Keto-enol tautomerism of gas-phase ions. Structure of reactive 1,3-cyclohexadien-5-one radical cations

1978 ◽  
Vol 100 (19) ◽  
pp. 6133-6137 ◽  
Author(s):  
D. H. Russell ◽  
M. L. Gross ◽  
N. M. M. Nibbering



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>



1987 ◽  
Vol 86 (4) ◽  
pp. 2081-2086 ◽  
Author(s):  
Robert C. Dunbar ◽  
Jyh Horung Chen ◽  
Hun Young So ◽  
Bruce Asamoto
Keyword(s):  




2018 ◽  
Vol 140 (2) ◽  
pp. 531-533 ◽  
Author(s):  
Luciano H. Di Stefano ◽  
Dimitris Papanastasiou ◽  
Roman A. Zubarev


2018 ◽  
Vol 90 (20) ◽  
pp. 11856-11862 ◽  
Author(s):  
Shiyu Dong ◽  
Nicole D. Wagner ◽  
David H. Russell


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