Anisotropic Self-Assembly of Organic-Inorganic Hybrid Microtoroids

被引:18
|
作者
Al-Rehili, Safa'a [1 ]
Fhayli, Karim [1 ]
Hammami, Mohamed Amen [1 ]
Moosa, Basem [1 ]
Patil, Sachin [1 ]
Zhang, Daliang [2 ]
Alharbi, Ohoud [2 ]
Hedhili, Mohamed Nejib [2 ]
Moehwald, Helmuth [3 ]
Khashab, Niveen M. [1 ]
机构
[1] KAUST, Adv Membranes & Porous Mat Ctr, Smart Hybrid Mat Lab SHMs, Thuwal 239556900, Saudi Arabia
[2] KAUST, Imaging & Characterizat Core Labs, Thuwal 239556900, Saudi Arabia
[3] Max Planck Inst Colloids & Interfaces, Muehlenberg 1, D-14476 Potsdam, Germany
关键词
BLOCK-COPOLYMERS; SIRNA DELIVERY; NANOPARTICLES; COMPLEXES; MICELLES; IRON; NANOSTRUCTURES; METALLACYCLES; METALLACAGES; FRAMEWORKS;
D O I
10.1021/jacs.6b10080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Toroidal structures based on self-assembly of predesigned building blocks are well-established in the literature, but spontaneous self-organization to prepare such structures has not been reported to date. Here, organic- inorganic hybrid microtoroids synthesized by simultaneous coordination-driven assembly of amphiphilic molecules and hydrophilic polymers are reported. Mixing amphiphilic molecules with iron(III) chloride and hydrophilic polymers in water leads, within minutes, to the formation of starlike nanostructures. A spontaneous self-organization of these nanostructures is then triggered to form stable hybrid microtoroids. Interestingly, the toroids exhibit anisotropic hierarchical growth, giving rise to a layered toroidal framework. These microstructures are mechanically robust and can act as templates to host metallic nanoparticles such as gold and silver. Understanding the nature of spontaneous assembly driven by coordination multiple non covalent interactions can help explain the well-ordered complexity of many biological organisms in addition to expanding the available tools to mimic such structures at a molecular level.
引用
收藏
页码:10232 / 10238
页数:7
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