Structural Characterization and Electronic Properties Determination by High-Field and High-Frequency EPR of a Series of Five-Coordinated Mn(II) Complexes

The isolation, structural characterization, and electronic properties of a series of high-spin mononuclear five-coordinated
Mn(II) complexes, [Mn(terpy)(X)2] (terpy = 2, 2‘:6‘,2‘ ‘-terpyridine; X = I- (1), Br- (2), Cl- (3), or SCN- (4)), are
reported. The X-ray structures of the complexes reveal that the manganese ion lies in the center of a distorted
trigonal bipyramid for complexes 1, 2, and 4, while complex 3 is better described as a distorted square pyramid.
The electronic properties of 1−4 were investigated by high-field and high-frequency EPR spectroscopy (HF-EPR)
performed between 5 and 30 K. The powder HF-EPR spectra have been recorded in high-field-limit conditions
(95−285 GHz) (D ≪ gβB). The spectra are thus simplified, allowing an easy interpretation of the experimental
data and an accurate determination of the spin Hamiltonian parameters. The magnitude of D varies between 0.26
and 1.00 cm-1 with the nature of the anionic ligand. Thanks to low-temperature EPR experiments, the sign of D
was unambiguously determined. D is positive for the iodo and bromo complexes and negative for the chloro and
thiocyano ones. A structural correlation is proposed. Each complex is characterized by a significant rhombicity with
E/D values between 0.17 and 0.29, reflecting the distorted geometry observed around the manganese. Finally, we
compared the spin Hamiltonian parameters of our five-coordinated complexes and those previously reported for
other analogous series of dihalo four- and six-coordinated complexes. The effect of the coordination number and
of the geometry of the Mn(II) complexes on the spin Hamiltonian parameters is discussed.