Radical cations of twisted acenes: chiroptical properties and spin delocalization

2019 ◽  
Vol 55 (43) ◽  
pp. 6022-6025 ◽  
Author(s):  
Anjan Bedi ◽  
Raanan Carmieli ◽  
Ori Gidron

A series of enantiopure twistacene radical cations display dependency of the chiroptical properties and the EPR signal on the backbone twist.

2019 ◽  
Vol 10 (19) ◽  
pp. 5708-5712
Author(s):  
Gabriel Moise ◽  
Lara Tejerina ◽  
Michel Rickhaus ◽  
Harry L. Anderson ◽  
Christiane R. Timmel

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>


1978 ◽  
Vol 43 (8) ◽  
pp. 2062-2067
Author(s):  
Slavomír Bystrický ◽  
Tibor Sticzay ◽  
Pavol Kováč

1975 ◽  
Vol 40 (3) ◽  
pp. 670-680 ◽  
Author(s):  
R. Bognár ◽  
Gy. Gaál ◽  
P. Kerekes ◽  
A. Lévai ◽  
S. Makleit ◽  
...  

1988 ◽  
Vol 53 (3) ◽  
pp. 497-505 ◽  
Author(s):  
Stanislav Luňák ◽  
Aleksandr I. Kokorin ◽  
Eva Mácová ◽  
Pavel Lederer

It has been found that [VO(acac)2] and [Co(acac)3] increase the rate of t-BuOOH photolysis, whereas [Fe(acac)3] has the opposite effect. Redox changes of the catalytically active [VO(acac)2] were followed using the EPR technique. An EPR signal from a free radical intermediate of photochemical decomposition of t-BuOOH was recorded, and the concentration of the intermediate was monitored during the reaction.


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