Sterically-Hindered and Strongly Sigma-Donating Triazole NHC Ligands Technology

 

General structure of classical NHCs and the present invention


Invention Summary:

NHC ligands (NHC = N-heterocyclic carbene) are the most popular ligands in transition-metal-catalysis, organocatalysis, organic synthesis and materials science, among other applications.

Rutgers researchers have developed a novel sterically-hindered and strongly sigma-donating NHC ligands on 1H-1,2,3-triazol-5-ylidene architecture. The ligands belong to a class of abnormal N-heterocyclic carbenes, where the metal is bound to the C4 or C5 position of the heterocyclic ring rather than in the typical C2 position. This results in an overwhelmingly stronger s-donation as compared to the classical imidazol-2-ylidenes, a property that is critical for transition-metal-catalysis using a variety of metals, catalytic reactions, and mechanisms.

Market Applications:

  • Pharmaceutical synthesis
  • Fine chemical production
  • Functional materials and polymers synthesis
  • Development of catalysts for various synthetically-valuable reactions

Advantages:

  • Higher stability to the metal-NHC bond and the complex itself
  • Adjusts the reactivity of metals through the steric demand
  • Offers stronger s-donation and p-acceptance compared to phosphine ligands
  • Provides unique umbrella shape of the steric bulk around the donor center
  • Facilitates peripheral N-wingtip and scaffold modification to tune steric and electronic properties of the ligand
  • TEP up to 2046.8 cm-1, %Vbur up to 48.2%
  • High activity in Au, Cu, Ag, Pd, Ir, Rh catalysis

Intellectual Property & Development Status: Provisional patent application filed, patent pending. Available for licensing and/or research collaboration. For any business development and other collaborative partnerships contact marketingbd@research.rutgers.edu.

Patent Information:
Contact:
Deborah Perez Fernandez
Acting Executive Director
Rutgers, The State University of New Jersey
848-932-4467
dpp80@rutgers.edu
Keywords: