ライフサイエンスコーパス: EPR

1 EPR (ESR) is a suitable noninvasive oximetry technique.

2 EPR analysis confirms the presence of the [5Fe-5S] clust

3 EPR analysis of the oxidized Gd-MoFeP P-cluster confirme

4 EPR and UV/vis spectroscopy as well as cyclic voltammetr

5 EPR confirmed the presence of Cu and Mn, further providi

6 EPR experiments and computational analysis support a rad

7 EPR measurements establish that the channels are inserte

8 EPR measurements show a distinct pattern of mobilities a

9 EPR measurements were carried out to establish starch su

10 EPR showed that a spin label inserted near the N-terminu

11 EPR spectra and Cl K-edge XAS for 3 are consistent with

12 EPR spectra collected over a range of potentials were de

13 EPR spectra exhibited signals similar to those of brain,

14 EPR spectra of the Cu(II) complexes exhibit an axially e

15 EPR spectra of the S2 state and flash-induced FTIR spect

16 EPR spectra were obtained for the spin-labeled ligands b

17 EPR spectra yield zero-field splitting parameters that a

18 EPR spectroscopy and headspace GC-MS analysis indicate t

19 EPR spectroscopy applying stable hydrophilic and hydroph

20 EPR spectroscopy confirms the presence of Mn(III) bound

21 EPR spectroscopy of 1 provides the first detailed study

22 EPR spectroscopy on Li[1] reveals hyperfine coupling of

23 EPR spectroscopy reveals both kinetic and thermodynamic

24 EPR spectroscopy shows that rotational motion of a nitro

25 EPR spectroscopy, SQUID magnetometry, and DFT calculatio

26 EPR studies exhibited a higher amount of free radicals f

27 EPR studies suggest the protein contains two Cu(II) spec

28 EPR, ENDOR, Mossbauer, and EXAFS analysis, coupled with

29 EPR/ENDOR/photophysical measurements on wild type (WT) M

30 The model was tested basing on 75 EPR spectroscopy measurements.

31 ic and spectroscopic (electronic absorbance, EPR) properties of KsHDH in comparison with the well def

32 probed extensively by UV-vis-NIR absorption, EPR, and electron nuclear double resonance (ENDOR) spect

33 d by cyclic voltammetry, optical absorption, EPR spectroscopy, X-ray crystallography, and DFT calcula

34 X-ray absorption, EPR, and resonance Raman spectroscopy highlight the chem

35 ut in situ 450 nm photolysis of E4(4H) in an EPR cavity at temperatures below 20 K.

36 Both UV-vis absorption and EPR spectroscopic studies suggest that the Nmar1307 can

37 polymerization of glyoxal/glyoxylic acid and EPR shows the formation of radical structures.

38 roups as follows: (i) EGF, amphiregulin, and EPR; and (ii) betacellulin, TGFalpha, and epigen.

39 hemistry, stopped-flow kinetic analyses, and EPR measurements were supported by the structural charac

40 Our FRET, biochemical and EPR analysis suggests that this fully closed conformatio

41 haracterization by X-ray crystallography and EPR spectroscopy of the nitrogenase molybdenum iron (MoF

42 ENDOR and EPR measurements show that photolysis generates a new Fe

43 yano species (S = 3/2), while IR, EXAFS, and EPR spectroscopies indicate [3](1-) to be an end-on supe

44 investigated by UV-vis-NIR, fluorescence and EPR spectroscopy, spectroelectrochemistry, and quantum c

45 and HbA is supported based on functional and EPR spectroscopic studies.

46 ical oxidation, and probed by vis-NIR-IR and EPR spectroscopies.

47 AM carboxylate-oxygen is an M(+) ligand, and EPR and circular dichroism spectroscopies reveal that bo

48 ns and confirmed with SQUID magnetometry and EPR spectroscopy, showing easy-axis or easy-plane magnet

49 Squid magnetometry and EPR studies yield data that are consistent with a single

50 electron and atomic force microscopies, and EPR.

