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Spin Switching with Triazolate-Strapped Ferrous Porphyrins.

Morten K PetersSebastian HamerTorben JäkelFynn RöhrichtFrank D SönnichsenCarolina von EssenManu K LahtinenChristian NätherKari T RissanenRainer Herges
Published in: Inorganic chemistry (2019)
Fe(III) porphyrins bridged with 1,2,3-triazole ligands were synthesized. Upon deprotonation, the triazolate ion coordinates to the Fe(III) ion, forming an overall neutral high-spin Fe(III) porphyrin in which the triazolate serves both as an axial ligand and as the counterion. The second axial coordination site is activated for coordination and binds p-methoxypyridine, forming a six-coordinate low-spin complex. Upon addition of a phenylazopyridine as a photodissociable ligand, the spin state of the complex can be reversibly switched with ultraviolet and visible light. The system provides the basis for the development of switchable catalase- and peroxidase-type catalysts and molecular spin switches.
Keyphrases
  • room temperature
  • visible light
  • density functional theory
  • single molecule
  • transition metal
  • metal organic framework
  • photodynamic therapy
  • ionic liquid
  • aqueous solution