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1 derived from density functional theory with extended X-ray absorption fine structure.
2 , reflecting their oxidation states, and the extended X-ray absorption fine structure amplitudes and
4 near edge structure (XANES) spectroscopy and extended X-ray absorption fine structure analyses demons
5 By x-ray absorption near edge structure and extended x-ray absorption fine structure analyses of iso
6 re of Fe(2+) changed upon increasing the pH; extended X-ray absorption fine structure analysis found
9 nalysis of the cobalt-containing protein and extended X-ray absorption fine structure analysis of the
12 and nuclear magnetic resonance spectroscopy, extended x-ray absorption fine structure analysis, and q
15 ransmission electron microscopy coupled with extended X-ray absorption fine structure and first-princ
16 n MMO reaction intermediate Q, obtained from extended x-ray absorption fine structure and Mossbauer a
17 (III) has been studied by means of ultrafast extended x-ray absorption fine structure and optical tra
20 experiments (X-ray and neutron diffraction, extended X-ray absorption fine structure) and result in
23 e errors of the two techniques; however, the extended X-ray absorption fine structure data allow the
27 tion spectroscopic data, including polarized extended X-ray absorption fine structure data of oriente
31 Such interactions are supported further by extended X-ray absorption fine structure (EXAFS) analyse
34 ctivation intermediate using Fe- and Mn-edge extended X-ray absorption fine structure (EXAFS) analysi
35 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analysi
36 ructure (XANES) and Fourier transformed (FT) extended X-ray absorption fine structure (EXAFS) analysi
37 lysis is reported that uses a combination of extended X-ray absorption fine structure (EXAFS) analysi
38 nce of Sr-Si(Al) bond distances in Sr K-edge extended X-ray absorption fine structure (EXAFS) analysi
40 s of the reaction were determined along with extended X-ray absorption fine structure (EXAFS) and IR
41 e of Pinal Creek, AZ, was investigated using extended X-ray absorption fine structure (EXAFS) and mic
43 anosarcina thermophila were characterized by extended X-ray absorption fine structure (EXAFS) and the
45 6, 32, 64, x = n/2), was studied by means of extended X-ray absorption fine structure (EXAFS) and X-r
54 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) data in
62 adiation photoemission spectroscopy (SRPES), extended X-ray absorption fine structure (EXAFS) measure
64 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) methodo
65 may contain information not provided by the extended X-ray absorption fine structure (EXAFS) part of
72 ral clay, and to explain the measured K-edge extended X-ray absorption fine structure (EXAFS) spectra
74 pping and Ag speciation was determined using extended X-ray absorption fine structure (EXAFS) spectro
76 eing anchored by two Rh-O bonds, as shown by extended X-ray absorption fine structure (EXAFS) spectro
79 y spectrometry (EDS), UV-vis absorption, and extended X-ray absorption fine structure (EXAFS) spectro
80 d site-specific mutagenesis with zinc K-edge extended X-ray absorption fine structure (EXAFS) spectro
81 ite in VanX, electronic absorption, EPR, and extended x-ray absorption fine structure (EXAFS) spectro
82 H) MCD, X-ray absorption (XAS) pre-edge, and extended X-ray absorption fine structure (EXAFS) spectro
83 X-ray absorption near edge spectroscopy and extended X-ray absorption fine structure (EXAFS) spectro
84 s in lead adsorption to hematite by coupling extended X-ray absorption fine structure (EXAFS) spectro
85 etailed structural characterization using Mn extended X-ray absorption fine structure (EXAFS) spectro
87 ry, high-energy X-ray scattering (HEXS), and extended X-ray absorption fine structure (EXAFS) spectro
88 r Hg(0) oxidation activity and analyzed with extended X-ray absorption fine structure (EXAFS) spectro
89 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectro
90 d by synchrotron X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) spectro
91 absorption near edge structure (XANES), and extended X-ray absorption fine structure (EXAFS) spectro
92 rization of trace elements in minerals using extended X-ray absorption fine structure (EXAFS) spectro
93 tion experiments combined with Mossbauer and extended X-ray absorption fine structure (EXAFS) spectro
94 bined with surface complexation modeling and extended X-ray absorption fine structure (EXAFS) spectro
95 nation of the solid phase using Hg LIII-edge extended X-ray absorption fine structure (EXAFS) spectro
96 ) and Mn(III) hydrous oxides] was studied by extended X-ray absorption fine structure (EXAFS) spectro
