EPR spectra and structure of certain phosphorus-containing nitroxyl radicals

1976 ◽  
Vol 11 (5) ◽  
pp. 515-520 ◽  
Author(s):  
A. V. Il'yasov ◽  
Ya. A. Levin ◽  
A. Sh. Mukhtarov ◽  
M. S. Skorobogatova
1976 ◽  
Vol 7 (4) ◽  
pp. no-no
Author(s):  
A. V. IL'YASOV ◽  
YA. A. LEVIN ◽  
A. SH. MUKHTAROV ◽  
M. S. SKOROBOGATOVA

1987 ◽  
Vol 26 (16) ◽  
pp. 2618-2620 ◽  
Author(s):  
Kundalika M. More ◽  
Gareth R. Eaton ◽  
Sandra S. Eaton

1977 ◽  
Vol 13 (2) ◽  
pp. 141-145
Author(s):  
L. I. Antsiferova ◽  
N. N. Korst ◽  
A. N. Ivanova ◽  
N. S. Nazemets

1981 ◽  
Vol 36 (2) ◽  
pp. 195-197 ◽  
Author(s):  
Karl E. Schwarzhans ◽  
Alfons Stuefer

Abstract The stable free radical 4,4,5,5-tetramethylimidazoline-1-oxyl-2-m-pyridyl-3-oxide has been prepared and used as a ligand in platinum(II), palladium(II) and copper(II) complexes. The magnetic moments and the EPR spectra of the complexes and the free radical have been investigated. The complexes show a considerable interaction between the nitroxyl radicals of the ligands.


1980 ◽  
Vol 35 (1) ◽  
pp. 68-70 ◽  
Author(s):  
Richard Fedrigolli ◽  
Karl E. Schwarzhans

Abstract The stable free radicals 4-carboxy-2,2,6,6-tetramethylpiperidinooxyl, 4-carboxy-methylene-2,2,6,6-tetramethylpiperidinooxyl, 4-carboxymethyl-2,2,6,6-tetramethylpipe-ridinooxyl and 3′-carboxy-2,2,6,6-tetramethylpiperidine-4-spiro-2′-oxirane-l-yloxyl have been prepared and used as ligands in copper(II) complexes. The magnetic moments and the EPR spectra of the complexes and the free radicals have been investigated and compared with complexes containing diamagnetic cyclohexanecarboxylic acid or cyclo -hexaneacetic acid ligands. One of the copper(II) complexes shows a considerable inter-action between the nitroxyl radicals of the ligands.


1980 ◽  
Vol 34 (3) ◽  
pp. 268-275 ◽  
Author(s):  
Marsha J. Heinig ◽  
G. R. Eaton ◽  
S. S. Eaton

Electron paramagnetic resonance (EPR) spectra of a homologous series of nitroxyl radicals derived from cyclic alkanones with 6 to 15 carbons in the ring have been obtained as a function of temperature. Long-range hyperfine coupling (0.7 to 2.2 G) was observed in the low-temperature spectra for rings with 6, 7, and 9 to 15 carbons. Deuteration of the 11- to 14-membered rings indicated that the long-range coupling was to one of the protons on the carbons adjacent to the point of attachment of the nitroxyl radical. For the 9- to 15-membered rings, there was a temperature region in which the hyperfine coupling decreased rapidly. This decrease is attributed to rapid conformational averaging on the EPR time scale. For the 12-, 13-, and 15-membered rings, the high temperature spectra exhibited resolved hyperfine coupling which can be computer-simulated, assuming four equivalent protons. The activation energies estimated from the coalescence temperatures in the EPR spectra fall in the range estimated by nuclear magnetic resonance and show similar influences of ring size on rigidity.


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