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1 e-based dioxygenase characterized by EPR and Mossbauer spectroscopy.
2 (1)H NMR, X-ray crystallography, and (57)Fe Mossbauer spectroscopy.
3 ray crystallography and (1)H NMR, XANES, and Mossbauer spectroscopy.
4 +), which is characterized by NMR and (57)Fe Mossbauer spectroscopy.
5 ants was explored by stopped-flow UV-vis and Mossbauer spectroscopy.
6 site was not detected by crystallography or Mossbauer spectroscopy.
7 acterized the photolyzed products by EPR and Mossbauer spectroscopy.
8 aracterized both NH(dark) and NH(light) with Mossbauer spectroscopy.
9 netics methodologies using optical, EPR, and Mossbauer spectroscopy.
10 haracterized by electrochemistry and EPR and Mossbauer spectroscopy.
11 have studied anaerobically purified FNR with Mossbauer spectroscopy.
12 to suppress Doppler dephasing in analogy to Mossbauer spectroscopy.
13 iffraction, elemental analysis, and (119) Sn Mossbauer spectroscopy.
14 Gentle cell lysis was demonstrated using Mossbauer spectroscopy.
15 efOM disrupted the Fh structure, as noted by Mossbauer spectroscopy.
16 g of minerals in the soil matrix with (57)Fe Mossbauer spectroscopy.
17 aracterized using FTIR, resonance Raman, and Mossbauer spectroscopy.
18 tu X-ray absorption spectroscopy and ex situ Mossbauer spectroscopy.
19 oil-free nuclear resonance effect similar to Mossbauer spectroscopy.
20 erized by X-ray crystallography, UV-Vis, and Mossbauer spectroscopy.
21 sA cells under these growth conditions using Mossbauer spectroscopy.
22 detect transformation products using (57)Fe-Mossbauer spectroscopy.
23 ose obtained from CO pulse chemisorption and Mossbauer spectroscopy.
24 xo diferric complex in VlmB, as supported by Mossbauer spectroscopy.
25 ies are tracked using UV-vis-NIR, FT-IR, and Mossbauer spectroscopy.
26 ption near-edge structure (XANES) and (57)Fe Mossbauer spectroscopy.
27 s was characterized by UV/Vis absorption and Mossbauer spectroscopy.
28 and abiotic oxidation products by XANES and Mossbauer spectroscopy.
29 ation of certain iron sites in comparison to Mossbauer spectroscopy.
30 elective extractions, X-ray diffraction, and Mossbauer spectroscopy.
31 3600 to 4400 kelvin, analyzed by synchrotron Mossbauer spectroscopy.
32 y diffraction, and electronic absorption and Mossbauer spectroscopy.
33 racterized the resulting solids using (57)Fe Mossbauer spectroscopy.
34 from (57)Fe-enriched mice were evaluated by Mossbauer spectroscopy.
35 spin Fe(III) species was confirmed by (57)Fe Mossbauer spectroscopy.
36 amagnetic resonance spectroscopy, and (57)Fe Mossbauer spectroscopy.
37 he Fe(4)S(4) clusters as indicated by (57)Fe Mossbauer spectroscopy.
38 upolar splitting of Fe(2+), as determined by Mossbauer spectroscopy.
39 -ray diffraction and NMR, UV-vis, and (57)Fe Mossbauer spectroscopy.
40 circular dichroism, EPR, resonance Raman and Mossbauer spectroscopies.
41 by electron paramagnetic resonance (EPR) and Mossbauer spectroscopies.
42 terized kinetically and by optical, EPR, and Mossbauer spectroscopies.
43 e-quench electron paramagnetic resonance and Mossbauer spectroscopies.
44 i-bonding as measured by infrared and (57)Fe Mossbauer spectroscopies.
45 quench electron paramagnetic resonance, and Mossbauer spectroscopies.
