Hemilabile and Bimetallic Coordination in Rh and Ir Complexes of NCN Pincer Ligands

• Published in: Inorganic chemistry Vol. 53; no. 19; pp. 10159 - 10170
• Main Authors: Mancano, Giulia, Page, Michael J, Bhadbhade, Mohan, Messerle, Barbara A
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 06.10.2014
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic501158x

Two new pincer ligands have been developed that contain a central N-heterocyclic carbene (NHC) moiety linked to two pendant pyrazole groups by either a methylene (NCNme) or ethylene (NCNet) chain. The coordination of these two ligands to rhodium and iridium resulted in a variety of binding modes. Tridentate coordination of the ligands was observed in the complexes [Rh(NCNme)(COD)]BPh4 (8), [Ir(NCNme)(COD)]BPh4 (10), [Rh(NCNet)(CO)2]BPh4 (13), and [Ir(NCNme)(CO)2]BPh4 (14), and monodentate NHC coordination was observed for [Ir(NCNme)2(COD)]BPh4 (11) and [Ir(NCNet)2(COD)]BPh4 (12). Both tridentate and bidentate coordination modes were characterized for [Rh(NCNet)(COD)]BPh4 (9) in the solution and solid state, respectively, while an unusual bridging mode was observed for the bimetallic complex [Rh(μ-NCNme)(CO)]2(BPh4)2 (15). The impact of this diverse coordination chemistry on the efficiency of the complexes as catalysts for the addition of NH, OH, and SiH bonds to alkynes was explored.