Abstract
Abstract The infrared spectra of potassium and cesium hexafluorotechnetate (IV) and -rhenate(IV) show a D4h-distortion of the octahedral complex ions. The splitting of degeneracies is not due to site symmetry. The linear combinations of the force constants of the irreducible representations A2u and Eu are determined in the valence force field on the basis of D4h-symmetry. As expected the force constants of stretching vibrations of [TcF6]-- are then smaller than those of [ReF6]--.
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