No abstract

The syntheses of novel dimethylbis(2-pyridyl)borate nickel(II) complexes 4 and 6 are reported. These complexes were unambiguously characterized by X-ray analysis. In dichloromethane solvent, complex 4 undergoes a unique square-planar to square-planar rotation around the nickel(II) center, for which activation parameters of ΔH⧧ = 12.2(1) kcal mol–1 and ΔS⧧ = 0.8(5) eu were measured via NMR inversion recovery experiments. Complex 4 was also observed to isomerize via a relatively slow ring flip: ΔH⧧ = 15.0(2) kcal mol–1; and ΔS⧧ = −4.2(7) eu. DFT studies support the experimentally measured rotation activation energy (cf. calculated ΔH⧧ = 11.1 kcal mol–1) as well as the presence of a high-energy triplet intermediate (ΔH = 8.8 kcal mol–1).

Rhodium(I) and Iridium(I) borate complexes of the structure [Me2B(2-py)2]ML2 (L2 = (tBuNC)2, (CO)2, (C2H4)2, cod, dppe) were prepared and structurally characterized (cod = 1,5-cyclooctadiene; dppe = 1,2-diphenylphosphinoethane). Each contains a boat-configured chelate ring that participates in a boat-to-boat ring flip. Computational evidence shows that the ring flip proceeds through a transition state that is near planarity about the chelate ring. We observe an empirical, quantitative correlation between the barrier of this ring flip and the π acceptor ability of the ancillary ligand groups on the metal. The ring flip barrier correlates weakly to the Tolman and Lever ligand parameterization schemes, apparently because these combine both σ and π effects while we propose that the ring flip barrier is dominated by π bonding. This observation is consistent with metal-ligand π interactions becoming temporarily available only in the near-planar transition state of the chelate ring flip and not the boat-configured ground state. Thus, this is a first-of-class observation of metal-ligand π bonding governing conformational dynamics.

Ruthenium(III) chloride hydrate is a convenient catalyst for the addition of active methylene compounds to aryl alkynes. These reactions are rapid, operationally simple, and high yielding in cases. Most significantly, no precautions are required to exclude air or water from the reactions. All reagents are commercially available at reasonable prices, and the reactions can be conducted in disposable glassware with minimal solvent.

A Ruthenium-Catalyzed Coupling of Alkynes with 1,3-Diketones. -Ene-type coupling reactions of alkynes with 1,3-diketones proceed at mild temperatures under air and in the presence of water. -(PENNINGTON-BOGGIO, M. K.; CONLEY, B. L.; WILLIAMS*, T. J.; J. Organomet. Chem. 716 (2012) 6-10, http://dx.