Formation of Chlorine in the Atmosphere by Reaction of Hypochlorous Acid with Seawater.

The highly reactive dihalogens play a significant role in the oxidative chemistry of the troposphere. One of the main reservoirs of these halogens is hypohalous acids, HOX, which produce dihalogens in the presence of halides (Y-), where X, Y = Cl, Br, I. These reactions occur in and on aerosol particles and seawater surfaces and have been studied experimentally and by field observations. However, the mechanisms of these atmospheric reactions are still unknown. Here, we establish the atomistic mechanism of HOCl + Cl- → Cl2 + OH- at the surface of the water slab by performing ab initio molecular dynamics (AIMD) simulations. Main findings are (1) This reaction proceeds by halogen-bonded complexes of (HOCl)···(Cl-)aq surrounded with the neighboring water molecules. (2) The halogen bonded (HOCl)···(Cl-)aq complexes undergo charge transfer from Cl- to OH- to form transient Cl2 at neutral pH. (3) The addition of a proton to one proximal water greatly facilitates the Cl2 formation, which explains the enhanced rate at low pH.

Energy transfer, pre-reactive complex formation and recombination reactions during the collision of peroxy radicals.

In this paper we study collisions between polyatomic radicals - an important process in fields ranging from biology to combustion. Energy transfer, formation of intermediate complexes and recombination reactions are treated, with applications to peroxy radicals in atmospheric chemistry. Multi-reference perturbation theory, supplemented by coupled-cluster calculations, describes the potential energy surfaces with high accuracy, including the interaction of singlet and triplet spin states during radical recombination. Our multi-reference molecular dynamics (MD) trajectories on methyl peroxy radicals confirm the reaction mechanism postulated in earlier studies. Specifically, they show that if suitable pre-reactive complexes are formed, they will rapidly lead to the formation and subsequent decomposition of tetroxide intermediates. However, generating multi-reference MD trajectories is exceedingly computationally demanding, and we cannot adequately sample the whole conformational space. To answer this challenge, we promote the use of a novel simplified semi-empirical MD methodology. It assumes the collision is governed by two states, a singlet (S0) and a triplet (T1) state. The method predicts differences between collisions on S0 and T1 surfaces, and qualitatively includes not only pre-reactive complex formation, but also recombination processes such as tetroxide formation. Finally, classical MD simulations using force-fields for non-reactive collisions are employed to generate thousands of collision trajectories, to verify that the semi-empirical method is sampling collisions adequately, and to carry out preliminary investigations of larger systems. For systems with low activation energies, the experimental rate coefficient is surprisingly well reproduced by simply multiplying the gas-kinetic collision rate by the simulated probability for long-lived complex formation.

Preparation and Characterization of the Halogen-Bonding Motif in the Isolated Cl-·IOH Complex with Cryogenic Ion Vibrational Spectroscopy.

In the presence of a halide ion, hypohalous acids can adopt two binding motifs upon formation of the ion-molecule complexes [XHOY]- (X, Y = Cl, Br, I): a hydrogen (HB) bond to the acid OH group and a halogen (XB) bond between the anion and the acid halogen. Here we isolate the X-bonded Cl-·IOH ion-molecule complex by collisions of I-·(H2O)n clusters with HOCl vapor and measure its vibrational spectrum by IR photodissociation of the H2-tagged complex. Anharmonic analysis of its vibrational band pattern reveals that formation of the XB complex results in dramatic lowering of the HOI bending fundamental frequency and elongation of the O-I bond (by 168 cm-1 and 0.13 Å, respectively, relative to isolated HOI). The frequency of the O-I stretch (estimated 436 cm-1) is also encoded in the spectrum by the weak v = 0 → 2 overtone transition at 872 cm-1.

Structures, Stability, and Decomposition Dynamics of the Polynitrogen Molecule N5+B(N3)4- and Its Dimer [N5+]2[B(N3)4-]2.

There is much current interest in materials that are made entirely or mostly of nitrogen atoms. Such materials, polynitrogens, may reveal new aspects of nitrogen chemistry, and are believed to provide a possible basis for novel energetic substances. An interesting family of such materials, in which the N5+ group appears as a cation, was prepared by K. O. Christe and co-workers. Little is known as yet on the microscopic properties of these materials. In this paper, we report theoretical calculations to predict the structure, energetic stability and decomposition dynamics of the polynitrogen molecule N5+B(N3)4-, the building block of a solid prepared by Christe, and of the dimer of this molecule. The structures are computed at the B3LYP-D3 level of DFT. ab initio molecular dynamics simulations are used to explore the thermal stability of the species and the decomposition mechanism. It is found that the N5+B(N3)4- ion-pair decomposes on a picosecond time scale at T = 200 K, with an ultrafast release of four N2 molecules, which is very exothermic. The species B(N3)3 is a product. The dimer is considerably more stable. Sensitivity of the process to temperature and to an applied force is reported. Possible applications of this material are briefly discussed.