional Isomers

DOI: 10.12677/amc.2026.143035, PP. 375-390

Keywords: 位点异构,螺芴咪唑,咔唑,光致发光量子产率,荧光寿命
Positional Isomerism
, Spirofluorene-Imidazole, Carbazole, Photoluminescence Quantum Yield, Fluorescence Lifetime

Full-Text   Cite this paper   Add to My Lib

Abstract:

为探究连接位点对螺芴咪唑–咔唑类有机荧光材料发光行为的影响,本文以螺芴咪唑为核心骨架、二苯基咔唑为给体单元,设计并合成了两种位点异构型蓝绿光荧光材料DP-CA和SP-CA。两种化合物组成单元相同,但给体连接位置不同,可作为研究位点异构效应的模型分子。通过1H NMR和HRMS对目标化合物结构进行了确认,并结合DFT计算、紫外–可见吸收光谱、荧光光谱、时间分辨荧光、循环伏安法和热重分析系统研究其结构与性能关系。结果表明,DP-CA和SP-CA均表现出蓝绿光发射,最大发射波长分别为498 nm和489 nm,但其光致发光量子产率差异显著,分别为81.52%和5.11%。时间分辨荧光测试显示,二者积分寿命分别为10.46 ns和10.69 ns,说明发光效率差异并非主要由激发态寿命决定,而与辐射跃迁效率及非辐射失活过程密切相关。DFT计算表明,DP-CA中给体与受体之间保持适度电子耦合,有利于辐射跃迁;而SP-CA中HOMO/LUMO空间分离程度较高,可能削弱辐射跃迁并增强非辐射失活,从而导致PLQY明显降低。热重分析显示,SP-CA的热分解温度为540℃,高于DP-CA的434℃,表明热稳定性与发光效率并不必然同步。上述结果说明,连接位点不仅影响螺芴咪唑–咔唑类材料的分子构型和能级分布,还会调控轨道重叠及辐射/非辐射过程的竞争关系,为位点异构调控蓝绿光有机荧光材料性能提供了参考。
To investigate the influence of connection sites on the luminescence behavior of spirofluorene-imidazole/carbazole-based organic fluorescent materials, two positional isomeric blue-green fluorescent materials, DP-CA and SP-CA, were designed and synthesized using spirofluorene-imidazole as the core skeleton and diphenylcarbazole as the donor unit. The two compounds possess identical structural units but differ in the donor connection sites, making them suitable model molecules for studying positional isomerism effects. The structures of the target compounds were confirmed by 1H NMR and HRMS, and their structure-property relationships were systematically investigated by DFT calculations, UV-vis absorption spectroscopy, photoluminescence spectroscopy, time-resolved fluorescence measurements, cyclic voltammetry, and thermogravimetric analysis. The results show that both DP-CA and SP-CA exhibit blue-green emission, with maximum emission wavelengths of 498 nm and 489 nm, respectively. However, their photoluminescence quantum yields differ significantly, reaching 81.52% and 5.11%, respectively. Time-resolved fluorescence measurements reveal that their integrated lifetimes are 10.46 ns and 10.69 ns, indicating that the difference in luminescence efficiency is not mainly determined by the excited-state lifetime, but is closely related to radiative transition efficiency and nonradiative decay processes. DFT calculations indicate that DP-CA maintains moderate electronic coupling between the donor and acceptor units, which is favorable for radiative transition, whereas SP-CA exhibits a higher degree of HOMO/LUMO spatial separation, which may weaken radiative transition and enhance nonradiative decay, resulting in a markedly reduced PLQY. Thermogravimetric analysis

