Effect of the Distant Substituent to Slow Magnetic Relaxation of Pentacoordinate Fe(III) Complexes.

Abstract

Pentacoordinate Fe(III) complexes [Fe(LMeO)2X] and [Fe(LEtO)2X], X = Cl and Br, show the slow magnetic relaxation that is enhanced by the applied static magnetic field. A substitution of the distant ethoxy group to the methoxy group residing at the phenyl ring of a Schiff base N,O-donor ligand (LMeO vs LEtO) considerably influences the relaxation characteristics. In the chlorido complex [Fe(LMeO)2Cl], the following three slow relaxation channels are recognized as possessing different relaxation times: τLF = 0.47 s, τIF = 13 ms, and τHF = 26 μs at the static field BDC = 0.2 T and T = 1.9 K. In the bromido complex [Fe(LMeO)2Br], only the following two relaxation channels are seen: τLF = 0.30 ms and τHF = 139 μs at BDC = 0.15 T and T = 1.9 K. Due to D > 0, the Orbach relaxation mechanism does not apply, and the temperature dependence of the high-frequency relaxation time can be described by two Raman-like terms.