Mechanistic Study of Competitive sp3-sp3 and sp2-sp3 Carbon−Carbon Reductive Elimination from a Platinum (IV) Center and the Isolation of a C−C Agostic Complex
Journal of the American Chemical Society2007Vol. 129(31), pp. 9538–9539
Citations Over TimeTop 14% of 2007 papers
Abstract
The addition of methyl triflate to an [NCN]PtCH3 pincer complex 1 ([NCN] = 2,6-bis(diethylaminomethyl)phenyl) results in kinetically controlled competitive reductive eliminations to generate both sp3-sp3 coupling products (ethane and [NCN]Pt(OTf), 3) and an sp2-sp3 coupling product, [[NC(CH3)N]PtCH3][OTf] (4). The last is a cationic complex that could either be formulated as an arenium species or, more likely, as a C−C agostic complex. The addition of CD3OTf to 1 affords 3, CH3CD3, and 4-d3, with the deuterated label in 4-d3 distributed between the arene methyl group and the platinum-bound methyl group, implicating the intermediacy of the five coordinate intermediate [[NCN]Pt(CH3)(CD3)]+ (I-d3).
Related Papers
- → Mechanism and energetics of reductive elimination of ethane from some tetramethylplatinum(IV) complexes(1989)61 cited
- → Quantitative synthesis and full characterization of the first isolated and stable pincer palladium(iv) complexes. Quantitative and regioselective synthesis of the C–X (X = Cl, Br) reductive elimination products(2010)49 cited
- → Computational and Experimental Investigation of Alkene Hydrogenation by a Pincer-Type [P2Si]Rh Complex: Alkane Release via Competitive σ-Bond Metathesis and Reductive Elimination(2019)16 cited
- → An Agostic Iridium Pincer Complex as a Highly Efficient and Selective Catalyst for Monoisomerization of 1‐Alkenes to trans‐2‐Alkenes(2017)14 cited
- → Revisiting C–C and C–H Bond Activation in Rhodium Pincer Complexes: Thermodynamics and Kinetics Involving a Common Agostic Intermediate(2022)6 cited