Issue 18, 2024

A planar electronic acceptor motif contributing to NIR-II AIEgen with combined imaging and therapeutic applications

Abstract

Designing molecules with donor–acceptor–donor (D–A–D) architecture plays an important role in obtaining second near-infrared region (NIR-II, 1000–1700 nm) fluorescent dyes for biomedical applications; however, this always comes with a challenge due to very limited electronic acceptors. On the other hand, to endow NIR-II fluorescent dyes with combined therapeutic applications, trivial molecular design is indispensable. Herein, we propose a pyrazine-based planar electronic acceptor with a strong electron affinity, which can be used to develop NIR-II fluorescent dyes. By structurally attaching two classical triphenylamine electronic donors to it, a basic D–A–D module, namely Py-NIR, can be generated. The planarity of the electronic acceptor is crucial to induce a distinct NIR-II emission peaking at ∼1100 nm. The unique construction of the electronic acceptor can cause a twisted and flexible molecular conformation by the repulsive effect between the donors, which is essential to the aggregation-induced emission (AIE) property. The tuned intramolecular motions and twisted D–A pair brought by the electronic acceptor can lead to a remarkable photothermal conversion with an efficiency of 56.1% and induce a type I photosensitization with a favorable hydroxyl radical (OH˙) formation. Note that no additional measures are adopted in the molecular design, providing an ideal platform to realize NIR-II fluorescent probes with synergetic functions based on such an acceptor. Besides, the nanoparticles of Py-NIR can exhibit excellent NIR-II fluorescence imaging towards orthotopic 4T1 breast tumors in living mice with a high sensitivity and contrast. Combined with photothermal imaging and photoacoustic imaging caused by the thermal effect, the imaging-guided photoablation of tumors can be well performed. Our work has created a new opportunity to develop NIR-II fluorescent probes for accelerating biomedical applications.

Graphical abstract: A planar electronic acceptor motif contributing to NIR-II AIEgen with combined imaging and therapeutic applications

Supplementary files

Article information

Article type
Edge Article
Submitted
22 Dec 2023
Accepted
28 Mar 2024
First published
01 Apr 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2024,15, 6777-6788

A planar electronic acceptor motif contributing to NIR-II AIEgen with combined imaging and therapeutic applications

M. Chen, Z. Zhang, R. Lin, J. Liu, M. Xie, X. He, C. Zheng, M. Kang, X. Li, H. Feng, J. W. Y. Lam, D. Wang and B. Z. Tang, Chem. Sci., 2024, 15, 6777 DOI: 10.1039/D3SC06886B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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