Spin Switching with Triazolate-Strapped Ferrous Porphyrins
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Updated: Jan 26, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Morten K Peters1, Sebastian Hamer1, Torben Jäkel1
1Otto-Diels-Institut für Organische Chemie , Christian Albrechts-Universität , Otto-Hahn-Platz 4 , 24098 Kiel , Germany.
Abstract:
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.
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