A family of dimeric, peroxo-containing heteropolytungstates, [M2(O2)2(XW11O39)2]12− [M = Zr4+, X = Si (1), Ge (2); M = Hf4+, X = Si (3)], have been synthesized by reacting ZrCl4/HfCl4 with the respective monolacunary Keggin precursor [XW11O39]8− (X = Si, Ge) in an aqueous acidic medium (pH 4.8). The isostructural polyanions 1−3 are composed of two (XW11O39) Keggin units encapsulating a central diperoxo−dimetal fragment {M2(O2)2}4+ (M = Zr4+, Hf4+). Cyclic voltammetry and exhaustive electrolysis studies indicate fast reductive release of the peroxo ligands upon reduction of 1−3. Stoichiometric oxo-transfer studies from 1−3 to the substrate l-methionine were performed, and the reactions were monitored by 1H NMR.
Peroxo-Zr/Hf-Containing Undecatungstosilicates and -Germanates
CARRARO, MAURO;SARTOREL, ANDREA;SCORRANO, GIANFRANCO;BONCHIO, MARCELLA;
2010
Abstract
A family of dimeric, peroxo-containing heteropolytungstates, [M2(O2)2(XW11O39)2]12− [M = Zr4+, X = Si (1), Ge (2); M = Hf4+, X = Si (3)], have been synthesized by reacting ZrCl4/HfCl4 with the respective monolacunary Keggin precursor [XW11O39]8− (X = Si, Ge) in an aqueous acidic medium (pH 4.8). The isostructural polyanions 1−3 are composed of two (XW11O39) Keggin units encapsulating a central diperoxo−dimetal fragment {M2(O2)2}4+ (M = Zr4+, Hf4+). Cyclic voltammetry and exhaustive electrolysis studies indicate fast reductive release of the peroxo ligands upon reduction of 1−3. Stoichiometric oxo-transfer studies from 1−3 to the substrate l-methionine were performed, and the reactions were monitored by 1H NMR.Pubblicazioni consigliate
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