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Self-assembled capsules based on tetrafunctionalized calix[4]resorcinarene cavitands.
Kenji Kobayashi1, Masamichi Yamanaka
1Department of Chemistry, Graduate School of Science, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan. skkobay@ipc.shizuoka.ac.jp.
Chemical Society Reviews
|June 19, 2014
Summary
Methylene-bridge cavitands, a type of calix[4]resorcinarene, form self-assembled capsules. These capsules are created using hydrogen bonds, metal-coordination bonds, and dynamic covalent bonds for various applications.
Area of Science:
- Supramolecular Chemistry
- Organic Chemistry
Background:
- Calix[4]resorcinarene derivatives are versatile scaffolds for creating molecular capsules.
- Two main categories exist based on functionalization at the upper rim: bridged and methylene-bridge derivatives.
Purpose of the Study:
- This review focuses on self-assembled capsules formed by methylene-bridge cavitands.
- It explores the assembly mechanisms and structural features of these specific cavitands.
Main Methods:
- The review synthesizes information on methylene-bridge cavitands.
- It discusses the non-covalent and dynamic covalent interactions driving capsule formation.
Main Results:
- Methylene-bridge cavitands self-assemble into well-defined capsular structures.
- Assembly is achieved through predictable intermolecular forces like hydrogen bonding and metal coordination.
Conclusions:
- Methylene-bridge cavitands offer a tunable platform for designing self-assembled supramolecular capsules.
- The review highlights their potential in host-guest chemistry and materials science.

