1968
DOI: 10.1039/c19680001260
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The crystal structure of dipyridinium µ-oxo-tetraperoxodioxobis(aquo)-dimolybdate(VI) and dipyridinium di-µ-hydroperoxo-tetraperoxo-dioxodimolybdate(IV)

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Cited by 8 publications
(2 citation statements)
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“…In the calculations this signal could be explained by a Mo 2 X 6 2Ϫ (2,2,6,0) complex. This composition is in accordance with the crystal structure found by Le Carpentier et al 28 and Mitschler et al, 29 having four side-on (η 2 ) peroxo groups, two terminal oxygens and two bridging hydroperoxo (OOH) groups. The absence of a chemical shift change for the terminal oxygen signal in this pH-interval can be explained by the fact that there are no likely protonation sites on this complex, since the hydroperoxo groups cannot be protonated.…”
supporting
confidence: 91%
“…In the calculations this signal could be explained by a Mo 2 X 6 2Ϫ (2,2,6,0) complex. This composition is in accordance with the crystal structure found by Le Carpentier et al 28 and Mitschler et al, 29 having four side-on (η 2 ) peroxo groups, two terminal oxygens and two bridging hydroperoxo (OOH) groups. The absence of a chemical shift change for the terminal oxygen signal in this pH-interval can be explained by the fact that there are no likely protonation sites on this complex, since the hydroperoxo groups cannot be protonated.…”
supporting
confidence: 91%
“…94 The only confirmed "triperoxomolybdate" is the salt reported as (Hpy)2[Mo2Oii]-2H20293 and later shown to contain bridging hydroperoxo ligands, [MoO (02)2(00H) ] a2-. [95][96] As shown in Figure 5, the structure consists of a pair of edge-shared pentagonal bipyramids. Each hydroperoxo ligand occupies an axial position in one bipyramid and an equatorial position in the other with O-Mo distances of 2.39 and 2.04 A, respectively.…”
Section: A 4:1 Complexesmentioning
confidence: 99%