Assessing the Viability of the Methylsulfinyl Radical-Ozone Reaction.

Although integral to remote marine atmospheric sulfur chemistry, the reaction between methylsulfinyl radical (CH3 SO) and ozone poses challenges to theoretical treatments. The lone theoretical study on this reaction reported an unphysically large barrier of 66 kcal mol-1 for abstraction of an oxygen atom from O3 by CH3 SO. Herein, we demonstrate that this result stems from improper use of MP2 with a single-reference, unrestricted Hartree-Fock (UHF) wavefunction. We characterized the potential energy surface using density functional theory (DFT), as well as multireference methodologies employing a complete active-space self-consistent field (CASSCF) reference. Our DFT PES shows, in contrast to previous work, that the reaction proceeds by forming an addition adduct [CH3 S(O3 )O] in a deep potential well of 37 kcal mol-1 . An O-O bond of this adduct dissociates via a flat, low barrier of 1 kcal mol-1 to give CH3 SO2 +O2 . The multireference computations show that the initial addition of CH3 SO+O3 is barrierless. These results provide a more physically intuitive and accurate picture of this reaction than the previous theoretical study. In addition, our results imply that the CH3 SO2 formed in this reaction can readily decompose to give SO2 as a major product, in alignment with the literature on CH3 SO reactions.

Prototypical Transition-Metal Carbenes, (CO)5Cr═CH2, (CO)4Fe═CH2, (CO)3Ni═CH2, (CO)5Mo═CH2, (CO)4Ru═CH2, (CO)3Pd═CH2, (CO)5W═CH2, (CO)4Os═CH2, and (CO)3Pt═CH2: Challenge to Experiment.

Transition-metal carbenes are useful in organometallic chemistry due to their demonstrated use as catalysts in carbon-carbon bond-forming reactions. Yet the prototypical transition-metal carbenes, consisting of a single metal center doubly bonded to a methylene ligand and surrounded by carbonyls, have been elusive to experimental synthesis. This theoretical work examines the structures and properties of nine prototypical transition-metal carbenes. Optimized values for M═CH2 bond lengths, dissociation energies, and vibrational frequencies are reported. The M═CH2 bond distances range from 1.81 (Ni) to 2.05 Š(Pd). The M═CH2 dissociation energies fall in the range of 16.4 (Pd) to 92.3 kcal mol-1 (Os). The spectroscopic observation of several of these molecules should be possible.

Radicals derived from acetaldehyde and vinyl alcohol.

Vinyl alcohol and acetaldehyde are isoelectronic products of incomplete butanol combustion. Along with the radicals resulting from the removal of atomic hydrogen or the hydroxyl radical, these species are studied here using ab initio methods as complete as coupled cluster theory with single, double, triple, and perturbative quadruple excitations [CCSDT(Q)], with basis sets as large as cc-pV5Z. The relative energies provided herein are further refined by including corrections for relativistic effects, the frozen core approximation, and the Born-Oppenheimer approximation. The effects of anharmonic zero-point vibrational energies are also treated. The syn conformer of vinyl alcohol is predicted to be lower in energy than the anti conformer by 1.1 kcal mol-1. The alcoholic hydrogen of syn-vinyl alcohol is found to be the easiest to remove, requiring 84.4 kcal mol-1. Five other radicals are also carefully considered, with four conformers investigated for the 1-hydroxyvinyl radical. Beyond energetics, we have conducted an overhaul of the spectroscopic literature for these species. Our results also provide predictions for fundamental modes yet to be reported experimentally. To our knowledge, the ν3 (3076 cm-1) and ν4 (2999 cm-1) C-H stretches for syn-vinyl alcohol and all but one of the vibrational modes for anti-vinyl alcohol (ν1-ν14) are yet to be observed experimentally. For the acetyl radical, ν6 (1035 cm-1), ν11 (944 cm-1), ν12 (97 cm-1), and accounting for our changes to the assignment of the 1419.9 cm-1 experimental mode, ν10 (1441 cm-1), are yet to be observed. We have predicted these unobserved fundamentals and reassigned the experimental 1419.9 cm-1 frequency in the acetyl radical to ν4 rather than to ν10. Our work also strongly supports reassignment of the ν10 and ν11 fundamentals of the vinoxy radical. We suggest that the bands assigned to the overtones of these fundamentals were in fact combination bands. Our findings may be useful in constructing improved combustion models of butanol and in spectroscopically characterizing these molecules further.

Correction: The methylsulfinyl radical CH3SO examined.

Correction for 'The methylsulfinyl radical CH3SO examined' by Marissa L. Estep et al., Phys. Chem. Chem. Phys., 2016, 18, 22293-22299.

The methylsulfinyl radical CH3SO examined.

Methylsulfinyl radical, a key intermediate in marine atmospheric chemistry, plays a central role in the oxidation of dimethyl sulfide. CH3SO has been extensively studied here with ab initio quantum mechanical methods, with methods as complete as CCSDT(Q) in conjunction with basis sets as large as cc-pV(5+d)Z. In this research, we report high-level computations for the ground and first excited electronic states of the methylsulfinyl radical. The structures of the X[combining tilde] (2)A'' and à (2)A' states are quite different with S-O distances of 1.499 and 1.652 Å, respectively. The X[combining tilde] to à adiabatic energy difference is predicted to be 45.1 kcal mol(-1), compared to 21.1 kcal mol(-1) for the analogous well-characterized methylperoxy radical CH3OO. The CH3SO barrier to internal rotation is 0.92 kcal mol(-1). The unknown X[combining tilde] (2)A'' torsional vibrational frequency τ is predicted to be 142 cm(-1) (harmonic) and 128 cm(-1) (anharmonic). Our predictions of the à (2)A' excited state vibrational frequencies are the first to be reported.

Investigating the Effects of Basis Set on Metal-Metal and Metal-Ligand Bond Distances in Stable Transition Metal Carbonyls: Performance of Correlation Consistent Basis Sets with 35 Density Functionals.

Density functional theory (DFT) is a widely used method for predicting equilibrium geometries of organometallic compounds involving transition metals, with a wide choice of functional and basis set combinations. A study of the role of basis set size in predicting the structural parameters can be insightful with respect to the effectiveness of using small basis sets to optimize larger molecular systems. For many organometallic systems, the metal-metal and metal-carbon distances are the most important structural features. In this study, we compare the equilibrium metal-ligand and metal-metal distances of six transition metal carbonyl compounds predicted by the Hood-Pitzer double-ζ polarization (DZP) basis set, against those predicted employing the standard correlation consistent cc-pVXZ (X = D,T,Q) basis sets, for 35 different DFT methods. The effects of systematically increasing the basis set size on the structural parameters are carefully investigated. The Mn-Mn bond distance in Mn2(CO)10 shows a greater dependence on basis set size compared to the other M-M bonds. However, the DZP predictions for re(Mn-Mn) are closer to experiment than those obtained with the much larger cc-pVQZ basis set. Our results show that, in general, DZP basis sets predict structural parameters with an accuracy comparable to the triple and quadruple-ζ basis sets. This finding is very significant, because the quadruple-ζ basis set for Mn2(CO)10 includes 1308 basis functions, while the equally effective double-ζ set (DZP) includes only 366 basis functions. Overall, the DZP M06-L method predicts structures that are very consistent with experiment.