ライフサイエンスコーパス: paramagnetic

1 th heterometallic metal-metal bonds that are paramagnetic.

2 of single-crystal X-ray crystallography and paramagnetic (1)H NMR spectroscopy, the results of which

3 Paramagnetic (1)H NMR studies establish that this valenc

4 In solution, both paramagnetic 3 and diamagnetic [3][GaCl(4)] exhibit simi

5 he photohole leads to conversion of Ag(+) to paramagnetic Ag(2+).

6 The addition of a paramagnetic agent increased the signal to noise ratio p

7 change in large protein complexes by using a paramagnetic agent to accelerate (15)N R(1rho) relaxatio

8 The magnetisation increase is strange as paramagnetic Al addition dilutes the ferromagnetic Fe/Co

9 We study the change in magnetisation with paramagnetic Al addition in the CoFeNi(0.5)Cr(0.5)-Al(x)

10 s subsequently probed in more detail using a paramagnetic alignment strategy, which revealed partial

11 Here we introduce a paramagnetic analog of the drug muscimol that enables ta

12 Biochemical, structural and paramagnetic analysis of two evolutionarily related SODs

13 milar absorption and emission mechanisms for paramagnetic and diamagnetic forms.

14 iplet ground state diatomic O(2) molecule is paramagnetic and exists in air as a free radical, constr

15 tic field-tuned tricritical point separating paramagnetic, antiferromagnetic, and metamagnetic phases

16 Ferrofluids, although reconfigurable, are paramagnetic at room temperature and lose their magnetiz

17 , based on conventional miniprep columns and paramagnetic bead-based purification, without the need t

18 is accomplished by conjugating substrates to paramagnetic beads and measuring the conversion of subst

19 microflow reactor is demonstrated by moving paramagnetic beads between two spatially separate soluti

20 ty of up to 10(-2) S/cm and room-temperature paramagnetic behavior with a spin concentration of ~10%.

21 gnetic HAp, all HAp:RE(3+) powders exhibited paramagnetic behavior.

22 Herein we report a paramagnetic beryllium radical cation, [(CAAC)(2)Be](+*)

23 Here, we report the synthesis of paramagnetic bidentate polypyridyl-ligated Ni halide and

24 We isolated a paramagnetic bimetallic Ni(III) intermediate featuring a

25 Manganese, a biologically active paramagnetic calcium analogue, provides novel intracellu

26 as in diamagnetic (SiP(3))Fe=CCH(3) and the paramagnetic cation S = 1/2 [(SiP(3))Fe=CCH(3)](+).

27 Remarkably, the inclusion of a paramagnetic center in the peptide increases the spin po

28 gnificant differences between the spectra of paramagnetic centers in two polymorphs, showing a potent

29 focused on the ligand shell surrounding the paramagnetic centre, seeking to increase rigidity or rem

30 We report a cobalt-based paramagnetic chemical exchange saturation transfer (PARA

31 Paramagnetic chemical exchange saturation transfer (para

32 nt field, the study of the CISS effect using paramagnetic chiral molecules, which could introduce ano

33 The substitution of paramagnetic chlorine atoms for IAEs proves the magnetic

34 Three paramagnetic Co(II) macrocyclic complexes containing 2-h

35 nd split H(2) have been extensively studied, paramagnetic complexes that exhibit this behavior remain

36 complex [(tBuO)(3)Mo=Mo(OtBu)(3)] and a new paramagnetic compound, [Mo(OtBu)(5)].

37 with dexmedetomidine/isoflurane and infused paramagnetic contrast (Gd-DOTA) into the cisterna magna

38 is problem, we synthesized a manganese-based paramagnetic contrast agent, ManICS1-AM, designed to per

39 or tracking glymphatic system transport with paramagnetic contrast such as gadoteric acid (Gd-DOTA) a

40 hancement (sPRE) in the presence of an inert paramagnetic cosolute allows the assessment of protein d

41 e translational diffusion coefficient of the paramagnetic cosolute, and the other residue specific.

