Synthesis and Photophysical Properties of a Water‐Soluble Tetrabenzotetraaza[8]Circulene Derivative With Long Lifetime Phosphorescence

ABSTRACT [8]Circulenes, a class of intriguing polycyclic aromatic hydrocarbons, have garnered considerable attention due to their aesthetically pleasing structures. Despite their unique structural features, the applications of these rigid π‐conjugated systems remain far from fully explored due to the inherent challenges in functionalizing them. In this study, we report the synthesis of a water‐soluble tetrabenzotetraaza[8]circulene derivative ( 3 ) through the introduction of four 2,5,8,11‐tetraoxatridecane substituents. The optical properties of 3 were systematically studied in THF/water mixtures, revealing its water‐fraction‐dependent fluorescence. At 77 K, compound 3 exhibits distinctive phosphorescence with an exceptionally long lifetime of 2.08 s and a phosphorescence quantum yield of 12.3%, both among the highest values of reported hetero[8]circulenes. Additionally, 3 displays a pronounced yellow‐green afterglow luminescence that persists for 7.6 s, underscoring its potential for persistent emission applications. This study presents an effective method to modulate the optoelectronic properties of hetero[8]circulene derivatives, offering new opportunities for hetero[8]circulenes as promising functional materials.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2026-02-01
DOI
https://doi.org/10.1002/ajoc.70318
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis and Photophysical Properties of a Water‐Soluble Tetrabenzotetraaza[8]Circulene Derivative With Long Lifetime Phosphorescence

Fengkun Chen, Rashid R. Valiev, Shijun Gu, Glib Baryshnikov et al.
Asian Journal of Organic Chemistry
Synthesis and Properties of Aromatic Compounds
article

Synthesis and Photophysical Properties of a Water‐Soluble Tetrabenzotetraaza[8]Circulene Derivative With Long Lifetime Phosphorescence

Fengkun Chen, Rashid R. Valiev, Shijun Gu, Glib Baryshnikov, Li Jiang
article en

Abstract

ABSTRACT [8]Circulenes, a class of intriguing polycyclic aromatic hydrocarbons, have garnered considerable attention due to their aesthetically pleasing structures. Despite their unique structural features, the applications of these rigid π‐conjugated systems remain far from fully explored due to the inherent challenges in functionalizing them. In this study, we report the synthesis of a water‐soluble tetrabenzotetraaza[8]circulene derivative ( 3 ) through the introduction of four 2,5,8,11‐tetraoxatridecane substituents. The optical properties of 3 were systematically studied in THF/water mixtures, revealing its water‐fraction‐dependent fluorescence. At 77 K, compound 3 exhibits distinctive phosphorescence with an exceptionally long lifetime of 2.08 s and a phosphorescence quantum yield of 12.3%, both among the highest values of reported hetero[8]circulenes. Additionally, 3 displays a pronounced yellow‐green afterglow luminescence that persists for 7.6 s, underscoring its potential for persistent emission applications. This study presents an effective method to modulate the optoelectronic properties of hetero[8]circulene derivatives, offering new opportunities for hetero[8]circulenes as promising functional materials.

Asian Journal of Organic ChemistryVol. 15(2)
University of Helsinki (FI), Donghua University (CN), Department of Science,Technology and Innovation (ZA), Department of Science and Technology and Biotechnology (IN)
European Commission, National Natural Science Foundation of China, National Science Council, Linköpings Universitet, Vetenskapsrådet, National Supercomputer Centre, Linköpings Universitet
Clean water and sanitation
Openalex Percentile: Top 66%
Synthesis and Properties of Aromatic Compounds
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Synthesis and Photophysical Properties of a Water‐Soluble Tetrabenzotetraaza[8]Circulene Derivative With Long Lifetime Phosphorescence — Fengkun Chen, Rashid R. Valiev, et al. · Asian Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS