Combining discotic mesogens with AIE luminogens for advanced optoelectronic applications: Design, synthesis, mesomorphism, self-assembly and optical properties of tetraphenylethylene-triphenylene oligomeric conjugates

The combination of different molecular entities with their own and specific functionalities within a single molecule enables the generation of potentially original multifunctional materials with unique properties and a broad range of applications across various fields. In this work, tetraphenylethylene (TPE) and triphenylene (TP) molecules are combined within a single oligomeric structure to yield original mesmorphic materials: TPE was chosen for its exceptional optical properties (AIE—aggregation-induced emission), while TP was included to ensure columnar self-assembly and mesomorphism. Two tetraphenylethylene-triphenylene tetrads, TPE-TP4 and TPE-ThTP4 , with a crossed-shaped molecular structure, with the central TPE connecting 4 radial TP subunits, have been synthesized by the Suzuki-Miyaura coupling reaction. Both compounds exhibit high thermal stability, above 340°C. While TPE-TP4 shows only crystalline behaviour before reversibly melting into the isotropic liquid, TPE-ThTP4 , which includes an additional thiophene ring bridging the central TPE and the peripheral TPs, exhibits a rectangular “multicolumnar” phase (Col rec ), over a large temperature range of approximately 300°C. They also both self-assemble in fibers when mixed in various solvents to form organic gels. UV-visible absorption and fluorescence emission spectra reveal that both compounds have strong fluorescence properties in solutions and thin films, with emission wavelengths ranging between 460 and 550 nm. The absolute emission quantum yield is highly solvent-dependent, reaching a maximum of 84.5% in cyclohexane. These tetrameric compounds also present significant aggregation induction emission behaviour. Overall, the combination of discotic mesogens and AIE-gens within a single molecular framework holds great promises for the development of next-generation optoelectronic materials. Combining tetraphenylethylene (AIE luminogen) with triphenylene (discotic mesogen) into single oligomers, enables the creation of multifunctional materials with unique and modulable properties. They exhibit a rectangular multicolumnar phase over a broad temperature range, form organogels in nonpolar solvents, display strong fluorescence in solution and thin films, and exhibit aggregation-induced emission behavior, highlighting their potential for next-generation optoelectronic materials.

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Publication Details

Journal
Giant
Published
2025-05-18
DOI
https://doi.org/10.1016/j.giant.2025.100362
Citations
4
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
2.07

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article

Combining discotic mesogens with AIE luminogens for advanced optoelectronic applications: Design, synthesis, mesomorphism, self-assembly and optical properties of tetraphenylethylene-triphenylene oligomeric conjugates

Bi‐Qin Wang, Ke‐Qing Zhao, Bertrand Donnio, Ping Hu et al.
4 citations
Giant
Luminescence and Fluorescent Materials
2.07
article

Combining discotic mesogens with AIE luminogens for advanced optoelectronic applications: Design, synthesis, mesomorphism, self-assembly and optical properties of tetraphenylethylene-triphenylene oligomeric conjugates

Bi‐Qin Wang, Ke‐Qing Zhao, Bertrand Donnio, Ping Hu, Ke-Xiao Zhao, Hang Lin
article en
4 citations

Abstract

The combination of different molecular entities with their own and specific functionalities within a single molecule enables the generation of potentially original multifunctional materials with unique properties and a broad range of applications across various fields. In this work, tetraphenylethylene (TPE) and triphenylene (TP) molecules are combined within a single oligomeric structure to yield original mesmorphic materials: TPE was chosen for its exceptional optical properties (AIE—aggregation-induced emission), while TP was included to ensure columnar self-assembly and mesomorphism. Two tetraphenylethylene-triphenylene tetrads, TPE-TP4 and TPE-ThTP4 , with a crossed-shaped molecular structure, with the central TPE connecting 4 radial TP subunits, have been synthesized by the Suzuki-Miyaura coupling reaction. Both compounds exhibit high thermal stability, above 340°C. While TPE-TP4 shows only crystalline behaviour before reversibly melting into the isotropic liquid, TPE-ThTP4 , which includes an additional thiophene ring bridging the central TPE and the peripheral TPs, exhibits a rectangular “multicolumnar” phase (Col rec ), over a large temperature range of approximately 300°C. They also both self-assemble in fibers when mixed in various solvents to form organic gels. UV-visible absorption and fluorescence emission spectra reveal that both compounds have strong fluorescence properties in solutions and thin films, with emission wavelengths ranging between 460 and 550 nm. The absolute emission quantum yield is highly solvent-dependent, reaching a maximum of 84.5% in cyclohexane. These tetrameric compounds also present significant aggregation induction emission behaviour. Overall, the combination of discotic mesogens and AIE-gens within a single molecular framework holds great promises for the development of next-generation optoelectronic materials. Combining tetraphenylethylene (AIE luminogen) with triphenylene (discotic mesogen) into single oligomers, enables the creation of multifunctional materials with unique and modulable properties. They exhibit a rectangular multicolumnar phase over a broad temperature range, form organogels in nonpolar solvents, display strong fluorescence in solution and thin films, and exhibit aggregation-induced emission behavior, highlighting their potential for next-generation optoelectronic materials.

GiantVol. 23
Sichuan Normal University (CN)
National Natural Science Foundation of China, Université de Strasbourg, Centre National de la Recherche Scientifique
Openalex Percentile: Top 13%
Luminescence and Fluorescent Materials
2.07
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