A new β-cyclodextrin-based nickel as green and water-soluble supramolecular catalysts for aqueous Suzuki reaction

Abstract

Abstract A water-soluble nickel complex based on amino-β-CD was developed using a facile method and exhibits excellent catalytic performance in the Suzuki reaction in water. This synthesized complex has been characterized using UV–Vis, AAS, TGA, and FT-IR techniques. The easily synthesized novel supramolecular catalysts have been applied as a green and eco-friendly catalyst in the Suzuki coupling for preparing diverse biaryls. This result indicates that using 2.5 mol% of nickel, K2CO3 as the best base, and water as the green solvent are the best reaction conditions. This new catalyst features easy handling, low-cost, mild, and simple protocol. The use of low-cost and accessibility of the reagents, modest conditions, and good yields of products are notable characteristics of this method. Using aqueous media with this catalyst as a proper catalyst makes the presented process a fascinating method compared to most reports. Under mild reaction conditions, this green Ni(II)-β-CD catalyst displayed recyclable behavior seven times with minor loss in its catalytic activity.