42 The complement of paramagnetic Cu(II) ions in the Mnx protein complex was

43 The paramagnetic cyano-bridged complex PhB((t)BuIm)(3)Fe-NC-

44 e greater physical proximity between surface paramagnetic defects and outer nuclei to efficiently pol

45 nd offer an appealing platform because these paramagnetic defects can be optically polarized efficien

46 and nuclear spin relaxation induced by other paramagnetic defects set practical constraints difficult

47 The key intermediate is a paramagnetic dihydride complex, trans-Fe(III)(H)(2)(+),

48 quantum critical scaling place UTe(2) at the paramagnetic end of this ferromagnetic superconductor se

49 gle-resolved photoemission spectroscopy that paramagnetic EuRh(2)Si(2) has a large FS essentially sim

50 sition of the product cluster to one or more paramagnetic Fe(III) species over several hours explains

51 eports have shown that intracellular, (super)paramagnetic ferritin nanoparticles can gate TRPV1, a no

52 n spin resonance (ESR) spectroscopy measures paramagnetic free radicals, or electron spins, in a vari

53 v device, a cuvette containing a solution of paramagnetic gadolinium(III) chelate in a non-polar solv

54 We used a dinuclear paramagnetic gadolinium(III) complex chelate that change

55 single-molecule conductance measurements in paramagnetic heterometallic molecular wires.

56 The pK(a)(MeCN)([MHL(n)](+)/[ML(n)) of paramagnetic hydrides in MeCN are estimated for the firs

57 Twenty paramagnetic hydrides prepared in bulk all have pK(a)(LA

58 Remarkably, the paramagnetic-induced shift of water (1) H NMR resonances

59 resence of magnetic interactions between the paramagnetic interlayer V ions and a Kondo screening of

60 xpel N(2) only above 60 degrees C, affording paramagnetic intermediates that convert to the correspon

61 cking include labelling the cells with Super Paramagnetic Iron Oxide nanoparticles (SPIOs).

62 d P2RY12, and phagocytosed micron-size super-paramagnetic iron oxides.

63 ent of NMR perturbations after site-specific paramagnetic labeling.

64 ntly, there is significant interest in novel paramagnetic labels for enhanced NMR studies on biomolec

65 Alignment of the helix by a paramagnetic lanthanide ion attached to its N-terminal r

66 menon of levitating particles suspended in a paramagnetic liquid under a nonuniform magnetic field, i

67 etic susceptibility effects arising from the paramagnetic lithium metal were used to distinguish betw

68 c polarizations of quantum paraelectrics and paramagnetic materials have in many cases been found to

69 t because they are shielded by an opaque and paramagnetic matrix.

70 The results presented show that MAS-DNP from paramagnetic metal ion dopants provides an efficient app

71 Recently, an alternative in the form of paramagnetic metal ions has emerged.

72 arkable relaxation effects in the absence of paramagnetic metal ions.

73 he 3D perovskite LaNiO(3), an unconventional paramagnetic metal, and the layered Ruddlesden-Popper ph

74 ions behave like the fermionic carriers of a paramagnetic metal.

75 novel protonated compound of HSrRuO(3) with paramagnetic metallic as ground state.

76 ble artificial food particles, consisting of paramagnetic microscopic beads coated with dietary polys

77 suitable for chemical trace gas detection of paramagnetic molecules such as nitric oxide, nitrogen di

78 nly capable of detecting and quantifying one paramagnetic MRI contrast agent at a time.

79 unoassay based on fluorescence relocation to paramagnetic nanoparticles aligned to form beadlines in

80 s and longer peripentacene polymers reveal a paramagnetic nature and feature Kondo fingerprints at ea

81 lly synthesizing and characterizing a common paramagnetic Ni intermediate and establishing its cataly

82 entate polypyridyl-ligated Ni catalysts, and paramagnetic Ni(I) halide or aryl species are proposed i

83 metalloenzymes, but well-defined examples of paramagnetic nickel hydride complexes are largely limite

84 The reactivity of two paramagnetic nickel(I) compounds, CpNi(NHC) (where Cp=cy

85 actosidase, respectively, converts them into paramagnetic NiL(0) , which displays a single (19) F NMR

86 l laccase from Streptomyces coelicolor using paramagnetic NMR and electron paramagnetic resonance spe

87 Herein, a paramagnetic NMR strategy designed to detect the putativ

88 To elucidate the effect of the paramagnetic nuclei, monolayers of the peptide coordinat

89 clei, monolayers of the peptide coordinating paramagnetic or diamagnetic ions are prepared.

