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1 2NiO4+delta as a model system for a combined paramagnetic (17)O NMR and DFT methodology, the approach
3 In this system, a gadolinium-based nonionic paramagnetic agent is used in conjunction with magnetic
6 studying the local environment of Li ions in paramagnetic battery materials, the use of (17)O NMR in
8 netic sticks that capture protein A/G-coated paramagnetic beads bound to antibody-luciferase-labeled
9 s, were chemically coupled to the surface of paramagnetic beads for the sensitive detection of ricin
10 ceeding 0.2 eV, indicating that the observed paramagnetic behavior around 10K is due to superparamagn
11 Magnetization studies revealed nearly ideal paramagnetic behavior at high temperatures for both radi
13 displays Pauli-like temperature independent paramagnetic behavior, with chiTIP = 6 x 10(-4) emu mol(
14 he pyrene knots, enabling the formation of a paramagnetic carbon structure with high spin density.
15 s by selectively doping one component with a paramagnetic center in order to measure the domain size
18 the existence of exchange coupling among the paramagnetic centers mediated by the conduction electron
19 the nanostructure, the photoluminescence and paramagnetic characteristic of Gd2O3:Eu(3+) nanorods wer
20 c exchange coupling to enable observation of paramagnetic chemical exchange saturation transfer (PARA
21 us solid-solid transition in a 2D crystal of paramagnetic colloidal particles is induced by a magneti
22 /EDTA extracts of a grassland soil, of which paramagnetic contaminations were removed with sodium sul
23 Es) and heteronuclear (1)H-(15)N NOEs if the paramagnetic contribution to the longitudinal relaxation
24 ysis reveals the dominating influence of the paramagnetic contribution yielding a highly deshielded a
27 hancement (sPRE) in the presence of an inert paramagnetic cosolute allows the assessment of protein d
30 al (delta(orb), temperature-independent) and paramagnetic (delta(para), temperature-dependent) contri
32 In magnetically doped semiconductors, where paramagnetic dopants (such as Mn(2+), Co(2+) and so on)
33 onance tuning (MRET), which occurs between a paramagnetic 'enhancer' and a superparamagnetic 'quenche
35 ne-electron reduction yields a spin-coupled, paramagnetic Fe(III)/Fe(IV) intermediate, denoted X, who
38 prosthetic groups of the globin chains: from paramagnetic ferrous Hb to diamagnetic ferrous oxyhemogl
39 s that coat the entire enzyme surface with a paramagnetic field of sufficient strength to determine i
42 it qualitatively resembles V(CO)6 , the only paramagnetic homoleptic metal carbonyl isolable under am
43 e technique transfers spin polarization from paramagnetic impurities at nanodiamond surfaces to (1)H
44 atial and temporal properties of the surface paramagnetic impurities provide insight to prolonging th
45 -field theory (LDA+DMFT) we characterize its paramagnetic insulating and metallic phases, showing the
46 ctron spectroscopy-the band structure of the paramagnetic insulating phase of Ca2RuO4 and show how it
47 resence of magnetic interactions between the paramagnetic interlayer V ions and a Kondo screening of
48 hich phases have different concentrations of paramagnetic ions, the phases can provide different reso
50 a have recently been discovered in oxides of paramagnetic Ir(4+) ions, widely known as 'iridates'.
52 he same sample preparation (i.e., mutations, paramagnetic labeling, and reconstitution in lipid bilay
54 are invoked by the covalent attachment of a paramagnetic lanthanoid chelating tag to the ligand of i
55 e induced throughout a 40-nm-thick amorphous paramagnetic layer through proximity to ferromagnets, me
56 that probe the local environment around O in paramagnetic Li-ion cathode materials are essential in o
59 l nitronyl nitroxides via the interaction of paramagnetic lithium derivatives as C-nucleophiles with
60 ic materials, such as diamagnetic copper and paramagnetic manganese, to overcome the Stoner criterion
61 levitation (MagLev) of diamagnetic or weakly paramagnetic materials suspended in a paramagnetic solut
63 nd magnetic properties of giant 3d and 3d/4f paramagnetic metal clusters in moderate oxidation states
64 In nuclear magnetic resonance (NMR), the paramagnetic metal ion interacting with the sugars cause
66 ntiferromagnetic insulator SrMnO3 and the 5d paramagnetic metal SrIrO3 is enormously strong, yielding
67 resonance (EPR) spectroscopy to characterize paramagnetic metal-organic and free radical species from
72 ted aggregation of fluorescent reporters and paramagnetic nanoparticle in a sandwich immunoassay was
79 ith some success for many decades to explain paramagnetic NMR pseudocontact shifts, and has been the
82 developed a novel docking strategy guided by paramagnetic NMR that positions a triple-helical collage
86 The simple, rapid magnetic manipulation of paramagnetic particles (PMPs) paired with the wide range
93 a recently developed multifunctional trityl paramagnetic probe and electron paramagnetic resonance (
95 ight-controlled effects observed for GNRs on paramagnetic properties and activities of surrounding mo
99 d-state quenching via (1) energy transfer or paramagnetic quenching by the Co(II) species and (2) exc
100 henylazoimidazole-based PDLs that switch the paramagnetic ratio of the investigated nickel species by
102 The structure was modeled using long-range paramagnetic relaxation enhancement (PRE) distance restr
105 1)H nuclear Overhauser enhancement (NOE) and paramagnetic relaxation enhancement (PRE) techniques.
