Isomeric organic ligand dominating polyoxometalate-based hybrid compounds: synthesis and as electrocatalysts and pH-sensitive probes

Abstract

<p>By introducing isomeric organic ligands into polyoxometalate (POM) systems, two new POM-based hybrid compounds, [Cu<sub>6</sub>(<i>m</i>-pyttz)<sub>2</sub>(H<sub>2</sub>O)][HPMo<sub>12</sub>O<sub>40</sub>] (<b>1</b>) and [Ag<sub>3</sub>(<i>p</i>-H<sub>2</sub>pyttz)(<i>p</i>-Hpyttz)Cl][H<sub>2</sub>PMo<sub>12</sub>O<sub>40</sub>]·6H<sub>2</sub>O (<b>2</b>) (<i>m</i>-/<i>p</i>-H<sub>2</sub>pyttz = 3-(pyrid-3/4-yl)-5(1H-1,2,4-triazol-3-yl)-1,2,4-triazolyl), have been hydrothermally synthesized and characterized. Single-crystal structural analysis shows the <i>m</i>-pyttz ligands link Cu<sup>I</sup> ions to generate a two-dimensional layer with hanger-like rhombus, which is pillared by the PMo<sub>12</sub> anions in <b>1</b>. Compound <b>2</b> exhibits a three-dimensional supramolecular framework, in which PMo<sub>12</sub> anions are building blocks facilitating the extension of the whole structure. The influence of the coordination modes of <i>m</i>-/<i>p</i>-H<sub>2</sub>pyttz on the structures is discussed in detail. Furthermore, electrochemical properties of <b>1</b> and <b>2</b> have been studied and they display excellent electrocatalytic activities toward the reduction of nitrite and hydrogen peroxide and pH-dependent electrochemical behaviors.</p

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