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介孔磁性负载铜配合物用于在绿色介质中一锅法合成5-取代-1H-四唑及硫化物的氧化反应

Mesoporous magnetic supported Cu complex for one-pot synthesis of 5-substituted 1H-tetrazoles in green media and the oxidation of sulfides.

作者信息

Molaei Somayeh, Ghadermazi Mohammad

机构信息

Department of Chemistry, Faculty of Science, University of Kurdistan, Sanandaj, Iran.

出版信息

Sci Rep. 2025 May 9;15(1):16175. doi: 10.1038/s41598-025-97420-6.

Abstract

We used the copper Phthalocyanine (Pc) on magnetic mesoporous silica nanoparticles. Therefore, several coordination sites became available which enhance chelating potency to load appropriate amounts of Gadolinium (Gd). This improves the catalytic activity in converting nitrile to tetrazole and selective oxidation of sulfides. Gadolinium (Gd) with incompletely occupied 4f and empty 5d orbitals can be used as the active component or as the promoter of the catalyst. Here, we outline the synthesis, characterization, and catalytic activity of a novel Gd(III) copper Phthalocyanine (Pc) coordination on the CoFeO/SBA-15 (CoFeO/SBA-15/CuPc@Gd). The prepared material was characterized using powder X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, elemental mapping, vibrating-sample magnetometer (VSM), Inductively coupled plasma atomic emission spectroscopy (ICP-AES), Fourier transform infrared spectroscopy, and nitrogen adsorption-desorption isotherm. The CoFeO/SBA-15/CuPc@Gd composite consists of a mesoporous structure with a surface area by BET and t-plot of 122.2 m/g and 86.28 m/g respectively, with a mean pore size of 5.37 nm, and pore volume of 0.164 cm/g. The CoFeO/SBA-15/CuPc@Gd was successfully applied as a powerful catalyst for green synthesis of 5-substituted 1H-tetrazoles in water and selective oxidation of sulfides at room temperature. This catalyst was recovered and reused several times without a significant decrease in efficiency and stability. The catalyst could be fully recovered by an external magnetic field and showed good reusability.

摘要

我们将铜酞菁(Pc)用于磁性介孔二氧化硅纳米颗粒上。因此,产生了几个配位位点,这增强了螯合能力,从而能够负载适量的钆(Gd)。这提高了将腈转化为四唑以及硫化物选择性氧化的催化活性。具有未完全占据的4f轨道和空的5d轨道的钆(Gd)可作为活性成分或催化剂的促进剂。在此,我们概述了一种新型的钆(III)铜酞菁(Pc)在CoFeO/SBA - 15(CoFeO/SBA - 15/CuPc@Gd)上的配位的合成、表征及催化活性。使用粉末X射线衍射、场发射扫描电子显微镜、透射电子显微镜、元素映射、振动样品磁强计(VSM)、电感耦合等离子体原子发射光谱(ICP - AES)、傅里叶变换红外光谱和氮吸附 - 解吸等温线对制备的材料进行了表征。CoFeO/SBA - 15/CuPc@Gd复合材料具有介孔结构,通过BET和t - 图测得的表面积分别为122.2 m²/g和86.28 m²/g,平均孔径为5.37 nm,孔体积为0.164 cm³/g。CoFeO/SBA - 15/CuPc@Gd成功地用作在水中绿色合成5 - 取代的1H - 四唑以及在室温下硫化物选择性氧化的高效催化剂。该催化剂可以回收并重复使用多次,而效率和稳定性不会显著降低。该催化剂可以通过外部磁场完全回收,并显示出良好的可重复使用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5197/12064759/6ebc3214bcfa/41598_2025_97420_Fig1_HTML.jpg

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