Efficient reduction of nitro compounds and domino preparation of 1-substituted-1<i>H</i>-1,2,3,4-tetrazoles by Pd(<scp>ii</scp>)-polysalophen coated magnetite NPs as a robust versatile nanocomposite

Abstract

A new, versatile, and green methodology has been developed for the efficient NaBH₄-reduction of nitroarenes as well as the domino/reduction MCR preparation of 1-substituted-1<i>H</i>-1,2,3,4-tetrazoles using Pd(ii)-polysalophen coated magnetite NPs as an efficient heterogeneous magnetically recyclable nanocatalyst. Polysalophen was firstly prepared based on a triazine framework with a high degree of polymerization, then coordinated to Pd ions and, finally, the resulting hybrid was immobilized on magnetite NPs. The catalyst was characterized by various instrumental and analytical methods, including GPC, DLS, N₂ adsorption-desorption, TGA, VSM, TEM, HRTEM, EDX, XPS, XRD, and ICP analyses. The catalyst possesses dual-functionality including the reduction of nitroarenes and the construction of tetrazole rings all in one step <i>via</i> a domino protocol. High to excellent yields were obtained for both nitro reduction and the direct preparation of 1-substituted-1<i>H</i>-1,2,3,4-tetrazoles from nitro compounds. Insight into the mechanism was conducted by XPS <i>in situ</i> as well as DLS <i>in situ</i> along with several control experiments. Recyclability of the catalyst was studied for 6 consecutive runs along with metal leaching measurements in each cycle.