2004
DOI: 10.1016/j.jallcom.2003.11.052
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Properties of molecular lanthanide crystals spectra in the near-IR region

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Cited by 17 publications
(11 citation statements)
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“…The most intense, wide bands that were located in the spectral range between 2500 and 3750 cm -1 were attributed to the ν NH and ν OH oscillations and to the 2ν CO , 2δ NH 2 , and 2δ OH 2 overtones. [31] A difference in the ν OH positions was observed for I and II. The broadening of the ν OH band at approximately 3380 cm -1 for I, in comparison with that at approximately 3420 cm -1 for II, is consistent with the presence of a coordinated water molecule.…”
Section: Ir Spectra Of the Crystalline Lanthanide Carbonatesmentioning
confidence: 96%
“…The most intense, wide bands that were located in the spectral range between 2500 and 3750 cm -1 were attributed to the ν NH and ν OH oscillations and to the 2ν CO , 2δ NH 2 , and 2δ OH 2 overtones. [31] A difference in the ν OH positions was observed for I and II. The broadening of the ν OH band at approximately 3380 cm -1 for I, in comparison with that at approximately 3420 cm -1 for II, is consistent with the presence of a coordinated water molecule.…”
Section: Ir Spectra Of the Crystalline Lanthanide Carbonatesmentioning
confidence: 96%
“…Recently, we have shown that the f-f transitions in this spectral region are seriously affected by coincident combination and/or overtone bands. [21,22] The present data also reveal that these bands strongly dominate the f-f transitions of the Nd III ion in the NIR region and this domination is different for the three non-isomorphic crystals studied. As can be seen from the equilibria variations between different species for sodium salts of Nd III -TTHA solutions, exemplified by the 4 I 9/2 Ǟ 2 P 1/2 transition in Figure 3, the shape and intensity of these bands do not change further when the pH of the solution exceeds 4.…”
Section: Ir and Raman Spectra Of Crystalsmentioning
confidence: 49%
“…The FT-IR spectrum of amminolysed yttrium (Fig. 4b) shows that the absorption intensity of C-H bands at 2800 cm −1 [3,15,44,51,52] decreases in comparison with the same bands reported in the spectrum of the commercial triethylamine [N(C 2 H 5 ) 3 ] (Fig. 4a).…”
Section: Amminolysis Of Yttrium Trichloridementioning
confidence: 57%
“…The FTIR spectra of both commercial reagent and silylated product are reported in Fig. 2. www.interscience.wiley.com/journal/aoc [19,30,51] Si-C deformation in Si-methyl group [36,40,59] IR band positions in hydrated yttrium acetate and the specific IR bands in silylated yttrium acetate, prepared with a dehydrated product, are reported in Tables 1 and 2, respectively. First, compared with the silylated product, the IR spectrum of hydrated yttrium acetate (Fig. 2a) exhibits an evolution of the stretching γ (C-C) (960 and 945 cm −1 ) [19] .…”
Section: Silylation Of Yttrium Triacetatementioning
confidence: 99%