On the Dissociation of Aromatic Radical Anions in Solution. 2. Reaction Path and Rate Constant Analysis

2003 ◽  
Vol 107 (51) ◽  
pp. 11292-11306 ◽  
Author(s):  
Irene Burghardt ◽  
Damien Laage ◽  
James T. Hynes
1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars

It has been found that the decay in dimethylformamide and dimethylformamide-water mixtures of radical anions in five of the investigated 5-nitrofurans is governed by a second-order reaction. Only the decay of the radical anion generated from 5-nitro-2-furfural III may be described by an equation including parallel first- and second-order reactions; this behaviour is evidently caused by the relatively high stability of the corresponding dianion, this being an intermediate in the reaction path. The presence of a larger conjugated system in the substituent in position 2 results in a decrease of the unpaired electron density in the nitro group and, consequently, an increase in the stability of the corresponding radical anions.


1993 ◽  
Vol 34 (26) ◽  
pp. 4223-4226 ◽  
Author(s):  
Masaaki Mishima ◽  
Chul Huh ◽  
Hirotaka Nakamura ◽  
Mizue Fujio ◽  
Yuho Tsuno

ChemInform ◽  
1990 ◽  
Vol 21 (3) ◽  
Author(s):  
Y. KUBOZONO ◽  
M. ATA ◽  
M. AOYAGI ◽  
T. FUJITA ◽  
N. FUKAMI ◽  
...  

1995 ◽  
Vol 36 (13) ◽  
pp. 2265-2268 ◽  
Author(s):  
Masaaki Mishima ◽  
Chul Huh ◽  
Hai Whang Lee ◽  
Hirotaka Nakamura ◽  
Mizue Fujio ◽  
...  

1984 ◽  
Vol 88 (11) ◽  
pp. 2368-2372 ◽  
Author(s):  
Yukio Yamamoto ◽  
Shoichi Nishida ◽  
Katsuyoshi Yabe ◽  
Koichiro Hayashi ◽  
Seishi Takeda ◽  
...  

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