Aggregation-induced emission in novel multilayered 3D polymers: development of a fluorescent probe for selective metal ion detection

被引:0
|
作者
Zhang, Sai [1 ]
Yuan, Qingkai [2 ]
Xu, Qingzheng [3 ]
Yan, Shenghu [1 ]
Zhang, Yue [1 ]
Li, Guigen [2 ]
机构
[1] Changzhou Univ, Sch Pharm, Continuous Flow Engn Lab Natl Petr & Chem Ind, Changzhou 213164, Jiangsu, Peoples R China
[2] Texas Tech Univ, Dept Chem, Lubbock, TX 79415 USA
[3] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Conducting polymers - Elastomers - Fluorescence spectroscopy - Metal ions;
D O I
10.1039/d4ra08548e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study presents the characterization of a novel multilayered three-dimensional (3D) polymer exhibiting aggregation-induced emission (AIE) properties when excited at a low wavelength of 280 nm. Utilizing fluorescence spectroscopy, we demonstrate that the polymer displays a marked enhancement in luminescence upon aggregation, a characteristic behavior that distinguishes AIE-active materials from conventional fluorophores. Furthermore, we explore the potential application of this multilayered 3D polymer as a fluorescent probe for the selective detection of specified metal ions. By incorporating chelating functional groups into the polymer matrix, we facilitate specific interactions with target metal ions, leading to significant fluorescence intensity changes that correlate with ion concentration. According to their cyclic voltammetry characteristics, the polymers have potential applications in cutting-edge electrical and optoelectronic systems. Our findings indicate that this multilayered 3D polymer serves as an effective fluorescent sensor and offers tunable optical properties, paving the way for innovative applications in environmental monitoring and biomedical diagnostics. The results underscore the utility of AIE-active polymers in developing advanced materials for sensitive and selective detection of metal ions, contributing to the growing field of smart sensing technologies.
引用
收藏
页码:2242 / 2249
页数:8
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