90 usive limits for magnetophoresis wherein the paramagnetic particles either aggregate near the magnet

91 Paramagnetic particles heavily decorated with anti-ERalp

92 The region of the localization of paramagnetic particles near the magnet decreases with in

93 Ferumoxytol is an ultrasmall super paramagnetic particles of iron oxide (USPIO) agent recen

94 elative magnetic energy of the suspension of paramagnetic particles.

95 tively consistent with the above scenario: a paramagnetic phase at large densities, a spontaneous tra

96 rly large in the high-temperature insulating paramagnetic phase near the Neel transition.

97 nsity, leading to an exotic ferromagnetic to paramagnetic phase transition.

98 spin-ordered and high temperature disordered paramagnetic phases.

99 ossover region between the ferromagnetic and paramagnetic phases.

100 transition from the rotationally disordered paramagnetic plastic crystal, Me-AZADO, to the ordered d

101 s large 4f-derived Fermi surface (FS) in the paramagnetic (PM) regime should be similar in shape and

102 inistered MRI contrast agent consisting of a paramagnetic polymer coating encapsulating a superparama

103 ments; (iv) structure determination; and (v) paramagnetic probe titration (PPT) to characterize the m

104 ints to the remarkable chemical stability of paramagnetic probes in historical bitumen in ancient Egy

105 carbonaceous radicals, which can be used as paramagnetic probes to investigate embalming materials w

106 reversible exchange processes as functional paramagnetic probes.

107 allows us to overcome the "blind sphere" in paramagnetic proteins, and to observe and assign (1)H, (

108 ormance in a molecular separation system for paramagnetic rare-earth cations.

109 ess in the understanding of melanin optical, paramagnetic redox, and conductivity properties, includi

110 ated Pin1 interdomain interactions using NMR paramagnetic relaxation enhancement (PRE) and molecular

111 Paramagnetic relaxation enhancement (PRE) is commonly us

112 Here we use paramagnetic relaxation enhancement (PRE) measured by NM

113 Paramagnetic relaxation enhancement (PRE) NMR and chemic

114 perturbations and intra- and intermolecular paramagnetic relaxation enhancement (PRE) NMR data revea

115 o study KRAS dimerization on nanodiscs using paramagnetic relaxation enhancement (PRE) NMR spectrosco

116 1)H nuclear Overhauser enhancement (NOE) and paramagnetic relaxation enhancement (PRE) techniques.

117 We have, moreover, used paramagnetic relaxation enhancement (PRE) to characteriz

118 how that the accurate measurement of solvent paramagnetic relaxation enhancement (sPRE) in the presen

119 n protein-cosolute interactions from solvent paramagnetic relaxation enhancement (sPRE) measurements.

120 simulated annealing driven by intermolecular paramagnetic relaxation enhancement data.

121 NMR paramagnetic relaxation enhancement experiments demonstr

122 chemical shifts, residual dipolar couplings, paramagnetic relaxation enhancement, and NMR relaxation

123 nment allows the use of previously published paramagnetic relaxation enhancements to evaluate placeme

124 n the two regions using a combination of NMR paramagnetic relaxation enhancements, residual dipolar c

125 nsumption experiments, coupled with electron paramagnetic resonance (EPR) analyses and DFT calculatio

126 zacyclotetradecane-1-acetato) using electron paramagnetic resonance (EPR) and (57)Fe Mossbauer spectr

127 radical species through the use of electron paramagnetic resonance (EPR) and electron nuclear double

