Phenylimino Indolinone: A Green-Light-Responsive T-Type Photoswitch Exhibiting Negative Photochromism

Open Access
Authors
  • S. Crespi
  • N.A. Simeth
  • M. Di Donato
  • S. Doria
  • C.N. Stindt
  • M.F. Hilbers
  • F.L. Kiss
  • R. Toyoda
  • S. Wesseling
  • W.J. Buma ORCID logo
  • B.L. Feringa
  • W. Szymanski
Publication date 22-11-2021
Journal Angewandte Chemie, International Edition
Volume | Issue number 60 | 48
Pages (from-to) 25290-25295
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract
Imines are photoaddressable motifs useful in the development of new generations of molecular switches, but their operation with low-energy photons and control over isomer stability remain challenging. Based on a computational design, we developed phenylimino indolinone (PIO), a green-light-addressable T-type photoswitch showing negative photochromism. The isomerization behavior of this photoactuator of the iminothioindoxyl (ITI) class was studied using time-resolved spectroscopies on time scales from femtoseconds to the steady state and by quantum-chemical analyses. The understanding of the isomerization properties and substituent effects governing these photoswitches opens new avenues for the development of novel T-type visible-light-addressable photoactuators based on C=N bonds.
Document type Article
Language English
Related publication Phenylimino Indolinone: A Green-Light-Responsive T-Type Photoswitch Exhibiting Negative Photochromism
Published at https://doi.org/10.1002/anie.202111748 https://doi.org/10.1002/ange.202111748
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Phenylimino Indolinone-Intern. ed (Final published version)
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