Related Experiment Video
Updated: May 1, 2026

10:23
Self-assembly of Complex Two-dimensional Shapes from Single-stranded DNA Tiles
Published on: May 8, 2015
10.9K
A shape-persistent quadruply interlocked giant cage catenane with two distinct pores in the solid state
Gang Zhang1, Oliver Presly, Fraser White
1Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg (Germany).
Angewandte Chemie (International Ed. in English)
|April 8, 2014
Summary
Researchers synthesized complex, shape-persistent interlocked organic cages using dynamic covalent chemistry. This breakthrough creates novel porous materials with nanoscale dimensions, mimicking natural structures.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Organic Synthesis
Background:
- Discrete interlocked three-dimensional structures are challenging to synthesize using traditional methods.
- Nature utilizes interlocked hollow structures (e.g., in viruses), but synthetic analogues are rare.
- Dynamic covalent chemistry offers a pathway to thermodynamically stable, interlocked products.
Purpose of the Study:
- To develop a synthetic route for creating shape-persistent, interlocked organic cage compounds.
- To achieve nanometer-scale dimensions for these synthetic structures.
- To explore the potential of these structures as novel porous materials.
Main Methods:
- Utilizing dynamic covalent chemistry for bond formation.
- Employing crystallization-induced self-assembly.
- Forming complex structures through the precise formation of 96 covalent bonds.
Main Results:
- High yields of shape-persistent interlocked organic cage compounds were achieved.
- Structures with dimensions in the nanometer regime were successfully synthesized.
- An unprecedented porous material featuring both intrinsic and extrinsic micropores and mesopores was formed.
Conclusions:
- Dynamic covalent chemistry is a powerful tool for constructing complex, discrete interlocked structures.
- The synthesized interlocked cages represent a novel class of porous materials with potential applications.
- This work bridges the gap between natural and synthetic molecular architectures.
More Related Videos
Related Concept Videos
Catenins
2.2K
Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the...
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the...
2.2K
Ionic Crystal Structures
18.0K
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
18.0K
Aromatic Hydrocarbon Cations: Structural Overview
3.5K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
Removing one hydrogen from the intervening CH2 group...
3.5K
Conformations of Cyclohexane
12.2K
Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts non-planar chair and boat conformations.
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
12.2K
Metallic Solids
16.4K
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and...
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and...
16.4K
Chair Conformation of Cyclohexane
16.2K
The chair conformation is the most stable form of cyclohexane due to the absence of angle and torsional strain. The absence of angle strain is a result of cyclohexane’s bond angle being very close to the ideal tetrahedral bond angle of 109.5° in its chair conformer. Similarly, the torsional strain is also absent owing to the perfectly staggered arrangement of bonds.
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
16.2K