References

[1]  Tang, C.W. and VanSlyke, S.A. (1987) Organic Electroluminescent Diodes. Applied Physics Letters, 51, 913-915.
https://doi.org/10.1063/1.98799
[2]  Hong, G., Gan, X., Leonhardt, C., Zhang, Z., Seibert, J., Busch, J.M., et al. (2021) A Brief History of OLEDS—Emitter Development and Industry Milestones. Advanced Materials, 33, Article 2005630.
https://doi.org/10.1002/adma.202005630
[3]  Lee, J.H., Chen, C.H., Lee, P.H., et al. (2019) Blue Organic Light-Emitting Diodes: Current Status, Challenges, and Future Outlook. Journal of Materials Chemistry C, 7, 5874-5888.
[4]  Ha, J.M., Hur, S.H., Pathak, A., Jeong, J. and Woo, H.Y. (2021) Recent Advances in Organic Luminescent Materials with Narrowband Emission. NPG Asia Materials, 13, Article No. 53.
https://doi.org/10.1038/s41427-021-00318-8
[5]  Chen, W.C., Zhu, Z.L. and Lee, C.S. (2018) Organic Light‐Emitting Diodes Based on Imidazole Semiconductors. Advanced Optical Materials, 6, Article 1800258.
https://doi.org/10.1002/adom.201800258
[6]  Zhao, L., Li, J., Li, L. and Hu, W. (2024) Recent Advances in Small-Molecule Organic Fluorescent Semiconductors. Journal of Materials Chemistry C, 12, 13745-13761.
https://doi.org/10.1039/d4tc01801j
[7]  Prabhu, C.P.K., Naveen, K.R. and Hur, J. (2024) Acceptor-Donor-Acceptor Based Thermally Activated Delayed Fluorescent Materials: Structure-Property Insights and Electroluminescence Performances. Materials Chemistry Frontiers, 8, 769-784.
https://doi.org/10.1039/d3qm01125a
[8]  Xu, Y., Xu, P., Hu, D. and Ma, Y. (2021) Recent Progress in Hot Exciton Materials for Organic Light-Emitting Diodes. Chemical Society Reviews, 50, 1030-1069.
https://doi.org/10.1039/d0cs00391c
[9]  Chen, X., Ma, D., Liu, T., Chen, Z., et al. (2022) Hybridized Local and Charge-Transfer Excited-State Fluorophores through the Regulation of the Donor-Acceptor Torsional Angle for Highly Efficient Organic Light-Emitting Diodes. CCS Chemistry, 4, 1285-1295.
[10]  Tian, X., Sheng, J., Zhang, S., Xiao, S., Gao, Y., Liu, H., et al. (2021) A Novel Deep Blue Le-Dominated HLCT Excited State Design Strategy and Material for OLED. Molecules, 26, Article 4560.
https://doi.org/10.3390/molecules26154560
[11]  Liu, Y., Tao, T., Hu, H., Li, H. and Ouyang, X. (2021) Fine Regulation of Linker and Donor Moieties to Construct Benzimidazole-Based Blue Emitters for High-Efficient Organic Light-Emitting Diodes. Dyes and Pigments, 188, Article 109191.
https://doi.org/10.1016/j.dyepig.2021.109191
[12]  Liu, Y., Yang, L., Bai, Q., Li, W., et al. (2021) Highly Efficient Non-Doped Blue Electroluminescence Based on Hybridized Local and Charge-Transfer Emitter Bearing Pyrene-Imidazole and Pyrene. Chemical Engineering Journal, 420, Article 129939.
[13]  Kumar, K. and Thakur, D. (2024) Overview of Imidazole-Based Fluorescent Materials with Hybridized Local and Charge Transfer and Hot-Exciton Pathway Characteristics in Excited States. Soft Matter, 20, 1669-1688.
https://doi.org/10.1039/d3sm01005h
[14]  Yu, P. and Xiao, Y. (2021) Non-Doped Deep-Blue OLEDs Based on Carbazole-π-Imidazole Derivatives. Materials, 14, Article 2349.
https://doi.org/10.3390/ma14092349
