Sheikh Safoora, Bhattacharyya Aditya, Henriquez Marco A, Nasseri Mohammad Ali, Chahkandi Mohammad, Allahresani Ali, Reiser Oliver
Department of Chemistry, University of Birjand, P.O. Box 97175-615 Birjand, Iran.
Institut für Organische Chemie, Universität Regensburg, Universitätsstraße 31, Regensburg 93053, German.
ACS Omega. 2024 Jul 9;9(29):31393-31400. doi: 10.1021/acsomega.3c10462. eCollection 2024 Jul 23.
A cobalt catalyst supported on an iron oxide core, denoted as γ-FeO@PEG@THMAM-Co, has been prepared and characterized by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray mapping, thermogravimetry differential thermogravimetry, vibrating sample magnetometry, and inductively coupled plasma. Polyhydroxy end groups in the shell make the catalyst particles dispersible in water, allowing Hiyama, Suzuki, and C-N cross-coupling reactions of aryl iodides and bromides. The catalyst could be recovered by magnetic decantation and reused for at least five successive runs with a negligent decrease in its activity or changes in its morphology. Water as a solvent without requiring additives, surfactants, or organic co-solvents, as well as an abundant and low-cost cobalt catalyst combined with facile recovery, low leaching, and scalability, provides an environmentally and economically attractive alternative to established palladium-catalyzed C-C and C-N coupling reactions.
一种负载在氧化铁核上的钴催化剂,记为γ-FeO@PEG@THMAM-Co,已通过傅里叶变换红外光谱、X射线衍射、场发射扫描电子显微镜、透射电子显微镜、能量色散X射线映射、热重差示热重法、振动样品磁强计和电感耦合等离子体进行了制备和表征。壳层中的多羟基端基使催化剂颗粒可分散在水中,从而实现芳基碘化物和溴化物的日山、铃木和C-N交叉偶联反应。该催化剂可通过磁倾析回收,并至少连续重复使用五次,其活性仅有轻微下降,形态也无变化。水作为溶剂,无需添加剂、表面活性剂或有机共溶剂,以及丰富且低成本的钴催化剂,再加上易于回收、低浸出率和可扩展性,为已有的钯催化C-C和C-N偶联反应提供了一种环境和经济上具有吸引力的替代方案。