Suspending Polyrotaxane Dissociation via Photo-Reversible Capping of Terminals

Macromol Rapid Commun. 2019 Oct;40(20):e1900323. doi: 10.1002/marc.201900323. Epub 2019 Aug 20.

Abstract

Reversible covalent bonds yield polymeric materials with functional characteristics such as self-healing, shape memory, stress relaxation, and stimuli-responsiveness. Here, photo-reversibly cappable polyrotaxanes are designed and the on-off controlled dissociation of their supramolecular architectures is demonstrated. The polyrotaxanes are synthesized by capping dithiobenzoates at both terminals of polyethylene glycol threaded through multiple α-cyclodextrins. Since dethreading of the α-cyclodextrins is prevented by the dithiobenzoate stoppers, the supramolecular dissociation is induced by their photo-cleavage. Subsequently, the cleaved dithiobenzoates spontaneously re-cap the polyrotaxane terminals in darkness. Thus, the supramolecular dissociation can be modulated by photo-reversible capping of the dithiobenzoate stoppers. These polyrotaxanes with dithiobenzoate stoppers are promising functional materials for photo-controlling physical properties and structures.

Keywords: dithiobenzoate; photo-reversible capping; polyrotaxanes; supramolecular dissociation.

MeSH terms

  • Benzoates / chemistry
  • Cyclodextrins / chemical synthesis
  • Cyclodextrins / chemistry*
  • Light*
  • Poloxamer / chemical synthesis
  • Poloxamer / chemistry*
  • Polyethylene Glycols / chemistry
  • Rotaxanes / chemical synthesis
  • Rotaxanes / chemistry*
  • alpha-Cyclodextrins / chemistry

Substances

  • Benzoates
  • Cyclodextrins
  • Rotaxanes
  • alpha-Cyclodextrins
  • polyrotaxane
  • Poloxamer
  • Polyethylene Glycols