128 ption and rapid freeze-quench (RFQ) electron paramagnetic resonance (EPR) and magnetic circular dichr

129 Electron paramagnetic resonance (EPR) at the X-band, combining in

130 Electron paramagnetic resonance (EPR) distance measurements are m

131 o the recent progress in biomedical electron paramagnetic resonance (EPR) due to their unmatched stab

132 Variable-temperature electron paramagnetic resonance (EPR) experiments show that the n

133 Electron paramagnetic resonance (EPR) has become an important too

134 A focus on electron paramagnetic resonance (EPR) imaging shows the validatio

135 Pulse electron paramagnetic resonance (EPR) is being applied to ever mo

136 ht into the catalytic mechanism via electron paramagnetic resonance (EPR) is not generally possible.

137 Variable-temperature electron paramagnetic resonance (EPR) measurements and relaxation

138 5 nm) activation of NADH coupled to electron paramagnetic resonance (EPR) measurements to study elect

139 ic beverages is determined using an electron paramagnetic resonance (EPR) method, which is based on a

140 re shown to correlate directly with electron paramagnetic resonance (EPR) parameters such as the tyro

141 a spectrum of the modulation of an electron paramagnetic resonance (EPR) signal by a tuneable optica

142 The S(3)' electron paramagnetic resonance (EPR) signal is significantly bro

143 from the observation of a multiline electron paramagnetic resonance (EPR) signal with effective total

144 Combined with X-band electron paramagnetic resonance (EPR) spectral analysis, this ind

145 vestigated based on mutagenesis and electron paramagnetic resonance (EPR) spectroscopic approaches.

146 Although the optical and electron paramagnetic resonance (EPR) spectroscopic signatures of

147 t 85 K, and time-resolved and pulse electron paramagnetic resonance (EPR) spectroscopies are used to

148 biothiols in a single sample, using electron paramagnetic resonance (EPR) spectroscopy and a trityl-r

149 ble radicals was investigated using electron paramagnetic resonance (EPR) spectroscopy and compared w

150 Electron paramagnetic resonance (EPR) spectroscopy indicates the

151 el was fitted to 180 data points of electron paramagnetic resonance (EPR) spectroscopy measurements o

152 ng several techniques, we show that electron paramagnetic resonance (EPR) spectroscopy of oligonucleo

153 ing site-directed spin labeling and electron paramagnetic resonance (EPR) spectroscopy of protein bou

154 Electron-paramagnetic resonance (EPR) spectroscopy of stretched r

155 Electron paramagnetic resonance (EPR) spectroscopy proved that th

156 sive highlights of the results from Electron Paramagnetic Resonance (EPR) spectroscopy to explain the

157 spin qubits are studied with pulsed electron paramagnetic resonance (EPR) spectroscopy under electric

158 In the current study, electron paramagnetic resonance (EPR) spectroscopy was employed t

159 ermeation chromatography (GPC), and electron paramagnetic resonance (EPR) spectroscopy were used to e

160 bsorption, cyclic voltammetry (CV), electron paramagnetic resonance (EPR) spectroscopy, and theoretic

161 itored by UV-vis microspectroscopy, electron paramagnetic resonance (EPR) spectroscopy, and X-ray cry

162 Electron paramagnetic resonance (EPR) spectroscopy, coupled with

163 ution three-dimensional structures, electron paramagnetic resonance (EPR) spectroscopy, quantum mecha

164 Magnetic susceptibility, electron paramagnetic resonance (EPR) spectroscopy, X-ray absorpt

165 at room temperature as observed by electron paramagnetic resonance (EPR) spectroscopy.

166 in all 18 white wines analysed by electronic paramagnetic resonance (EPR) spectroscopy.

167 Mnx protein complex was examined by electron paramagnetic resonance (EPR) spectroscopy.

168 (IVIS), and quantified ex vivo via electron paramagnetic resonance (EPR) spectroscopy.

