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In situ green synthesis of Cu‐Ni bimetallic nanoparticles supported on reduced graphene oxide as an effective and recyclable catalyst for the synthesis of N ‐benzyl‐ N ‐aryl‐5‐amino‐1 H ‐tetrazoles
Author(s) -
Nasrollahzadeh Mahmoud,
Sajjadi Mohaddeseh,
Komber Hartmut,
Khonakdar Hossein Ali,
Sajadi S. Mohammad
Publication year - 2019
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.4938
Subject(s) - bimetallic strip , chemistry , graphene , catalysis , aryl , oxide , nanocomposite , nanoparticle , nuclear chemistry , inorganic chemistry , nanotechnology , organic chemistry , materials science , alkyl
In the present work, for the first time we have designed a novel approach for the synthesis of N ‐benzyl‐ N ‐aryl‐5‐amino‐1 H ‐tetrazoles using reduced graphene oxide (rGO) decorated with Cu‐Ni bimetallic nanoparticles (NPs). In situ synthesis of Cu/Ni/rGO nanocomposite was performed by a cost efficient, surfactant‐free and environmentally benign method using Crataegus azarolus var. aronia L. leaf extract as a stabilizing and reducing agent. Phytochemicals present in the extract can be used to reduce Cu 2+ and Ni 2+ ions and GO to Cu NPs, Ni NPs and rGO, respectively. Analyses by means of FT‐IR, UV–Vis, EDS, TEM, FESEM, XRD and elemental mapping confirmed the Cu/Ni/rGO formation and also FT‐IR, NMR, and mass spectroscopy as well as elemental analysis were used to characterize the tetrazoles. The Cu/Ni/rGO nanocomposite showed the superior catalytic activity for the synthesis of N ‐benzyl‐ N ‐aryl‐5‐amino‐1 H ‐tetrazoles within a short reaction time and high yields. Furthermore, this protocol eliminates the need to handle HN 3 .