Abstract
Highly unsaturated mono(N-heterocyclic carbene) Ir(iii) systems have been targeted via ligand abstraction protocols. Hydrogenation of Ir(IPr)(cod)Cl (1a) leads to the formation of the highly reactive (fluxional) trimer [Ir(IPr)(H)2Cl]3, while the related IMes system undergoes further C-H bond activation. Chloride abstraction from 1aprior to hydrogenation allows access to sources of the 12-electron [Ir(IPr)(H)2]+ fragment, which, in the absence of a suitable donor, dimerizes to give [{Ir(IPr)(H)(μ-H)}2]2+.
| Original language | English |
|---|---|
| Pages (from-to) | 2523-2525 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 47 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 7 Mar 2011 |
| Externally published | Yes |