TY - JOUR
T1 - Smart stimuli-responsive spherical nanostructures constructed from supramolecular metallodendrimers via hierarchical self-assembly
AU - Chen, Li Jun
AU - Zhao, Guang Zhen
AU - Jiang, Bo
AU - Sun, Bin
AU - Wang, Ming
AU - Xu, Lin
AU - He, Jiuming
AU - Abliz, Zeper
AU - Tan, Hongwei
AU - Li, Xiaopeng
AU - Yang, Hai Bo
PY - 2014/4/23
Y1 - 2014/4/23
N2 - In this article, we present the design and construction of a series of supramolecular poly(benzyl ether) metallodendrimers featuring a well-defined hexagonal metallacycle at their cores via coordination-driven self-assembly. It was found that the second generation metallodendrimer 3c was able to hierarchically self-assemble into the regular vesicle-like structures. These nanoscale vesicles were monodisperse in shape and relatively monodisperse in size as detected in SEM, TEM, AFM, and DLS experiments. Notably, this kind of hierarchically formed vesicle-like nanostructure adopted a discrete metallacycle as the main skeleton, which is obviously different from many previous reports of nanoscale spherical architectures. Moreover, such supramolecular vesicle-like structures could encapsulate some fluorescent molecules, like BODIPY and SRB, etc. By taking advantage of the dynamic nature of metal-ligand bonds, the disassembly and reassembly of the hexagonal cavity core could be reversibly controlled by the addition and removal of bromide ions, resulting in the transition from the vesicles to micelles. Thus, the controlled release of fluorescence dye was successfully realized by the halide-induced vesicles-micelles transition. These findings not only enrich the library of supramolecular metallodenrimers but also provide a new avenue to the construction of novel "smart" nanomaterials, which have potential application in functional molecules delivery and release.
AB - In this article, we present the design and construction of a series of supramolecular poly(benzyl ether) metallodendrimers featuring a well-defined hexagonal metallacycle at their cores via coordination-driven self-assembly. It was found that the second generation metallodendrimer 3c was able to hierarchically self-assemble into the regular vesicle-like structures. These nanoscale vesicles were monodisperse in shape and relatively monodisperse in size as detected in SEM, TEM, AFM, and DLS experiments. Notably, this kind of hierarchically formed vesicle-like nanostructure adopted a discrete metallacycle as the main skeleton, which is obviously different from many previous reports of nanoscale spherical architectures. Moreover, such supramolecular vesicle-like structures could encapsulate some fluorescent molecules, like BODIPY and SRB, etc. By taking advantage of the dynamic nature of metal-ligand bonds, the disassembly and reassembly of the hexagonal cavity core could be reversibly controlled by the addition and removal of bromide ions, resulting in the transition from the vesicles to micelles. Thus, the controlled release of fluorescence dye was successfully realized by the halide-induced vesicles-micelles transition. These findings not only enrich the library of supramolecular metallodenrimers but also provide a new avenue to the construction of novel "smart" nanomaterials, which have potential application in functional molecules delivery and release.
UR - https://www.scopus.com/pages/publications/84899567930
U2 - 10.1021/ja500152a
DO - 10.1021/ja500152a
M3 - 文章
C2 - 24684256
AN - SCOPUS:84899567930
SN - 0002-7863
VL - 136
SP - 5993
EP - 6001
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 16
ER -