54
Views
0
CrossRef citations to date
0
Altmetric
Research Articles

Synthesis and catalytic activity of silver N-heterocyclic carbene complexes based on bis(3,5-dimethylpyrazol-1-yl)methyl-substituted pyridylimidazole

, , , , , & show all
Pages 375-391 | Received 14 Dec 2023, Accepted 05 Feb 2024, Published online: 05 Mar 2024
 

Abstract

A series of N-heterocyclic carbene (NHC) silver complexes derived from 6-[bis(3,5-dimethylpyrazol-1-yl)methyl]-2-pyridylimidazole have been synthesized and characterized by physico-chemical and spectroscopic methods, and the structures of four complexes have been confirmed by X-ray structural analyses. The functionalized NHC is a monodentate ligand in (NHC)AgCl through the carbene carbon atom, and a bridging [C,N,N] tridentate ligand in (NHC)2Ag2(BF4)2 and (NHC)2Ag2(PF6)2 through two pyrazolyl nitrogens and the carbene carbon to form a metallomacrocycle, in which a head (carbene)– to tail (nitrogen) coordination mode to two silver atoms is observed. Preliminary catalytic tests show that these newly synthesized Ag–NHC complexes exhibit excellent catalytic activity at a low catalyst loading (0.1–1 mol%) in the aldehyde–amine–alkyne coupling reaction.

Disclosure statement

There are no conflicts of interest to declare.

Additional information

Funding

This work is partly supported by Petrochemical Research Institute of PetroChina Company Limited (PRIKY22004).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.