ライフサイエンスコーパス: Mossbauer

1 Mossbauer analyses revealed small quantities (<5%) of Fe

2 Mossbauer analysis and density functional theory (DFT) c

3 Mossbauer and electron paramagnetic resonance spectrosco

4 Mossbauer and EPR analyses show that 6b is a diiron(IV)

5 Mossbauer and EPR spectroscopies, along with X-ray struc

6 Mossbauer and infrared spectra are consistent with parti

7 Mossbauer and magnetic susceptibility data demonstrate t

8 Mossbauer data for the tetrameric complexes 1-3 demonstr

9 Mossbauer hyperfine parameters for Fe(II)-reacted NAu-1

10 Mossbauer spectra collected in the presence of a high ap

11 Mossbauer spectra of equivalent (57)Fe-enriched samples

12 Mossbauer spectra of whole cells were dominated by HS Fe

13 Mossbauer spectra show that the intermediate contains a

14 Mossbauer spectroscopic characterization of (57)Fe-enric

15 Mossbauer spectroscopic data for a set of reference dini

16 Mossbauer spectroscopy analysis of minerals precipitated

17 Mossbauer spectroscopy analysis revealed that nearly all

18 Mossbauer spectroscopy and ac magnetic susceptibility re

19 Mossbauer spectroscopy and magnetometry reveal strong ma

20 Mossbauer spectroscopy confirmed the formation of transi

21 Mossbauer spectroscopy illustrates that the triflate sal

22 Mossbauer spectroscopy measurements confirmed that iron

23 Mossbauer spectroscopy of magnetite reacted with (56)Fe(

24 Mossbauer spectroscopy revealed the presence of two dist

25 Mossbauer spectroscopy suggests that substrate binding t

26 Mossbauer spectroscopy supports the structural observati

27 Mossbauer spectroscopy was used to detect pools of Fe in

28 Mossbauer spectroscopy, kinetic isotope effect, and gas

29 Mossbauer spectroscopy, magnetometry, and variable-tempe

30 Mossbauer studies of the peroxo state reveal a diferric

31 Mossbauer, EPR, magnetic susceptibility, and DFT studies

32 Mossbauer, EXAFS, and XANES results give no indication t

33 (PS-Fe(II)/Fe(III) ratio approximately 1.2 (Mossbauer) or 0.8 (XAS)).

34 After reconstitution with 57Fe2+, Mossbauer studies of NfuA showed a broad quadrupole doub

35 ields the complete vibrational spectrum of a Mossbauer isotope, and provides a valuable probe that is

36 Here we report a Mossbauer investigation on whole cells overexpressing PF

37 been characterized by electronic absorption, Mossbauer, and NMR spectroscopies, as well as X-ray crys

38 been demonstrated by UV-visible absorption, Mossbauer, and resonance Raman spectroscopies, using dit

39 pic methods including UV-visible absorption, Mossbauer, EPR, and HYSCORE spectroscopies that these ad

40 For ((iPr)PDI)FeN(2)Ad, Mossbauer spectroscopy also supports spin crossover beha

41 spectroscopy, single crystal X-ray analysis, Mossbauer spectroscopy, and magnetic susceptibility meas

42 y, the first exhibits optical absorption and Mossbauer spectra similar to those of J and, like J, a l

43 X-ray absorption and Mossbauer spectroscopy results indicate that reduction o

44 ation of density functional calculations and Mossbauer spectroscopy, we have examined chloroperoxidas

45 ron X-ray diffraction, DFT calculations, and Mossbauer spectroscopy, a unified understanding of the N

46 signatures for the iron-oxo chromophore, and Mossbauer and XAS measurements establish the presence of

47 l details, magnetic susceptibility data, and Mossbauer spectra demonstrate that 1 has a low-spin (S =

48 Both X-ray diffraction and Mossbauer analyses further confirm that increased nanopa

49 X-ray diffraction and Mossbauer spectroscopy confirm that the reduction occurs

50 K using single-crystal X-ray diffraction and Mossbauer spectroscopy in laser-heated diamond anvil cel

51 yA)2Fe2(L)](3+), where X-ray diffraction and Mossbauer spectroscopy indicate a metal-centered oxidati

52 s, in conjunction with X-ray diffraction and Mossbauer spectroscopy, reveal the presence of weak ferr

53 of magnetochemistry, X-ray diffraction, and Mossbauer spectroscopic and computational studies establ

54 h sediment chemistry, X-ray diffraction, and Mossbauer spectroscopy on sediments retrieved from an or

55 , as revealed by detailed magnetic, DSC, and Mossbauer studies.

