Abstract

We report stable and heterogeneous graphene oxide (GO)–intercalated copper as an efficient catalyst for the organic transformations in green solvents. The GO-intercalated copper(II) complex of bis(1,4,7,10-tetraazacyclododecane) [Cu(II)-bis-cyclen] was prepared by a facile synthetic approach with a high dilution technique. The as-prepared GO-Cu(II)-bis-cyclen nanocomposite was used as a click catalyst for the 1,3 dipolar Huisgen cycloaddition reaction of terminal alkyne and azide substrates. On directing a great deal of attention toward the feasibility of the rapid electron transfer rate of the catalyst in proliferating the yield of 1,2,3-triazole products, the click catalyst GO-Cu(II)-bis-cyclen nanocomposite was designed and synthesized via non-covalent functionalization. The presence of a higher coordination site in an efficient 2D nanocomposite promotes the stabilization of Cu(I) L-acetylide intermediate during the catalytic cycle initiated by the addition of reductants. From the XRD analysis, the enhancement in the d-interlayer spacing of 1.04 nm was observed due to the intercalation of the Cu(II)-bis-cyclen complex in between the GO basal planes. It was also characterized by XPS, FT-IR, RAMAN, UV, SEM, AFM, and TGA techniques. The recyclability of the heterogeneous catalyst [GO-Cu(II)-cyclen] with the solvent effect has also been studied. This class of GO-Cu(II)-bis-cyclen nanocomposite paves the way for bioconjugation of macromolecules through the click chemistry approach.

Highlights

  • The Cu(I)-catalyzed [3 + 2] cycloaddition reaction between the terminal alkynes and azides, popularly known as “click reaction,” was developed by Sharpless and Meldal, which have emerged in various branches of research (Kolb et al, 2001; Meldal and Schoffelen, 2016)

  • Despite the success of coppercatalyzed azide–alkyne cycloaddition (CuAAC), it depicts certain demerits such as i) contamination of click products are inferred due to the use of copper(II)–based catalyst, like in few cases, copper prefers to coordinate with the available heteroatoms in the substrates such as macromolecules or macrocycles, ii) in situ formation of unstable Cu(I) species by the addition of the reducing agent which become the salient prerequisite in the click reaction (Meldal and Tornøe, 2008), and iii) the copper directly coordinates with the available heteroatoms in the case of macromolecules or macrocycles and thereby the efficiency is reduced

  • Graphene oxide consists of different oxygencontaining functional groups such as -OH, -COOH, and -C-O-C possessing exceptional properties on intercalation proven to enhance the electron mobility of graphene, thereby facilitating the fast electron transfer during the catalytic reactions improving its catalytic activity in CuAAC (Dreyer et al, 2010)

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Summary

Introduction

The Cu(I)-catalyzed [3 + 2] cycloaddition reaction between the terminal alkynes and azides, popularly known as “click reaction,” was developed by Sharpless and Meldal, which have emerged in various branches of research (Kolb et al, 2001; Meldal and Schoffelen, 2016). In order to enhance the catalytic activity of CuAAC by the stabilization of Cu(I) species, click reaction requires certain auxiliary reagents such as ligands, bases, and oxidizing/reducing agents depending on the copper source material used (Wang et al, 2016). We report the highly stable, dispersible, recyclable, and heterogeneous copper-based GO nanocomposites [GO-Cu(II)-bis-cyclen nanocomposite] as an efficient click catalyst for the 1,3-dipolar cycloaddition of the terminal alkynes and azides without the need of base or excess of co-catalysts. The graphene oxide/poly(vinyl imidazole) nanocomposite as heterogeneous polymeric catalyst was reported for the click synthesis of 1,2,3-triazole derivatives in excellent yields via onepot three-component cycloaddition of halides, terminal alkynes, and sodium azide (Pourjavadi et al, 2015). The catalytic properties of metals and metal nanoparticles were improved when the graphene oxide (GO) was used as a catalytic support due to their increased surface area and stability (Shabestari et al, 2020)

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