-
aminoxyl radical TEMPO, a
commonly encountered organic aminoxyl radical Fremy's salt, an
inorganic aminoxyl radical Sterically unhindered aminoxyls bearing...
- This
heterocyclic compound is a red-orange,
sublimable solid. As a
stable aminoxyl radical, it has
applications in
chemistry and biochemistry.
TEMPO is used...
- oxidation. By
these reactions HALS are
oxidised to
their corresponding aminoxyl radicals (R2NO• c.f. TEMPO),
however they are able to
return to
their initial...
- bio-membranes and
membrane biophysics. For example,
stearic acid
labelled with
aminoxyl spin
label moiety at
various carbons (5, 7, 9, 12, 13, 14 and 16) with...
- is used as a
catalyst and
chemical oxidant by
virtue of
being a
stable aminoxyl radical. Its
major appeal over
TEMPO is that it is less expensive, being...
- NR2OH
Phosphine oxide, PR3=O Sulfoxide, R2S=O Azoxy, RN=N+(O−)R RN=N+RO−
Aminoxyl group,
radicals with the
general structure R2N–O• Category:Amine oxides...
-
molecules for this task. [citation needed]
Nitroxyl radicals (also
called aminoxyl radicals) —
chemical species containing the R2N−O•
functional group "Nitroxyl"...
- may be
explained by the
formation of
aminoxyl radicals through a
process known as the
Denisov Cycle. The
aminoxyl radical (N-O•)
combines with free radicals...
- more
quickly than the
ozone can
react with the rubber. This
process forms aminoxyl radicals and was
first thought to
degrade only to the
quinone diimine,...
- O-ethylhydroxylamine. A
variety of
functional groups can be
oxidized with the
aminoxyl radical (phthalimide-N-oxyl, PINO)
formed by the
abstraction of a hydrogen...