Patra Sagarika, Panda Smitabala, Acharya Swadhin Swaraj, Phaomei Ganngam, Parida Bibhuti Bhusan
Organic Synthesis Laboratory, P. G. Department of Chemistry, Berhampur University, Bhanja Bihar, Odisha 760007, India.
Department of Chemistry, Dhanamanjari University, Imphal, Manipur 795001, India.
ACS Omega. 2025 Jun 5;10(23):24105-24116. doi: 10.1021/acsomega.4c10467. eCollection 2025 Jun 17.
Herein, we report the synthesis of novel LaPO·Pd nanocatalyst, characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and X-ray photoelectron spectroscopy (XPS) studies. The newly prepared nanocatalyst has been utilized as an efficient catalyst for synthesizing biaryls through Suzuki-Miyaura cross-coupling reactions of haloarenes and phenylboronic acids. The salient features of the protocol include the aqueous medium synthesis of biaryls, broad substrate scope, high yield of the products, gram-scale synthesis of biaryl , recyclability, and reusability of the nanocatalyst for five consecutive runs without significant loss in its catalytic efficiency and yield. The aforementioned features account for the green and sustainable aspect of the protocol in the biaryl synthesis.
在此,我们报道了新型LaPO·Pd纳米催化剂的合成,并通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、粉末X射线衍射(PXRD)和X射线光电子能谱(XPS)研究对其进行了表征。新制备的纳米催化剂已被用作通过卤代芳烃与苯基硼酸的铃木-宫浦交叉偶联反应合成联芳基的高效催化剂。该方法的显著特点包括在水介质中合成联芳基、底物范围广、产物收率高、联芳基的克级合成、纳米催化剂的可回收性以及连续五次重复使用而其催化效率和收率无显著损失。上述特点体现了该联芳基合成方法的绿色可持续性。