51 cts were analyzed by UV/vis, NMR, GC-MS, and EPR.

52 ents and variable temperature UV-Vis-NIR and EPR spectroscopic data indicate that, relative to the sm

53 fibril core, we recorded solid-state NMR and EPR data on fibrils formed by the first 88 residues of O

54 The direct (13)C NMR and EPR spectra of the nitroxide free radicals and the oxoam

55 ces are observed in their respective NMR and EPR spectra of these species.

56 NMR and EPR spectroscopies are shown to be valuable tools to obs

57 rmination, vibrational spectroscopy, NMR and EPR spectroscopies, electrochemistry, X-ray absorption s

58 The structure, solved by solution NMR and EPR spectroscopy in membrane-mimetic environments, consi

59 ination of comprehensive mechanistic NMR and EPR studies, isolation of a key Ni(I) intermediate, and

60 Optical and EPR measurements highlight the presence of a Cu-Scys bon

61 4S] cluster was characterized by optical and EPR spectroscopies; it has a reduction potential of -370

62 Using spin probes and EPR spectroscopy, we have determined that both O2(*-) an

63 o CYP121 proceeds in a two-step process, and EPR spectroscopy indicates that the binding induces acti

64 The resonance Raman and EPR investigations reveal that 3 contains a low spin cob

65 lography, (57)Fe Mossbauer spectroscopy, and EPR spectroscopy were used to fully characterize these n

66 eaction, we report the crystal structure and EPR analysis of HydG.

67 at 100 K as well as at room temperature and EPR spectroscopy on a spin-labeled single crystal allows

68 pic techniques (IR absorption, NMR, VCD, and EPR) we gained clear evidence that both compounds adopt

69 In turn, combined UV-vis and EPR spectroscopic studies showed that a novel Cu(2+) sit

70 atrixes and characterized by IR, UV-vis, and EPR spectroscopies.

71 trix isolation spectroscopy (IR, UV-vis, and EPR) in combination with QM and QM/MM calculations.

72 We used UV-visible and EPR spectroscopy to characterize heme binding to DnrF an

73 ulation of muscle pain-related behaviors and EPRs after BAO.

74 R spectroscopy and in MTHF glasses by W-band EPR and Q-band ENDOR spectroscopy.

75 in argon matrices by IR, UV-vis, and X-band EPR spectroscopy and in MTHF glasses by W-band EPR and Q

76 X-band EPR was used to monitor the oxidation of DNA-bound Dps a

77 mounts, by comparing the correlation between EPR and AAS/ICP data for Mn(2+) standards with that for

78 Mg(2+)-bound and Mg(2+)-free conditions, but EPR spectroscopic studies reveal large Mg(2+)-driven qua

79 Compounds 1-3 were analyzed by EPR and NMR spectroscopy, DFT calculations, and X-ray cr

80 d derivative allowed its characterization by EPR, UV-vis, and CD spectroscopies, validating spin-delo

81 stable Rh(IV) form, which we characterize by EPR and UV-visible spectroscopy as well as X-ray crystal

82 ron traps were observed and characterized by EPR and optical spectroscopies.

83 radicals to be detected and characterized by EPR spectroscopy for the first time.

84 air-stable monoradicals and characterized by EPR spectroscopy.

85 (NO2)(N3PyS)](+), which was characterized by EPR, FTIR, UV-vis, and CSI-MS.

86 airs (3, 2; 5, 6) have been characterized by EPR, zero-field (57)Fe Mossbauer, magnetometry, single c

87 e alpha-carbon, enabling direct detection by EPR of peptide backbone structural dynamics.

88 s, the structures of which are determined by EPR spectroscopy.

89 r)L)Fe(NMes), respectively, as determined by EPR, zero-field (57)Fe Mossbauer, magnetometry, and sing

90 ...U(V) super-exchange coupling in dimers by EPR.

