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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
Published on: August 2, 2012
Nonamphiphilic assembly in water: polymorphic nature, thread structure, and thermodynamic incompatibility
Lei Wu1, Jyotsana Lal, Karen A Simon
1Department of Chemistry, Syracuse University, Syracuse, New York 13244, USA.
Journal of the American Chemical Society
|May 9, 2009
Summary
Researchers designed water-soluble molecules that self-assemble into liquid crystals. This discovery offers new insights into nonamphiphilic molecular assembly and liquid crystal formation in aqueous solutions.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Physical Chemistry
Background:
- Self-assembly of water-soluble molecules is entropically difficult.
- Understanding nonamphiphilic assemblies in water is crucial for developing new materials.
Purpose of the Study:
- To design and synthesize water-soluble aromatic molecules capable of forming nonamphiphilic assemblies and chromonic liquid crystals.
- To investigate the assembly behavior and liquid crystal phase formation in aqueous solutions.
Main Methods:
- Synthesis of novel water-soluble dichromonyl molecules.
- Characterization of liquid crystal phases using birefringence.
- Small-angle neutron scattering (SANS) to determine assembly structures.
- Investigating the effect of adding monoanionic and dianionic molecules.
Main Results:
- A new molecule, 5'DSCG-diviol, was synthesized and exhibits a large birefringent phase.
- Nonamphiphilic assemblies and chromonic liquid crystal phases were formed in water.
- SANS revealed concentration-independent rod-shaped assemblies.
- Monoanionic molecules disrupted the liquid crystal phase, while dianionic molecules retained it.
Conclusions:
- A novel assembly structure for nonamphiphilic molecules in water, termed molecular threads, was proposed.
- These threads consist of small molecules linked by salt bridges and stacked aromatic groups, heavily hydrated.
- Mixing different molecules can lead to new liquid crystals or phase segregation due to thermodynamic incompatibility.
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