4.8 Article

Tristability in a Light-Actuated Single-Molecule Magnet

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 42, Pages 15880-15884

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja407332y

Keywords

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Funding

  1. National Science Foundation [CHE-1010002]
  2. Centre National de la Recherche Scientifique (CNRS)
  3. University of Bordeaux
  4. Conseil Regional d'Aquitaine
  5. GIS Advanced Materials in Aquitaine (COMET Project)
  6. ANR [NT09_469563]
  7. Institut Universitaire de France (IUF)
  8. NSF Grant [DMR-1157490]
  9. State of Florida
  10. Direct For Mathematical & Physical Scien [1111900] Funding Source: National Science Foundation
  11. Division Of Chemistry [1111900] Funding Source: National Science Foundation

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Molecules exhibiting bistability have been proposed as elementary binary units (bits) for information storage, potentially enabling fast and efficient computing. In particular, transition metal complexes can display magnetic bistability via either spin-crossover or single-molecule magnet behavior. We now show that the octahedral iron(II) complexes in the molecular salt [Fe(1-propyltetrazole)(6)](BF4)(2), when placed in its high-symmetry form, can combine both types of behavior. Light irradiation under an applied magnetic field enables fully reversible switching between an S = 0 state and an S = 2 state with either up (M-S = +2) or down (M-S = -2) polarities. The resulting tristability suggests the possibility of using molecules for ternary information storage in direct analogy to current binary systems that employ magnetic switching and the magneto-optical Kerr effect as write and read mechanisms.

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