Rare examples of C(sp(3))-F reductive elimination were observed from several cis-F(2)Au(R)(IPr) intermediates generated by oxidation of (IPr)AuR complexes with XeF(2). For R groups bearing β-hydrogens, β-hydride elimination was competitive with C(sp(3))-F reductive elimination. For strained cyclic R groups and most acyclic R groups lacking β-hydrogens, carbocation-like rearrangements occurred prior to C(sp(3))-F reductive elimination. Kinetics of the decay of one cis-F(2)Au(R)(IPr) species, stereochemical analysis of reductive elimination with a chiral R group, and DFT analysis collectively suggest C(sp(3))-F reductive elimination proceeding through transient cationic [(IPr)Au(F)(R)](+) intermediates with significant ionization of the Au-alkyl bonds.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3474378 | PMC |
| http://dx.doi.org/10.1039/C1SC00515D | DOI Listing |
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