A synergistic {Cu2-W12O40} catalyst with high conversion for homo-coupling of terminal alkynes

By the strategy of replacing the H2O ligands in the paddle wheel shaped copper dimer Cu-2(OAc)(4)(H2O)(2) with polyoxometalate (POM) [H2W12O40](6-) {W12O40} pro-ligands, a novel nano porous 2D network {[Cu-2(OAc)(4)](2)(W12O40)}(n) was obtained. The POM - copper centered redox reactions and stability of the compound were studied by cyclic voltammetry. Furthermore, the compound was found to be a super-efficient homogeneous catalyst (almost 100% conversion) in homo-coupling of terminal alkynes compared with its components and physical mixture under mild conditions with low amounts. The in situ Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) results clearly show the changes of alkyne substances in the catalytic process and the X-ray photoelectron spectroscopy (XPS) results reveal the electron transfer from {W12O40} to Cu(ii) to promote the C-H activation step during the homo-coupling of terminal alkynes. The synergistic Cu(ii)-POM catalytic mechanism was proposed.

Automated summary

By replacing the H2O ligands with polyoxometalate (POM) [H2W12O40](6-) {W12O40} pro-ligands, a novel nano porous 2D network {[Cu-2(OAc)(4)](2)(W12O40)}(n) was synthesized. The compound exhibited high efficiency as a homogeneous catalyst in the homo-coupling of terminal alkynes under mild conditions and low amounts. In situ DRIFTS results revealed the changes of alkyne substances during the catalytic process, while XPS results showed electron transfer from {W12O40} to Cu(ii) to promote the C-H activation step. A synergistic Cu(ii)-POM catalytic mechanism was proposed.