ESR spectra of radical anions ? Products of the reaction of fullerene with alkali metals

1992 ◽  
Vol 41 (12) ◽  
pp. 2234-2236
Author(s):  
S. P. Solodovnikov ◽  
V. V. Bashilov ◽  
V. I. Sokolov
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 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

1976 ◽  
Vol 7 (50) ◽  
pp. no-no
Author(s):  
F. GERSON ◽  
W. B. JUN. MARTIN ◽  
G. PLATTNER ◽  
F. SONDHEIMER ◽  
H. N. C. WONG
Keyword(s):  

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

1971 ◽  
Vol 54 (1) ◽  
pp. 361-369 ◽  
Author(s):  
F. Gerson ◽  
G. Moshuk ◽  
M. Schwyzer
Keyword(s):  

2002 ◽  
Vol 80 (11) ◽  
pp. 1393-1397 ◽  
Author(s):  
Maneesh Bahadur ◽  
Christopher W Allen ◽  
William E Geiger ◽  
Adam Bridges

The syntheses of the dicobalt hexacarbonyl complexes, N3P3F6-n(C[Formula: see text]CPhCo2(CO)6)n (n = 1 (3), n = 2 (4)), is reported. The introduction of the organometallic fragment allows for simplification of the NMR spectra and separation of the isomers of the disubstituted (4) derivatives. Electrochemical studies show that 3 undergoes a reversible one-electron reduction. At 233 K, the geminal isomer of 4 undergoes two separate reversible one-electron reductions. The ESR spectra of the radical anions of 3 and 4 have been obtained and show the absence of delocalization of unpaired spin density from the organometallic cluster to the phosphazene.Key words: cyclophosphazenes, cobalt–alkyne clusters, electrochemistry, ESR.


Sign in / Sign up

Export Citation Format

Share Document