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1 al motion of the water proton spins past the nitroxide radical.
2 ron C-N bonds analogous to the N-O bond of a nitroxide radical.
3 l state and hence the electroactivity of the nitroxide radical.
4 ds to its corresponding catalytically active nitroxide-radical.
5 -aromatics, iron coordination complexes, and nitroxide radicals.
6 e-coupled clusters of copper(II) with stable nitroxide radicals.
7 ganic solvents in the presence of paramagnet nitroxide radicals.
8 MeO or EtO) supported by air-stable nitronyl nitroxide radicals.
9 ates when used at the same concentrations as nitroxide radicals.
10 gle crystal ascertains the grafting of three nitroxide radicals.
11                                     A stable nitroxide radical, 1-oxyl-4-bromo-2,2,5,5-tetramethylpyr
12 eling of these plasma activities by a stable nitroxide radical, 2,2,6, 6-tetramethyl-1-piperidinyloxy
13  trapping studies show the intermediacy of a nitroxide radical and a C-nitroso species during this re
14 nthesized two series of compounds in which a nitroxide radical and a fullerene C(60) moiety were kept
15 mechanistic model that includes the observed nitroxide radical and C-nitroso compound intermediates h
16         The ORCA is based on spirocyclohexyl nitroxide radicals and poly(ethylene glycol) chains conj
17 al based on an oxoverdazyl core and nitronyl nitroxide radicals and successfully synthesized it using
18 eptide-based battery, in which viologens and nitroxide radicals are incorporated as redox-active grou
19                                              Nitroxide radicals are introduced into the reverse micel
20                                              Nitroxide radicals are paramagnetic contrast agents, use
21                                       Stable nitroxide radicals are potent antioxidants and are among
22                            Structures of the nitroxide radicals are supported by X-ray crystallograph
23 d their one-electron oxidation products, the nitroxide radicals, as intermediates in this pathway.
24 ements larger than 10 were obtained with bis-nitroxide radical at 14.1 T and low temperature ( approx
25 space coupling is found between the diagonal nitroxide radicals at the conformationally constrained N
26 tic resonance (EPR) spectroscopy of a stable nitroxide radical attached site-specifically to a macrom
27                                        These nitroxide radical-based nanostructures have longitudinal
28 arization of solvent molecules that approach nitroxide radical-based spin labels within <5-10 A.
29 g both axial and equatorial hydroxyl groups, nitroxide-radical-based reagents should be the first cho
30 ound, which is transformed into a persistent nitroxide radical by further photolysis.
31  recent reports that the coupling factor for nitroxide radicals cannot be quantified due to the diffi
32 ween the chloroacetamide 2,6-diazaadamantane nitroxide radical (ClA-DZD) and cucurbit[7]uril (CB-7),
33 n ubiquitin in the presence of two different nitroxide radical cosolutes, at multiple static magnetic
34                                              Nitroxide radicals could be converted to their correspon
35  bulky N-substituents R(1) and R(2) prevents nitroxide radical dimerization, ensuring their kinetic s
36                  With one model 2,2,6,6-TMPi nitroxide radical, evidence for an alternate pathway, wh
37 ical, consisting of oxoverdazyl and nitronyl nitroxide radical fragments, with a quartet ground state
38 orous volumes up to 80% and concentration of nitroxide radicals grafted in the bulk matrix up to 285
39 e examine a family of polythiophenes bearing nitroxide radical groups, showing that while both specie
40 TEMPO oxoammonium salts and three homologous nitroxide radicals have been prepared and characterized.
41                      This is ascribed to the nitroxide radicals having different orientations with re
42                                    We attach nitroxide radicals (i.e., spin labels) to multiple phosp
43 ument, a technique was developed for imaging nitroxide radicals in the whole stomach.
44 tation of PTH1R[168-198] was determined from nitroxide-radical induced relaxation of NMR signals util
45                              On the basis of nitroxide radical-induced relaxation studies, the centra
46   Through-bond coupling between the adjacent nitroxide radicals is mediated by the nitroxide-m-phenyl
47 romophores (E(red) = -1158 mV) with nitronyl nitroxide radical moieties via selective deprotection/ox
48 standing of the redox chemistry of a pair of nitroxide radicals-oxoammonium cations.
49 the buffer solution, respectively, and (B) a nitroxide radical partitioning between polar (aqueous) a
50                                              Nitroxide radicals possess important antioxidant activit
51 x at room temperature, the bis-spiro-oxetane nitroxide radical possesses electron spin coherence time
52 ylpiperidine (PP-H), which produces a stable nitroxide radical (PP(*)) product upon reaction with O(2
53            An improved method that employs a nitroxide radical probe (3AP) has been developed and uti
54 tane and bis-spiro-tetrahydrofuran pyrroline nitroxide radicals relies on the Mitsunobu reaction-medi
55 tetramethylrhodamine (5-TAMRA) and the small nitroxide radical TEMPO were synthesized and tested to i
56 I) chromophore covalently linked to a stable nitroxide radical (TEMPO) by optical and electron parama
57 ected spin labeling (SDSL) utilizes a stable nitroxide radical to obtain structural and dynamic infor
58 tilizes site-specific attachment of a stable nitroxide radical to probe the structure and dynamics of
59 rand 6 (Val-95), due to the proximity of the nitroxide radical to the backbone 15N and NH nuclei of t
60                        The ability of stable nitroxide radicals to detoxify hypervalent heme proteins
61                            The conversion of nitroxide radicals to the 2,2-DMPy products by CYP3A4 or
62                                   Use of the nitroxide radical trap TEMPO affords phosphonate 10, pre
63 cleotide-independent labeling scheme, stable nitroxide radicals were attached to eight specific pRNA
64 pening metathesis polymerization (ROMP), and nitroxide radicals were incorporated at three different
65                                              Nitroxide radicals were introduced at selected positions
66 DI) chromophores covalently linked to stable nitroxide radicals were synthesized and investigated by
67 ad portion of XJB-5-131 consists of a stable nitroxide radical, which has been extensively investigat
68  (EPR) spectra of natural-isotopic-abundance nitroxide radicals, which are ubiquitously used as repor
69 lutathionyl radical (GS(*)), interactions of nitroxide radicals with GS(*) and thiols have not been s
70 ys, a mechanism involving interaction of the nitroxide radicals with heme iron (Fe(III)), followed by
71 determined whether this novel interaction of nitroxide radicals with heme iron has any relevance in r