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

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‐addressab...

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Detalles Bibliográficos
Autores principales: Crespi, Stefano, Simeth, Nadja A., Di Donato, Mariangela, Doria, Sandra, Stindt, Charlotte N., Hilbers, Michiel F., Kiss, Ferdinand L., Toyoda, Ryojun, Wesseling, Sammo, Buma, Wybren Jan, Feringa, Ben L., Szymański, Wiktor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298291/
https://www.ncbi.nlm.nih.gov/pubmed/34609785
http://dx.doi.org/10.1002/anie.202111748
Descripción
Sumario: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.