56 x is trapped and characterized using EPR and Mossbauer (MB) spectroscopies.

57 EPR and Mossbauer quantification of the various iron products, r

58 Quantitative interpretation of EPR and Mossbauer spectroscopic data indicates the presence of t

59 ative zero field splitting and other EPR and Mossbauer spectroscopic properties reminiscent of previo

60 Here, EPR and Mossbauer spectroscopies allow electronic characterizati

61 errous heme species in cyt c(554) by EPR and Mossbauer spectroscopies during the HAO catalyzed oxidat

62 e-based dioxygenase characterized by EPR and Mossbauer spectroscopy.

63 EPR and Mossbauer studies show that the iron remains ferric thro

64 ch electron paramagnetic resonance (EPR) and Mossbauer spectroscopies have been used to obtain eviden

65 by electron paramagnetic resonance (EPR) and Mossbauer spectroscopies.

66 r has been characterized by UV-vis, EPR, and Mossbauer spectroscopies.

67 Optical, EPR, and Mossbauer studies show that the enzyme contains a nonhem

68 X-ray absorption fine structure (EXAFS) and Mossbauer spectroscopy combined with macroscopic sorptio

69 yperfine sublevel correlation (HYSCORE), and Mossbauer spectroscopies as well as protein-film electro

70 IR and Mossbauer spectroscopy, and elemental analysis on 2 and

71 ons of these structures gave values of J and Mossbauer parameters in agreement with experiment.

72 ent magnetic susceptibility measurements and Mossbauer data show that the boron-centered Fe(14) clust

73 A combination of analytical methods and Mossbauer and EPR spectroscopies showed that reconstitut

74 despite differences between its optical and Mossbauer spectroscopic parameters and those of other pe

75 The magnetic properties and Mossbauer spectroscopy indicate that they undergo long-r

76 together with published resonance Raman and Mossbauer data suggest that the high-valent iron center

77 circular dichroism, EPR, resonance Raman and Mossbauer spectroscopies.

78 Characterization by resonance Raman and Mossbauer spectroscopy provides complementary insights i

79 nd electron microscopy, as well as Raman and Mossbauer spectroscopy, reveal magnetite nanoparticles i

80 V-visible absorption/CD, resonance Raman and Mossbauer) have been used to investigate the mechanism o

81 -edge X-ray absorption, resonance Raman, and Mossbauer data collected for these complexes conclusivel

82 UV-visible absorption, resonance Raman, and Mossbauer properties but differ in terms of redox proper

83 mperature arises from cation reordering, and Mossbauer spectroscopy supports this interpretation.

84 e-quench electron paramagnetic resonance and Mossbauer spectroscopies to the mouse R2 reaction to eva

85 isible, electron paramagnetic resonance, and Mossbauer spectroscopic features of the homodimeric QueE

86 sis of X-ray diffraction, Raman spectra, and Mossbauer spectra confirm the presence of Fe(III) center

87 , XRD, X-ray photoelectron spectroscopy, and Mossbauer spectroscopy confirm the relationship between

88 Magnetic susceptibility and Mossbauer spectroscopy reveal the +1 oxidation state and

89 The UV-vis and Mossbauer spectroscopic properties of the intermediate a

90 both oxygenated intermediates by UV-vis and Mossbauer spectroscopy, proposed structures from DFT and

91 ants was explored by stopped-flow UV-vis and Mossbauer spectroscopy.

92 Infrared, UV-vis, and Mossbauer spectroscopies, together with magnetic suscept

93 Both UV-visible and Mossbauer experiments provide unambiguous evidence that

94 UV-visible and Mossbauer spectra of both samples indicated the presence

95 ray crystallography and (1)H NMR, XANES, and Mossbauer spectroscopy.

