Peroxo-Zr/Hf-Containing Undecatungstosilicates and -Germanates

被引:68
作者
Mal, Sib Sankar [2 ]
Nsouli, Nadeen H. [2 ]
Carraro, Mauro [3 ]
Sartorel, Andrea [3 ]
Scorrano, Gianfranco [3 ]
Oelrich, Holger [1 ]
Walder, Lorenz [1 ]
Bonchio, Marcella [3 ]
Kortz, Ulrich [2 ]
机构
[1] Univ Osnabruck, Inst Chem, D-49069 Osnabruck, Germany
[2] Jacobs Univ, Sch Sci & Engn, D-28725 Bremen, Germany
[3] Univ Padua, Dept Chem Sci, CNR, ITM, I-35131 Padua, Italy
关键词
U-VI IONS; ORGANIC-LIGANDS; ZR-IV; SUBSTITUTED POLYOXOTUNGSTATES; CRYSTAL-STRUCTURES; PROTON-TRANSFER; TH-IV; COMPLEXES; ZIRCONIUM(IV); THORIUM(IV);
D O I
10.1021/ic902203p
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A family of dimeric, peroxo-containing heteropolytungstates, [M(2)(O(2))(2)(XW(11)O(39))(2)](12-) [M = Zr(4+), X = Si (1), Ge (2); M = Hf(4+), X = Si (3)], have been synthesized by reacting ZrCl(4)/HfCl(4) with the respective monolacunary Keggin precursor [XW(11)O(39)](8-) (X=Si, Ge) in an aqueous acidic medium (pH 4.8). The isostructural polyanions 1-3 are composed of two (XW(11)O(39)) Keggin units encapsulating a central diperoxo-dimetal fragment {M(2)(O(2))(2)}(4+) (M=Zr(4+), Hf(4+)). 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 (1)H NMR.
引用
收藏
页码:7 / 9
页数:3
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