An Acetate-Functionalized Tetranuclear Zirconium Sandwiching Polyoxometalate Complex
The dimeric, zirconium‐sandwiching compound K4H6[Zr4(OH)6(CH3COO)2(α‐PW10O37)2]·23H2O (1) was obtained by the reaction of lacunary [PW11O39]7– and ZrCl4 in a 1 M potassium acetate buffer. It was characterized by elemental and thermogravimetric analysis, X‐ray crystallography, solution 183W NMR, FTIR...
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Published in: | European Journal of Inorganic Chemistry Vol. 2010; no. 22; pp. 3473 - 3477 |
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Main Authors: | , , , , , , |
Format: | Book Review Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
01-08-2010
WILEY‐VCH Verlag |
Subjects: | |
Online Access: | Get full text |
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Summary: | The dimeric, zirconium‐sandwiching compound K4H6[Zr4(OH)6(CH3COO)2(α‐PW10O37)2]·23H2O (1) was obtained by the reaction of lacunary [PW11O39]7– and ZrCl4 in a 1 M potassium acetate buffer. It was characterized by elemental and thermogravimetric analysis, X‐ray crystallography, solution 183W NMR, FTIR, and UV spectroscopy, and cyclic voltammetry (CV). All the studies indicate that compound 1 is stable both in the solid state and in solution. The cyclic voltammograms indicate good electrocatalytic activity in the reduction of nitrite.
Dimeric zirconium‐sandwiching polyoxometalate complex K4H6[Zr4(OH)6(CH3COO)2(α‐PW10O37)2]·23H2O (1) was prepared from ZrCl4 and K7[PW11O39] and characterized by single‐crystal X‐ray, thermogravimetric, and elemental analysis, IR, UV, and NMR spectroscopy, and cyclic voltammetry. It is stable in a wide pH range for a long time and has good electrocatalytic activity in the reduction of nitrite. |
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Bibliography: | National Nature Science Foundation of China (NSFC) - No. 20871027; No. 20973035 ark:/67375/WNG-FTD6HSLK-B Program for New Century Excellent Talents in University - No. NCET-07-0169 istex:45B66BB4898F8E41B579F67DB2B4B6E8C5DAB0B3 ArticleID:EJIC201000043 Program for Changjiang Scholars and Innovative Research Team in University |
ISSN: | 1434-1948 1099-0682 |
DOI: | 10.1002/ejic.201000043 |