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pH as a Structure Director in the Synthesis of Copper Molybdates

机译:pH值在钼酸铜合成中的结构指导

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This paper deals with the investigation of the reactions of aqueous molybdates in the presence of copper ions under varying pH to obtain new copper molybdates and rationalize the structures formed in terms of the self-assembling nano-building blocks of polyoxomolybdates (POMs). The reactions led to the precipitation of porous copper molybdates: 1D polymeric anions in (NH_4)_6[{Cu(H_2O)_4} {Mo_(36)O_(112)(H_2O)_(16)}]_(21)H_2O,1, a 3D framework bimetallic oxide in Cu_3Mo_2O_g, 2. Our results reported here clearly suggest that copper complexes formed during the initial stages of the reaction probably dictate the architecture of the final solids. Interestingly the magnetic properties studied on these compounds showed that 1 shows paramagnetic ordering since magnetically active centres i.e. Cu(ll) are separated by large diamagnetic centres of {Mo_(36)} cluster anions where as 2 shows the dominance of antiferromagnetic near-neighbor interaction.
机译:本文研究了在不同pH值下铜离子存在下钼酸水溶液在反应中的反应,以获得新的钼酸铜,并根据聚氧钼酸根(POMs)的自组装纳米结构单元合理化了结构。反应导致了多孔钼酸铜的沉淀:(NH_4)_6 [{Cu(H_2O)_4} {Mo_(36)O_(112)(H_2O)_(16)}] _(21HH_2O中的一维聚合阴离子,1,是在Cu_3Mo_2O_g,2中的3D框架双金属氧化物。我们在这里报告的结果清楚地表明,反应初始阶段形成的铜络合物可能决定了最终固体的结构。有趣的是,研究这些化合物的磁性能表明1显示顺磁有序,因为磁活性中心,即Cu(II)被{Mo_(36)}团簇阴离子的大抗磁中心隔开,其中2显示反铁磁近邻相互作用的优势。

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