91 the mono-radicals have been distinguished by EPR spectroscpy and the ground state of the diradicals h

92 reaction has unequivocally been evidenced by EPR spectroscopy.

93 fic spin labeling of the Q-helix followed by EPR-based interspin distance analyses, closure and reope

94 -NN, PTP-NN, and PPP-NN were investigated by EPR and optical spectroscopy combined with DFT calculati

95 pping ability of 3 and 4 was investigated by EPR for oxygen- and carbon-centered radicals.

96 Preliminary mechanistic investigation by EPR spectroscopy and density functional theory calculati

97 nt as H-complexes (H-Mn(2+)), as measured by EPR of live, nonirradiated Mn-replete cells, is now the

98 und catenated sulfur products is provided by EPR and resonance Raman spectroscopy in addition to dens

99 Analysis of the copper-binding site by EPR showed a signal signature more similar to those obse

100 ons of the singly reduced radical species by EPR spectroscopy and DFT calculations verified delocaliz

101 These conclusions were substantiated by EPR data, isotopic labeling studies, and the use of radi

102 This notion is supported by EPR studies of the reaction mixtures.

103 (C5Me5)3Th, which has a characteristic EPR spectrum consistent with a d(1) ground state, has th

104 et band and appearance of the characteristic EPR signal at g = 4.3 during the oxidation, showing the

105 ared to WT Dps in forming the characteristic EPR signal at g = 4.3, consistent with W52 acting as an

106 lated from solution and fully characterized (EPR, X-ray crystallography).

107 As revealed by quantum chemistry, EPR measurements and transient absorption spectroscopy,

108 crystallography on all titanocene complexes, EPR and NMR spectroscopy, and DFT were used to support o

109 In contrast, EPR spectra of 2 show g values consistent with the DFT-c

110 of the FeMo-cofactor, and the corresponding EPR data shows a new S = 3/2 spin system with spectral f

111 responding complex by X-ray crystallography, EPR, and XAS spectroscopic methods.

112 Continuous-wave (CW) EPR spectra of samples of Mnx, prepared in atmosphere an

113 nt, analytical ultracentrifugation, and DEER EPR, indicate that the transmembrane domain is monomeric

114 ng double electron-electron resonance (DEER) EPR spectroscopy are generally limited to the 15-60 A ra

115 No age-dependent EPR trends were apparent.

116 Comparison of the dimer EPR spectra to those of Cu porphyrin monomers shows evid

117 rature photolysis of Ni-C yields distinctive EPR-active states, collectively termed Ni-L, that are at

118 ral artery disease (PAD) show an exaggerated EPR, sometimes report pain when walking and are at risk

119 oxygen species (ROS) mediate the exaggerated EPR associated with PAD.

120 f these catalytic mixtures generally exhibit EPR signals arising from two S = 1/2 intermediates, a hi

121 Computational simulation of the experimental EPR spectra, using a developed algorithm for J modulatio

122 The experimental EPR spectrum of copper-bound SliLPMO10E requires the sim

123 Although the lower-field EPR signals from the organic free radicals in fossil fue

124 ling the sample to cryogenic temperature for EPR analysis.

125 n states and (iii) mono- vs. multi-frequency EPR spectra.

126 Here, EPR and Mossbauer spectroscopies allow electronic charac

127 yferrous form, displays a ferric-hydroperoxo EPR signal, in contrast to the cryoreduced oxy-wild-type

128 tions of the measurements, specifically: (i) EPR spectra recorded under high vs. low frequency condit

129 ns with respect to magnetic anisotropy, (ii) EPR spectra of non-integer (Kramers) vs. integer (non-Kr

130 For paramagnetic Cr(III), EPR (HYSCORE) spectroscopy shows hyperfine coupling to n

131 In EPR studies of the oxidation of ferrous iron-loaded Dps

132 compounds are fully characterized, including EPR and CV studies for the radicals.

