scholarly journals Interaction of HCO+ Cations With Interstellar Negative Grains. Quantum Chemical Investigation and Astrophysical Implications

Author(s):  
Albert Rimola ◽  
Cecilia Ceccarelli ◽  
Nadia Balucani ◽  
Piero Ugliengo

In cold galactic molecular clouds, dust grains are coated by icy mantles and are prevalently charged negatively, because of the capture of the electrons in the gas. The interaction of the charged grains with gaseous cations is known to neutralize them. In this work, we focus on the chemical consequences of the neutralization process of HCO+, often the most abundant cation in molecular clouds. More specifically, by means of electronic structure calculations, we have characterized the energy and the structure of all possible product species once the HCO+ ion adsorbs on water clusters holding an extra electron. Two processes are possible: (i) electron transfer from the negative water cluster to the HCO+ ion or (ii) a proton transfer from HCO+ to the negative water cluster. Energetic considerations favor electron transfer. Assuming this scenario, two limiting cases have been considered in astrochemical models: (a) all the neutralized HCO+ is retained as neutral HCO adsorbed on the ice and (b) all the neutralized HCO+ gets desorbed to the gas phase as HCO. None of the two limiting cases appreciably contribute to the HCO abundance on the grain surfaces or in the gas.

2020 ◽  
Vol 92 (3) ◽  
pp. 473-484
Author(s):  
Zoi Salta ◽  
Agnie M. Kosmas ◽  
Oscar N. Ventura

AbstractElectronic structure calculations have been performed to determine the thermochemistry and kinetics of the reaction between OH and the radicals of the S enantiomer of the herbicide Metolachlor, 2-chloro-N-(2-methyl-6-ethylphenyl)-N(2-methoxy-1-methylethyl) acetamide (MC), produced by photoinduced breaking of the C–Cl bond. Both density functional and ab initio composite methods were employed to calculate the structure of reactants, intermediates, transition states and products, in gas phase and in aqueous solution. The expected relative abundance of each product was calculated and compared to the experimentally observed concentrations. It is shown that a combination of thermodynamic and kinetic characteristics interplay to produce the expected theoretical abundances, which turn out to be in agreement with the experimentally observed distribution of products.


2015 ◽  
Vol 51 (27) ◽  
pp. 5856-5859 ◽  
Author(s):  
C. S. Cooper ◽  
R. J. Oldman ◽  
C. R. A. Catlow

Mechanism of C–H bond cleavage, involving electron transfer to adsorbed oxygen on YSZ by electronic structure calculations.


2019 ◽  
Vol 217 ◽  
pp. 414-433 ◽  
Author(s):  
Bo Xu ◽  
Tamar Stein ◽  
Utuq Ablikim ◽  
Ling Jiang ◽  
Josie Hendrix ◽  
...  

Synchrotron based mass spectrometry coupled with theoretical calculations provides insight into polycyclic aromatic hydrocarbon water interactions.


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