BODIPY directed one-dimensional self-assembly of gold nanorods

被引:2
|
作者
Hemant [1 ]
Rahman, Atikur [1 ]
Sharma, Priyanka [1 ]
Shanavas, Asifkhan [1 ]
Neelakandan, Prakash P. [1 ,2 ]
机构
[1] Inst Nano Sci & Technol, Sect 81, Mohali 140306, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
关键词
NANOPARTICLES; OLIGOMERS; GROWTH; METAL;
D O I
10.1039/d4nr02161d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The assembly of anisotropic nanomaterials into ordered structures is challenging. Nevertheless, such self-assembled systems are known to have novel physicochemical properties and the presence of a chromophore within the nanoparticle ensemble can enhance the optical properties through plasmon-molecule electronic coupling. Here, we report the end-to-end assembly of gold nanorods into micrometer-long chains using a linear diamino BODIPY derivative. The preferential binding affinity of the amino group and the steric bulkiness of BODIPY directed the longitudinal assembly of gold nanorods. As a result of the linear assembly, the BODIPY chromophores positioned themselves in the plasmonic hotspots, which resulted in efficient plasmon-molecule coupling, thereby imparting photothermal properties to the assembled nanorods. This work thus demonstrates a new approach for the linear assembly of gold nanorods resulting in a plasmon-molecule coupled system, and the synergy between self-assembly and electronic coupling resulted in an efficient system having potential biomedical applications. Self-assembly of gold nanorods is facilitated by plasmon-molecule interactions between gold and BODIPY, and the chemical structure of BODIPY plays a crucial role in forming a linear chain.
引用
收藏
页码:12127 / 12133
页数:7
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