Abstract
Halide abstraction from the ruthenium N-heterocyclic carbene complex Ru(IPr)2(CO)HCl (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene) with NaBAr4F (BAr4F = B{C6H3(3,5-CF3)2}4) gave the salt [Ru(IPr)2(CO)H]BAr4F (2), which was shown through a combined X-ray/neutron structure refinement and quantum theory of atoms in molecules (QTAIM) study to contain a bifurcated Ru···η3-H2C ξ-agostic interaction involving one iPr substituent of the IPr ligand. This system complements the previously reported [Ru(IMes)2(CO)H]+ cation (IMes =1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene), where a non-agostic form is favored. Treatment of 2 with CO, H2, and the amine–boranes H3B·NR2H (R = Me, H) gave [Ru(IPr)2(CO)3H]BAr4F (3), [Ru(IPr)2(CO)(η2-H2)H]BAr4F (4), and [Ru(IPr)2(CO)(κ2-H2BH·NR2H)H]BAr4F (R = Me, 5; R = H, 6), respectively. Heating 5 in the presence of Me3SiCH═CH2 led to alkene hydroboration and formation of the C–H activated product [Ru(IPr)(IPr)′(CO)]BAr4F (7). X-ray characterization of 3 and 5–7 was complemented by DFT calculations, and the mechanism of H2/H exchange in 4 was also elucidated. Treatment of 2 with HBcat resulted in Ru–H abstraction to form the boryl complex [Ru(IPr)2(CO)(Bcat)] BAr4F (8), which proved to be competent in the catalytic hydroboration of 1-hexene. In 8, a combined X-ray/neutron structure refinement and QTAIM analysis suggested the presence of a single Ru···η2-HC ξ-agostic interaction.