An immobilized Schiff base-Mn complex as a hybrid magnetic nanocatalyst for green synthesis of biologically active [4,3-d]pyrido[1,2-a]pyrimidin-6-ones

一种固定化的席夫碱-锰配合物作为混合磁性纳米催化剂用于绿色合成具有生物活性的[4,3-d]吡啶并[1,2-a]嘧啶-6-酮

阅读:1

Abstract

The immobilization of metal ions on inorganic supports has garnered significant attention due to its wide range of applications. These immobilized metal ions serve as catalysts for chemical reactions and as probes for studying biological processes. In this study, we successfully prepared Fe(3)O(4)@SiO(2)@Mn-complex by immobilizing manganese onto the surface of magnetic Fe(3)O(4)@SiO(2) nanoparticles through a layer-by-layer assembly technique. The structure of these hybrid nanoparticles was characterized by various analytical techniques, including Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM), and inductively coupled plasma-optical emission spectrometry (ICP-OES). Fe(3)O(4)@SiO(2)@Mn-complex was successfully utilized in the synthesis of biologically active 7-aryl[4,3-d]pyrido[1,2-a]pyrimidin-6(7H)-one derivatives in an aqueous medium, providing environmentally friendly conditions. The desired products were manufactured in high yields (81-95%) without the formation of side products. The heterogeneity of the solid nanocatalyst was assessed using a hot filtration test that confirmed minimal manganese leaching during the reaction. This procedure offers numerous advantages, including short reaction times, the use of a green solvent, the ability to reuse the catalyst without a significant decrease in catalytic activity, and easy separation of the catalyst using an external magnet. Furthermore, this approach aligns with environmental compatibility and sustainability standards.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。