Abstract
The pincer ligand PhN(CH2CH2PiPr2)2 (iPrPNPhP) was treated with [Ir(coe)2(μ-Cl)]2 (coe = cyclooctene) under H2 to generate (iPrPNPhP)IrH2Cl (1). Reaction of 1 with LiBHEt3 formed (iPrPNPhP)IrH3 (2). The solid-state structures of 1 and 2 were determined. Compound 2 catalyzes CO2 hydrogenation to formate and formic acid dehydrogenation but gives inferior performance to systems with RN(CH2CH2PiPr2)2 (R = H or Me) ligands, demonstrating the importance of the substituent on the nitrogen donor.
Cite
CITATION STYLE
Curley, J. B., Hert, C., Bernskoetter, W. H., Hazari, N., Mercado, B. Q., & Wedal, J. C. (2025). Flash Communication: Ir Complexes with a PhN(CH2CH2PiPr2)2 Pincer Ligand for Reversible CO2 Hydrogenation. Organometallics. https://doi.org/10.1021/acs.organomet.5c00153
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