Reactions of a Stable Phosphinyl Radical with Stable Aminoxyl Radicals

2015 ◽  
Vol 44 (1) ◽  
pp. 94-96 ◽  
Author(s):  
Shintaro Ishida ◽  
Fumiya Hirakawa ◽  
Takeaki Iwamoto
Keyword(s):  
1982 ◽  
Vol 60 (21) ◽  
pp. 2725-2733 ◽  
Author(s):  
Edward G. Janzen ◽  
Gregory A. Coulter ◽  
Uwe M. Oehler ◽  
John P. Bergsma

The nitrogen and β-hydrogen hyperfine splitting constants (hfsc) for phenyl, 4-nitrophenyl, 4-pyridyl, benzoyl, and trichloromethyl spin adducts of α-phenyl tert-butyl nitrone (PBN) as well as for the tert-butoxyl adduct of 5,5-dimethylpyrroline-N-oxide (DMPO) have been obtained as a function of solvent (30 solvents). A useful linear relationship between the β-H hfsc and the N-hfsc of each aminoxyl is found except for the benzoyl adduct of PBN. Some speculations regarding the structural significance of these correlations is presented.


1991 ◽  
Vol 45 ◽  
pp. 949-952 ◽  
Author(s):  
Carl Lagercrantz ◽  
Kostas Karagiannis ◽  
Dimitrios Vynios ◽  
Dionissios Papaioannou ◽  
Dagfinn W. Aksnes ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (6) ◽  
pp. e0157944 ◽  
Author(s):  
Marcos de Oliveira ◽  
Robert Knitsch ◽  
Muhammad Sajid ◽  
Annika Stute ◽  
Lisa-Maria Elmer ◽  
...  

1992 ◽  
pp. 573-583 ◽  
Author(s):  
Edward G. Janzen ◽  
Rheal A. Towner

2007 ◽  
pp. 145-182 ◽  
Author(s):  
A. rockenbauer ◽  
M. Györ ◽  
H. O. Hankovszky ◽  
K. Hideg
Keyword(s):  

1993 ◽  
Vol 48 (4) ◽  
pp. 505-510 ◽  
Author(s):  
Yong-Kang Zhang ◽  
De-Kang Shen

A novel dihydroxy-substituted aminoxyl spin label, 4-hydroxy-3-(3'-hydroxypropyl)-2,2,6,6-tetramethylpiperidine-1-oxy (5), has been prepared. From this aminoxyl radical, a spin-labeled crown ether, 16,16,18,18-tetramethyl-2,5,8,11-tetraoxa-17-azabicyclo[ 13,4,0]-nonadecane-17-oxy (12), and a spin-labeled cyclic diester, 16,16,18,18-tetramethyl-3,10-dioxo-2,5,8,11-tetraoxa-17-azabicyclo[13,4,o]nonadecane-17-oxy (13), have been acquired. Other four new stable aminoxyl radicals 8,9,10, and 11 have also been obtained within the synthetic approach. It has been demonstrated that the cyclic ether compound (7) is generated by the reduction of its corresponding lactone which is sidely derived from the oxo-reduced species of 3 by intramolecular cyclization.


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