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制备负载有环氧氯丙烷和环糊精的金纳米颗粒修饰的UiO-66-NH,作为交叉偶联和羰基化反应中的新型高效催化剂。

Preparation of gold nanoparticles decorated UiO-66-NH incorporated epichlorohydrin and cyclodextrin as novel efficient catalyst in cross coupling and carbonylative reactions.

作者信息

Mohammadi Leila, Vaezi Mohammadreza

机构信息

Department of Nano Technology and Advanced Materials, Materials and Energy Research Center, Karaj, Iran.

出版信息

Sci Rep. 2025 Apr 25;15(1):14544. doi: 10.1038/s41598-025-97624-w.

DOI:10.1038/s41598-025-97624-w
PMID:40280973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12032121/
Abstract

This study presents a new, highly effective, and reusable catalyst: UiO-66-NH@Epichlorohydrin@Cyclodextrin@Au-NPs. This innovative catalyst starts with the Zr-based UiO-66 material, which is functionalized with amino groups (-NH). We enhanced its surface compatibility by modifying it with epichlorohydrin and cyclodextrin via a post-synthesis modification method. Gold nanoparticles were then stabilized on this modified composite, resulting in the UiO-66-NH@Epichlorohydrin@Cyclodextrin@Au-NPs complex. We used this catalyst for C-C coupling and Carbonylative Sonogashira reactions in mild conditions. Its effectiveness was underscored by various analytical techniques, including XRD, EDS, SEM, FT-IR, TEM, BET, ICP, TGA, and elemental mapping. The catalyst exhibited exceptional performance in Sonogashira, Heck, Suzuki coupling, and Carbonylative reactions, achieving good to excellent yields. It proved to be highly recyclable, maintaining its catalytic activity for up to nine cycles with minimal loss.

摘要

本研究提出了一种新型、高效且可重复使用的催化剂:UiO-66-NH@环氧氯丙烷@环糊精@金纳米粒子。这种创新型催化剂始于基于锆的UiO-66材料,该材料用氨基(-NH)进行了功能化。我们通过后合成改性方法用环氧氯丙烷和环糊精对其进行改性,增强了其表面兼容性。然后将金纳米粒子稳定在这种改性复合材料上,得到UiO-66-NH@环氧氯丙烷@环糊精@金纳米粒子复合物。我们在温和条件下将这种催化剂用于碳-碳偶联反应和羰基化Sonogashira反应。包括XRD、EDS、SEM、FT-IR、TEM、BET、ICP、TGA和元素映射在内的各种分析技术都突出了其有效性。该催化剂在Sonogashira、Heck、Suzuki偶联反应和羰基化反应中表现出优异的性能,产率达到良好至优异。事实证明它具有高度可回收性,在催化活性损失极小的情况下可保持九个循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/9d6c9a64fd8a/41598_2025_97624_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/49bf85d630ea/41598_2025_97624_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/fcbb81bef8e7/41598_2025_97624_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/9760905a34f4/41598_2025_97624_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/ff80c3b644ac/41598_2025_97624_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/fc4277ac70f3/41598_2025_97624_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/bf2ca1e9c419/41598_2025_97624_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/e8b98009386a/41598_2025_97624_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/2badcd9c691b/41598_2025_97624_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/8093fbe5171c/41598_2025_97624_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/9d6c9a64fd8a/41598_2025_97624_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/49bf85d630ea/41598_2025_97624_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/fcbb81bef8e7/41598_2025_97624_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/9760905a34f4/41598_2025_97624_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/ff80c3b644ac/41598_2025_97624_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/fc4277ac70f3/41598_2025_97624_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/bf2ca1e9c419/41598_2025_97624_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/e8b98009386a/41598_2025_97624_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/2badcd9c691b/41598_2025_97624_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/8093fbe5171c/41598_2025_97624_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/12032121/9d6c9a64fd8a/41598_2025_97624_Fig10_HTML.jpg

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本文引用的文献

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Gold-Catalyzed C-O Cross-Coupling Reactions of Aryl Iodides with Silver Carboxylates.金催化的芳基碘化物与羧酸银的碳-氧交叉偶联反应
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Highly Efficient Photocatalytic Degradation of Tetracycline by Modifying UiO-66 via Different Regulation Strategies.
通过不同调控策略修饰UiO-66实现四环素的高效光催化降解
ACS Omega. 2023 Jul 24;8(30):27375-27385. doi: 10.1021/acsomega.3c02762. eCollection 2023 Aug 1.
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Stabilization of Pd NPs over the surface of β-cyclodextrin incorporated UiO-66-NH for the C-C coupling reaction.在β-环糊精掺杂的UiO-66-NH表面上稳定钯纳米颗粒用于碳-碳偶联反应。
RSC Adv. 2023 Jun 7;13(25):17143-17154. doi: 10.1039/d2ra08347g. eCollection 2023 Jun 5.
5
Gold nanoparticle decorated post-synthesis modified UiO-66-NH for A-coupling preparation of propargyl amines.金纳米颗粒修饰后合成改性 UiO-66-NH 用于 A-偶联制备炔丙胺。
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6
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