A Raman spectroscopic study of the uranyl mineral rutherfordine - revisited

The molecular structure of the uranyl mineral rutherfordine has been investigated by the measurement of the near-infrared (NIR) and Raman spectra and complemented with infrared spectra including their interpretation. The spectra of rutherfordine show the presence of both water and hydroxyl units in the structure as evidenced by IR bands at 3562 and 3465 cm(-1) (O-H) and 3343, 3185 and 2980 cm(-1) (H(2)O). Raman spectra show the presence of four sharp bands at 3511, 3460, 3329 and 3151 cm(-1). Corresponding molecular water bending vibrations were only observed in both Raman and infrared spectra of one of two studied rutherfordine samples. The second rutherfordine sample studied contained only hydroxyl ions in the equatorial uranyl plane and did not contain any molecular water. The infrared spectra of the (CO(3))(2-) units in the antisymmetric stretching region show complexity with three sets of carbonate bands observed. This combined with the observation of multiple bands in the (CO(3))(2-) bending region in both the Raman and IR spectra suggests that both monodentate and bidentate (CO(3))(2-) units may be present in the structure. This cannot be exactly proved and inferred from the spectra; however, it is in accordance with the X-ray crystallographic studies. Complexity is also observed in the IR spectra Of (UO(2))(2+) antisymmetric stretching region and is attributed to non-identical UO bonds. U-O bond lengths were calculated using wavenumbers of the nu(3) and nu(1) (UO(2))(2+) and compared with data from X-ray single crystal structure analysis of rutherfordine. Existence of solid solution having a general formula (UO(2))(CO(3))(1-x)(OH)(2x)center dot yH(2)O (x, y >= 0) is supported in the crystal structure of rutherfordine samples studied. Copyright (C) 2009 John Wiley & Sons, Ltd.