169 Thermosynechococcus elongatus using electron paramagnetic resonance (EPR) spectroscopy: E(m) Q(B)/Q(B

170 able triarylmethyl spin probe whose electron paramagnetic resonance (EPR) spectrum is highly sensitiv

171 Electron paramagnetic resonance (EPR) studies of the rhenium(II)

172 Detailed electron paramagnetic resonance (EPR) studies, isotopic labeling,

173 we have performed an integrated NMR/electron paramagnetic resonance (EPR) study into the detailed asp

174 turbid media, the properties of the electron paramagnetic resonance (EPR) technique make it suitable

175 on products of Cp*(2)Co using pulse electron paramagnetic resonance (EPR) techniques at low temperatu

176 ly undergo bioconjugation, by using electron paramagnetic resonance (EPR) to measure conformational d

177 ization was carried out via UV-vis, electron paramagnetic resonance (EPR), (57)Fe Mossbauer, Fe X-ray

178 niques including UV-vis absorption, electron paramagnetic resonance (EPR), and X-ray absorption spect

179 tes in addition to O(2) Here, using electron paramagnetic resonance (EPR), Mossbauer, and UV-visible

180 magnetic circular dichroism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption,

181 ay, dynamic light scattering (DLS), electron paramagnetic resonance (EPR), UV-vis, fluorescence, and

182 or winemaking) were investigated by electron paramagnetic resonance (EPR).

183 13)CN-labeled enzyme as verified by electron paramagnetic resonance (EPR)/electron nuclear double-res

184 High-frequency and -field electron paramagnetic resonance (HFEPR) spectroscopy confirms thi

185 a combination of X-ray scattering, electron paramagnetic resonance (in the case where the metal cati

186 UV-visible spectroscopy and electron paramagnetic resonance analyses confirmed the formation

187 use combined mutagenesis and pulse electron paramagnetic resonance analyses to establish histidine-4

188 rial homolog leucine transporter by electron paramagnetic resonance analysis and X-ray crystallograph

189 Electron paramagnetic resonance analysis further revealed that ad

190 aled more perfusion, and functional electron paramagnetic resonance analysis revealed more oxygen in

191 In line with these observations, electron paramagnetic resonance analysis suggested that 10E8 inhi

192 Electron paramagnetic resonance and density functional theoretica

193 ando X-ray absorption spectroscopy, electron paramagnetic resonance and density-functional theory sim

194 According to electron paramagnetic resonance and diffuse-reflectance infrared

195 (4+) was unambiguously confirmed by electron paramagnetic resonance and magnetometry.

196 Electron paramagnetic resonance and X-ray absorption spectroscopi

197 Biochemical and continuous wave electron paramagnetic resonance data demonstrate the inability of

198 high resolution in double electron-electron paramagnetic resonance distance measurements.

199 d-state NMR data and newly acquired electron paramagnetic resonance double electron-electron resonanc

200 We make predictions for electron paramagnetic resonance experiments and analyze experimen

201 Electron paramagnetic resonance experiments provide critical vali

202 Electron paramagnetic resonance experiments show that the extent

203 eveloped new hyperpolarized MRI and electron paramagnetic resonance imaging procedures that allow mor

204 nd the ability to label and perform electron paramagnetic resonance in cells is expected to be applic

205 a cryoreduction approach coupled to electron paramagnetic resonance measurements to study electron tr

206 etermination of CntA and subsequent electron paramagnetic resonance measurements uncover the molecula

207 y means of transient absorption and electron paramagnetic resonance measurements.

208 distance measurements derived from electron paramagnetic resonance of a bifunctional spin label (BSL

209 previous study from continuous-wave electron paramagnetic resonance of myosin labeled at specific sit

210 ermination, were investigated using electron paramagnetic resonance of spin probes doped into the mic

211 In the electron paramagnetic resonance spectra, at least two forms are o

212 l of this spin qubit with a 240 GHz electron paramagnetic resonance spectrometer powered by a free el

213 We present biochemical and electron paramagnetic resonance spectroscopic characterization mo

214 UV-visible and electron paramagnetic resonance spectroscopies are consistent wit

215 quantification, and UV-visible and electron paramagnetic resonance spectroscopies to investigate Uvr

216 ure, using stopped-flow optical and advanced paramagnetic resonance spectroscopies.

