scholarly journals Intracluster Sulphur Dioxide Oxidation by Sodium Chlorite Anions: A Mass Spectrometric Study

Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7114
Author(s):  
Chiara Salvitti ◽  
Federico Pepi ◽  
Anna Troiani ◽  
Giulia de Petris

The reactivity of [NaL·ClO2]− cluster anions (L = ClOx−; x = 0–3) with sulphur dioxide has been investigated in the gas phase by ion–molecule reaction experiments (IMR) performed in an in-house modified Ion Trap mass spectrometer (IT-MS). The kinetic analysis revealed that SO2 is efficiently oxidised by oxygen-atom (OAT), oxygen-ion (OIT) and double oxygen transfer (DOT) reactions. The main difference from the previously investigated free reactive ClO2− is the occurrence of intracluster OIT and DOT processes, which are mediated by the different ligands of the chlorite anion. This gas-phase study highlights the importance of studying the intrinsic properties of simple reacting species, with the aim of elucidating the elementary steps of complex processes occurring in solution, such as the oxidation of sulphur dioxide.

2019 ◽  
Vol 490 (3) ◽  
pp. 3498-3507
Author(s):  
Junfeng Zhen ◽  
Weiwei Zhang ◽  
Yuanyuan Yang ◽  
Qingfeng Zhu

ABSTRACT It is possible that fullerene–polycyclic aromatic hydrocarbon (PAH) clusters or associations of fullerenes with PAHs contain a large fraction of interstellar fullerenes in the interstellar medium. Herein, we report the formation and photofragmentation behaviour of fullerene–PAH derivatives, fullerene/9-vinylanthracene (C16H12) and fullerene/9-methylanthracene (C15H12) cluster cations. Experiments are carried out using a quadrupole ion trap in combination with time-of-flight mass spectrometry in the gas phase. The results show that fullerene (C60)/9-vinylanthracene (e.g. [(C16H12)3C60]+), fullerene (C56 and C58)/9-vinylanthracene (e.g. [(C16H12)4C56]+ and [(C16H12)4C58]+), fullerene (C60)/9-methylanthracene (e.g. [(C15H12)3C60]+), and fullerene (C56 and C58)/9-methylanthracene (e.g. [(C15H12)4C56]+ and [(C15H12)4C58]+) cluster cations, i.e. large fullerene-derived molecules, are formed in the gas phase through the ion–molecule reaction pathway. With irradiation, all fullerene–PAH-derived cluster cations lose their monomolecular groups without other fragmentation channels (e.g. dehydrogenation). The structure of newly formed fullerene–PAH-derived cluster cations and the bond energy for these adduction formation pathways are investigated with theoretical calculations. The obtained results provide a general molecular growth route towards large fullerene–PAH derivatives (e.g. large fullerene-derived molecules) with functional PAHs in a bottom-up formation process and insights into the effect of functional groups (e.g. vinyl, –C2H3, and methyl, –CH3) on their formation and photoevolution behaviours. In addition, the fullerene–PAH-derived clusters (from 83 to 170 atoms in total, or ∼2 nm in size) offer a good model of carbon dust grains, and the relevance to the nanometre-sized carbon dust grain in space is briefly discussed.


2020 ◽  
Author(s):  
Oisin Shiels ◽  
P. D. Kelly ◽  
Cameron C. Bright ◽  
Berwyck L. J. Poad ◽  
Stephen Blanksby ◽  
...  

<div> <div> <div> <p>A key step in gas-phase polycyclic aromatic hydrocarbon (PAH) formation involves the addition of acetylene (or other alkyne) to σ-type aromatic radicals, with successive additions yielding more complex PAHs. A similar process can happen for N- containing aromatics. In cold diffuse environments, such as the interstellar medium, rates of radical addition may be enhanced when the σ-type radical is charged. This paper investigates the gas-phase ion-molecule reactions of acetylene with nine aromatic distonic σ-type radical cations derived from pyridinium (Pyr), anilinium (Anl) and benzonitrilium (Bzn) ions. Three isomers are studied in each case (radical sites at the ortho, meta and para positions). Using a room temperature ion trap, second-order rate coefficients, product branching ratios and reaction efficiencies are reported. </p> </div> </div> </div>


2000 ◽  
Vol 96 ◽  
pp. 445-475 ◽  
Author(s):  
Wan Yong Feng ◽  
Scott Gronert
Keyword(s):  

ChemInform ◽  
2010 ◽  
Vol 31 (17) ◽  
pp. no-no
Author(s):  
Wan Yong Feng ◽  
Scott Gronert
Keyword(s):  

2015 ◽  
Vol 21 (41) ◽  
pp. 14305-14308 ◽  
Author(s):  
Shaodong Zhou ◽  
Maria Schlangen ◽  
Jilai Li ◽  
Xiao-Nan Wu ◽  
Helmut Schwarz

2010 ◽  
Vol 29 (13) ◽  
pp. 3001-3006 ◽  
Author(s):  
Robert F. Höckendorf ◽  
Yali Cao ◽  
Martin K. Beyer

1986 ◽  
Vol 69 (4) ◽  
pp. 806-815 ◽  
Author(s):  
Jean-Claude Tabet ◽  
Chantal Prevost ◽  
Anne Bouillot ◽  
Josette Bastard ◽  
Due Do Khae Manh ◽  
...  
Keyword(s):  

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