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用于铃木耦合反应的可回收LaF·Pd纳米催化剂:由卤代芳烃和苯硼酸绿色合成联芳基化合物

Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids.

作者信息

Panda Smitabala, Patra Sagarika, Acharya Swadhin Swaraj, Phaomei Ganngam, Parida Bibhuti Bhusan

机构信息

Department of Chemistry, Berhampur University Bhanja Bihar-760007 Odisha India

出版信息

RSC Adv. 2024 Jul 5;14(30):21269-21276. doi: 10.1039/d4ra00686k.

Abstract

Herein we prepared the novel LaF·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the presence of KCO as the base at 70 °C. The present method is capable of giving the C-C coupled product in good to excellent yields (up to 97%). The reactions were conducted under green conditions in aqueous medium and the nanocatalyst used in this study was recyclable. The recyclability and reusability of the catalyst was checked for seven consecutive cycles without significant loss in reactivity.

摘要

在此,我们制备了通过XRD和TEM分析表征的新型LaF·Pd纳米催化剂。该纳米催化剂应用于铃木偶联反应,在70℃下,以碳酸钾为碱,从易得的芳基卤化物(溴化物和碘化物)和取代苯硼酸在水介质中合成联芳基。本方法能够以良好至优异的产率(高达97%)得到C-C偶联产物。反应在水介质中的绿色条件下进行,本研究中使用的纳米催化剂可回收。检查了催化剂的可回收性和可重复使用性,连续七个循环,反应活性没有明显损失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a826/11224950/5c0406af7c49/d4ra00686k-f1.jpg

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