Quinoxaline N-oxide ion radicals. 2. Structures of anion radicals of N-oxides of hydroxymethyl derivatives of quinoxaline and products of their electrochemical reduction

1985 ◽  
Vol 21 (10) ◽  
pp. 1164-1168
Author(s):  
V. M. Kazakova ◽  
O. G. Sokol ◽  
G. G. Dvoryantseva ◽  
I. S. Musatova ◽  
A. S. Elina
1996 ◽  
Vol 32 (7) ◽  
pp. 800-806
Author(s):  
Ya. Stradyn' ◽  
L. Baumane ◽  
R. Gavars ◽  
B. Vigante ◽  
G. Duburs

1981 ◽  
Vol 46 (2) ◽  
pp. 498-502 ◽  
Author(s):  
Jozef Černák ◽  
František Tomanovič ◽  
Andrej Staško ◽  
Anna Fedosyevna Oleinikova ◽  
Jaroslav Kováč

para Substituted chloro, bromo, and nitro derivatives of 2-acyl-5-phenylfurane are reduced polarographically in a one-electron wave to the corresponding anion radicals, which were studied by the EPR method. The reduction of nitro derivatives, studied by the Kalousek switch, is reversible and leads to a stable anion radical with an unpaired electron center on the nitrogen nucleus; the reduction of the halogen derivatives is only partly reversible and leads to unstable ketyl radicals. The bromo derivatives give polarographic maxima typical for concurrent reactions.


1997 ◽  
Vol 33 (2) ◽  
pp. 184-189 ◽  
Author(s):  
Ya. Stradyn' ◽  
R. Gavar ◽  
L. Baumane ◽  
B. Vigante ◽  
G. Dubur

1974 ◽  
Vol 14 (4) ◽  
pp. 678-681 ◽  
Author(s):  
V. M. Kazakova ◽  
V. B. Piskov

1993 ◽  
Vol 29 (8) ◽  
pp. 918-925
Author(s):  
Ya. Stradyn' ◽  
R. Gavars ◽  
L. Baumane ◽  
B. Vigante ◽  
G. Duburs

1973 ◽  
Vol 7 (2) ◽  
pp. 213-216
Author(s):  
S. S. Gitis ◽  
I. M. Sosonkin ◽  
A. Ya. Kaminskii

Sign in / Sign up

Export Citation Format

Share Document