133 Indeed, EPR hyperspectral images provide spatial and spectral in

134 ed clusters display nearly indistinguishable EPR features, X-ray absorption spectroscopy/extended X-r

135 ction, and H/D exchange), spectroscopic (IR, EPR), and structural properties of the enzyme.

136 Kinetic EPR was employed to measure rate constants and Arrhenius

137 A well-known EPR-active state produced under H2 and known as Ni-C is

138 findings, in combination with spin-labeling/EPR spectroscopic measurements in reconstituted-membrane

139 pical of a Mn-peroxide species and a 29-line EPR signal typical of a Mn(II) Mn(III) entity.

140 te of Sc is also indicated by the eight-line EPR spectra arising from the I=7/2 (45) Sc nucleus.

141 he nitrones gave rise to a standard six-line EPR spectrum whose values were in agreement with the lit

142 Recent spectroscopic studies, mainly EPR, have come closest to obtaining a molecular mechanis

143 Moreover, EPR and ENDOR spectroscopies show that charge is equally

144 R, UV-vis-NIR, infra-red, (57) Fe-Mossbauer, EPR), X-ray crystallographic characterization of the clu

145 Use of Mossbauer, EPR, NMR, UV/Vis, and IR spectroscopy, in conjunction wi

146 presence of air, followed by HPLC, HPLC-MS, EPR, and UV-VIS spectroscopy analysis of the resulting m

147 Experimental (NMR, IR, MS, EPR, XAS, XRD) and computational data (DFT) support an o

148 of a combination of magnetic multiresonance (EPR) spectroscopies, comparison to biochemical models an

149 hophosphate, peptides), which exhibit narrow EPR signals (small zero-field splitting).

150 The new EPR spectroscopic probe of the diferric state indicated

151 complementary techniques, such as FTIR, NMR, EPR, and MALDI-ToF, were employed.

152 V-vis absorption, resonance Raman, (1)H NMR, EPR, and X-ray absorption (near-edge) spectroscopy, ESI

153 uctures are supported by (1)H and (17)O NMR, EPR, resonance Raman and UV-vis spectra, electrophoresis

154 ized by various spectroscopies (UV-vis, NMR, EPR, XAS, resonance Raman) and DFT calculations, followi

155 and UV-vis spectra as well as the absence of EPR signals demonstrate a singlet ground state of the zw

156 cating that ROS mediates the exaggeration of EPR in rats with simulated PAD.

157 It is now demonstrated, based on EPR and infrared spectroscopic studies, that the Ni-C to

158 ak homodimers and the lipid bilayer based on EPR spectroscopy topology studies.

159 These results, together with other EPR and in situ IR spectroscopic and kinetic isotope eff

160 Mechanistic and electron paramagnetic (EPR) spectroscopic data supports the conclusion that the

161 The peak EPR in 'ligated' rats during saline infusion averaged 31

162 The peak EPR in 'ligated' rats was also attenuated (n = 7; P < 0.

163 ion averaged 31 +/- 4 mmHg, whereas the peak EPR in these rats during tiron infusion averaged 13 +/-

164 The solution-phase EPR spectra of the radical cations have Gaussian linesha

165 We present EPR spin-trapping proof that: (i) EBN is an efficient pr

166 were determined by measurements of the probe EPR g-factor and of the fluorescence quenching of pyrene

167 Pulse EPR data reveal an exchangeable deuterium hyperfine coup

168 Pulse EPR, in the form of pulsed electron-electron double reso

169 nnel proteins are of great interest as pulse EPR reports on functionally significant but distinct con

170 ur work demonstrates the capability of pulse EPR methods for providing detailed information on the pr

171 Pulsed EPR spectroscopy experiments on 3 revealed quantum coher

172 Here we demonstrate use of pulsed EPR spectroscopy to measure the interaction between two

173 pin labeling to enable application of pulsed EPR techniques.

