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基于非发射性杂芳烃设计具有新型核心结构的红色聚集诱导发光材料。

Rational design of red AIEgens with a new core structure from non-emissive heteroaromatics.

作者信息

Chen Ming, Hu Xianglong, Liu Junkai, Li Baixue, Leung Nelson L C, Viglianti Lucia, Cheung Tsz Shing, Sung Herman H Y, Kwok Ryan T K, Williams Ian D, Qin Anjun, Lam Jacky W Y, Tang Ben Zhong

机构信息

Department of Chemistry , Hong Kong Branch of Chinese National Engineering , Research Center for Tissue Restoration and Reconstruction , Institute of Advanced Study , State Key Laboratory of Molecular Nanoscience , Division of Life Science and Diversion of Biomedical Engineering , The Hong Kong University of Science and Technology , Clear Water Bay, Kowloon , Hong Kong , China . Email:

MOE Key Laboratory of Laser Life Science , Institute of Laser Life Science , College of Biophotonics , South China Normal University , Guangzhou , 510631 , China.

出版信息

Chem Sci. 2018 Aug 21;9(40):7829-7834. doi: 10.1039/c8sc02810a. eCollection 2018 Oct 28.

DOI:10.1039/c8sc02810a
PMID:30429992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6194487/
Abstract

The development of new aggregation-induced emission (AIE) systems is a hot research topic, from which functional materials with diversified structures and properties are derived. Here, based on rare, non-emissive and highly electron-withdrawing heteroaromatics of 1,4,5,8-tetraazaanthracene (TAA), experimental and theoretical studies reveal that attaching phenyl rotors to TAA is crucial to creating a new N-type AIE core structure. Furthermore, by covalent attachment of electron-donating aromatic amines to the peripheries of the AIE core, red AIEgens could be obtained readily, which exhibit excellent photostability for long-term lysosome tracking. This work not only provides a new strategy to design heterocycle-containing AIEgens from non-emissive heteroaromatics but also stimulates more their applications as bio-imaging materials.

摘要

新型聚集诱导发光(AIE)体系的开发是一个热门研究课题,从中衍生出具有多样结构和性质的功能材料。在此,基于1,4,5,8-四氮杂蒽(TAA)这种稀有、无发射且具有强吸电子性的杂芳烃,实验和理论研究表明,将苯基转子连接到TAA上对于创建一种新的N型AIE核心结构至关重要。此外,通过将给电子芳香胺共价连接到AIE核心的外围,可以很容易地获得红色AIEgens,它们在长期溶酶体追踪中表现出优异的光稳定性。这项工作不仅提供了一种从无发射杂芳烃设计含杂环AIEgens的新策略,还激发了它们作为生物成像材料的更多应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ac13a824e4a9/c8sc02810a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ff9d57cee832/c8sc02810a-c1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/19d130a18e28/c8sc02810a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/4892becc8a0f/c8sc02810a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ae1bfd66a607/c8sc02810a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ac13a824e4a9/c8sc02810a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ff9d57cee832/c8sc02810a-c1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/19d130a18e28/c8sc02810a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/4892becc8a0f/c8sc02810a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ae1bfd66a607/c8sc02810a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daea/6194487/ac13a824e4a9/c8sc02810a-f4.jpg

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