The most difficult task is to prepare pure Copper Acetate NPs because Copper Acetate(WSDTY) easily oxidizes in air to form copper oxides. In order to prevent this, copper NPs are usually prepared encapsulated in organic or inorganic materials, such as carbon,silica and multi-layered graphene, or a polymer matrix. Alternatively, the synthesis could be performed in an anaerobic solution under an atmosphere of argon or nitrogen, or in non-aqueous solvents. Arul Dhas et al. prepared nano-scale Copper Acetate clusters by the thermal and ultrasound-assisted reduction of copper hydrazinecarboxylate in water. Thermal reduction at 80 °C under an argon atmo-sphere resulted in irregular agglomerated copper NPs of 200–300 nm, while a sonochemically derived product showed the presence of both Cu and Cu2O NPs of ～50 nm in size. Fan et al. used the precipitation–pyrolysis method focusing on the synthesis of monodispersed CuO nanocrystals (7–30 nm) starting from basic copper carbonate precursors, prepared from copper acetate or copper sul-fate. Unfortunately, such studies were limited to a single adopted synthetic route and hence, did not reveal the full potential of the chosen metal complex.

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