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Published on: June 18, 2013
Ionic self-assembled wormlike nanowires and their cyclodextrin inclusion-tuned transition
Qiuhong Li1, Xiao Chen, Xudong Wang
1Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan, 250100, China.
The Journal of Physical Chemistry. B
|August 13, 2010
Summary
Ionic self-assembly successfully created novel wormlike nanowires from ferrocenylmethyl)trimethylammonium iodide (FcMI) and sodium bis(2-ethyl-1-hexyl)sulfosuccinate (AOT). These redox-active nanowires form complex structures and can transform into vesicles.
Area of Science:
- Materials Science
- Supramolecular Chemistry
- Nanotechnology
Background:
- Ionic self-assembly (ISA) is a powerful technique for creating ordered nanostructures.
- Ferrocene-containing compounds offer unique redox properties.
- Controlling self-assembly is key to designing advanced materials.
Purpose of the Study:
- To synthesize and characterize novel wormlike nanowires using ISA.
- To investigate the structural and redox properties of the resulting complexes.
- To explore the transformation of these nanostructures into vesicles.
Main Methods:
- Ionic self-assembly of (ferrocenylmethyl)trimethylammonium iodide (FcMI) and sodium bis(2-ethyl-1-hexyl)sulfosuccinate (AOT).
- Characterization of FcM-AOT complexes using techniques like X-ray diffraction (implied by lattice spacing).
- Transmission electron microscopy (TEM) and dynamic light scattering (DLS) for vesicle analysis.
Main Results:
- Successful preparation of wormlike nanowires with an ordered hexagonal columnar structure (D = 2.49 nm).
- FcM-AOT complexes exhibit redox activity due to ferrocene incorporation.
- Nanowires form intricate net-like structures, some with high-order crystallinity.
- Transformation into vesicles achieved by complexation with beta-cyclodextrins.
Conclusions:
- ISA provides a versatile route to fabricate redox-active nanowires.
- The self-assembly and vesicle formation are governed by noncovalent interactions.
- This work demonstrates a pathway for creating complex supramolecular architectures with tunable properties.