174 IM) Yb(trensal), by isotope selective pulsed EPR spectroscopy on an oriented single crystal.

175 Using pulsed EPR (PELDOR or DEER) to measure interdomain distances in

176 ture, along with co-sedimentation and pulsed-EPR measurements, demonstrates that high-affinity bindin

177 rosine (F2Y) at Y356 and rapid freeze-quench EPR analysis of its reaction with Y731F-alpha2, CDP, and

178 Finally, rapid freeze-quench EPR experiments indicated that both WT and W321F KatG pr

179 Using rapid freeze-quenching EPR, we observed the formation of a high-spin intermedia

180 based exploration and preferential return (r-EPR) mechanism that incorporates space in the EPR model.

181 ature by UV-vis absorption, resonance Raman, EPR, ESI-MS, and XAS analyses.

182 Recent EPR and crystallographic studies have observed that oxid

183 f muscle evokes the exercise pressor reflex (EPR), which is expressed partly by increases in heart ra

184 e nociception and exercise pressor reflexes (EPRs), and P2Y1 has been linked to heat responsiveness a

185 Here we report EPR spectroscopic studies of cryoreduced oxy-F33Y-CuBMb,

186 (pi1*)(1)(pi2*)(2), consistent with reported EPR g values.

187 Time-resolved EPR measurements and time-dependent density functional t

188 oth DFT and electron paramagnetic resonance (EPR) analyses further indicate that, upon T-TET, the tri

189 Electron paramagnetic resonance (EPR) analysis detected signals of organic radical interm

190 Electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) spect

191 n contrast, electron paramagnetic resonance (EPR) and nuclear magnetic resonance (NMR) on the isolate

192 me-resolved electron paramagnetic resonance (EPR) and quantum chemical calculations.

193 ) and pulse electron paramagnetic resonance (EPR) characterization.

194 e show that electron paramagnetic resonance (EPR) combined with atomic absorption spectroscopy (AAS)

195 st time, on electron paramagnetic resonance (EPR) imaging data sets that will furnish the distributio

196 Pulse electron paramagnetic resonance (EPR) is being applied to ever more complex biological sy

197 Pulsed electron paramagnetic resonance (EPR) measurements enabled the investigation of the coher

198 Using electron paramagnetic resonance (EPR) of a bifunctional spin label (BSL) bound stereospec

199 Electron paramagnetic resonance (EPR) of biomolecules spin-labeled with nitroxides can of

200 GHz) pulse electron paramagnetic resonance (EPR) of the NH2Y*s reported the gx values with unprecede

201 hemical and electron paramagnetic resonance (EPR) spectroscopic analyses demonstrate that CP outcompe

202 d hyperfine electron paramagnetic resonance (EPR) spectroscopic methods, combined with site-directed

203 e dependent electron paramagnetic resonance (EPR) spectroscopic studies show that the active reducing

204 optical and electron paramagnetic resonance (EPR) spectroscopies and modelling.

205 n (XES) and electron paramagnetic resonance (EPR) spectroscopies in the solid state.

206 and pulsed electron paramagnetic resonance (EPR) spectroscopies revealed that the effectiveness of t

207 orption and electron paramagnetic resonance (EPR) spectroscopies support a mechanism in which an Fe(I

208 e (NMR) and Electron Paramagnetic Resonance (EPR) spectroscopies to distinguish the reaction of a mod

209 (DEER) and electron paramagnetic resonance (EPR) spectroscopies.

210 , by pulsed electron paramagnetic resonance (EPR) spectroscopy and compared the performance of these

211 bination of electron paramagnetic resonance (EPR) spectroscopy and computational approaches has provi

212 nation with electron paramagnetic resonance (EPR) spectroscopy at defined electrochemical potentials

213 using both electron paramagnetic resonance (EPR) spectroscopy for its experimental determination and

214 Electron paramagnetic resonance (EPR) spectroscopy is a powerful method to elucidate mole

215 a points of electron paramagnetic resonance (EPR) spectroscopy measurements of various food products.

