Hierarchical self-assembly of triangular metallodendrimers into the ordered nanostructures

被引:29
|
作者
Jiang, Bo [1 ]
Chen, Li-Jun [1 ]
Zhang, Ying [2 ]
Tan, Hong-Wei [2 ]
Xu, Lin [1 ]
Yang, Hai-Bo [1 ]
机构
[1] E China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[2] Beijing Normal Univ, Dept Chem, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
Coordination-driven self-assembly; Hierarchical self-assembly; Metallodendrimers; Ordered nanostructures; Triangular metallacycles; RESPONSIVE SUPRAMOLECULAR GELS; MOLECULAR ELECTRONICS; DENDRIMERS; METALLACYCLES; CATALYSIS; COMPLEXES; STRATEGY; LIGANDS;
D O I
10.1016/j.cclet.2016.03.017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We designed and constructed a new family of 60 dendritic dipyridyl donors, from which two novel triangular metallodendrimers were successfully prepared via coordination-driven self-assembly. Inspired by the existence of multiple intermolecular interactions (e.g., pi-pi stacking and CH-pi interactions) imposed by the DMIP-functionalized poly(benzyl ether) dendrons, their hierarchical self assembly behaviors were studied in various mixed solvents by using scanning electron microscopy (SEM). Interestingly, it was found that the morphologies of the obtained metallodendrimers were highly depended on the dendron generation. For example, the first-generation metallodendrimer was able to hierarchically self-assemble into the spherical nanostructures in various mixed solvents, However, the nanofibers were observed for the second-generation metallodendrimer under the similar conditions. Furthermore, the driven force for the formation of such ordered nanostructures was investigated by using H-1 NMR and fluorescence spectroscopy. (C) 2016 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:607 / 612
页数:6
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