Electron spin resonance of .beta.-chloroalkyl nitroxides. Angular dependence of .beta.-chlorine hyperfine coupling

1970 ◽  
Vol 74 (15) ◽  
pp. 3025-3027 ◽  
Author(s):  
Edward G. Janzen ◽  
Bruce R. Knauer ◽  
Lewis T. Williams ◽  
William B. Harrison

1970 ◽  
Vol 74 (9) ◽  
pp. 2037-2038 ◽  
Author(s):  
Edward G. Janzen ◽  
Bruce R. Knauer ◽  
John L. Gerlock ◽  
Kenneth J. Klabunde


1986 ◽  
Vol 64 (4) ◽  
pp. 769-772 ◽  
Author(s):  
Donald R. Arnold ◽  
A. Martin de P. Nicholas ◽  
Kent M. Young

The linear relationship between the electron spin resonance hyperfine coupling constants (hfc) of the α- and β-hydrogens of para-substituted α-phenethyl radicals provides experimental evidence that the magnitude of both the α- and β -hfc is determined largely by the extent of spin delocalization in these benzylic systems. The [Formula: see text] scale, developed using substituted benzyl radicals, is shown to apply to phenethyl radicals as well.



1981 ◽  
Vol 59 (1) ◽  
pp. 156-163 ◽  
Author(s):  
D. Plancherel ◽  
D. R. Eaton

Electron spin resonance spectra are reported from a number of radicals derived from 2,4-pentadione substituted at the 3 position with nitroxide-containing groups. If the substituent is t-butyl nitroxide no metal complexes are formed. This is attributed to steric factors which prevent the formation of the enol form of the β-diketone. If the substituent is trifluoromethyl nitroxide two types of metal complex have been observed. The esr spectra of the first type are very similar to that of the uncomplexed radical. Such complexes are formed with Co(III) and Al(III). The esr spectra of the second type show considerably increased 14N and 19F hyperfine coupling constants and in some cases large couplings to the metal nucleus. Complexes for the second type have been observed with Pd(II), Pt(II), and Rh(III). The possible structures of these radicals are discussed.



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.



1980 ◽  
Vol 41 (2) ◽  
pp. 229-239 ◽  
Author(s):  
O Claesson ◽  
A Lund ◽  
J.-P Jørgensen ◽  
E Sagstuen


1991 ◽  
Vol 43 (4) ◽  
pp. 2531-2540 ◽  
Author(s):  
Shin-ichi Kuroda ◽  
Keiichi Ikegami ◽  
Yuka Tabe ◽  
Kazuhiro Saito ◽  
Mitsuyoshi Saito ◽  
...  


Sign in / Sign up

Export Citation Format

Share Document