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Solid-State Self-Assembly: Exclusive Formation and Dynamic Interconversion of Discrete Cyclic Assemblies Based on
Koki Okabe1, Masahiro Yamashina1, Eiji Tsurumaki1
1Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8551, Japan.
The Journal of Organic Chemistry
|June 24, 2024
Summary
Solid-state self-assembly of molecular tweezers yields cyclic hexamers and porous networks. This strategy enables tunable solid-state properties and dynamic interconversion, overcoming challenges in solid-state construction.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Organic Chemistry
Background:
- Solid-state self-assembly is challenging compared to solution-based systems.
- Molecular tweezers are versatile building blocks for supramolecular structures.
Purpose of the Study:
- To develop a solid-state self-assembly strategy for molecular tweezers.
- To investigate the formation of well-defined assemblies in the solid state.
- To explore tunable properties and dynamic behavior of solid-state assemblies.
Main Methods:
- Classical recrystallization of molecular tweezers.
- Exposure of molecular tweezers powders to solvent vapor.
- Characterization of solid-state assemblies and their properties.
Main Results:
- Exclusive and quantitative formation of cyclic hexamers or porous networks from flexible molecular tweezers.
- Cyclic hexamers exhibit high thermal stability and moderate solid-state fluorescence.
- Heterologous assemblies allow tuning of properties; solvent vapor induces dynamic interconversion.
Conclusions:
- Demonstrated a novel solid-state self-assembly strategy for molecular tweezers.
- Achieved controlled formation of discrete and extended solid-state architectures.
- Established a platform for dynamic control over solid-state supramolecular structures.
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