[15]  Bezvikonnyi, O., Bernard, R.S., Andruleviciene, V., Volyniuk, D., Keruckiene, R., Vaiciulaityte, K., et al. (2022) Derivatives of Imidazole and Carbazole as Bifunctional Materials for Organic Light Emitting Diodes. SSRN Electronic Journal.
https://doi.org/10.2139/ssrn.4110014
[16]  Ravi, S., Nithiasri, P.R., Karthikeyan, S., Pannipara, M., Al-Sehemi, A.G., Moon, D., et al. (2023) Carbazole Fluorophore with an Imidazole/Thiazole Unit: Contrasting Stimuli-Induced Fluorescence Switching, Water-Sensing and Deep-Blue Emission. RSC Advances, 13, 12476-12482.
https://doi.org/10.1039/d3ra01897k
[17]  Peng, H.N., Liu, J.L., Li, G.Z., Zhao, B., et al. (2024) Efficient Deep Blue Fluorescent Emitters Based on Bipolar Phenanthroimidazole-Carbazole Hybrid for Non-Doped Electroluminescent Device with Small Ciey. Dyes and Pigments, 222, Article 111885.
https://doi.org/10.1016/j.dyepig.2023.111885
[18]  Keerthika, P., Kumar, A., Selvaganesan, A., Moon, J., Nutalapati, V., Lee, J.Y., et al. (2025) Overcoming the 5% EQE Ceiling in Deep-Blue Fluorescent OLEDs with Hybridized Local and Charge Transfer Featured Phenanthroimidazole-Carbazole Emitters. Journal of Materials Chemistry C, 13, 20540-20548.
https://doi.org/10.1039/d5tc02737c
[19]  Wang, Y., Du, C., Cheng, Z., Ge, S., Feng, Z., Wan, L., et al. (2024) Rational Molecular Design of Phenanthroimidazole-Based Fluorescent Materials toward High-Efficiency Deep-Blue Oleds by Molecular Isomer Engineering. ACS Applied Materials & Interfaces, 16, 51201-51211.
https://doi.org/10.1021/acsami.4c05510
[20]  Sun, H., Chen, S., Zhong, A., Sun, R., Jin, J., Yang, J., et al. (2023) Tuning Photophysical Properties via Positional Isomerization of the Pyridine Ring in Donor-Acceptor-Structured Aggregation-Induced Emission Luminogens Based on Phenylmethylene Pyridineacetonitrile Derivatives. Molecules, 28, Article 3282.
https://doi.org/10.3390/molecules28073282
[21]  Zhang, D., Song, X., Cai, M., Kaji, H. and Duan, L. (2018) Versatile Indolocarbazole‐Isomer Derivatives as Highly Emissive Emitters and Ideal Hosts for Thermally Activated Delayed Fluorescent OLEDs with Alleviated Efficiency Roll‐Off. Advanced Materials, 30, Article 1705406.
https://doi.org/10.1002/adma.201705406
[22]  Zeng, S., Xie, Y., Huang, W., Wei, C., et al. (2026) Spiro-Fluoreno-Imidazole Emitters Efficiently Harvesting Hot Excitons for Deep-Blue Organic Light-Emitting Diodes with CIEy below 0.046. Angewandte Chemie International Edition, 2026, e202524293.
[23]  Allen, L.A.T. and Natho, P. (2023) Trends in Carbazole Synthesis—An Update (2013-2023). Organic & Biomolecular Chemistry, 21, 8956-8974.
https://doi.org/10.1039/d3ob01605f
[24]  Tagare, J. and Vaidyanathan, S. (2018) Recent Development of Phenanthroimidazole-Based Fluorophores for Blue Organic Light-Emitting Diodes (OLEDs): An Overview. Journal of Materials Chemistry C, 6, 10138-10173.
https://doi.org/10.1039/c8tc03689f
[25]  Chen, W.C., Yuan, Y., Xiong, Y., Rogach, A.L., Tong, Q. and Lee, C. (2017) Aromatically C6-and C9-Substituted Phenanthro[9,10-d]imidazole Blue Fluorophores: Structure-Property Relationship and Electroluminescent Application. ACS Applied Materials & Interfaces, 9, 26268-26278.
https://doi.org/10.1021/acsami.7b06547

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133