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Photoinduced host-to-guest electron transfer in a self-assembled coordination cage.
Ganta, Sudhakar; Borter, Jan-Hendrik; Drechsler, Christoph; Holstein, Julian J; Schwarzer, Dirk; Clever, Guido H.
Afiliação
  • Ganta S; Department of Chemistry and Chemical Biology, TU Dortmund University Otto-Hahn Straße 6 44227 Dortmund Germany guido.clever@tu-dortmund.de.
  • Borter JH; Max-Planck-Institute for Multidisciplinary Sciences Am Fassberg 11 37077 Göttingen Germany.
  • Drechsler C; Department of Chemistry and Chemical Biology, TU Dortmund University Otto-Hahn Straße 6 44227 Dortmund Germany guido.clever@tu-dortmund.de.
  • Holstein JJ; Department of Chemistry and Chemical Biology, TU Dortmund University Otto-Hahn Straße 6 44227 Dortmund Germany guido.clever@tu-dortmund.de.
  • Schwarzer D; Max-Planck-Institute for Multidisciplinary Sciences Am Fassberg 11 37077 Göttingen Germany.
  • Clever GH; Department of Chemistry and Chemical Biology, TU Dortmund University Otto-Hahn Straße 6 44227 Dortmund Germany guido.clever@tu-dortmund.de.
Org Chem Front ; 9(20): 5485-5493, 2022 Oct 11.
Article em En | MEDLINE | ID: mdl-36324316
ABSTRACT
A [Pd2L4] coordination cage, assembled from electron-rich phenothiazine-based ligands and encapsulating an electron-deficient anthraquinone-based disulfonate guest, is reported. Upon excitation at 400 nm, transient absorption spectroscopy unveils photoinduced electron transfer from the host's chromophores to the guest, as indicated by characteristic spectral features assigned to the oxidized donor and reduced acceptor. The structure of the host-guest complex was characterized by NMR spectroscopy, mass spectrometry and single-crystal X-ray analysis. Spectroelectrochemical experiments and DFT calculations both agree with the proposed light-induced charge separation. A kinetic analysis of the involved charge transfer channels reveals, besides a guest-independent LMCT path, 44% efficiency for the host-guest charge transfer (HGCT).

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Chem Front Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Chem Front Ano de publicação: 2022 Tipo de documento: Article