1991
DOI: 10.1016/s0020-1693(00)85449-3
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X-ray and spectroscopic investigations of the structure of yttrium acetate tetrahydrate

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1991
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Cited by 65 publications
(36 citation statements)
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“…The 13 C CP-MAS spectrum of the silylated yttrium acetate illustrates, in comparison with the hydrated yttrium acetate, the deformation of the set of three resonance at 24 ppm corresponding to the methyl group. [19] This deformation corresponds to the decreasing and the modification of the intensities of the different resonances. Moreover, the intensity of the second set at around 185 ppm assigned to an acetate bonded to a metal atom strongly decreased.…”
Section: Silylation Of Yttrium Triacetatementioning
confidence: 98%
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“…The 13 C CP-MAS spectrum of the silylated yttrium acetate illustrates, in comparison with the hydrated yttrium acetate, the deformation of the set of three resonance at 24 ppm corresponding to the methyl group. [19] This deformation corresponds to the decreasing and the modification of the intensities of the different resonances. Moreover, the intensity of the second set at around 185 ppm assigned to an acetate bonded to a metal atom strongly decreased.…”
Section: Silylation Of Yttrium Triacetatementioning
confidence: 98%
“…1. F. Ribot et al [19,30] indicate that, in the case of hydrated rare earth acetate crystals, there are four kinds of coordination modes of acetate groups: monodentate, chelating, bridging and polymeric. 13 C CP-MAS appears to be very appropriate to define the coordination modes.…”
Section: Silylation Of Yttrium Triacetatementioning
confidence: 99%
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