217 ic resonance, (57)Fe Mossbauer, and electron paramagnetic resonance spectroscopies.

218 modes was done by using UV/Vis and Electron Paramagnetic Resonance spectroscopies.

219 Electron paramagnetic resonance spectroscopy (EPR) is a uniquely

220 thesized and analyzed by UV-vis and electron paramagnetic resonance spectroscopy and by X-ray crystal

221 of the surfactants' monolayer using electron paramagnetic resonance spectroscopy and dynamic light sc

222 mation of the former is inferred by electron paramagnetic resonance spectroscopy and its abstraction

223 ed recombinantly produced HoxEFU by electron paramagnetic resonance spectroscopy and kinetic assays w

224 As shown by combined high-field electron paramagnetic resonance spectroscopy and magnetization me

225 Electron paramagnetic resonance spectroscopy and X-ray photoelect

226 Electron paramagnetic resonance spectroscopy and X-ray photoelect

227 Electron paramagnetic resonance spectroscopy confirms that the te

228 cent advances in the application of electron paramagnetic resonance spectroscopy have demonstrated th

229 er after 7 d as determined from the electron paramagnetic resonance spectroscopy measurements of inta

230 As determined by electron paramagnetic resonance spectroscopy of intermediates, th

231 by site-directed spin labeling and electron paramagnetic resonance spectroscopy of melanopsin, the r

232 rium-exchange mass spectrometry and electron paramagnetic resonance spectroscopy reveal an asymmetry

233 Time-resolved electron paramagnetic resonance spectroscopy shows that the (T(1)

234 ) and D(*+) spin states using pulse electron paramagnetic resonance spectroscopy shows that the spin

235 Applying cryogenic infrared and electron paramagnetic resonance spectroscopy to an [FeFe] model h

236 time-resolved mass spectrometry and electron paramagnetic resonance spectroscopy to determine how the

237 we used site-directed spin-labeling electron paramagnetic resonance spectroscopy to examine the inter

238 ing site-directed spin labeling and electron paramagnetic resonance spectroscopy to improve protein s

239 oit species-selective scavengers in electron paramagnetic resonance spectroscopy to sequester specifi

240 Continuous wave and pulsed electron paramagnetic resonance spectroscopy was used to study th

241 cryogenic X-ray diffraction at 6 K, electron paramagnetic resonance spectroscopy, and correlated elec

242 haracterized by means of UV-vis and electron paramagnetic resonance spectroscopy, cyclic voltammetry,

243 association by variable-temperature electron paramagnetic resonance spectroscopy, determining the mod

244 We sampled blood for oxidative (electron paramagnetic resonance spectroscopy, HPLC), nitrosative

245 ic modeling, X-ray crystallography, electron paramagnetic resonance spectroscopy, protein electrochem

246 ), as determined by magnetometry or electron paramagnetic resonance spectroscopy, respectively.

247 (*) and [LCuOOH](-) on the basis of electron paramagnetic resonance spectroscopy, the production of H

248 lf-decomposition, while detected by electron paramagnetic resonance spectroscopy, was unlikely to be

249 protein film electrochemistry, and electron paramagnetic resonance spectroscopy, we confirm the prev

250 re assessed by variable-temperature electron paramagnetic resonance spectroscopy, X-ray absorption sp

251 lecular structure determination and electron paramagnetic resonance spectroscopy.

252 elicolor using paramagnetic NMR and electron paramagnetic resonance spectroscopy.

253 (1)H nuclear magnetic resonance and electron paramagnetic resonance spectroscopy.

254 onfocal fluorescence microscopy and electron paramagnetic resonance spectroscopy.

255 y delocalized spin, as evidenced by electron paramagnetic resonance spectroscopy.

256 troscopies, cyclic voltammetry, and electron paramagnetic resonance spectroscopy.

