Reactions of water with radical cations of guanine, 9-methylguanine, 2′-deoxyguanosine and guanosine: keto–enol isomerization, C8-hydroxylation, and effects of N9-substitution

2018 ◽  
Vol 20 (43) ◽  
pp. 27510-27522 ◽  
Author(s):  
Yan Sun ◽  
Wenjing Zhou ◽  
May Myat Moe ◽  
Jianbo Liu

The reactions of D2O with guanine radical cations in nucleobases and nucleosides were studied in the gas phase using the guided-ion-beam experiment and computational modeling.




2009 ◽  
Vol 131 (2) ◽  
pp. 024306 ◽  
Author(s):  
J. M. Lucas ◽  
J. de Andrés ◽  
J. Sogas ◽  
M. Albertí ◽  
J. M. Bofill ◽  
...  


2009 ◽  
Vol 113 (52) ◽  
pp. 14766-14773 ◽  
Author(s):  
J. M. Lucas ◽  
J. de Andrés ◽  
E. López ◽  
M. Albertí ◽  
J. M. Bofill ◽  
...  






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>





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