O. Yazidi

Electronic states of MgO: Spectroscopy, predissociation, and cold atomic Mg and O production

We used multiconfigurational methods and a large basis set to compute the potential energy curves of the valence and valence-Rydberg electronic states of MgO molecule. New bound electronic states are found. Using these highly correlated wave functions, we evaluated their mutual spin-orbit couplings and transition moment integrals. For the bound electronic states of MgO, we deduced an accurate set of spectroscopic constants that agree remarkably well with experimental results. Moreover, our potentials, transition moments, and spin-orbit coupling evolutions are incorporated into Fermi golden rule calculations to deduce the radiative lifetimes of MgO(B (1)Σ(+)) rovibrational levels and the natural lifetimes of MgO(A (1)Π) vibrational levels, where a good agreement is found with experimental values. Finally, we suggest new routes for the production of cold Mg and O atoms and cold MgO molecules.

Theoretical investigations of the MgO+ cation: spectroscopy, spin–orbit coupling and single ionization spectrum

We used ab initio methodology for the computation of the potential energy curves of the doublet and quartet electronic states of the MgO+ cation correlating with the four lowest dissociation limits. Using these highly correlated wavefunctions, we calculated their spin–orbit coupling and transition moments. We deduced an accurate set of spectroscopic constants for this cation. Most of the data relative to the electronic excited states of this cation are predictive in nature. Moreover, our potentials, transition moments and spin–orbit coupling evolutions are incorporated into Fermi golden rule calculations to deduce the natural lifetimes of the lowest MgO+(12Σ+) ro-vibrational levels. Finally, our potentials were used for the prediction of the single ionization spectrum of MgO.

Structure, Reactivity, and Fragmentation of Small Multi-Charged Methane Clusters

Small methane clusters (CH4)n are irradiated using intense femtosecond laser excitation at 624 nm. The ionized species and those resulting from their fragmentation are detected via time-of-flight mass spectrometry (TOF MS). We find evidence of bound, multiply charged methane molecules and clusters resulting from Coulomb explosion upon exposure to highly energetic, ultrafast radiation. The assignment of the mass spectra is done after first-principles calculations (at the (R)MP2/aug-cc-pVXZ (X = D,T) level) on the charged (CH4)n(q+) clusters (n = 1-4, q = 1-4). We also considered the cluster stabilities and fragments that may result from intracluster molecular reactivity. Complex intracluster ion-molecule reactions induced by photoionization are expected to occur. Interestingly, we show that multi charged small methane clusters undergo intracluster reactions and fragmentations which are different from those observed for isolated methane ions or for large ionized methane clusters.

Full-Dimensional Theory of Pair-Correlated HNCO Photofragmentation

Full-dimensional semiclassical dynamical calculations combining classical paths and Bohr quantization of product internal motions are reported for the prototype photofragmentation of isocyanic acid in the S1 state. These calculations allow one to closely reproduce for the first time key features of state-of-the-art imaging measurements at photolysis wavelengths of 201 and 210 nm while providing insight into the underlying dissociation mechanism. Quantum scattering calculations being beyond reach for most polyatomic fissions, pair-correlated data on these processes are much more often measured than predicted. Our theoretical approach can be used to fill this gap.

Theoretical investigations of the IO,q+ (q = 2, 3, 4) multi-charged ions: Metastability, characterization and spectroscopy

Using ab initio methodology, we studied the IO(q+) (q = 2, 3, 4) multi-charged ions. Benchmark computations on the IO(X(2)Π) neutral species allow validate the current procedure. For IO(2+), several potential wells were found on the ground and the electronic excited states potentials with potential barriers with respect to dissociation, where this dication can exist in the gas phase as long-lived metastable molecules. We confirm hence the recent observation of the dication by mass spectrometry. Moreover, we predict the existence of the metastable IO(3+) trication, where a shallow potential well along the IO internuclear distance is computed. This potential well supports more than 10 vibrational levels. The IO(3+) excited states are repulsive in nature, as well as the computed potentials for the IO(4+) tetracation. For the bound states, we give a set of spectroscopic parameters including excitation transition energies, equilibrium distances, harmonic and anharmonic vibrational terms, and rotational constants. At the MRCI + Q/aug-cc-pV5Z(-PP) level, the adiabatic double and triple ionization energies of IO are computed to be ~28.1 eV and ~55.0 eV, respectively.

Electronic structure of the [MgO3]+ cation

Accurate ab initio calculations are performed to investigate the stable isomers of [MgO(3)](+) and its lowest electronic states at both molecular and asymptotic regions. The calculations are done using large basis sets and configuration interaction methods including the complete active space self-consistent field, the internally contracted multi-reference configuration interaction, the standard coupled cluster (RCCSD(T)) approaches and the newly implemented explicitly correlated coupled cluster method (RCCSD(T)-F12). The presence of three stable forms is predicted: a cyclic global minimum c-MgO(3)(+), which is followed by a quasi-linear isomer, l2-MgO(3)(+). A third isomer of C(s) symmetry (l1-MgO(3)(+)) is also found. Moreover, we computed the one-dimensional cuts of the six-dimensional potential energy surfaces of the lowest doublet and quartet electronic states of [MgO(3)](+) along the R(MgO) and R(OO) stretching coordinates covering both the molecular and the asymptotic regions. These curves are used later for discussing the metastability of this cation and to propose plausible mechanisms for the Mg(+) + O(3) atmospherically important ion-molecule reaction and related reactive channels.

Ab initio study of the photodissociation of radical molecules of astrochemical interest

Plenary lecture given at the 8th Mid-European Clay Conference, held in Kosice (Slovakia) on July 4-8th, 2016.COST MOLIM WG3 Meeting, Algorithm Development and High-performance Computing in Chemistry and Physics; Bratislava, March 21-22, 2016; http://web4.umb.sk/molim2016/Oral presentation given at the 8th Mid-European Clay Conference, held in Kosice (Slovakia) on July 4-8th, 2016. S6: application and treatment of clays and other industrial minerals.Cost Action Molim, Molecules in Motions, CM 1405; University Paris-Est Marne-La-Vallee, France, 27-29 August 2015This chapter provides an overview of the main biochemical transformations of major elements, including carbon, nitrogen, sulfur, iron and phosphorus in anaerobic digesters. Mineralization of organic matter during anaerobic digestion processes results in the production of inorganic carbonate, ammonium, sulfide, and phosphate species, which are involved in a complex network of chemical and biological reactions through interaction with available macro and micro nutrients as well as microbial processes with profound effects on the efficiency and stability of the anaerobic digester performance. The interplay of iron, phosphorus and sulfur cycles has recently attracted attention in the frame of research developed for the recovery of phosphorus on one hand and in the frame of the

Stereoisomers of hydroxymethanes: Probing structural and spectroscopic features upon substitution

Ab initio studies on CHx(OH)4-x (x = 0-3) polyols are carried out to derive their structural and spectroscopic features. Several stereoisomers (both equilibrium structures and transition states) are found. Some are predicted here for the first time. We determined hence their geometrical parameters, vibrational frequencies, electronic excitation energies for the singlet manifold, and IR spectra. While the IR spectra for all polyols present similar shapes, their UV spectra exhibit however distinct band origin that are specific to each polyol and more interestingly to each diasteroisomer. Stereoelectronic effects are also noticed and discussed. It is suggested that UV spectroscopy is an efficient probe to experimentally identify polyols in mixtures involving polyols.