A mononuclear iron(iii) complex with unusual changes of color and magneto-structural properties with temperature: synthesis, structure, magnetization, multi-frequency ESR and DFT study

From the reaction of 2-hydroxy-6-methylpyridine (L) with iron(ii) tetrafluoroborate, a new mononuclear iron(iii) octahedral complex [FeL6](BF4)(3) has been isolated. The color of the complex reversibly changed from red at room temperature to yellow-orange at the liquid nitrogen temperature. Magnetization measurements indicate that iron(iii) in [FeL6](BF4)(3) is in a high-spin state S = 5/2, from room temperature to 1.8 K. The high-spin ground state of iron(iii) is also confirmed by DFT calculations. Although the spin-crossover of the complex is not observed, X-band and multifrequency high-field/high-frequency electron spin resonance (ESR) spectroscopy shows rather uncommon iron(iii) spectra at room temperature and an unusual change with cooling. Spectral simulations reveal that the S = 5/2 ground state multiplet of the complex can be characterized by the temperature independent axial zero-field splitting parameter of |D| = +2 GHz (0.067 cm(-1)) while the value of the rhombic parameter E of the order of some tenths MHz increases on lowering the temperature. Single crystal X-ray diffraction (SCXRD) shows that the iron(iii) coordination geometry does not change with temperature while supramolecular interactions are temperature dependent, influencing the iron(iii) rhombicity. Additionally, the DFT calculations show temperature variation of the HOMO-LUMO gap, in agreement with the changes of color and ESR-spectra of the iron(iii) complex with temperature.

Automated summary

A new mononuclear iron(iii) octahedral complex, [FeL6](BF4)3, has been synthesized from the reaction between 2-hydroxy-6-methylpyridine (L) and iron(ii) tetrafluoroborate. The color of the complex changes reversibly from red to yellow-orange with temperature. Magnetization measurements show that the iron(iii) in [FeL6](BF4)3 is in a high-spin state. Although spin-crossover is not observed, X-band and multifrequency high-field/high-frequency electron spin resonance (ESR) spectroscopy reveal unusual iron(iii) spectra at room temperature and changes with cooling.