Effects of Steric Congestion on Stilbene Radical Anions and Dianions:  DFT Calculations in the Interpretation of Stilbene Radical Anion ESR Spectra

1996 ◽  
Vol 61 (19) ◽  
pp. 6739-6743 ◽  
Author(s):  
James E. Gano ◽  
E. Jean Jacob ◽  
P. Sekher ◽  
Girija Subramaniam ◽  
Leif A. Eriksson ◽  
...  
1979 ◽  
Vol 44 (12) ◽  
pp. 3632-3643 ◽  
Author(s):  
Karel Mach ◽  
Igor Janovský ◽  
Karel Vacek

Total yields of paramagnetic species, their optical bleaching and thermal annealing in acetic, propionic, a-butyric, isobutyric, and pivalic acid γ-irradiated at 77 K were followed by ESR spectroscopy. Radical anions, always found after irradiation, disappear during optical bleaching without formation of any paramagnetic product. During thermal annealing they are converted almost quantitatively into the α-radicals of the respective acid, with the exception of pivalic acid. Amounts of radical anions were estimated from the difference of integrated ESR spectra taken before and after optical bleaching. The results show that approximately equal amounts of the reduction and oxidation paramagnetic products of the γ-irradiation can be detected.


1980 ◽  
Vol 45 (2) ◽  
pp. 369-375 ◽  
Author(s):  
Stanislav Miertuš ◽  
Ondrej Kyseľ

The 4-nitrobenzophenone radical anion prepared by electrolysis was studied by ESR spectroscopy. On the basis of the interpretation of ESR spectra, the conformation of this system was estimated. The effect of the concentration of supporting electrolyte and of the presence of a proton-donor agent (C2H5OH) was examined. It is assumed that changes in hyperfine splitting constants are caused by association.


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.


1980 ◽  
Vol 9 (6) ◽  
pp. 611-612 ◽  
Author(s):  
Akinori Hasegawa ◽  
Takatoshi Yamaguchi ◽  
Michiro Hayashi

ChemInform ◽  
2010 ◽  
Vol 23 (18) ◽  
pp. no-no
Author(s):  
A. G. DAVIES ◽  
A. G. NEVILLE

2017 ◽  
Vol 41 (14) ◽  
pp. 6866-6874 ◽  
Author(s):  
Dmitri V. Konarev ◽  
Maxim A. Faraonov ◽  
Alexey V. Kuzmin ◽  
Salavat S. Khasanov ◽  
Yoshiaki Nakano ◽  
...  

Radical anion salts of metal phthalocyanines (M = CuII, PbII, VIVO and SnIVCl2) with the {cryptand(Na+)} cations have been obtained and studied.


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