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淀粉介导并粘结滑石的致密磁铁矿涂层,从而产生一种用于咪唑并[1,2-c]喹唑啉三组分合成的高效纳米催化剂。

Starch mediates and cements densely magnetite-coating of talc, giving an efficient nano-catalyst for three-component synthesis of imidazo[1,2-c]quinazolines.

作者信息

Hosseinzadeh Hedyeh, Rad-Moghadam Kurosh, Mehrdad Morteza, Rouhi Somayeh

机构信息

Chemistry Department, University of Guilan, Rasht, 41335-1914, Iran.

出版信息

Sci Rep. 2024 Jan 5;14(1):666. doi: 10.1038/s41598-023-51123-y.

DOI:10.1038/s41598-023-51123-y
PMID:38182779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10770035/
Abstract

Hot-water-soluble starch (HWSS) was used as a powerful cementing material to produce nano-size conglomerates of talc and magnetite nanoparticles. Coordination of HWSS hydroxyl groups to iron atoms at surface of magnetite leads to grafting and encapsulation of its nanoparticles. The resulting nano-complex showed a higher loading capacity on talc than pristine magnetite nanoparticles. Only a minute amount of HWSS was detected in the fabricated nano-composite Talc\HWSS@FeO. XPS study suggests a considerable interaction between HWSS and FeO nanoparticles, upon which some of the Fe atoms on surface of FeO are reduced into Fe atoms. ATR FT-IR spectra of the nano-composite revealed significant delamination of talc sheets on interaction with HWSS-coated FeO nanoparticles. The nano-composite displayed an efficient catalytic activity in the synthesis of new imidazo[1,2-c]quinazoline derivatives via Grobke-Blackburn-Bienaymé three-component reaction of 4-aminoquinazoline, arylaldehydes and isocyanide. The efficiency of the method was exemplified by synthesizing 7 new products in fairly high yields (68-83%) within short reaction times (24-30 min) using a catalytic amount of the catalyst under solvent-free condition at 120 °C. Clean and fast synthesis of the products and convenient separation of the robust nano-catalyst are the prominent advantages of the present method. The nano-catalyst was properly characterized.

摘要

热水溶性淀粉(HWSS)被用作一种强力胶凝材料,以制备滑石和磁铁矿纳米颗粒的纳米级团聚体。HWSS的羟基与磁铁矿表面的铁原子配位,导致其纳米颗粒的接枝和包封。所得的纳米复合物对滑石的负载能力比原始磁铁矿纳米颗粒更高。在制备的纳米复合材料滑石\HWSS@FeO中仅检测到微量的HWSS。X射线光电子能谱(XPS)研究表明HWSS与FeO纳米颗粒之间存在相当大的相互作用,在此作用下,FeO表面的一些铁原子被还原为铁原子。纳米复合材料的衰减全反射傅里叶变换红外光谱(ATR FT-IR)显示,滑石片层与HWSS包覆的FeO纳米颗粒相互作用时发生了显著的分层。该纳米复合材料在通过4-氨基喹唑啉、芳醛和异腈的格罗布克-布莱克本-比内梅三组分反应合成新型咪唑并[1,2-c]喹唑啉衍生物中表现出高效的催化活性。该方法的效率通过在120℃无溶剂条件下使用催化量的催化剂在短反应时间(24-30分钟)内以相当高的产率(68-83%)合成7种新产物得到例证。产物的清洁快速合成以及坚固的纳米催化剂的便捷分离是本方法的突出优点。对该纳米催化剂进行了适当的表征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/882b7af5f260/41598_2023_51123_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/e51f12cb74bd/41598_2023_51123_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/95472c051c28/41598_2023_51123_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/eb2e5cb951d6/41598_2023_51123_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/411cb1a5f03c/41598_2023_51123_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/ca917e19f0f1/41598_2023_51123_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/78188ee59c59/41598_2023_51123_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/03d6d51b6bbd/41598_2023_51123_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/882b7af5f260/41598_2023_51123_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/e51f12cb74bd/41598_2023_51123_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/95472c051c28/41598_2023_51123_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/eb2e5cb951d6/41598_2023_51123_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/411cb1a5f03c/41598_2023_51123_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/ca917e19f0f1/41598_2023_51123_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/78188ee59c59/41598_2023_51123_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/03d6d51b6bbd/41598_2023_51123_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bce/10770035/882b7af5f260/41598_2023_51123_Fig8_HTML.jpg

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