216 ion-display electron paramagnetic resonance (EPR) spectroscopy of nonirradiated cells is highly diagn

217 high-field electron paramagnetic resonance (EPR) spectroscopy to characterize paramagnetic metal-org

218 with pulsed electron paramagnetic resonance (EPR) spectroscopy to determine their coherence times.

219 y (1)H NMR, electron paramagnetic resonance (EPR) spectroscopy, equilibrium dialysis, intrinsic trypt

220 teady-state electron paramagnetic resonance (EPR) spectroscopy.

221 examined by electron paramagnetic resonance (EPR) spectroscopy.

222 and pulsed electron paramagnetic resonance (EPR) spectroscopy.

223 uency pulse electron paramagnetic resonance (EPR) spectroscopy.

224 examined by electron paramagnetic resonance (EPR) spectroscopy.

225 imaging and electron paramagnetic resonance (EPR) spectroscopy.

226 exhibits an electron paramagnetic resonance (EPR) spectrum with an unusually large gzz value of 2.44

227 an in situ electron paramagnetic resonance (EPR) spin trapping technique and radical trapping with p

228 c probe and electron paramagnetic resonance (EPR) technique for in vivo concurrent assessment of thes

229 zation from electron paramagnetic resonance (EPR) to NMR.

230 d and pulse electron paramagnetic resonance (EPR) with laser excitation.

231 Electron paramagnetic resonance (EPR), absorption, and magnetic circular dichroism (MCD)

232 V-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear magnetic resonance (NMR) spectrosco

233 synthesis, electron paramagnetic resonance (EPR), and circular dichroism to detect and analyze the s

234 oism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption, and X-ray absorption spe

235 bination of electron paramagnetic resonance (EPR), stopped flow freeze quench on a millisecond-second

236 nation with electron paramagnetic resonance (EPR)-based spectroscopy and imaging techniques provide a

237 The electron spin resonance (EPR) spin-trapping technique allows detection of radical

238 Using electron paramagnetic spin resonance (EPR), we show that this rotation aligns the two membrane

239 ctroscopic (electron paramagnetic resonance [EPR] and UV-vis) and theoretical (density functional the

240 to nitrite, and an analysis of the resulting EPR hyperfine parameters confirms that mARC is remarkabl

241 of the enhanced permeability and retention (EPR) effect and the tumor microenvironment, the optimal

242 nounced enhanced permeability and retention (EPR) effect in and the heterogeneity of human tumors as

243 tion by enhanced permeability and retention (EPR) effect with concomitant increase in efficacy.

244 on the enhanced permeability and retention (EPR) effect, which refers to the ability of macromolecul

245 nt with enhanced permeability and retention (EPR) effects.

246 elling electron paramagnetic resonance (SDSL EPR) spectroscopy.

247 However, to reliably deploy soluble EPR probes as oxygen sensors in complex biological syste

248 lectron paramagnetic resonance spectroscopy (EPR).

249 X-ray photoelectron spectroscopy, EPR, and magnetometry support this assignment.

250 en substrate deuterium atoms and the stable, EPR-active iron-nitrosyl adduct, a surrogate for reactio

251 suite of methods, including kinetic studies, EPR spectroscopy, and computational methods.

252 ng the fate of deuterium-labeled substrates, EPR, trapping experiments, and LA-LDI mass spectrometry

253 basis of Mossbauer, magnetic susceptibility, EPR, and X-ray absorption in conjunction with density fu

254 nation of advanced spectroscopic techniques (EPR, IR, XAS, UV-vis, NMR, luminescence spectroscopies).

255 = 2) from 70 to 4 K in variable-temperature EPR measurements.

