Orthogonal photoswitching in a multifunctional molecular system

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Abstract

The wavelength-selective, reversible photocontrol over various molecular processes in parallel remains an unsolved challenge. Overlapping ultraviolet-visible spectra of frequently employed photoswitches have prevented the development of orthogonally responsive systems, analogous to those that rely on wavelength-selective cleavage of photo-removable protecting groups. Here we report the orthogonal and reversible control of two distinct types of photoswitches in one solution, that is, a donor-acceptor Stenhouse adduct (DASA) and an azobenzene. The control is achieved by using three different wavelengths of irradiation and a thermal relaxation process. The reported combination tolerates a broad variety of differently substituted photoswitches. The presented system is also extended to an intramolecular combination of photoresponsive units. A model application for an intramolecular combination of switches is presented, in which the DASA component acts as a phase-transfer tag, while the azobenzene moiety independently controls the binding to alpha-cyclodextrin.

Original languageEnglish
Article number12054
Number of pages10
JournalNature Communications
Volume7
DOIs
Publication statusPublished - Jul-2016

Keywords

  • WAVELENGTH-SELECTIVE CLEAVAGE
  • VISIBLE-LIGHT
  • AZOBENZENE PHOTOSWITCHES
  • PROTECTING GROUPS
  • SUBSTITUTED AZOBENZENES
  • CHEMISTRY
  • CYCLODEXTRIN
  • PHOTOPHARMACOLOGY
  • OLIGONUCLEOTIDES
  • ISOMERIZATION

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