Light-Induced Cyclization of a Daisy-Chain Rotaxane

  • ChemPubSoc Europe Logo
  • Author: Asian Journal of Organic Chemistry
  • Published Date: 24 May 2018
  • Source / Publisher: Asian Journal of Organic Chemistry/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: Light-Induced Cyclization of a Daisy-Chain Rotaxane

So-called [c2]daisy-chain rotaxanes (pictured top) are excellent candidates for building functional artificial molecular "muscles". This is due to their unique ability of generating muscle-like contraction and extension motions upon external stimuli such as light or pH changes.


Most [c2]daisy-chain rotaxanes can perform a one-dimensional linear contraction/extension. One interesting strategy to achieve other modes of movement would be to transform [c2]daisy-chain rotaxanes into a "double-lasso macrocycle" (pictured bottom) by cyclization. However, there are very few examples of such systems.


Da-Hui Qu and colleagues, East China University of Science and Technology, have synthesized a [c2]daisy-chain-rotaxane-based double-lasso macrocycle. First, they prepared a precursor rotaxane which contained a [c2]daisy chain and two terminal coumarin groups using a copper(I)-catalyzed azide alkyne cycloaddition (CuAAC) reaction. Then, a [2+2]cycloaddition between the two coumarin groups was performed under UV light (λ = 365 nm), and a double-lasso macrocycle was obtained.


In the presence of acid/base stimuli, the [c2]daisy-chain unit showed reversible muscle-like extension/contraction (pictured bottom). The size of the double-lasso macrocycle could, thus, be tuned. This double-lasso macrocycle could be a useful addition to the family of mechanically interlocked molecules (MIMs).


 

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