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Investigating the effect of immobilization of yttrium-Schiff base onto magnetite nanoparticles: enhanced catalytic activity in the synthesis of dihydropyrimidinones under solvent-free conditions

机译:研究将钇席夫碱固定在磁铁矿纳米颗粒上的作用:在无溶剂条件下合成二氢嘧啶酮的催化活性增强

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摘要

A new complex of yttrium-salpr was synthesized through the reaction of Y(NO3)(3)center dot 6(H2O) and salpr Schiff base (salpr = N,N'-bis(3-salicylidenaminopropyl) amine). The prepared complex was characterized by Mid and Far-IR, C-13-NMR, H-1-NMR, UV-Vis, XRF, and CHN. The obtained data suggested a binuclear structure for this compound. To our surprise, the catalytic activity of this complex was even lower than its precursor, Y(NO3)(3)center dot 6(H2O), in one-pot synthesis of dihydropyrimidinones under solvent-free conditions. As one of the reasons of this reduced activity should pertain to the binuclear structure of the complex that reduces the availability of yttrium in the reaction, the complex was immobilized on modified Fe3O4 nanoparticles, which not only increases the surface to the volume ratio of the compound, but also hinders the formation of binuclear structure due to site (Schiff base) isolation. These prepared nanoparticles depicted noticeably high catalytic activity as well as good recyclability and very easy separation.
机译:通过Y(NO3)(3)中心点6(H2O)和salpr Schiff碱(salpr = N,N'-双(3-salicylidenaminopropyl)胺)的反应合成了新的钇-salpr配合物。制备的络合物通过中红外和远红外,C-13-NMR,H-1-NMR,UV-Vis,XRF和CHN进行表征。获得的数据表明该化合物具有双核结构。令我们惊讶的是,在无溶剂条件下一锅合成二氢嘧啶酮时,该络合物的催化活性甚至低于其前体Y(NO3)(3)中心点6(H2O)。由于这种活性降低的原因之一应该是该复合物的双核结构降低了反应中钇的利用率,因此将该复合物固定在改性的Fe3O4纳米颗粒上,这不仅增加了化合物的表面积与体积比,但由于位点(席夫碱)的隔离,也阻碍了双核结构的形成。这些制备的纳米颗粒表现出显着的高催化活性以及良好的可回收性和非常容易的分离。

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