Abstract
IridiumIII complexes are attractive candidates for direct functionalization of abundant alkanes, such as methane. However, iridium catalysts have received little attention. This study focuses on iridium complexes containing η5-C5Me5 (Cp*) and monodentate N-heterocyclic carbene (NHC) ligands. The complexes [Cp*IrIII(NHC)(Me)]+[MeB(C6F5)3]- activate the C-H bonds of hydrocarbons and activate molecular oxygen. The latter reaction forms the unusual oxo-bridged dimer [{Cp*Ir(NHC)(Me)}2(μ-O)]2+[2{MeB(C6F5)3}]2-, which has been characterized by NMR and optical spectroscopies as well as single crystal X-ray diffraction analysis.
| Original language | English |
|---|---|
| Journal | ACS National Meeting Book of Abstracts |
| State | Published - 2011 |
| Event | 241st ACS National Meeting and Exposition - Anaheim, CA, United States Duration: 27 Mar 2011 → 31 Mar 2011 |
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