磺酸负载香兰素/双吲哚甲烷功能化Fe3O4@SiO2-propyl NPs作为合成咪唑喹唑啉类、咪唑喹唑啉类和噻唑喹唑啉类绿色、高效、磁可回收催化剂

IF 2.1 3区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Journal of Sulfur Chemistry Pub Date : 2024-03-03 DOI:10.1080/17415993.2023.2253345
Leila Zare Fekri , Zahra Mohammadi , Atefeh Alijani
{"title":"磺酸负载香兰素/双吲哚甲烷功能化Fe3O4@SiO2-propyl NPs作为合成咪唑喹唑啉类、咪唑喹唑啉类和噻唑喹唑啉类绿色、高效、磁可回收催化剂","authors":"Leila Zare Fekri ,&nbsp;Zahra Mohammadi ,&nbsp;Atefeh Alijani","doi":"10.1080/17415993.2023.2253345","DOIUrl":null,"url":null,"abstract":"<div><p>Sulfonic acid-supported vanillin/bis indolylmethane-functionalized Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>-Propyl NPs were prepared and characterized by FT-IR, XRD, FE-SEM, TEM, VSM, EDX, DLS, and TGA-DTG. The catalytic efficiency of the prepared nanoparticles was subsequently investigated for the effective synthesis of imidazoquinazolines via the one-pot condensation of 2-aminobenzimidazole, aryl aldehydes, and cyclohexanone or dimedone under solvent-free condition. Some thiazoquinazolines also were prepared via the multicomponent reaction of aldehydes, dimedone, and 2-aminobenzothiazol under solvent-free condition,. This avenue is really suitable because it makes a high yield of product, doesn’t take too long, doesn’t need harmful materials and solvents, its work-up is easy and the catalyst is reusable.</p></div>","PeriodicalId":17081,"journal":{"name":"Journal of Sulfur Chemistry","volume":"45 2","pages":"Pages 198-216"},"PeriodicalIF":2.1000,"publicationDate":"2024-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sulfonic acid-supported vanillin/bis indolylmethane-functionalized Fe3O4@SiO2-propyl NPs as green, effective, and magnetically recoverable catalysts for the synthesis of imidazoquinazolines and thiazoquinazolines\",\"authors\":\"Leila Zare Fekri ,&nbsp;Zahra Mohammadi ,&nbsp;Atefeh Alijani\",\"doi\":\"10.1080/17415993.2023.2253345\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Sulfonic acid-supported vanillin/bis indolylmethane-functionalized Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>-Propyl NPs were prepared and characterized by FT-IR, XRD, FE-SEM, TEM, VSM, EDX, DLS, and TGA-DTG. The catalytic efficiency of the prepared nanoparticles was subsequently investigated for the effective synthesis of imidazoquinazolines via the one-pot condensation of 2-aminobenzimidazole, aryl aldehydes, and cyclohexanone or dimedone under solvent-free condition. Some thiazoquinazolines also were prepared via the multicomponent reaction of aldehydes, dimedone, and 2-aminobenzothiazol under solvent-free condition,. This avenue is really suitable because it makes a high yield of product, doesn’t take too long, doesn’t need harmful materials and solvents, its work-up is easy and the catalyst is reusable.</p></div>\",\"PeriodicalId\":17081,\"journal\":{\"name\":\"Journal of Sulfur Chemistry\",\"volume\":\"45 2\",\"pages\":\"Pages 198-216\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-03-03\",\"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/S1741599323000892\",\"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/S1741599323000892","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

制备了磺酸支持的香兰素/双吲哚甲烷功能化 Fe3O4@SiO2-Propyl NPs,并通过 FT-IR、XRD、FE-SEM、TEM、VSM、EDX、DLS 和 TGA-DTG 对其进行了表征。随后,在无溶剂条件下,研究了所制备纳米粒子在通过 2-氨基苯并咪唑、芳基醛、环己酮或二甲基酮的一锅缩合反应有效合成咪唑喹唑啉类化合物中的催化效率。一些噻唑喹啉类化合物也是在无溶剂条件下通过醛、二咪酮和 2-氨基苯并噻唑的多组分反应制备的。这种方法非常适合,因为它产率高,耗时短,不需要有害材料和溶剂,操作简单,催化剂可重复使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Sulfonic acid-supported vanillin/bis indolylmethane-functionalized Fe3O4@SiO2-propyl NPs as green, effective, and magnetically recoverable catalysts for the synthesis of imidazoquinazolines and thiazoquinazolines

Sulfonic acid-supported vanillin/bis indolylmethane-functionalized Fe3O4@SiO2-Propyl NPs were prepared and characterized by FT-IR, XRD, FE-SEM, TEM, VSM, EDX, DLS, and TGA-DTG. The catalytic efficiency of the prepared nanoparticles was subsequently investigated for the effective synthesis of imidazoquinazolines via the one-pot condensation of 2-aminobenzimidazole, aryl aldehydes, and cyclohexanone or dimedone under solvent-free condition. Some thiazoquinazolines also were prepared via the multicomponent reaction of aldehydes, dimedone, and 2-aminobenzothiazol under solvent-free condition,. This avenue is really suitable because it makes a high yield of product, doesn’t take too long, doesn’t need harmful materials and solvents, its work-up is easy and the catalyst is reusable.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Sulfur Chemistry
Journal of Sulfur Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
4.10
自引率
9.10%
发文量
38
审稿时长
6-12 weeks
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.
期刊最新文献
A green and efficient synthesis of alkyl 2-((5-hydroxy-1H-pyrazole-4-carbonothioyl)thio)acetates via a one-pot, solvent-free reaction Synthesis of novel isoxazole/dihydroisoxazole tethered β-lactam hybrids via regiospecific 1,3-dipolar cycloaddition methodology on 3-phenylthio-β-lactams Thiazole derivatives: prospectives and biological applications Synthesis of benzothioamide derivatives from benzonitriles and H2S-based salts in supercritical CO2 Synthesis and biological evaluation of 2-(2-hydrazinyl) thiazole derivatives with potential antibacterial and antioxidant activity
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1