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Issue 8, 2015
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Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism

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Abstract

Valence tautomeric (VT) metal complexes are highly promising bistable molecular compounds for applications as molecular switches in molecular electronics and spintronics. Although VT species can be switched with light, the photoswitching in all reported systems requires very low temperatures (usually below 20 K) because photoinduced states are highly unstable at room temperature. The thermal instability hinders any practical application of these complexes in genuine devices. In this report, for the first time we demonstrate photoswitching of VT species and associated magnetic properties at room temperature. The bidirectional photoswitching in solution is due to cistrans photoisomerizable 4-styrylpyridine ligands deliberately integrated into cobalt dioxolene molecular complexes. The novel type of photoswitching has been coined Ligand-Driven Light-Induced Valence Tautomerism (LD-LIVT). The photoconversion of VT states of 28% has been achieved in solution at room temperature. The photoinduced states show extraordinary thermal stability for hours at room temperature, as compared to common nanoseconds reported previously. The switching proceeds at molecular level with the effective photoswitching rate of 3 × 1013 molecules per s under our conditions. Consequently, this work may open new horizons in applications of molecular switches based on VT metal complexes in molecular devices functioning at room temperature.

Graphical abstract: Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism

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Publication details

The article was received on 13 Jan 2015, accepted on 22 May 2015 and first published on 22 May 2015


Article type: Edge Article
DOI: 10.1039/C5SC00130G
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Chem. Sci., 2015,6, 4599-4609
  • Open access: Creative Commons BY-NC license
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    Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism

    A. Witt, F. W. Heinemann and M. M. Khusniyarov, Chem. Sci., 2015, 6, 4599
    DOI: 10.1039/C5SC00130G

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