Wydział Chemii

Yuzhuo Sha

Wenchao Chu

Tongliang Zhou

Roger Lalancette

Roman Szostak

Michal Szostak

2025

Organometallics

44

1100-1107

10.1021/acs.organomet.5c00093

Naukowa

Angielski

Artykuł

Imidazol-2-ylidenes, IPr and IMes, represent by far the most important and widely utilized N-heterocyclic carbenes in organic synthesis and catalysis. Herein, we report the synthesis, catalytic activity, and structural and electronic characterization of ImPyDippDipp and ImPyMesMes, sterically bulky and easily accessible biaryl L-shaped N-heterocyclic carbene analogues of IPr and IMes. These ligands exploit the rigid imidazo[1,5-a]pyridin-3-ylidene architecture to merge the properties of the biaryl scaffold with the electron-rich characteristics of the carbene center. The catalytic activity is evaluated in the gold(I)-catalyzed hydration of alkynes and cyclization N-propargylamides, two model reactions for π-activation of alkynes that have found broad application in organic synthesis. Structural and electronic evaluation indicates that biaryl L-shaped ImPyDippDipp and ImPyMesMes ligands are more sterically demanding and more electron σ-donating and π-accepting than the classical imidazol-2-ylidnes, IPr and IMes. Both of these L-shaped ligands show excellent catalytic activity in gold(I)-catalyzed hydration of alkynes and cyclization of N-propargylamides compared to their imidazol-2-ylidene congeners, IPr and IMes. Considering the tremendous impact of imidazol-2-ylidenes in homogeneous catalysis, we anticipate that this class of biaryl L-shaped NHCs will be rapidly and widely adopted to complement IPr and IMes N-heterocyclic carbenes.

Carbene compounds, Catalytic activity, Hydration, Hydrocarbons, Ligands

http://dx.doi.org/10.1021/acs.organomet.5c00093

https://www.acs.org/content/acs/en.html