Photoactivation of Aggregation-Induced Emission Molecules for Fast and Efficient Synthesis of Highly Fluorescent Single-Chain Nanoparticles

被引:7
作者
De-La-Cuesta, Julen [1 ,2 ]
Pomposo, Jose A. [1 ,2 ,3 ,4 ]
机构
[1] Univ Basque Country, CSIC, Ctr Fis Mat, Paseo Manuel de Lardizabal 5, E-20018 San Sebastian, Spain
[2] MPC, Paseo Manuel de Lardizabal 5, E-20018 San Sebastian, Spain
[3] Univ Basque Country, UPV EHU Apartado, Dept Fis Mat, Apartado 1072, E-20800 San Sebastian, Spain
[4] Basque Fdn Sci, IKERBASQUE, Maria Diaz Haro 3, E-48013 Bilbao, Spain
来源
ACS OMEGA | 2018年 / 3卷 / 11期
关键词
LUMINESCENT POLYMERIC NANOPARTICLES; BIOMEDICAL APPLICATIONS; ORGANIC NANOPARTICLES; FABRICATION; CONSTRUCTION; STRATEGY; DELIVERY; SYSTEMS; DESIGN;
D O I
10.1021/acsomega.8b02374
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-chain nanoparticles (SCNPs) are ultrasmall soft nanomaterials constructed via intrachain cross-linking of individual precursor polymer chains, with promising prospects for nanomedicine, catalysis, and sensing, among other different fields. SCNPs are versatile building blocks for the construction of new fluorescent probes with ultrasmall size, higher brightness, and better photostability than previous particle-based systems. Herein, we report on a new, fast, and efficient method to produce SCNPs with intense fluorescence emission in solution which is based on the photoactivation of appropriate aggregation-induced emission (AIE) cross-linking molecules containing azide functional groups. Remarkably, the presence of the azide moiety- that can be transformed to highly reactive nitrene species upon UV irradiation-was found to be essential for the SCNPs to display intense fluorescence emission. We attribute the fluorescence properties of the SCNPs to the immobilization of the initially nonfluorescent AIE molecules via intrachain cross-linking upon photoactivation. Such cross-linking-induced immobilization process activates the AIE mechanism and, hence, leads to fluorescent SCNPs in both solution and solid state.
引用
收藏
页码:15193 / 15199
页数:7
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