Probing Magnetic Excitations in CoII Single-Molecule Magnets by Inelastic Neutron Scattering

Eur J Inorg Chem. 2019;2019(8):10.1002/ejic.201900142. doi: 10.1002/ejic.201900142.

Abstract

Co(acac)2(H2O)2 (1, acac = acetylacetonate), a transition metal complex ( S = 3 / 2 ), displays field-induced slow magnetic relaxation as a single-molecule magnet. For 1 and its isotopologues Co(acac)2(D2O)2 (1-d 4 ) and Co(acac-d 7)2(D2O)2 (1-d 18 ) in approximately D 4 h symmetry, zero-field splitting of the ground electronic state leads to two Kramers doublets (KDs): lower energy M S = ± 1 / 2 ϕ 1 , 2 and higher energy M S = ± 3 / 2 ϕ 3 , 4 states. This work employs inelastic neutron scattering (INS), a unique method to probe magnetic transitions, to probe different magnetic excitations in 1-d 4 and 1-d 18 . Direct-geometry, time-of-flight Disk-Chopper Spectrometer (DCS), with applied magnetic fields up to 10 T, has been used to study the intra-KD transition as a result of Zeeman splitting, M S = - 1 / 2 ϕ 1 M S = + 1 / 2 ϕ 2 , in 1-d 18 . This is a rare study of the M S = - 1 / 2 M S = + 1 / 2 excitation in transition metal complexes by INS. Indirect-geometry INS spectrometer VISION has been used to probe the inter-KD, ZFS transition, M S = ± 1 / 2 ϕ 1 , 2 M S = ± 3 / 2 ( ϕ 3 , 4 ) in both 1-d 4 and 1-d 18 , by variable-temperature (VT) properties of this excitation. The INS spectra measured on VISION also give phonon features of the complexes that are well described by periodic DFT phonon calculations.

Keywords: Cobalt; DFT phonon calculations; Inelastic neutron scattering; Phonons; Zero-field splitting.