Interface Properties of the Partially Oxidized Pt(111) Surface Using Hybrid DFT-Solvation Models.

This article reports a theoretical-computational effort to model the interface between an oxidized platinum surface and aqueous electrolyte. It strives to account for the impact of the electrode potential, formation of surface-bound oxygen species, orientational ordering of near-surface solvent molecules, and metal surface charging on the potential profile along the normal direction. The computational scheme is based on the DFT/ESM-RISM method to simulate the charged Pt(111) surface with varying number of oxygen adatoms in acidic solution. This hybrid solvation method is known to qualitatively reproduce bulk metal properties like the work function. However, the presented calculations reveal that vital interface properties such as the electrostatic potential at the outer Helmholtz plane are highly sensitive to the position of the metal surface slab relative to the DFT-RISM boundary region. Shifting the relative position of the slab also affects the free energy of the system. It follows that there is an optimal distance for the first solvent layer within the ESM-RISM framework, which could be found by optimizing the position of the frozen Pt(111) slab. As it stands, manual sampling of the position of the slab is impractical and betrays the self-consistency of the method. Based on this understanding, we propose the implementation of a free energy optimization scheme of the relative position of the slab in the DFT-RISM boundary region. This optimization scheme could considerably increase the applicability of the hybrid method.

Photoinduced O2-Dependent Stepwise Oxidative Deglycination of a Nonheme Iron(III) Complex.

The iron(III) complex [Fe(tpena)]2+ (tpena = N, N, N'-tris(2-pyridylmethyl)ethylendiamine- N'-acetate) undergoes irreversible O2-dependent N-demethylcarboxylation to afford [FeII(SBPy3)(MeCN)]2+ (SBPy3 = N, N-bis(2-pyridylmethyl)amine- N-ethyl-2-pyridine-2-aldimine), when irradiated with near-UV light. The loss of a mass equivalent to the glycyl group in a process involving consecutive C-C and C-N cleavages is documented by the measurement of the sequential production of CO2 and formaldehyde, respectively. Time-resolved UV-vis absorption, Mössbauer, EPR, and Raman spectroscopy have allowed the spectroscopic characterization of two iron-based intermediates along the pathway. The first of these, proposed to be a low-spin iron(II)-radical ligand complex, reacts with O2 in the rate-determining step to produce a putative alkylperoxide complex. DFT calculations suggest that this evolves into an Fe(IV)-oxo species, which can abstract a hydrogen atom from a cis methylene group of the ligand to give the second spectroscopically identified intermediate, a high-spin iron(III)-hydroxide of the product oxidized ligand, [FeIII(OH)(SBPy3)]2+. Reduction and exchange of the cohydroxo/water ligand produces the crystallographically characterized products [FeII(SBPy3)(X)]2+/3+, X = MeCN, [Zn(tpena)]+.

A DFT-based mechanistic proposal for the light-driven insertion of dioxygen into Pt(ii)-C bonds.

The photocatalyzed insertion of dioxygen into the Pt(ii)-methyl bond in terpyridine platinum complexes has been shown to proceed efficiently, but its mechanism remains a challenge. In particular, there are serious counter-intuitive differences in the reactivity of structurally similar complexes. M06 calculations in solvent with a valence double-ζ basis set supplemented by polarization and diffusion shells (benchmarked against ωB97x-D calculations with a larger basis set) are able to provide a satisfactory mechanistic answer. The proposed mechanism starts with the absorption of a photon by the metal complex, which then evolves into a triplet state that reacts with the triplet dioxygen fragment. A variety of possible reaction paths have been identified, some leading to the methylperoxo product and others reverting to the reactants, and the validity of some of these paths has been confirmed by additional experiments. The balance between the barriers towards productive and unproductive paths reproduces the diverging experimental behavior of similar complexes and provides a general mechanistic picture for these processes.

Computational characterization of the mechanism for the light-driven catalytic trichloromethylation of acylpyridines.

The computational characterization of the mechanism for complex reactions involving the photoactivation of transition metal compounds remains a challenge for theoretical chemistry. In this work we show how the application of DFT and ONIOM(DFT:MM) methods can characterize the photoinduced iridium-catalyzed enantioselective trichloromethylation of 2-acylpyridines that was recently reported by Meggers and co-workers. This is a complex process, as it involves two linked catalytic cycles and yields the product with high enantioselectivity. Calculations succeed in reproducing all available experimental data, including the sign and value of the enantiomeric excess. The detailed mechanistic picture that is obtained leads to the identification of the origin of selectivity as the steric repulsion between an attacking trichloromethyl radical and the ligands at iridium in the path leads to the minor enantiomer.

Light-Driven Enantioselective Organocatalytic ß-Benzylation of Enals.

A photochemical organocatalytic strategy for the direct enantioselective ß-benzylation of α,ß-unsaturated aldehydes is reported. The chemistry capitalizes upon the light-triggered enolization of 2-alkyl-benzophenones to afford hydroxy-o-quinodinomethanes. These fleeting intermediates are stereoselectively intercepted by chiral iminium ions, transiently formed upon condensation of a secondary amine catalyst with enals. Density functional theory (DFT) studies provided an explanation for why the reaction proceeds through an unconventional Michael-type addition manifold, instead of a classical cycloaddition mechanism and subsequent ring-opening.

Computational study with DFT and kinetic models on the mechanism of photoinitiated aromatic perfluoroalkylations.

A combination of DFT calculations and kinetic models is applied to fully elucidate the seemingly complex reactivity of α-cyano arylacetates toward metal-free photoinitiated aromatic perfluoroalkylation. The resulting mechanistic framework rationalizes the observed quantum yield as well as the differences in reactivity and/or selectivity of seemingly similar substrates. The use of a kinetic model for the chemical interpretation of the DFT-computed reaction constants is shown to be critical.

Pd-catalysed mono- and dicarbonylation of aryl iodides: insights into the mechanism and the selectivity.

The mechanism of the experimentally reported phosphine-free palladium-catalysed carbonylation of aryl iodides with amines in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as base was investigated at the DFT level. Paths were identified for both di- and monocarbonylation, and the calculated selectivity for three different substrates was in agreement with experiment. In dicarbonylation yielding α-ketoamides, formation of the second carbon-carbon bond occurs through reductive elimination in the Pd acyl amide intermediate after DBU-assisted nucleophilic attack of an amine at a terminal CO ligand. This path yields the major product with iodobenzene and the almost exclusive product with p-methoxyiodobenzene. Two different possible pathways yield the monocarbonylated amide product. In one of them, which affords the minor product for iodobenzene, base-assisted nucleophilic attack of the amine takes place on a Pd-bound acyl ligand. For substrates with electron-withdrawing substituents, such as p-cyanoiodobenzene, aryl migration to the CO ligand is disfavoured, and this allows base-assisted amine attack at a terminal CO ligand early in the catalytic cycle. From the resulting Pd amide aryl complex, the subsequent reductive elimination occurs easily, and monocarbonylation becomes favoured.