1993
DOI: 10.1016/0304-5102(93)87110-t
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Characterization of the compounds formed from the interaction of divalent cations with inorganic molecular metal—oxygen cluster compounds

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Cited by 19 publications
(22 citation statements)
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“…Reports of solid 12-tungstophosphoric acid salts containing divalent cations are quite rare [16,18,37,39,40]. Although such salts are often reported to be of low crystallinity [16] or to have not been formed at all [18], we have found that it is possible to obtain the salts of good crystallinity starting from a chloride solution of the corresponding cation and preserving the pH of an acid solution in the region from 1.0 to 1.2.…”
Section: Resultsmentioning
confidence: 73%
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“…Reports of solid 12-tungstophosphoric acid salts containing divalent cations are quite rare [16,18,37,39,40]. Although such salts are often reported to be of low crystallinity [16] or to have not been formed at all [18], we have found that it is possible to obtain the salts of good crystallinity starting from a chloride solution of the corresponding cation and preserving the pH of an acid solution in the region from 1.0 to 1.2.…”
Section: Resultsmentioning
confidence: 73%
“…Although such salts are often reported to be of low crystallinity [16] or to have not been formed at all [18], we have found that it is possible to obtain the salts of good crystallinity starting from a chloride solution of the corresponding cation and preserving the pH of an acid solution in the region from 1.0 to 1.2. Under such conditions Keggin anions are stable [41,42].…”
Section: Resultsmentioning
confidence: 92%
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“…[7,[13][14][15][16]. However, two fairly recent publications have suggested that soluble alkaline earth metal salts prepared by the reaction of H 3 [PMo 12 O 40 ] (and also H 3 [PW 12 O 40 ]) and the alkaline earth hydroxides, which were characterized by infrared spectroscopy, X-ray powder diffraction (XRD), differential thermal analysis and nitrogen adsorption-desorption measurements, are, in fact, a mixture of simple divalent salts and the parent acid itself [17,18]. Moreover, a single-crystal X-ray structural investigation of the product obtained from the Ba 2+ /[PMo 12 O 40 ] 3− system gave a unit cell effectively identical with that of the hydrated acid, H 3 [PMo 12 O 40 ]·(29-30)H 2 O [18][19][20] and, furthermore, the Ba 2+ ions could not be located within the unit cell, supporting the above conclusion.…”
Section: Introductionmentioning
confidence: 99%