96 ical techniques including TEM, SEM, XAS, and Mossbauer analyses.

97 t density functional calculations as well as Mossbauer and stopped-flow spectroscopic characterizatio

98 millitesla linewidth) were characterized by Mossbauer and EPR spectroscopy, respectively.

99 (2+), and the products were characterized by Mossbauer and EPR spectroscopy.

100 th Fe2+, Fe3+, and S2-, and characterized by Mossbauer, EPR, and visible spectroscopies.

101 and [4(57)Fe-4S]H HydA1 was characterized by Mossbauer, HYSCORE, ENDOR, and nuclear resonance vibrati

102 TFcP](2+) complexes was further confirmed by Mossbauer, IR, and XPS data.

103 The preceding paper demonstrates by Mossbauer and electron paramagnetic resonance (EPR) spec

104 place in pristine sediments as determined by Mossbauer spectroscopy (20 +/- 11% reduction).

105 4Fe-4S] (2+) configuration, as determined by Mossbauer spectroscopy, suggesting that it contained at

106 upolar splitting of Fe(2+), as determined by Mossbauer spectroscopy.

107 from (57)Fe-enriched mice were evaluated by Mossbauer spectroscopy.

108 scopic probes that have been interrogated by Mossbauer spectroscopy and high-field EPR spectroscopy,

109 iron silicate spinel, detected previously by Mossbauer spectroscopy, is seen in the calorimetric sign

110 acterization of the reconstituted protein by Mossbauer spectroscopy indicated the presence of only [4

111 amount of Fe(3+) ions that was quantified by Mossbauer spectroscopy and confirmed by the TN values of

112 distinct electronic structures, as shown by Mossbauer spectroscopy, although both are high spin (S =

113 structures of the compounds were studied by Mossbauer spectroscopy, NMR spectroscopy, magnetochemist

114 Analysis of TsrM by Mossbauer and HYSCORE spectroscopies suggests that SAM d

115 Whole cell Mossbauer analysis on cells induced with 0.5 mM arabinos

116 v2 has a S = 4 spin state and characteristic Mossbauer spectrum, a parallel mode g = 16.4 EPR signal,

117 Combined Mossbauer and crystallographic studies indicate that the

118 n explored via the collection of comparative Mossbauer data for all of the complexes featured and als

119 by X-ray crystallography, but complementary Mossbauer studies established the presence of divalent a

120 shifted to 765 cm(-1) in the (18)O complex; Mossbauer experiments show a signal with an delta = 0.02

121 Computational, Mossbauer, XAS, and NRVS studies indicate that protonati

122 dels of ToMOH and the theoretically computed Mossbauer spectra.

123 Conventional Mossbauer spectroscopy shows a diamagnetic ground state

124 Corresponding Mossbauer spectra exhibited two populations of A-cluster

125 r characterization by X-ray crystallography, Mossbauer spectroscopy, and high-field EPR spectroscopy.

126 etylene inhibitors by X-ray crystallography, Mossbauer, and nuclear magnetic resonance spectroscopy.

127 Here we report detailed Mossbauer and density functional theory (DFT) studies of

128 racteristic molecular structure differences, Mossbauer spectra, magnetic circular dichroism spectrosc

129 copy) and phase analyses (X-ray diffraction, Mossbauer spectroscopy) reveal the formation of Fe(3)O(4

130 ished by a combination of X-ray diffraction, Mossbauer spectroscopy, magnetochemistry, and open-shell

131 igh-energy x-ray diffraction and time-domain Mossbauer spectroscopy, we show that nematicity and magn

132 tional treatment with CO altered the doublet Mossbauer parameters, suggesting an interaction with CO,

133 We have employed Mossbauer spectroscopy to characterize the iron in our p

134 EPR, ENDOR, Mossbauer, and EXAFS analysis, coupled with a DFT study,

135 orption and CD, resonance Raman, EPR, ENDOR, Mossbauer, and EXAFS studies of [2Fe-2S] Grx3/4 homodime

136 EPR, Mossbauer spectroscopy, and electron microscopy were use

137 EPR, Mossbauer, and optical spectroscopies reveal that CmlA c

138 EPR, Mossbauer, and XAS spectroscopic results presented herei

139 terized using UV-vis absorption/CD/MCD, EPR, Mossbauer, and resonance Raman spectroscopies.

