Reactivity of Ir-NSiN Complexes: Ir-Catalyzed Dehydrogenative Silylation of Carboxylic Acids

This work describes the results from the studies on the potential of [Ir(μ‐Cl)(cod)]2 (cod=1,5‐cyclooctadiene) as metallic precursor for the preparation of Ir(NSiN) complexes (NSiN=fac‐bis‐(pyridine‐2‐yloxy)methylsilyl). The reaction of [Ir(μ‐Cl)(cod)]2 with bis‐(pyridine‐2‐yloxy)methylsilane enabled the synthesis of [Ir(H)(Cl)(NSiN)(η2‐cod)] with an uncommon η2‐coordination mode for the cod ligand. The application of Ir–NSiN species as catalysts precursors for the dehydrogenative silylation of carboxylic acids was also explored. The outcomes from these catalytic studies revealed a clear influence of the ancillary ligand on the catalytic activity of Ir–NSiN species. Thus, whereas [Ir(H)(CF3SO3)(NSiN)(coe)] shows poor catalytic activity, the related complex [Ir(H)(CF3CO2)(NSiN)(coe)] with a trifluoroacetate ligand was demonstrated to be a highly active catalyst precursor.
Financial support from MINECO/FEDER projects: CTQ2013‐42532‐P and CTQ2015‐67366‐P and DGA/FSE group E07) is gratefully acknowledged. Dr. P. García‐Orduña acknowledges CSIC, European Social Fund and Ministerio de Economía y Competitividad of Spain for a PTA contract. Authors would like to acknowledge the use of Servicio General de Apoyo a la Investigación‐SAI, Universidad de Zaragoza. The support of KFUPM is also appreciated.