Pd‐PEPPSI‐IHeptCl: A General‐Purpose,Highly Reactive Catalyst for the Selective Coupling of Secondary Alkyl Organozincs

Dichloro[1,3‐bis(2,6‐di‐4‐heptylphenyl)imidazol‐2‐ylidene](3‐chloropyridyl)palladium(II) (Pd‐PEPPSI‐IHept^Cl), a new, very bulky yet flexible Pd–N‐heterocyclic carbene (NHC) complex has been evaluated in the cross‐coupling of secondary alkylzinc reactants with a wide variety of oxidative addition partners in high yields and excellent selectivity. The desired, direct reductive elimination branched products were obtained with no sign of migratory insertion across electron‐rich and electron‐poor aromatics and all forms of heteroaromatics (five and six membered). Impressively, there is no impact of substituents at the site of reductive elimination (i.e., ortho or even di‐ortho), which has not yet been demonstrated by another catalyst system to date.     

Study of polymerizing styrene through depolarized light scattering

The thermal polymerization of clean styrene has been studied through Rayleigh-Brillouin light scattering. The frequency shifts, Rayleigh to Brillouin intensity ratios, Rayleigh depolarization ratios, and depolarized intensities were measured as the polymerization proceeded to completion at 90°C. The depolarized intensities decreased and the frequency shifts increased smoothly from the monomer to the polymer values. The Vv intensities and Rayleigh to Brillouin intensity ratios increase dramatically during the first stages of polymerization then decrease systematically to their final values. There is a large increase in the Rayleigh to Brillouin intensity ratio from the monomer to the final polymer value. The vertical depolarization ratio pv and the horizontal depolarization ratio pV were found to be respectively 0.4 and 1 for the polymer. Our observations are explained in terms of light being scattered from concentration fluctuations in the early stages of polymerization and from spherically symmetric strain fields in the polymer. We believe that the background, which we observed to embrace a wide range of frequencies, was due to rotational Raman transitions.     

Solvent Effect and Reactivity Trend in the Aerobic Oxidation of 1,3‐Propanediols over Gold Supported on Titania: NMR Diffusion and Relaxation Studies

In recent work, it was reported that changes in solvent composition, precisely the addition of water, significantly inhibits the catalytic activity of Au/TiO₂ catalyst in the aerobic oxidation of 1,4‐butanediol in methanol due to changes in diffusion and adsorption properties of the reactant. In order to understand whether the inhibition mechanism of water on diol oxidation in methanol is generally valid, the solvent effect on the aerobic catalytic oxidation of 1,3‐propanediol and its two methyl‐substituted homologues, 2‐methyl‐1,3‐propanediol and 2,2‐dimethyl‐1,3‐propanediol, over a Au/TiO₂ catalyst has been studied here using conventional catalytic reaction monitoring in combination with pulsed‐field gradient nuclear magnetic resonance (PFG‐NMR) diffusion and NMR relaxation time measurements. Diol conversion is significantly lower when water is present in the initial diol/methanol mixture. A reactivity trend within the group of diols was also observed. Combined NMR diffusion and relaxation time measurements suggest that molecular diffusion and, in particular, the relative strength of diol adsorption, are important factors in determining the conversion. These results highlight NMR diffusion and relaxation techniques as novel, non‐invasive characterisation tools for catalytic materials, which complement conventional reaction data.     

Oxidative Addition of Haloheteroarenes to Palladium(0): Concerted versus SNAr‐Type Mechanism

The kinetics of the oxidative additions of haloheteroarenes HetX (X=I, Br, Cl) to [Pd⁰(PPh₃)₂] (generated from [Pd⁰(PPh₃)₄]) have been investigated in THF and DMF and the rate constants have been determined. In contrast to the generally accepted concerted mechanism, Hammett plots obtained for substituted 2‐halopyridines and solvent effects reveal a reaction mechanism dependent on the halide X of HetX: an unprecedented S_NAr‐type mechanism for X=Br or Cl and a classical concerted mechanism for X=I. These results are supported by DFT studies.     

Graph Duality in Surface Dynamics

Journal of Nonlinear Science - We compare one-dimensional representations for the isotopy stable dynamics of homeomorphisms in two dimensions. We consider the skeleton graph representative, which...     

Applying the combined integral method to one-dimensional ablation

In this paper the combined integral method is applied to a simple one-dimensional ablation problem. One of the drawbacks of heat balance integral methods is how to choose the approximating function. It is common to use a polynomial form but even then it is not clear what the power of the highest order term should be. Previous studies have determined exponents either from exact solutions or from expansions valid over short time scales; neither approach is satisfactory nor very accurate for larger times. We combine the heat balance and refined integral methods to determine this exponent as part of the solution process, and conclude that it is in fact time-dependent in the ablation stage. From comparing the approximate solutions with numerical and exact analytical solutions whenever possible, we show that this new method greatly improves the accuracy on standard methods, without overcomplicating the method.