140 methods--XANES, EXAFS, X-ray, (1)H NMR, EPR, Mossbauer, and cyclic voltammetry--demonstrate that the

141 (II) state by rapid-freeze quench (RFQ) EPR, Mossbauer, and ENDOR spectroscopy.

142 mplex has been characterized by UV-vis, EPR, Mossbauer, and HRMS and shown to be capable of oxidizing

143 I over the pH range of 3.9-9.5, using EXAFS, Mossbauer, and resonance Raman spectroscopies.

144 uction with excess Ti(III)citrate, exhibited Mossbauer spectra consisting of two quadrupole doublets

145 er was undetectable by chemical extractions, Mossbauer or X-ray Absorption spectroscopies.

146 Specifically, (57) Fe Mossbauer and X-ray absorption spectroscopy provided uni

147 Analysis of the (57) Fe Mossbauer spectra revealed two spectral components that

148 In this study, we combined (57)Fe Mossbauer and Fe K-edge X-ray absorption spectroscopic (

149 Based on (57)Fe Mossbauer and infrared spectroscopy (IR) data, the elect

150 A combination of (57)Fe Mossbauer and magnetic circular dichroism (MCD) spectros

151 both variable-temperature zero-field (57)Fe Mossbauer and magnetometry with a spin reversal barrier

152 d characterized by X-ray diffraction, (57)Fe Mossbauer and multinuclear NMR spectroscopy, and combust

153 (57)Fe Mossbauer data of the extremely oxidation-sensitive comp

154 spectroscopic signatures such as low (57)Fe Mossbauer isomer shifts and linear Fe-N-O units with hig

155 Zero-field (57)Fe Mossbauer parameters obtained for ((Ar)L)FeCl(N(p-(t)BuC

156 The (57)Fe Mossbauer quadrupole splittings and (1)H and (13)C NMR c

157 The (57)Fe Mossbauer spectra of 2, 6, 8, and 9 show a clear trend i

158 (57)Fe Mossbauer spectrometry shows that up to 6% of the total

159 structural Fe(III) in the clays using (57)Fe Mossbauer spectrometry.

160 X-ray crystallographic and (57)Fe Mossbauer spectroscopic investigations indicated that 2

161 (57)Fe Mossbauer spectroscopy and DFT-calibrated Huckel calcula

162 land Gola di Lago (Switzerland) using (57)Fe Mossbauer spectroscopy and synchrotron X-ray techniques.

163 X-ray absorption spectroscopy (XAS), (57)Fe Mossbauer spectroscopy and X-ray diffraction, we followe

164 etween 1 and its reduction product by (57)Fe Mossbauer spectroscopy are discussed, and the reduction

165 otoelectron spectroscopy and in-field (57)Fe Mossbauer spectroscopy give unambiguous evidence that a

166 Results from (57)Fe Mossbauer spectroscopy indicate that both Al-substitutio

167 e observed in incubated sediments and (57)Fe Mossbauer spectroscopy revealed that Fe(III) associated

168 In addition, X-ray crystallography, (57)Fe Mossbauer spectroscopy, and EPR spectroscopy were used t

169 (57)Fe Mossbauer spectroscopy, X-ray photoelectron spectroscopy

170 racterized the resulting solids using (57)Fe Mossbauer spectroscopy.

171 amagnetic resonance spectroscopy, and (57)Fe Mossbauer spectroscopy.

172 he Fe(4)S(4) clusters as indicated by (57)Fe Mossbauer spectroscopy.

173 -ray diffraction and NMR, UV-vis, and (57)Fe Mossbauer spectroscopy.

174 (1)H NMR, X-ray crystallography, and (57)Fe Mossbauer spectroscopy.

