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A Top‐Down Approach to Synthesis of pH‐Controlled Cu NPs: Their Catalytic Activity toward the One‐Pot Preparation of α‐Aminonitriles and 5‐Substituted 1 <i>H</i> ‐Tetrazoles from Aldehydes

Zemin HeKey Laboratory of Organic Polymer Photoelectric Materials, School of Sciences Xijing University Xi'an 710123 ChinaLi FengSchool of Civil and Transportation Engineering Guangdong University of Technology, No100 Waihuan Xi Road, Guangzhou, Higher Education Mega Center, Panyu District Guangzhou 510006 Guangdong ChinaPei WuSchool of Civil Engineering and Architecture Chongqing University of Science and Technology Chongqing 401331 ChinaShiyao LiHuayue Institute of Ecological Environment Engineering Chongqing 401120 PR ChinaMilad KazemnejadiDepartment of Chemistry, College of Science Shiraz University Shiraz 7194684795 Iran
2020en
ABI

Аннотация

Abstract A new approach for the preparation of copper nanoparticles has been developed by the chemical decomposition of bulk‐waste copper wire using HNO 3 / DMSO/ NaOCl (HDN) reagent. This is a two‐steps synthesis via a top‐down approach for the preparation of NPs. A mixture of Cu NPs was obtained in high basic pHs (&gt;12) including CuO, Cu(OH) 2 and Cu 2 (OH) 3 Cl NPs. The Cu NPs demonstrated high dependent on pH, which each of copper NPs were selectively prepared with pH control. Selective preparation of copper NPs lead to pure Botallackite Cu 2 (OH) 3 Cl, Cu(OH) 2 , and Tenorite CuO structures at pH =7, pH&lt;7, and pH=11 respectively. The mixture and pure copper NPs were thoroughly characterized by various analytical techniques including XPS, EDX, XRD, DLS, FTIR, FE‐SEM, TEM, BET, and ICP methods. The resultant Cu NPs were used as an efficient heterogeneous, recyclable nanocatalyst for the preparation of α‐aminonitriles and 5‐substituted 1 H ‐tetrazoles with a synergistic effect. The nanocatalyst not only demonstrated high to excellent yields for the aminonitriles and tetrazoles under mild conditions, but also it can be recovered and reused for several times without considerable loss in activity. Kinetics for the preparation of α‐aminonitrile and 5‐substituted 1 H ‐tetrazole was studied and chemoselectivity of the method was evaluated by various combinations.

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