46 UV-vis, resonance Raman, and variable field Mossbauer spectroscopies.
47 aracterized by (19)F NMR, UV-vis, and (57)Fe Mossbauer spectroscopies.
48 ) (4), as evidenced by (1)H NMR, ATR-IR, and Mossbauer spectroscopies.
49 ectron-nuclear double resonance (ENDOR), and Mossbauer spectroscopies.
50 ve also been characterized by UV-visible and Mossbauer spectroscopies.
51 r has been characterized by UV-vis, EPR, and Mossbauer spectroscopies.
52 by X-ray diffraction and (1)H NMR and (57)Fe Mossbauer spectroscopies.
53 and characterized by a combination of (57)Fe Mossbauer spectroscopy, (1)H NMR spectroscopy, magnetome
55 ron X-ray diffraction, DFT calculations, and Mossbauer spectroscopy, a unified understanding of the N
57 UV-visible absorption, resonance Raman, and Mossbauer spectroscopies along with parallel analytical
60 distinct electronic structures, as shown by Mossbauer spectroscopy, although both are high spin (S =
63 mbination of magnetic resonance, near-IR and Mossbauer spectroscopies and electrochemical methods, we
65 Fe active sites are characterized by (57)Fe Mossbauer spectroscopy and aberration-corrected scanning
67 lso investigated by wet chemistry and (57)Fe Mossbauer spectroscopy and calculated by FactSage at the
68 ion in the presence of goethite using (57)Fe Mossbauer spectroscopy and changes in the isotopic compo
69 amount of Fe(3+) ions that was quantified by Mossbauer spectroscopy and confirmed by the TN values of
72 ng (LIESST) effect measurements, and, for 1, Mossbauer spectroscopy and diffuse reflectance data.
74 the heme iron dynamics in cytochrome c with Mossbauer spectroscopy and especially nuclear resonance
75 scopic probes that have been interrogated by Mossbauer spectroscopy and high-field EPR spectroscopy,
77 he nanoscale was studied by a combination of Mossbauer spectroscopy and magnetic characterization.
79 ing Tc oxidation is further supported by the Mossbauer spectroscopy and micro X-ray diffraction data
81 with H(2)S to FeS(2) was followed by (57)Fe Mossbauer spectroscopy and showed a clear biological tem
84 land Gola di Lago (Switzerland) using (57)Fe Mossbauer spectroscopy and synchrotron X-ray techniques.
85 volution of Fe and Zn speciation with (57)Fe Mossbauer spectroscopy and with bulk and micro-X-ray abs
88 d using combined high resolution synchrotron Mossbauer spectroscopy and x-ray diffraction techniques
89 ation was observed at high C/Fe ratios using Mossbauer spectroscopy and X-ray diffraction, and X-ray
90 X-ray absorption spectroscopy (XAS), (57)Fe Mossbauer spectroscopy and X-ray diffraction, we followe
91 its environment can be used to realize laser Mossbauer spectroscopy and, with it, new types of strain
92 neral composition were analyzed using (57)Fe Mossbauer spectroscopy and/or X-ray diffraction analysis
93 , electron paramagnetic resonance (EPR), and Mossbauer spectroscopies, and cryospray ionization mass
95 olarization surface enhanced NMR (DNP-SENS), Mossbauer spectroscopy, and computational chemistry were
100 In addition, X-ray crystallography, (57)Fe Mossbauer spectroscopy, and EPR spectroscopy were used t
101 Operando experiments by X-ray diffraction, Mossbauer spectroscopy, and galvanostatic intermittent t
102 iffraction, X-ray fluorescence spectroscopy, Mossbauer spectroscopy, and gas-phase DART mass spectrom
103 r characterization by X-ray crystallography, Mossbauer spectroscopy, and high-field EPR spectroscopy.
