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Redshifted and thermally bistable one-way quantitative hemithioindigo-derived photoswitches enabled by isomer-specific excited state intramolecular proton transfer.
Krell-Jørgensen, Mikkel; Zulfikri, Habiburrahman; Bonnevie, Magnus Grage; Bro, Frederik Simonsen; Dohn, Asmus Ougaard; Laraia, Luca.
Afiliação
  • Krell-Jørgensen M; Department of Chemistry, Technical University of Denmark, Kemitorvet 2800, Kongens Lyngby, Denmark. luclar@kemi.dtu.dk.
  • Zulfikri H; Science Institute and Faculty of Physical Sciences, University of Iceland, Reykjavík, Iceland.
  • Bonnevie MG; Department of Chemical Engineering, Faculty of Engineering, Universitas Indonesia, Depok 16424, Indonesia.
  • Bro FS; Department of Chemistry, Technical University of Denmark, Kemitorvet 2800, Kongens Lyngby, Denmark. luclar@kemi.dtu.dk.
  • Dohn AO; Department of Chemistry, Technical University of Denmark, Kemitorvet 2800, Kongens Lyngby, Denmark. luclar@kemi.dtu.dk.
  • Laraia L; Science Institute and Faculty of Physical Sciences, University of Iceland, Reykjavík, Iceland.
Chem Commun (Camb) ; 59(5): 563-566, 2023 Jan 12.
Article em En | MEDLINE | ID: mdl-36537010
We report bistable indole-containing hemithioindigos (HTIs) with one-way quantitative photoswitching properties. Supported by state-averaged CASPT2/CASSCF calculations, we propose a mechanism for the observed one-way photoswitching that involves an isomer-specific excited state intramolecular proton transfer (ESIPT). Additionally, we developed a thermally bistable oligomer-inspired bipyrrole-containing HTI, which displays large band separation and bidirectional near-quantitative photoisomerization in the near-infrared, bio-optical window.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article