What is it about?
Catalysts are used extremely widely to make the products we use daily. Though catalysts are not destroyed in the process, they are often lost into the products they form. Using a simple, hand-held magnet, this paper shows how immobilising the catalyst on a magnetic support allows repeated recovery and re-use of the catalyst in one of the most important and widely used reactions - the alkyne-azide cycloaddition (the most famous 'Click' reaction).
Featured Image
Why is it important?
We take one of the most active catalysts for this transformation and make it reusable and greener as it is far easier to separate from the products and requires little additional solvent use. It therefore satisfies the critera of 'click' chemistry in using benign solvents for the catalytic reaction (water, ethyl acetate) and does not require purification (by column or recrystallization). While copper itself is cheap, the removal of this metal from the products and the means to do this simply using magnetism is a real advantage.
Perspectives
Read the Original
This page is a summary of: Reusable and highly active supported copper(i)–NHC catalysts for Click chemistry, Chemical Communications, January 2013, Royal Society of Chemistry,
DOI: 10.1039/c3cc44371j.
You can read the full text:
Contributors
The following have contributed to this page