{"title":"将 L-缬氨酸固定在超顺磁性 Fe 3 O 4 纳米粒子上,作为合成新噻唑衍生物的新型、可回收和绿色纳米催化剂","authors":"Hamid Fallahi , Mojdeh Shojaei , Farhad Shirzaei , Hamid Reza Shaterian","doi":"10.1080/17415993.2024.2378784","DOIUrl":null,"url":null,"abstract":"<div><p>The novel immobilization of L-Valine on superparamagnetic Fe<sub>3</sub>O<sub>4</sub> nanoparticles was prepared using a simple protocol for the first time. This compound acts as a highly efficient and recyclable heterogeneous nanocatalyst for the synthesis of thiazole derivatives <em>via</em> a one-pot and multi-component condensation reaction of arylglyoxals monohydrate, cyclic 1,3-dicarbonyls, and thiobenzamides in a water solvent. The structure of the nanocatalyst was characterized and confirmed using various techniques, such as Fourier transform infrared spectroscopy (FT-IR), Energy Dispersive X-ray (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TG/DTA), and vibrating sample magnetometry (VSM). This heterogeneous nanocatalyst can be easily recovered from the reaction mixture by an external magnetic field and reused for subsequent reactions at least five times without losing significant catalytic activity.</p></div>","PeriodicalId":17081,"journal":{"name":"Journal of Sulfur Chemistry","volume":"45 5","pages":"Pages 657-677"},"PeriodicalIF":2.1000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The immobilization of L-Valine on superparamagnetic Fe3O4 nanoparticles as a novel, recoverable and green nanocatalyst for the synthesis of new thiazole derivatives\",\"authors\":\"Hamid Fallahi , Mojdeh Shojaei , Farhad Shirzaei , Hamid Reza Shaterian\",\"doi\":\"10.1080/17415993.2024.2378784\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The novel immobilization of L-Valine on superparamagnetic Fe<sub>3</sub>O<sub>4</sub> nanoparticles was prepared using a simple protocol for the first time. This compound acts as a highly efficient and recyclable heterogeneous nanocatalyst for the synthesis of thiazole derivatives <em>via</em> a one-pot and multi-component condensation reaction of arylglyoxals monohydrate, cyclic 1,3-dicarbonyls, and thiobenzamides in a water solvent. The structure of the nanocatalyst was characterized and confirmed using various techniques, such as Fourier transform infrared spectroscopy (FT-IR), Energy Dispersive X-ray (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TG/DTA), and vibrating sample magnetometry (VSM). This heterogeneous nanocatalyst can be easily recovered from the reaction mixture by an external magnetic field and reused for subsequent reactions at least five times without losing significant catalytic activity.</p></div>\",\"PeriodicalId\":17081,\"journal\":{\"name\":\"Journal of Sulfur Chemistry\",\"volume\":\"45 5\",\"pages\":\"Pages 657-677\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Sulfur Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1741599324000230\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Sulfur Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1741599324000230","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
本研究首次采用简单的方法在超顺磁性 Fe3O4 纳米粒子上制备了新型固定化 L-缬氨酸。该化合物可作为一种高效、可回收的异质纳米催化剂,用于在水溶剂中通过芳基乙二醛一水合物、环状 1,3 二甲基和硫代苯甲酰胺的一锅多组分缩合反应合成噻唑衍生物。利用傅立叶变换红外光谱(FT-IR)、能量色散 X 射线(XRD)、扫描电子显微镜(SEM)、热重分析(TG/DTA)和振动样品磁强计(VSM)等多种技术对该纳米催化剂的结构进行了表征和确认。这种异质纳米催化剂可在外部磁场的作用下从反应混合物中轻松回收,并可在后续反应中重复使用至少五次,而不会失去明显的催化活性。
The immobilization of L-Valine on superparamagnetic Fe3O4 nanoparticles as a novel, recoverable and green nanocatalyst for the synthesis of new thiazole derivatives
The novel immobilization of L-Valine on superparamagnetic Fe3O4 nanoparticles was prepared using a simple protocol for the first time. This compound acts as a highly efficient and recyclable heterogeneous nanocatalyst for the synthesis of thiazole derivatives via a one-pot and multi-component condensation reaction of arylglyoxals monohydrate, cyclic 1,3-dicarbonyls, and thiobenzamides in a water solvent. The structure of the nanocatalyst was characterized and confirmed using various techniques, such as Fourier transform infrared spectroscopy (FT-IR), Energy Dispersive X-ray (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TG/DTA), and vibrating sample magnetometry (VSM). This heterogeneous nanocatalyst can be easily recovered from the reaction mixture by an external magnetic field and reused for subsequent reactions at least five times without losing significant catalytic activity.
期刊介绍:
The Journal of Sulfur Chemistry is an international journal for the dissemination of scientific results in the rapidly expanding realm of sulfur chemistry. The journal publishes high quality reviews, full papers and communications in the following areas: organic and inorganic chemistry, industrial chemistry, materials and polymer chemistry, biological chemistry and interdisciplinary studies directly related to sulfur science.
Papers outlining theoretical, physical, mechanistic or synthetic studies pertaining to sulfur chemistry are welcome. Hence the target audience is made up of academic and industrial chemists with peripheral or focused interests in sulfur chemistry. Manuscripts that truly define the aims of the journal include, but are not limited to, those that offer: a) innovative use of sulfur reagents; b) new synthetic approaches to sulfur-containing biomolecules, materials or organic and organometallic compounds; c) theoretical and physical studies that facilitate the understanding of sulfur structure, bonding or reactivity; d) catalytic, selective, synthetically useful or noteworthy transformations of sulfur containing molecules; e) industrial applications of sulfur chemistry; f) unique sulfur atom or molecule involvement in interfacial phenomena; g) descriptions of solid phase or combinatorial methods involving sulfur containing substrates. Submissions pertaining to related atoms such as selenium and tellurium are also welcome. Articles offering routine heterocycle formation through established reactions of sulfur containing substrates are outside the scope of the journal.