106 nuclear magnetic resonance experiments using paramagnetic relaxation enhancement (PRE), which is sens
107 how that the accurate measurement of solvent paramagnetic relaxation enhancement (sPRE) in the presen
111 coupling data, amide protection factors, and paramagnetic relaxation enhancement distances, in combin
117 n with liposomes is mapped by intermolecular paramagnetic relaxation enhancement using Gd(3+)-tagged
119 are encounter complexes using intermolecular paramagnetic relaxation enhancement, a highly sensitive
121 r tags that can aid in the interpretation of paramagnetic relaxation enhancement, double electron-ele
126 of spin-label conformers against intradomain paramagnetic relaxation enhancements with a genetic algo
131 ted in more detail by time-resolved electron paramagnetic resonance (EPR) and quantum chemical calcul
134 of MCR-ALS, for the first time, on electron paramagnetic resonance (EPR) imaging data sets that will
144 family by magnetometry, optical and electron paramagnetic resonance (EPR) spectroscopies and modellin
145 ption (XAS), and emission (XES) and electron paramagnetic resonance (EPR) spectroscopies in the solid
146 and continuous wave (CW) and pulsed electron paramagnetic resonance (EPR) spectroscopies revealed tha
147 oupled to UV/visible absorption and electron paramagnetic resonance (EPR) spectroscopies support a me
148 uclear Magnetic Resonance (NMR) and Electron Paramagnetic Resonance (EPR) spectroscopies to distingui
150 (Ph4P)2[VO(C3S4O)2] (4), by pulsed electron paramagnetic resonance (EPR) spectroscopy and compared t
152 e been employed in combination with electron paramagnetic resonance (EPR) spectroscopy at defined ele
153 n of magnetic anisotropy using both electron paramagnetic resonance (EPR) spectroscopy for its experi
155 el was fitted to 180 data points of electron paramagnetic resonance (EPR) spectroscopy measurements o
156 , we report that absorption-display electron paramagnetic resonance (EPR) spectroscopy of nonirradiat
157 In the first use of high-field electron paramagnetic resonance (EPR) spectroscopy to characteriz
158 his series of molecules with pulsed electron paramagnetic resonance (EPR) spectroscopy to determine t
159 mplex, as demonstrated by (1)H NMR, electron paramagnetic resonance (EPR) spectroscopy, equilibrium d
167 n aqueous solution using an in situ electron paramagnetic resonance (EPR) spin trapping technique and
168 ional trityl paramagnetic probe and electron paramagnetic resonance (EPR) technique for in vivo concu
170 stigated by time-resolved and pulse electron paramagnetic resonance (EPR) with laser excitation.
172 visible-near-infrared (UV-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear magnetic re
173 We have used chemical synthesis, electron paramagnetic resonance (EPR), and circular dichroism to
174 magnetic circular dichroism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption,
175 Here, we used a combination of electron paramagnetic resonance (EPR), stopped flow freeze quench
176 at these probes in combination with electron paramagnetic resonance (EPR)-based spectroscopy and imag
178 as investigated with spectroscopic (electron paramagnetic resonance [EPR] and UV-vis) and theoretical
181 acterization of the intermediate by electron paramagnetic resonance and (13)C, (57)Fe electron nuclea
182 e/spin exchange rates determined by electron paramagnetic resonance and by molecular structural level
184 man cytochrome P450 3A4 (CYP3A4) by electron paramagnetic resonance and fluorescence spectroscopy.
