期刊
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
卷 66, 期 2, 页码 413-418出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2006.03.015
关键词
infrared and Raman spectra; ammonium metal(II) phosphate monohydrates; potassium metal(II) phosphate monohydrates; normal PO43- vibrations; distortion of the PO43- ions
类别
The IR and Raman spectra of the isostructural M'MPO4 center dot H2O compounds (M'= K+, NH4+; M = Mn2+ CO2+, Ni2+) are reported and discussed with respect to the normal vibrations of the PO43- ions. The vibrational behavior Of PO43- is in agreement with its low site symmetry C-s in the lattices-the symmetric v(1) and v(2) modes are activated in the IR spectra and the degeneration of the asymmetric v(3) and v(4) modes is lifted. A relatively large unit-cell group splitting is observed for v, in both the IR and Raman spectra and for v(3) in Raman spectra. It has been established that the mean wavenumbers of the P-O stretches (v(PO)) are not affected by the M2+ ions present, but they are lower for the NH4-series than for the K-one (predominant influence of both the smaller repulsion potential and the hydrogen bonds in the NH4-lattices over the influence of the M+-O interactions). The extent of the energetic distortion of the PO43- ions has been estimated based on the spectroscopic data for the site group splitting of the asymmetric modes (Delta v(3) and Delta v(4) the separation between the highest and the lowest wavenumbered P-O stretches (Delta v(max)) and the intensity of v(1) in the IR spectra. The data provide an evidence that the PO43- ions in KWPO4 center dot H2O are more distorted regarding the P-O bond lengths than those in NH4MPO4-H2O, but their angular distortion is the same in both series. The trends for the energetic distortion of the phosphate ions found from the spectroscopic data correspond to the data for their geometric distortion deduced from the values of the distortion indices DI(PO) and DI(OPO). (c) 2006 Elsevier B.V. All rights reserved.
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