Dynamics of mechanically bonded macrocycles in radial hetero[4]catenane isomers
Literature Information
Antony Wing Hung Ng, Yu Hin Leung
Radial [4]catenane isomers in which the dynamics of the interlocked macrocycles are encoded by the covalent structure of the central macrocyclic backbone are described. Shuttling motion of the interlocked β-cyclodextrin was found to be dependent on both the position and interaction strength of the interlocked cucurbit[6]urils on the central macrocycle. This work demonstrates that the dynamics of different mechanically bonded macrocycles in a hetero[n]catenane can be coordinated complementarily, suggesting the possible exploitation of higher-order [n]catenanes as the next level molecular machines in which more complex tasks can be performed with sophisticated intramolecular motions.
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Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry














