THE ELECTRON SPIN RESONANCE SPECTRA OF DINITRONAPHTHALENE ANION RADICALS

1965 ◽  
Vol 43 (12) ◽  
pp. 3400-3406 ◽  
Author(s):  
P. H. H. Fischer ◽  
C. A. McDowell

The radical anions of 1,4-dinitronaphthalene, 1,5-dinitronaphthalene, and 1,8-dinitronaphthalene have been generated by electrolytic means, and their e.s.r. spectra recorded. The spectra consist of 61, 111, and 85 lines respectively, and can be analyzed in terms of one nitrogen and three proton coupling constants, consistent with the full symmetry of the species giving rise to them. These constants are, for 1,4-dinitronaphthalene: aN = 0.97 G, aH2 = 1.69 G, aH5 = 0.53 G, and aH6 = 0.41 G; for 1,5-dinitronaphthalene: aN = 2.30 G, aH2 = 2.42 G, aH3 = 0.44 G, and aH4 = 2.82 G; for 1,8-dinitronaphthalene: aN = 3.03 G, aH2 = 3.63 G, aH3 = 0.95 G, and aH4 = 3.73 G. Whereas the nitrogen coupling constants can be unambiguously assigned, this, in the absence of deuteration studies say, is not the case for the three sets of equivalent protons. As an aid in the assignment of proton coupling constants, Hückel LCAO calculations and simplified SCFMO calculations by the method of McLachlan have been performed. The first mentioned of the above proton constants could thus be assigned with reasonable certainty, the remaining two aHi remain ambiguous.

1972 ◽  
Vol 25 (11) ◽  
pp. 2353 ◽  
Author(s):  
RFC Claridge ◽  
BM Peake

The hyperfine coupling constants for the radical anions of 2,3-dihydro- phenalene (perinaphthane) and 7,8,9,l0-tetrahydrocyclohepta[de]naphthalene have been determined from analysis of the electron spin resonance spectra in solution. The results are compared with data from other mono- and di-peri- substituted naphthalenes. A simple H�ckel molecular orbital treatment is used to describe the inductive effect of the aliphatic substituent.


1977 ◽  
Vol 55 (20) ◽  
pp. 3554-3558 ◽  
Author(s):  
J. P. Michaut ◽  
J. Roncin

Nitrogen and proton coupling tensors have been measured for the [Formula: see text] radical trapped in five different single crystal matrices. As all isotropic coupling constants are the same within experimental error (aN = 21.2 G, aH = 28.4 G), no measurable crystal field effect is found. In these solids the motions of the radical depend on the dimension of the trapping cage and the motions of the surrounding molecules.


1968 ◽  
Vol 46 (24) ◽  
pp. 3847-3856 ◽  
Author(s):  
P. H. H. Fischer ◽  
H. Zimmermann

Electron spin resonance spectra have been observed for anion radicals derived from 2-fluoro-nitro-benzene, 3-fluoro-nitrobenzene, 2,4-difluoro-nitrobenzene, 2,5-difluoro-nitrobenzene, 4-fluoro-2-nitro-phenol, 2-fluoro-6-nitrophenol, and 3-fluoro-6-nitrophenol. All radicals were generated electrolytically in dimethoxyethane/acetonitrile solution, acetonitrile, or dimethylformamide. The radicals are generally quite stable with the exception of those from 2-fluoro-6-nitrophenol and 3-fluoro-6-nitrophenol, the latter decaying with a half-life of approximately 6 min. All spectra can be interpreted completely, and coupling constants are assigned by comparison to related compounds and consistency arguments.


1966 ◽  
Vol 44 (5) ◽  
pp. 551-559 ◽  
Author(s):  
Raymond Wilson

Electron spin resonance observations on the photolytically generated ketyls of benzaldehyde, acetophenone, and benzophenone in protic solvents are reported. Proton coupling constants differ considerably from those reported by other workers for the same ketyls generated by other methods in aprotic solvents.Molecular orbital calculations of unpaired electron spin densities, in which the effective electronegativities of the oxygen atoms on the ketyls are assumed to be increased by hydrogen bonding in protic solvents, are reported. The calculated changes in spin densities agree qualitatively with the semi-empirical changes calculated by the McConnell relationship.Observations on the dynamics of solvation of the benzaldehyde ketyl in a mixture of a protic and an aprotic solvent are reported and discussed.


1974 ◽  
Vol 39 (15) ◽  
pp. 2276-2281 ◽  
Author(s):  
Reuben D. Rieke ◽  
Stephen E. Bales ◽  
Claude F. Meares ◽  
Loretta I. Rieke ◽  
Charles M. Milliren

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