Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7691105 | Vibrational Spectroscopy | 2016 | 9 Pages |
Abstract
The vibrational and reorientational dynamics of CH3 groups from (CH3)2SO ligands in the high- and low-temperature phases of [Cd(OS(CH3)2)6](ClO4)2 were investigated by Fourier transform infrared (FT-IR) and Raman (FT-Raman) spectroscopy, and quasielastic and inelastic incoherent neutron scattering (QENS and IINS) methods. The results show that in the high temperature phases the CH3 groups and ClO4â anions perform fast (ÏR â 10â12 s) reorientational motions. These molecular motions do not change significantly at low-temperature phase transition (detected earlier by differential scanning calorimetry (DSC) at TC4c=235K on cooling and at TC4c=242Kâon heating). Neutron powder diffraction (NPD) measurements, performed simultaneously with QENS and IINS, indicated that this phase transition is associated with a change of the crystal structure. The comparison of FT-IR, FT-Raman and the proton-weighted phonon density of states function G(ν) calculated from IINS experimental spectra at low temperature phase of [Cd(OS(CH3)2)6](ClO4)2 was made.
Keywords
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Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Elżbieta Szostak, Joanna HetmaÅczyk, Anna MigdaÅ-Mikuli,