-
Aminoxyl denotes a
radical functional group with
general structure R2N–O•. It is
commonly known as a
nitroxyl radical or a nitroxide,
however IUPAC discourages...
- This
heterocyclic compound is a red-orange,
sublimable solid. As a
stable aminoxyl radical, it has
applications in
chemistry and biochemistry.
TEMPO is used...
- weathering. Like most
compounds of this class, the
activated form is an
aminoxyl radical. It is
produced by the
diesterification of
sebacic acid with 4-Hydroxy-TEMPO...
- 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...
- 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...
- will
react with rubber. This
reaction converts it to the
corresponding aminoxyl radical (R2N–O•), with the
ozone being converted to a
hydroperoxyl radical...
- 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...
- 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...
- 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...
- 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...