104 spectroscopy, single crystal X-ray analysis, Mossbauer spectroscopy, and magnetic susceptibility meas
105 atography, transmission electron microscopy, Mossbauer spectroscopy, and magnetic susceptibility meas
106 y photoelectron spectroscopy (XPS), in-field Mossbauer spectroscopy, and magnetization measurements e
107 ion of methods including transient kinetics, Mossbauer spectroscopy, and mass spectrometry, we demons
108 characterized using X-ray diffraction (XRD), Mossbauer spectroscopy, and scanning electron microscopy
109 nt study, powder XRD, synchrotron-based XAS, Mossbauer spectroscopy, and TEM demonstrated unambiguous
110 tored temporally using UV-vis absorption and Mossbauer spectroscopy, and the intermediate [2Fe-2S](2+
111 diffraction, time-domain (151)Eu synchrotron Mossbauer spectroscopy, and X-ray absorption spectroscop
112 etween 1 and its reduction product by (57)Fe Mossbauer spectroscopy are discussed, and the reduction
113 yperfine sublevel correlation (HYSCORE), and Mossbauer spectroscopies as well as protein-film electro
114 ray crystallography, NMR-, FTIR-, and (57)Fe-Mossbauer spectroscopy as well as by electronic absorpti
116 estigated using transmission and synchrotron Mossbauer spectroscopy at high pressures and low tempera
117 he present study also demonstrates that 57Fe Mossbauer spectroscopy can be employed to study the in v
118 tration of laser-induced conversion electron Mossbauer spectroscopy (CEMS) of the (229)Th isomer in a
119 etic method is compared with low-temperature Mossbauer spectroscopy, CO pulse chemisorption, and elec
120 X-ray absorption fine structure (EXAFS) and Mossbauer spectroscopy combined with macroscopic sorptio
123 , XRD, X-ray photoelectron spectroscopy, and Mossbauer spectroscopy confirm the relationship between
126 tron paramagnetic resonance (EPR) and (57)Fe Mossbauer spectroscopy coupled with wave function based
127 een investigated using UV-vis absorption and Mossbauer spectroscopies, coupled with analytical studie
129 errous heme species in cyt c(554) by EPR and Mossbauer spectroscopies during the HAO catalyzed oxidat
131 ation state of Au was assigned using (197)Au Mossbauer spectroscopy, electron paramagnetic resonance,
133 ure of the accumulated Fe was examined using Mossbauer spectroscopy, EPR, electronic absorption spect
134 ata, as well as with spectroscopic data from Mossbauer spectroscopy, Fe K-edge high-energy resolution
138 otoelectron spectroscopy and in-field (57)Fe Mossbauer spectroscopy give unambiguous evidence that a
139 and solid-state magnetic studies, and (57)Fe Mossbauer spectroscopy has been applied to characterize
140 ess, variable-temperature and variable-field Mossbauer spectroscopy has been used to characterize the
142 ch electron paramagnetic resonance (EPR) and Mossbauer spectroscopies have been used to obtain eviden
143 es, including UV-visible absorption and 57Fe Mossbauer spectroscopies, have been used to investigate
144 gh a combination of electrochemistry, (57)Fe Mossbauer spectroscopy, high-resolution transmission ele
146 K using single-crystal X-ray diffraction and Mossbauer spectroscopy in laser-heated diamond anvil cel
147 yA)2Fe2(L)](3+), where X-ray diffraction and Mossbauer spectroscopy indicate a metal-centered oxidati
150 acterization of the reconstituted protein by Mossbauer spectroscopy indicated the presence of only [4
151 iron silicate spinel, detected previously by Mossbauer spectroscopy, is seen in the calorimetric sign
152 reactivity studies as well as in situ (57)Fe Mossbauer spectroscopy, key mechanistic features and spe
154 in (LS), as determined by the combination of Mossbauer spectroscopy, magnetic measurements, and singl
