ChemInform Abstract: Role of Defects in Radiation Chemistry of Crystalline Organic Materials. Part 3. Geometrical and Electronic Structures of Alkene Radical Anion and Cation in Alkene/n-Alkane Mixed Crystals as Studied by ESR Spectroscopy

ChemInform ◽  
2010 ◽  
Vol 23 (8) ◽  
pp. no-no
Author(s):  
K. MATSUURA ◽  
H. MUTO ◽  
K. NUNOME
Keyword(s):  
Electronic Structures ◽  
Radical Anion ◽  
Esr Spectroscopy ◽  
Organic Materials ◽  
Radiation Chemistry ◽  
Mixed Crystals

Association of radical anion with alkali cations. IV. ESR study of the 4-nitrobenzophenone radical anion

1980 ◽  
Vol 45 (2) ◽  
pp. 369-375 ◽  
Author(s):  
Stanislav Miertuš ◽  
Ondrej Kyseľ
Keyword(s):  
Hyperfine Splitting ◽  
Radical Anion ◽  
Esr Spectroscopy ◽  
Supporting Electrolyte ◽  
Esr Spectra ◽  
Proton Donor ◽  
Alkali Cations

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.

Stability of radical anions derived from substituted 5-nitrofurans investigated by ESR spectroscopy

1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars
Keyword(s):  
Radical Anion ◽  
High Stability ◽  
Esr Spectroscopy ◽  
Reaction Path ◽  
Order Reaction ◽  
Second Order ◽  
Radical Anions ◽  
Second Order Reaction ◽  
Unpaired Electron Density ◽  
The Stability

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.

On the Structure of Lead(II) Complexes in Aqueous Solutions. I. Trinuclear Clusters

1995 ◽  
Vol 60 (4) ◽  
pp. 527-536 ◽  
Author(s):  
Martin Breza ◽  
Alena Manová
Keyword(s):  
Quantum Chemistry ◽  
Aqueous Solutions ◽  
Electronic Structures ◽  
Mndo Method ◽  
Model Systems ◽  
Trinuclear Clusters ◽  
The Stability ◽  
Semiempirical Mndo

Using semiempirical MNDO method of quantum chemistry the optimal geometries and corresponding electronic structures of [Pb3(OH)n]6-n model systems as well as of their hydrated [Pb3(OH)n(H2O)8-n]6-n analogues (n = 4, 5) are investigated. The most stable trinuclear lead(II) complexes present in aqueous solutions correspond to cyclo-(μ3-OH)(μ2-OH)3Pb32+, Pb(μ-OH)2Pb(μ-OH)2Pb2+, cyclo-(μ3-OH)2(μ2-OH)3Pb3+, Pb(OH)(μ-OH)2Pb(μ-OH)Pb(OH)+ and Pb(OH)(μ-OH)2Pb(μ-OH)2Pb+ systems. The key role of OH bridges (by vanishing direct Pb-Pb bonds) on the stability of individual isomers is discussed.

A study of the radiation chemistry of poly(chlorotrifluoroethylene) by ESR spectroscopy

2003 ◽  
Vol 68 (5) ◽  
pp. 857-864 ◽  
Author(s):  
David J.T. Hill ◽  
Kristofer J. Thurecht ◽  
Andrew K. Whittaker
Keyword(s):  
Esr Spectroscopy ◽  
Radiation Chemistry

scholarly journals Reactivity of Superoxide Radical Anion with Cyclic Nitrones:  Role of Intramolecular H-Bond and Electrostatic Effects

2007 ◽  
Vol 129 (26) ◽  
pp. 8177-8191 ◽  
Author(s):  
Frederick A. Villamena ◽  
Shijing Xia ◽  
John K. Merle ◽  
Robert Lauricella ◽  
Beatrice Tuccio ◽  
...  
Keyword(s):  
Radical Anion ◽  
Superoxide Radical ◽  
Electrostatic Effects ◽  
Superoxide Radical Anion ◽  
Cyclic Nitrones
Sign in / Sign up

Export Citation Format

Share Document