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IR. and Raman spectra of LnONO3 (50–4,000 cm−1, LnLa, Gd, Eu, and Dy) are reported and discussed. The low frequency region of the spectra reflects the cubic structure of these compounds. The dimensions of the cubic unit cells determined by X‐Ray powder diagrams are: 12.81 ± 0.05 Å for EuONO3, 12.69 ± 0.05 Å for GdONO3, and 12.67 ± 0.05 Å for DyONO3. The vibrational frequencies of the nitrato group are consistent with a bidentate nitrate of C2v symmetry. The synthesis of anhydrous Ln (NO3)3 (LnLa, Gd, Eu, and Dy) by dehydration of the corresponding penta‐ or hexahydrates is described. The IR. and Raman spectra (50‐4,000 cm−1) are analysed. Splitting of the bands point to a complex structure of these compounds. All six vibrational modes of the nitrato group are observed and the data are again consistent with bidentate NO−3 moieties. Finally, an analytical control of the purity of Ln (NO3)3 is suggested.
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Bünzli et al. (1978) studied this question.
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