155 ished by a combination of X-ray diffraction, Mossbauer spectroscopy, magnetochemistry, and open-shell
157 ent analyses in conjunction with the EPR and Mossbauer spectroscopy measurements and the site-directe
161 peroxo) was monitored by rapid freeze-quench Mossbauer spectroscopy, multiple diferric mu-oxo/mu-hydr
162 structures of the compounds were studied by Mossbauer spectroscopy, NMR spectroscopy, magnetochemist
164 measurements, sequential Fe extractions, and Mossbauer spectroscopy of 12 h light-dark cycle incubate
165 hows remarkable success on the prediction of Mossbauer spectroscopy of alpha-Fe, chi-Fe5C2 and theta-
173 h sediment chemistry, X-ray diffraction, and Mossbauer spectroscopy on sediments retrieved from an or
175 ron paramagnetic resonance spectroscopy, and Mossbauer spectroscopy pinpoint the hexacoordinate Co(II
176 both oxygenated intermediates by UV-vis and Mossbauer spectroscopy, proposed structures from DFT and
177 Characterization by resonance Raman and Mossbauer spectroscopy provides complementary insights i
179 pecies, which we characterized by UV/vis and Mossbauer spectroscopies, quantum mechanical calculation
180 erived from transient-state enzyme kinetics, Mossbauer spectroscopy, reaction product analysis, X-ray
184 copy) and phase analyses (X-ray diffraction, Mossbauer spectroscopy) reveal the formation of Fe(3)O(4
185 nd electron microscopy, as well as Raman and Mossbauer spectroscopy, reveal magnetite nanoparticles i
186 s, in conjunction with X-ray diffraction and Mossbauer spectroscopy, reveal the presence of weak ferr
187 e observed in incubated sediments and (57)Fe Mossbauer spectroscopy revealed that Fe(III) associated
192 ing limitation using a combination of (57)Fe Mossbauer spectroscopy, SC-XRD (single-crystal X-ray dif
194 F(peroxo) accumulated at 70 ms determined by Mossbauer spectroscopy showed that F(peroxo) decays into
197 ray absorption spectroscopy (XAS) and (57)Fe Mossbauer spectroscopy showed the presence of mixed-vale
198 etic ordering below 70 K was found by (57)Fe Mossbauer spectroscopy, showing that a fraction of the F
199 xidation state of the metal sites by EPR and Mossbauer spectroscopies shows that the Rieske cluster a
203 ure magnetization and applied magnetic field Mossbauer spectroscopy studies revealed a very large dep
204 4Fe-4S] (2+) configuration, as determined by Mossbauer spectroscopy, suggesting that it contained at
207 mperature arises from cation reordering, and Mossbauer spectroscopy supports this interpretation.
208 ow here by SEC, circular dichroism (CD), and Mossbauer spectroscopies that iron binds to the assembly
211 analogous to the capabilities of traditional Mossbauer spectroscopy, the sensitivity of the nucleus t
212 e-quench electron paramagnetic resonance and Mossbauer spectroscopies to the mouse R2 reaction to eva
214 were combined with magnetic measurements and Mossbauer spectroscopy to elucidate the electronic and s
217 ray diffraction measurements supplemented by Mossbauer spectroscopy up to pressures ~ 150 GPa, we doc
218 g studies, cyclic voltammetry, magnetometry, Mossbauer spectroscopy, UV-vis-NIR spectroscopy, NMR spe
224 pectrometry, UV-visible absorption, EPR, and Mossbauer spectroscopies, we characterized nsp13 as an i
225 ation of density functional calculations and Mossbauer spectroscopy, we have examined chloroperoxidas
227 igh-energy x-ray diffraction and time-domain Mossbauer spectroscopy, we show that nematicity and magn
229 peciation are subsequently studied by (57)Fe Mossbauer spectroscopy, which exclusively detects (57)Fe
231 amagnetic quadrupole iron doublet appears in Mossbauer spectroscopy with delta = 0.06 mm/s and DeltaE
232 d characterization by X-ray crystallography, Mossbauer spectroscopy, X-ray absorption spectroscopy (X