256 The EPR measurements and mass spectrometry analyses further

257 The EPR spectrum of 7 suggests the presence of a Co(I) bound

258 The EPR spectrum of each spin-labeled peptide indicates nano

259 The EPR spectrum of Pt(pop-BF2)(5-) and UV-vis spectra of bo

260 The EPR spectrum of the singly reduced cage shows that the e

261 In addition, the EPR findings demonstrated that the Fermi contact term co

262 PR) mechanism that incorporates space in the EPR model.

263 Binding gave quantifiable changes in the EPR spectra from which binding profiles could be obtaine

264 ics the tumor microenvironment including the EPR effect.

265 eral other parameters known to influence the EPR effect were evaluated, such as blood and lymphatic v

266 ft tumors, we evaluated the influence of the EPR effect on liposomal distribution in vivo by injectio

267 he first part deals with the analysis of the EPR experiments as a function of the ions under investig

268 The use of the EPR g-factor for the determination of partition constant

269 H affect the DMPO-OH signal intensity of the EPR spectra.

270 Tiron infusion had no effect on the EPR in rats with patent femoral arteries (n = 9).

271 001); the attenuating effect of tiron on the EPR was partly reversed when saline was reinfused into t

272 To examine the effects of ROS on the EPR, we infused a superoxide scavenger, tiron, into the

273 s or predictions could be made regarding the EPR effect or liposomal uptake.

274 Microwave frequency sweeps through the EPR line shape are shown as a time domain strategy to si

275 derstandable to people who are laymen to the EPR field in anticipation of future progress and broad a

276 Their EPR parameters indicated they had planar pi-character.

277 rovide a purified defined system amenable to EPR, optical and vibrational spectroscopy, and fluoresce

278 ite-Directed Spin Labeling (SDSL) coupled to EPR spectroscopy, and enzymatic assays.

279 In this report, we apply an array of tools (EPR, NMR, transient absorption, and UV-vis spectroscopy;

280 netic assay using KO2 and direct freeze-trap EPR to follow its decay removed the rate-limiting substr

281 -dimethyl-1-pyrroline-N-oxide) spin-trapping EPR method at room temperature on a Bruker E500 spectrom

282 We report a unique EPR signal with g-tensor, gx = 2.30, gy = 2.18, and gz =

283 Using EPR spectroscopy, we have directly observed a Mn(IV) int

284 and the generated species were studied using EPR, UV-vis, IR, VCD, UHR-ESI-MS, and XANES/XAFS measure

285 Here, we utilize EPR spectroscopy to target the conformational changes th

286 cyano adducts were characterized by UV-vis, EPR, and ENDOR spectroscopies and X-ray crystallography.

287 (IV) dimer has been characterized by UV-vis, EPR, and Mossbauer spectroscopies.

288 emonstrated and characterized by IR, UV-vis, EPR, NMR, and single-crystal X-ray diffractions.

289 can be characterized by cyclic voltammetry, EPR spectroscopy, and X-ray crystallography.

290 To investigate, we used continuous wave EPR spectroscopy and site-specific spin labels that dire

291 pecies are relatively stable compounds whose EPR spectra represent "structural fingerprints" of the p

292 These structures, along with EPR analysis, allow us to propose a mechanism in which a

293 f [MgCl(THF)5][Fe8Me12], which combined with EPR and MCD studies is shown to be consistent with Kochi

294 yo-electron microscopy, which, combined with EPR spectroscopy and molecular dynamics simulations, unc

295 d, by combining structure determination with EPR (electron paramagnetic resonance) spectroscopy and s

296 The results obtained with EPR and UV-vis spectroscopy indicate that carbamates can

297 as statistical spectroscopy) in tandem with EPR spectroscopy are used to interpret the magnetic beha

298 -tagged forms of CYP144A1-FLV and -TRV, with EPR demonstrating cysteine thiolate coordination of heme

299 ion of stimuli and were studied by NMR, XRD, EPR spectroscopy, and DFT calculations.

300 Further reductions of Xn-Hex(*-) yield EPR signals (in frozen solutions) that can be assigned t