257 roxymethyl radical was evaluated by electron paramagnetic resonance spectroscopy.

258 xed valence dirhodium species whose electron paramagnetic resonance spectrum revealed a delocalizatio

259 Continuous-wave and pulse electron paramagnetic resonance techniques are used to verify the

260 Here, we use pulse electron paramagnetic resonance to examine the conformations of t

261 spin-labeling and variable-pressure electron paramagnetic resonance to reveal them in a membrane prot

262 dependent and can be controlled by electron-paramagnetic resonance, affecting device resistance and

263 ion of hydrogen-deuterium exchange, electron paramagnetic resonance, and NMR spectroscopy experiments

264 in-state ice in neutron scattering, electron paramagnetic resonance, and thermodynamic experiments.

265 reover, Fourier transform infrared, electron paramagnetic resonance, and UV-visible spectroscopy stud

266 fraction, continuous wave and pulse electron paramagnetic resonance, density-functional theory calcul

267 dence (e.g., X-ray crystallography, electron paramagnetic resonance, electrochemistry) demonstrates t

268 gested that the analysis by ESR (or electron paramagnetic resonance, EPR) is suitable to evaluate, ei

269 deuterium labeling, radical clock, electron paramagnetic resonance, high-resolution mass spectrometr

270 Using a combination of electron paramagnetic resonance, on spin-labeled protein, and dis

271 and computational methods, such as electron paramagnetic resonance, solid-state ultraviolet-visible

272 ly probed with 2-dimensional pulsed electron paramagnetic resonance.

273 experiments, mass spectrometry and electron paramagnetic resonance.

274 analytical ultracentrifugation, and electron paramagnetic resonance.

275 etric method and by continuous-wave electron paramagnetic resonance.

276 -ray photoelectron spectroscopy and electron paramagnetic resonance.

277 se of NbP up to 60 tesla and uncover a Berry paramagnetic response, characteristic of the topological

278 Paramagnetic rim lesions, rare in other neurological con

279 iable on magnetic resonance imaging by their paramagnetic rims, and increasing evidence supports thei

280 The first is a paramagnetic (S = 1/2) cobalt(III)-superoxo species that

281 ing in a large animal model shows an infarct paramagnetic shift associated with duration of coronary

282 er, with a maximum Curie constant and Li NMR paramagnetic shift near a composition of Li(0.60)TiNb(2)

283 muted conspire to mask modest changes in NMR paramagnetic shifts, but are evident in Yb EPR and Eu em

284 We present a strategy that combines sparse paramagnetic solid-state NMR restraints with physics-bas

285 rticles heated or cooled in certain polar or paramagnetic solvents may behave as if they carry an ele

286 EPR study identified a potassiated paramagnetic species and multistate density function the

287 Relevant electrochemical surrogates of these paramagnetic species have been isolated.

288 Detection of diverse paramagnetic species is important in applications rangin

289 but also a local change of concentration of paramagnetic species is realized.

290 NMR experiments using paramagnetic spin labels reveal how SspH1 binds Ube2D~Ub

291 Cs (iRBCs) is changed due to ferric (Fe(3+)) paramagnetic state in hemozoin crystallites which induce

292 ition temperature (between ferromagnetic and paramagnetic states) using very small fields (smaller th

293 nce revealed that termites contained several paramagnetic substances in their bodies, such as Fe(3+),

294 e habenula is more associated with increased paramagnetic (such as iron) rather than decreased diamag

295 t in some cases, the data from only a single paramagnetic tag are sufficient for accurate folding.

296 t that polymer nanodiscs functionalized with paramagnetic tags can be used to speed-up data acquisiti

297 However, the transition from the photonic paramagnetic to photonic glass phase is more subtle in t

298 Here, we show a reversible paramagnetic-to-ferromagnetic transformation of ferroflu

299 bled the understanding of and the search for paramagnetic topological materials(5,6).

300 The proposal that paramagnetic transition metal complexes could be used as

301 Understanding the thermodynamics of paramagnetic transition metal hydride complexes, especia