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A one‐pot method for synthesis of reduced graphene oxide‐supported Cu–Cu2O and catalytic application in tandem reaction of halides and sodium azide with terminal alkynes

Reduced graphene oxide (RGO)‐supported Cu–Cu2O nanocomposite material (Cu‐Cu2O@RGO) was prepared through a one‐pot reflux synthesis method. The morphology, crystal structure and composition of the prepared Cu‐Cu2O@RGO were characterized using transmission electron microscopy, X‐ray diffraction, and...

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Bibliographic Details
Published in:Applied organometallic chemistry 2018-04, Vol.32 (4), p.n/a
Main Authors: Li, Zhuofei, Zhao, Hongyan, Han, Huatao, Song, Jinyi, Liu, Yang, Guo, Weihao, Sun, Zhizhong, Chu, Wenyi
Format: Article
Language:English
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Summary:Reduced graphene oxide (RGO)‐supported Cu–Cu2O nanocomposite material (Cu‐Cu2O@RGO) was prepared through a one‐pot reflux synthesis method. The morphology, crystal structure and composition of the prepared Cu‐Cu2O@RGO were characterized using transmission electron microscopy, X‐ray diffraction, and X‐ray photoelectron, infrared and Raman spectroscopies. Cu‐Cu2O@RGO as a heterogeneous catalyst was applied to tandem reactions of halides and sodium azide with terminal alkynes to synthesize effectively 1,4‐disubstituted 1,2,3‐triazoles. Moreover, the catalyst showed excellent recyclability performance with very little leaching of the metal. Compared with homogeneous catalysts, Cu‐Cu2O@RGO as a green and efficient catalyst was recoverable, easy to separate and highly stable in the tandem method for the synthesis of 1,2,3‐triazole compounds. Reduced graphene oxide (RGO)‐supported Cu–Cu2O nanocomposite (Cu‐Cu2O@RGO) was prepared through one‐pot reflux synthesis. Cu‐Cu2O@RGO as a heterogeneous catalyst was applied to tandem reactions of halides and sodium azide with terminal alkynes to synthesize 1,4‐disubstituted 1,2,3‐triazoles. Cu‐Cu2O@RGO as a green and efficient catalyst was recoverable, easy to separate and highly stable in the tandem method for synthesis of 1,2,3‐triazole compounds.
ISSN:0268-2605
1099-0739
DOI:10.1002/aoc.4301