The dissociation dynamics of HOD via two-photon excitation to the C̃ state have been investigated using the H-atom Rydberg tagging time-of-flight (TOF) technique. The H-atom action spectrum for the C̃ ← X̃ transition shows resolved rotational structure. Product translational energy distributions and angular distributions have also been recorded for the H + OD channel for three excited levels each ...

Dissociative photoionization of methyl bromide (CH3Br) in an excitation energy range of 10.45-16.90 eV has been investigated by using threshold photoelectron-photoion coincidence (TPEPICO) velocity imaging. The coincident time-of-flight mass spectra indicate that the ground state X(2)E of CH3Br(+) is stable, and both A(2)A1 and B(2)E ionic excited states are fully dissociative to produce the un...

Synopsis We present a combined experimental and theoretical study focused on the ionic states of the N2O4 molecule. Experimental results regarding photoionization induced by the synchrotron radiation SOLEIL in the 13.5-15.5 eV energy range were obtained using the electron-ion velocity vector correlation method. The potential energy curves for the dissociation of the N-N bond were computed withi...

Dialumenes are neutral AlI compounds with Al=Al multiple bonds. We report the isolation of an amidophosphine-supported dialumene. Our X-ray crystallographic, spectroscopic, and computational DFT analyses reveal a long extreme trans-bent bond low dissociation energy order. In solution, dialumene can dissociate into monomeric species. Reactivity studies two modes reaction: as or aluminyl monomers.

The oxidation of phenols by HFeO4(-) proceeds via a hydrogen atom transfer (HAT) mechanism, as evidenced by a large deuterium isotope effect and a linear correlation between the log(rate constant) and bond dissociation free energy (BDFE) of phenols. The Marcus cross relation has been applied to predict the rate constant of HAT from hydroquinone to HFeO4(-).

The formation of an active 16-electron ruthenium sec-alkoxide complex via loss of the CO ligand is an important step in the mechanism of the racemization of sec-alcohols by (η(5)-Ph(5)C(5))Ru(CO)(2)X ruthenium complexes with X = Cl and O(t)Bu. Here we show with accurate DFT calculations the potential energy profile of the CO dissociation pathway for a series of relevant (η(5)-Ph(5)C(5))Ru(CO)(2...

A facile method for cross-linking organic molecules has been developed by computational modeling, instrumentation design, and experimental research. Briefly, organic molecules are hit by H2 with controllable kinetic energy in our novel apparatus where a high flux of hyperthermal H2 is generated. When a C–H bond of the organic molecule is hit by H2 at about 20 eV, efficient kinematic energy-tran...

The photodissociation dynamics of allyl chloride at 235 nm producing atomic Cl((2)P(J);J=1/2,3/2) fragments is investigated using a two-dimensional photofragment velocity ion imaging technique. Detection of the Cl((2)P(1/2)) and Cl((2)P(3/2)) products by [2+1] resonance enhanced multiphoton ionization shows that primary C-Cl bond fission of allyl chloride generates 66.8% Cl((2)P(3/2)) and 33.2%...

Ab initio electronic structure calculations are reported for S4. Geometric and energetic parameters are calculated using the singles and doubles coupled-cluster method, including a perturbutional correction for connected triple excitation, CCSD(T), together with systematic sequences of correlation consistent basis sets extrapolated to the complete basis set limit. The geometry for the ground st...