185 been characterized by 9 and 130 GHz electron paramagnetic resonance and high-field electron nuclear d
186 at pH 1, which is characterized by electron paramagnetic resonance and in situ X-ray absorption spec
187 derived from a combined analysis of electron paramagnetic resonance and inductively coupled plasma sp
188 analyzed by X-ray crystallography, electron paramagnetic resonance and optical spectroscopy, and den
189 and nitric oxide bioavailability by electron paramagnetic resonance and phosphorylation of vasodilato
191 obtained from variable-temperature electron paramagnetic resonance and ultraviolet-visible spectrosc
192 application of Raman spectroscopy, electron paramagnetic resonance and UV-vis absorption spectroscop
193 m nitrite in erythrocytes including electron paramagnetic resonance detection of nitrosyl hemoglobin,
195 erformance of nanometer-range pulse electron paramagnetic resonance distance measurements (pulsed ele
196 e probed the protomer arrangement by solvent paramagnetic resonance enhancement, analysis of chemical
197 of these mutants led us to a set of electron paramagnetic resonance experiments that provide evidence
198 is study, continuous-wave and pulse electron paramagnetic resonance in a native outer-membrane prepar
202 We have also characterized the electron paramagnetic resonance signal of the molybdenum center i
204 we are able to clearly identify the electron paramagnetic resonance signals for four of the iron/sulf
205 quency-domain Fourier-transform THz electron paramagnetic resonance spectra obtained on Mn2Os.7MeOH a
206 by pressure-induced changes in the electron paramagnetic resonance spectra of a nitroxide side chain
208 nfrared, electronic absorption, and electron paramagnetic resonance spectra of MeC3Me ((3)3) are comp
212 in-depth time-resolved optical and electron-paramagnetic resonance spectroscopic study of two crypto
219 pre-steady state kinetic analyses, electron paramagnetic resonance spectroscopy and single crystal X
220 of Singlet Oxygen Sensor Green, by electron paramagnetic resonance spectroscopy and the induction of
221 nd characterized by IR, UV-vis, and electron paramagnetic resonance spectroscopy as well as by quantu
224 molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a pivotal r
228 Electronic and variable-temperature electron paramagnetic resonance spectroscopy of the mixed-valence
229 on, near-UV circular dichroism, and electron paramagnetic resonance spectroscopy provide evidence tha
231 cavities, and variable-temperature electron paramagnetic resonance spectroscopy shows that a dilute
232 tion spectroscopy and freeze-quench electron paramagnetic resonance spectroscopy support the presence
233 rein, voltammetry was combined with electron paramagnetic resonance spectroscopy to identify and defi
234 we use site-directed spin-labeling electron paramagnetic resonance spectroscopy to investigate confo
235 he use of time-resolved optical and electron paramagnetic resonance spectroscopy to probe singlet fis
236 ) in its resting conformation using electron paramagnetic resonance spectroscopy together with bioche
237 is-copper six-porphyrin nanoring by electron paramagnetic resonance spectroscopy via measurement of t
238 e mechanism of maltose stimulation, electron paramagnetic resonance spectroscopy was used to study th
245 )-derived radical was identified by electron paramagnetic resonance spin trapping, immunospin trappin
252 ransmission electron microscopy and electron paramagnetic resonance to show that the presence of anio
253 directed spin labeling coupled with electron paramagnetic resonance to test the first 88 amino acids
254 e spectroscopically (UV/visible and electron paramagnetic resonance) distinct heme environments were
255 g structure determination with EPR (electron paramagnetic resonance) spectroscopy and simulation, sho
256 assessed by electronic absorption, electron paramagnetic resonance, and Mn K-edge X-ray absorption m
257 high-resolution mass spectrometry, electron paramagnetic resonance, and nuclear magnetic resonance s
258 n characterized by resonance Raman, electron paramagnetic resonance, and X-ray absorption spectroscop
259 its metallocofactors by UV-visible, electron paramagnetic resonance, hyperfine sublevel correlation (
260 oscopy, nuclear magnetic resonance, electron paramagnetic resonance, infrared and Raman spectroscopy,
261 terizations (electronic absorption, electron paramagnetic resonance, X-ray absorption spectroscopies)
263 n application example, droplets containing a paramagnetic salt and doxorubicin (leukemia drug) are ma
266 manipulation, where droplets instead contain paramagnetic salts with molar magnetic susceptibilities
267 the two radicals is imagined to react with a paramagnetic scavenger via spin-selective electron trans
268 etwork solid composed of Fe(III) centers and paramagnetic semiquinoid linkers, (NBu4)2Fe(III)2(dhbq)3
269 This work demonstrates that lanthanide-based paramagnetic shift reagents can be designed to detect im
270 7)Fe hyperfine coupling interaction with the paramagnetic signal, which indicates that the iron-sulfu
272 The methodology for studying (17)O shifts in paramagnetic solids described in this work will be usefu
273 weakly paramagnetic materials suspended in a paramagnetic solution in a magnetic field gradient provi
274 rticles heated or cooled in certain polar or paramagnetic solvents may behave as if they carry an ele
277 e to identify for the first time the various paramagnetic species present in the native state of thes
278 n-group and transition-metal diamagnetic and paramagnetic species, and to bind strongly to metal cent
281 ins usually lack reactive cysteines and that paramagnetic spin labels entering the periplasm are sele
282 e material of interest (doping/attachment of paramagnetic spin labels to biomolecules of interest).
285 Using ESR to trace the reactionary path of paramagnetic spins or spin-active proxy molecules provid
286 sing ferromagnetic La2/3Sr1/3MnO3 (LSMO) and paramagnetic SrIrO3 (SIO) are synthesized with the preci
288 ition temperature (between ferromagnetic and paramagnetic states) using very small fields (smaller th
289 the addition of exogenous superoxide via the paramagnetic superoxide donor potassium dioxide or super
291 rtant materials for electrical conductivity, paramagnetic susceptibility, optical nonlinearity, photo
296 tational manipulation of free-standing super-paramagnetic thin-film microplates using external magnet
297 lic chelates (e.g., DOTP(8-)) complexed with paramagnetic thulium (Tm(3+)), to generate pHe maps in r
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