A pillar[5]arene-based [1]rotaxane was simply prepared in a high yield of 73%. Its stucture was confirmed by (1)H NMR, 2D NMR spectra, mass spectra and theoretical calculation.

In this proof-of-concept study, an active-template coupling is used to demonstrate a novel kinetic self-sorting process. This process iteratively increases the yield of the target heterocircuit [3]rotaxane product at the expense of other threaded species.

The dynamics of mechanically interlocked molecules such as rotaxanes and catenanes have been studied in solution as examples of rudimentary molecular switches and machines, but in this medium, the molecules are randomly dispersed and their motion incoherent. As a strategy for achieving a higher level of molecular organization, we have constructed a metal-organic framework material using a [2]ro...

Interlocked molecules such as catenanes and rotaxanes, connected only via mechanical bonds have the ability to perform large-scale sliding and rotational movements, making them attractive components for the construction of artificial molecular machines and motors. We here demonstrate the realization of large, rigid rotaxane structures composed of DNA origami subunits. The structures can be easi...

The efficacy of many drugs can be limited by undesirable properties, such as poor aqueous solubility, low bioavailability, and off-target interactions. To combat this, various drug carriers have been investigated to enhance the pharmacological profile therapeutic agents. In this work, we demonstrate use mechanical protection cage a DNA-targeting metallodrug within photodegradable rotaxane. More...

Supramolecular copolymers with complex architectures and emergent functions constitute a class of challenging but enticing synthetic targets in polymer science. Individual building blocks can be tailored to endow a resulting supramolecular copolymer with increased structural and functional complexity. Herein, we describe the construction of a linear supramolecular copolymer comprising mechanica...

A series of new squaraine rotaxanes have been synthesized with a tetralactam macrocycle and stopper groups of varying sizes and functionalities. In chloroform solvent, the relative size of the stopper group appears to have little influence on the high mechanical stability of the rotaxane structure. There is no evidence for unthreading (sometimes referred to as deslipping), even in the presence ...

This tutorial review describes the evolution of the field of chemical templation, in particular, emphasising the impact its application has made to the synthesis of mechanically interlocked structures. Recent advances in the use of negatively charged template species for the synthesis of interlocked structures are detailed, with the main focus of this review describing the development of a gene...