175 +), which is characterized by NMR and (57)Fe Mossbauer spectroscopy.

176 spin Fe(III) species was confirmed by (57)Fe Mossbauer spectroscopy.

177 e3(mu(3)-NH) has a similar zero-field (57)Fe Mossbauer spectrum compared to previously reported [((tb

178 Moreover, the (57)Fe Mossbauer spectrum of 4 at 80K exhibits parameters (delt

179 e2Mn(THF) was determined by (1)H NMR, (57)Fe Mossbauer, and X-ray fluorescence.

180 Combined experimental data including (57)Fe Mossbauer, IR, UV-vis-NIR, NMR and Kbeta X-ray emission

181 ely, as determined by EPR, zero-field (57)Fe Mossbauer, magnetometry, and single crystal X-ray diffra

182 been characterized by EPR, zero-field (57)Fe Mossbauer, magnetometry, single crystal X-ray diffractio

183 n spectroscopic evidence from UV-vis, (57)Fe Mossbauer, resonance Raman, infrared, and (1)H/(19)F NMR

184 erized by X-ray diffraction analysis, (57)Fe Mossbauer, SQUID magnetometry, mass spectrometry, and co

185 perfine splitting in the zero-field (5)(7)Fe Mossbauer spectra at 4.2 K.

186 a ((1) H-NMR, UV-vis-NIR, infra-red, (57) Fe-Mossbauer, EPR), X-ray crystallographic characterization

187 his paper, we present field-dependent (57)Fe-Mossbauer and EPR data for Hase I, which, in conjunction

188 ray crystallography, NMR-, FTIR-, and (57)Fe-Mossbauer spectroscopy as well as by electronic absorpti

189 Zero- and applied-field Mossbauer spectroscopic measurements indicate diamagneti

190 High-field Mossbauer spectroscopy gave an (57)Fe A(dip) tensor of (

191 y photoelectron spectroscopy (XPS), in-field Mossbauer spectroscopy, and magnetization measurements e

192 ure magnetization and applied magnetic field Mossbauer spectroscopy studies revealed a very large dep

193 Variable-field Mossbauer spectroscopy of 1-O indicates an intermediate-

194 Structures, zero-field Mossbauer data, and redox potentials are presented for e

195 Finally, zero-field Mossbauer spectra collected for 1 and 4 also reveal the

196 ady-state investigation, including the first Mossbauer spectroscopic characterization of diiron redox

197 B-co-loaded form provided an opportunity for Mossbauer analysis of NifB-co.

198 compared to pure ferrihydrite (inferred from Mossbauer-derived blocking temperatures), these samples

199 g mass spectrometry as well as UV-vis, FTIR, Mossbauer, XAS, and parallel-mode EPR spectroscopies.

200 gation of solvent molecules and variation in Mossbauer spectra, spin ground state, and intracluster F

201 n integrative biophysical approach involving Mossbauer and electronic absorption spectroscopies, elec

202 first quantum chemical investigation of IPC Mossbauer and NMR spectroscopic properties, as well as t

203 h were characterized by UV-vis-NIR, MCD, IR, Mossbauer, and XPS spectroscopy.

204 Its Mossbauer spectra reveal that the intermediate possesses

205 as a high-spin iron(III) center based on its Mossbauer and EPR spectra and its quantitative reduction

206 The 4.2 K Mossbauer spectrum of 2b exhibits a quadrupole doublet w

207 5 K Mossbauer spectra of cells were dominated by a sextet du

208 ion of methods including transient kinetics, Mossbauer spectroscopy, and mass spectrometry, we demons

209 in Hhyd was demonstrated by an unusually low Mossbauer isomer shift of the distal Fe of the [2Fe]H su

210 Magnetic, Mossbauer, and crystallographic data are consistent with

211 g studies, cyclic voltammetry, magnetometry, Mossbauer spectroscopy, UV-vis-NIR spectroscopy, NMR spe

212 atography, transmission electron microscopy, Mossbauer spectroscopy, and magnetic susceptibility meas

213 ansmission and scanning electron microscopy, Mossbauer, UV-vis and FTIR spectroscopy and X-ray powder

214 high-resolution mass spectrometry, and NMR, Mossbauer, IR, and UV/Vis spectroscopy.