97 cale characterization of adsorbed U(VI) with extended X-ray absorption fine structure (EXAFS) spectro
98 n Fourier-Transform Infrared (ATR FT-IR) and Extended X-ray Absorption Fine Structure (EXAFS) spectro
99 gregates was determined by synchrotron-based extended X-ray absorption fine structure (EXAFS) spectro
102 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectro
104 r local (<6 A) structure by As and Fe K-edge extended X-ray absorption fine structure (EXAFS) spectro
106 ination of neutron and X-ray diffraction and extended X-ray absorption fine structure (EXAFS) spectro
108 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectro
109 capacity and the kinetics of adsorption and Extended X-ray Absorption Fine Structure (EXAFS) Spectro
110 e of phosphate and goethite were examined by extended X-ray absorption fine structure (EXAFS) spectro
112 ) interaction in Met121Cys was detectable by extended X-ray absorption fine structure (EXAFS) spectro
114 absorption near-edge structure (XANES), and extended X-ray absorption fine structure (EXAFS) suggest
115 by combining microscopy, chemisorption, and extended X-ray absorption fine structure (EXAFS) techniq
116 r distribution function (d-PDF) analysis and extended X-ray absorption fine structure (EXAFS) were us
117 eparations and x-ray spectroscopy, including extended x-ray absorption fine structure (EXAFS), allowe
118 r resonance vibrational spectroscopy (NRVS), extended X-ray absorption fine structure (EXAFS), and de
120 ay absorption near edge structure (XANES) or extended X-ray absorption fine structure (EXAFS), it all
121 y absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS), we fin
128 arisons between AP and NPP, we measured zinc extended x-ray absorption fine structure for AP and NPP
129 resonance, and X-ray absorption spectroscopy/extended X-ray absorption fine-structure investigation o
130 f the (14)N ENDOR data, together with recent extended X-ray absorption fine structure measurements of
131 t K-shell X-ray absorption spectroscopy, and extended X-ray absorption fine structure measurements.
132 X-ray diffraction and single-crystal EXAFS (Extended X-ray Absorption Fine Structure) measurements.
133 doublet peak in the Fourier transform of the extended x-ray absorption fine structure of the coral co
134 tion spectroscopy (specifically, analysis of extended X-ray absorption fine structure or EXAFS), we i
135 lpha fluorescence, we are able to extend the extended x-ray absorption fine structure range beyond th
143 ough direct comparisons with high-resolution extended X-ray absorption fine structure spectroscopic d
144 rom X-ray absorption near edge structure and extended X-ray absorption fine structure spectroscopies,
145 ligand at the Mo center, confirming earlier extended X-ray absorption fine structure spectroscopy (E
147 As demonstrated by atomic absorption and extended X-ray absorption fine structure spectroscopy (E
149 ucture (XANES) spectroscopy and Hg LIII-edge extended X-ray absorption fine structure spectroscopy (E
150 ma-Al(2)O(3) (gamma-alumina) at pH 7.5 using extended X-ray absorption fine structure spectroscopy (E
151 and Acid Birnessite (AB) were determined by Extended X-ray Absorption Fine Structure Spectroscopy (E
152 surface-associated U using grazing incidence extended X-ray absorption fine structure spectroscopy (G
154 Te/Sb2Te3] interfacial structure by means of Extended X-Ray Absorption Fine Structure spectroscopy an
156 nce vibrational spectroscopy (NRVS) aided by extended X-ray absorption fine structure spectroscopy an
158 ar magnetic resonance (NMR) spectroscopy and extended X-ray absorption fine structure spectroscopy of
159 Comparisons of iron-ligand geometry using extended x-ray absorption fine structure spectroscopy sh
162 f 0.02 A by means of ultrafast time-resolved extended x-ray absorption fine structure spectroscopy.
163 this complex was investigated via Ag K-edge extended X-ray absorption fine structure spectroscopy.
164 (Pt1/Co3O4), evidenced by in situ studies of extended X-ray absorption fine structure spectroscopy.
165 ction, transmission electron microscopy, and extended X-ray absorption fine structure spectroscopy.
168 usly proposed to bind Zn(2+) on the basis of extended X-ray absorption fine-structure spectroscopy.
172 an other MoFe proteins and has been shown by extended X-ray absorption fine structure studies to cont
174 ination of X-ray absorption spectroscopy and extended X-ray absorption fine structure, supported by d
175 duction to the Cu(I) form, which is shown by extended X-ray absorption fine structure to be composed
177 EPR features, X-ray absorption spectroscopy/extended X-ray absorption fine structure (XAS/EXAFS) spe
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