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Sulfate sulfato complexes

X-Ray diffraction studies of aqueous CdS04 solutions have clearly demonstrated the formation of O-sulfato complexes.668-670 These are of the general form [Cd(H20)6- (0S03) ](2-2")+, and appear to be the major species present in concentrated solutions. These results are fully in accord with tensimetric studies of the cadmium and magnesium sulfate aqueous systems, which indicate an increased interionic attraction at elevated temperatures.671 In contrast, X-ray diffraction studies on cadmium perchlorate solutions show no evidence for the coordination of the perchlorate ion to the metal, the only cationic species present being [Cd(H20)6]2+(Cd—O, 2.292 A, cf. Cd—O, 2.292 A in solid [Cd(H20)6][C104]2),670... [Pg.963]

As was observed in the case of the extraction of zirconium and hafnium from nitrate media, it is probable that the different tendencies of the metals towards hydrolysis has some effect on the selectivity observed,298 313 expecially in view of the proved extraction of hydroxo complexes. The extraction of both metals decreases markedly in the presence of sulfate ions in the aqueous phase (a feature that is utilized in the stripping of the loaded hafnium with sulfuric acid), although the selectivity for hafnium over zirconium is simultaneously increased on account of the higher stability constants of the inextractable sulfato complexes of zirconium.298... [Pg.813]

Sulfates and sulfites. Mono- and bis-sulfate complexes of actinyl ions, An02S04 and An02(S04)2 , are generally prepared from acidic solutions. The geometry about the actinide metal center is pentagonal biypyramidal from actinyl, sulfato, and aquo oxygen atoms. A tris(sulfato) complex has been reported, but it is very weak if it does exist. Ternary hydroxo, sulfato complexes have been reported for uranyl, but they have not been structurally characterized. [Pg.275]

The use of porphyrin complexes for the electrocatalytic detection of 8O2 is limited. Iron and titanium porphyrin peroxo complexes (TPPFe-O-FeTPP or TiP(02)) interact with 8O2 to give sulfato complexes of the porphyrins or to give free sulfate Carballo et al. showed that NiPPIX polymerized on GCE catalyzed the oxidation of 8O2, and the modified electrode was stable under hydro-dynamic conditions of a flow cell . ... [Pg.331]

Miksztal, A.R. and J.S. Valentine (1984). Reactivity of the peroxo hgand in metal-loporphyrin complxes Reaction of sulfur dioxide with iron and titanium porphyrin peroxo complxes to give sulfato complexes or sulfate. Inorg. Chem. 23(22), 3548-3552. [Pg.357]

There is IR evidence for bridging carboxylates in titania hydrolysates in the presence of carboxylic acids. " The IR spectra of V0(quin)(H20)3 and [V0(quin)2S04], where quin = quinic acid, (56), include Vs and Vas CO2 showing unidentate carboxylate. The sulfato complex gave bands from unidentate sulfate. ... [Pg.309]


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Sulfate complexes

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Sulfato complexes

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