215 on of a nitrido species that on the basis of Mossbauer, magnetic susceptibility, EPR, and X-ray absor

216 Using a combination of Mossbauer spectroscopy and density functional calculatio

217 in (LS), as determined by the combination of Mossbauer spectroscopy, magnetic measurements, and singl

218 hows remarkable success on the prediction of Mossbauer spectroscopy of alpha-Fe, chi-Fe5C2 and theta-

219 Use of Mossbauer, EPR, NMR, UV/Vis, and IR spectroscopy, in con

220 these catalysts, we have performed operando Mossbauer spectroscopic studies of a 3:1 Ni:Fe layered h

221 Optical, Mossbauer, resonance Raman spectroscopies and native mas

222 Previous Mossbauer spectra of unenriched diseased human hearts la

223 change is smaller than reported in previous Mossbauer investigations on a bacterial cytochrome c, an

224 flow UV-visible absorption and freeze-quench Mossbauer experiments identified a transient iron(IV)-ox

225 In situ freeze-quench Mossbauer spectroscopy during turnover reveals an iron-b

226 it by ultraviolet-visible, resonance Raman, Mossbauer and electrospray ionization mass spectrometric

227 haracterized by UV-visible, resonance Raman, Mossbauer, and EPR methods.

228 ysiological conditions, with optical, redox, Mossbauer, and NMR characteristics that are consistent w

229 This work reports Mossbauer and DFT studies of the diiron-N2 complex LMeFe

230 dichroism, electron paramagnetic resonance, Mossbauer and resonance Raman spectroscopies.

231 products by electron paramagnetic resonance, Mossbauer, and nuclear resonance vibrational spectroscop

232 electronic, electron paramagnetic resonance, Mossbauer, and X-ray absorption spectroscopic analyses f

233 olarization surface enhanced NMR (DNP-SENS), Mossbauer spectroscopy, and computational chemistry were

234 In the present study, in situ Mossbauer and magnetic circular dichroism spectroscopic

235 Using (119)Sn-Mossbauer spectroscopy, which is the most sensitive tool

236 Combined with freeze-trapped solution Mossbauer studies of reactions with primary alkyl halide

237 y UV/Visible and IR spectroelectrochemistry, Mossbauer and NMR spectroscopy, X-ray crystallography, a

238 Mass spectrometry, Mossbauer, electron paramagnetic resonance, and x-ray ab

239 to complementary structural, spectroscopic (Mossbauer, EPR/ENDOR, IR), and computational probes that

240 In this study, Mossbauer and EPR spectroscopies were used to characteri

241 Magnetic susceptibility, Mossbauer, and neutron diffraction data show that the ma

242 le crystal X-ray diffraction and synchrotron Mossbauer source spectroscopy.

243 -pressure optical absorption and synchrotron Mossbauer spectroscopic measurements of iron-enriched de

244 estigated using transmission and synchrotron Mossbauer spectroscopy at high pressures and low tempera

245 Here, we present synchrotron Mossbauer spectroscopy and X-ray diffraction combined wi

246 d using combined high resolution synchrotron Mossbauer spectroscopy and x-ray diffraction techniques

247 The room temperature Mossbauer spectrum of irradiated hematite shows the emer

248 The room-temperature Mossbauer spectrum confirms the 1:1 ratio of Fe(II) (del

249 CPO-I and P450-I using variable-temperature Mossbauer and X-ray absorption spectroscopies.

250 Variable-temperature Mossbauer data also corroborate a significant temperatur

251 r time scale, such that variable-temperature Mossbauer spectra reveal a thermally activated transitio

