Abstract

Longer switching wavelengths and good photochemical yields and stabilities of the cis isomers in reducing aqueous environments are achieved by introducing 2,2 -aminoalkyl substituents into 4,4 - diamido-substituted azobenzenes. The products are thus suitable for photocontrol of biomolecular structures in intracellular environments, such as switching between two peptide configurations (see pictures).

Original languageEnglish
Pages (from-to)1484-1486
Number of pages3
JournalAngewandte Chemie - International Edition
Volume48
Issue number8
DOIs
StatePublished - Feb 9 2009

Keywords

  • azo compounds
  • Isomerization
  • Peptides
  • Photoswitches

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