252 The Mossbauer data presented here provide direct spectroscop

253 The Mossbauer features are distinct for the two sites, with

254 The Mossbauer parameters for 1-O include an unusually small

255 The Mossbauer parameters of the minor component are indicati

256 The Mossbauer patterns observed in strong applied fields sho

257 The Mossbauer spectroscopy of iron carbides (alpha-Fe, gamma

258 The Mossbauer spectrum at 90 K of the EPR-silent intermediat

259 The Mossbauer spectrum in the as-isolated HbRC core shows th

260 The Mossbauer spectrum of 1 (S = 0) and TDDFT calculations,

261 The Mossbauer spectrum of CYP119-I is similar to that of chl

262 The Mossbauer studies reveal that 2 has distinct Fe(IV) site

263 ing Tc oxidation is further supported by the Mossbauer spectroscopy and micro X-ray diffraction data

264 absorption spectroscopy (XAS) confirmed the Mossbauer results, and bulk As XAS indicated the prevale

265 tric hyperfine interactions deduced from the Mossbauer analysis suggests that NifB-co is either a 4Fe

266 Furthermore, the Mossbauer spectra reveal that the [4Fe-4S](2+) cluster o

267 ne sample of 1 displays three sextets in the Mossbauer spectrum at 4.2 K (H(ext) = 0) which converge

268 he low quadrupole splitting parameter in the Mossbauer spectrum observed for a ToMOH(peroxo) intermed

269 cessful quantum chemical calculations of the Mossbauer and NMR properties in various S = 3/2 iron por

270 riflate salts corroborate the results of the Mossbauer and NMR spectroscopy and reveal substantial st

271 ation is associated with perturbation of the Mossbauer spectrum of the diferric cluster, especially t

272 lectron hopping is comparable to that of the Mossbauer time scale, such that variable-temperature Mos

273 The DFT calculations reproduce the Mossbauer parameters (A-tensors, electric field gradient

274 with internal fluctuations measured with the Mossbauer effect and neutron scattering.

275 We first explore the model with the Mossbauer effect.

276 f these enzymes to determine the theoretical Mossbauer parameters for the ferryl and protonated ferry

277 These Mossbauer parameters are comparable to those observed fo

278 Finally, field shift energies are related to Mossbauer isomer shifts, and equilibrium mass-independen

279 ronments that are reflected in their unusual Mossbauer parameters, including quadrupole-splitting val

280 Here, we use Mossbauer spectroscopy on (57)Fe-labeled complex I from

281 Here we used Mossbauer spectroscopy combined with selective chemical

282 Using Mossbauer and EPR spectroscopies, X-ray crystallography,

283 rt-butylureaylato)-N-ethylene]aminato) using Mossbauer and dual-frequency/dual-mode electron paramagn

284 ure of the accumulated Fe was examined using Mossbauer spectroscopy, EPR, electronic absorption spect

285 that we have characterized extensively using Mossbauer and parallel mode EPR spectroscopy.

286 treatment with chlorine and hydrogen, using Mossbauer and X-ray absorption spectroscopy.

287 protein by biochemical analysis and UV-vis, Mossbauer, resonance Raman, and EPR spectroscopy.

288 enzoic acid and characterized by UV-visible, Mossbauer and electron paramagnetic resonance spectrosco

289 UV/visible, Mossbauer, and X-ray absorption spectroscopies have been

290 ansitions to a new species (pKa = 13.1) with Mossbauer parameters that are indicative of an iron(IV)-

291 the heme iron dynamics in cytochrome c with Mossbauer spectroscopy and especially nuclear resonance

292 croscopic sorption experiments combined with Mossbauer and extended X-ray absorption fine structure (

293 The metrical parameters combined with Mossbauer spectroscopic and magnetic data for ((i)PrPDI)

294 ed, using analytical methods in concert with Mossbauer and electron paramagnetic resonance spectrosco

295 apid mixing technologies in conjunction with Mossbauer, ultraviolet/visible, and x-ray absorption spe

296 lved Fe(2+) release to solution coupled with Mossbauer spectra and XRD analysis of solid phase produc

297 sotope fractionations in other elements with Mossbauer isotopes, such as platinum and uranium.

298 In the present work, Mossbauer spectroscopy and electron microscopy indicate

299 nt study, powder XRD, synchrotron-based XAS, Mossbauer spectroscopy, and TEM demonstrated unambiguous

300 characterized using X-ray diffraction (XRD), Mossbauer spectroscopy, and scanning electron microscopy