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1 f and 6d electronic states by means of X-ray magnetic circular dichroism.
2 n behavior and geometry in solution by using magnetic circular dichroism.
3 opic methods, including X-ray absorption and magnetic circular dichroism.
4 orbital moment of Co, as observed with x-ray magnetic circular dichroism.
5 netometry, ferromagnetic resonance and X-ray magnetic circular dichroism.
6 sion electron microscopy combined with x-ray magnetic circular dichroism.
7 defined by electrodic reduction monitored by magnetic circular dichroism.
8 imagnetic material, the AOS is attributed to magnetic circular dichroism and angular momentum transfe
10 e trivalent Sm dopant, as confirmed by X-ray magnetic circular dichroism and first-principles calcula
11 ed by different probing depths, namely X-ray magnetic circular dichroism and photoelectron spectrosco
12 udy, we have examined these two enzymes with magnetic circular dichroism and UV-visible absorption sp
13 element-specific techniques, including X-ray magnetic circular dichroism and X-ray absorption spectro
14 /Pd trilayer system is investigated by x-ray magnetic circular dichroism and x-ray resonant magnetic
16 element-specific measurement technique x-ray magnetic circular dichroism, and determined the full mag
17 nge, we have employed electronic absorption, magnetic circular dichroism, and electron paramagnetic r
18 copic techniques, including resonance Raman, magnetic circular dichroism, and electron paramagnetic r
19 f wild-type nNOS with UV-visible absorption, magnetic circular dichroism, and electron paramagnetic r
20 yme variants by using electronic absorption, magnetic circular dichroism, and electron paramagnetic r
21 cterization (absorption, circular dichroism, magnetic circular dichroism, and electron paramagnetic r
22 tiometry and characterization by UV-visible, magnetic circular dichroism, and electron paramagnetic r
23 been characterized by electronic absorption, magnetic circular dichroism, and electron paramagnetic r
25 (2+)Cbi (+) by using electronic absorption, magnetic circular dichroism, and electron paramagnetic r
27 the CFeSP, we have combined resonance Raman, magnetic circular dichroism, and EPR spectroscopic metho
28 bauer, resonance Raman, variable-temperature magnetic circular dichroism, and EPR spectroscopies.
29 e using element specific time-resolved x-ray magnetic circular dichroism, and ferromagnetic resonance
31 UV-visible absorption, variable temperature magnetic circular dichroism, and resonance Raman data, i
35 s probed by UV-visible, variable temperature magnetic circular dichroism, and x-ray absorption spectr
36 ronic spectra of porphycenes: Absorption and magnetic circular dichroism are discussed, together with
37 oment, which was directly confirmed by X-ray magnetic circular dichroism, as an element-specific prob
40 produces a six-coordinate circular dichroism/magnetic circular dichroism (CD/MCD) spectra for ferrous
41 cterized by electron paramagnetic resonance, magnetic circular dichroism, circular dichroism, and ele
42 d resonant X-ray absorption spectroscopy and magnetic circular dichroism, combined with hard X-ray ph
45 examined the absorption, circular dichroism, magnetic circular dichroism, electron paramagnetic reson
46 of low-temperature electronic absorption and magnetic circular dichroism, electron paramagnetic reson
47 circular dichroism, and variable-temperature magnetic circular dichroism, electron paramagnetic reson
48 Electron Microscope (TEM) to obtain Electron Magnetic Circular Dichroism (EMCD) signals as a function
49 -visible absorption and variable-temperature magnetic circular dichroism, EPR, resonance Raman and Mo
51 nd atomic site specific Fe L(2,3)-edge X-ray magnetic circular dichroism indicated that MtoA directly
55 using electronic absorption, low-temperature magnetic circular dichroism (MCD) and variable-temperatu
64 itored by atomic absorption spectrometry and magnetic circular dichroism (MCD) shows that the enzyme
68 Ferrous M79A and H229A HtsA mutants possess magnetic circular dichroism (MCD) spectra that are simil
70 consistent with circular dichroism (CD) and magnetic circular dichroism (MCD) spectroscopic data and
71 ave employed electronic absorption (Abs) and magnetic circular dichroism (MCD) spectroscopic techniqu
72 variable-temperature, variable-field (VTVH) magnetic circular dichroism (MCD) spectroscopies (FeII s
74 aramagnetic resonance (EPR), absorption, and magnetic circular dichroism (MCD) spectroscopies show th
79 n-deficient bulk SrTiO3-delta crystals using magnetic circular dichroism (MCD) spectroscopy and SQUID
80 s heme identity for LPO, we used comparative magnetic circular dichroism (MCD) spectroscopy of LPO ve
82 ectronic absorption and variable-temperature magnetic circular dichroism (MCD) spectroscopy to experi
83 is described with an emphasis on the use of magnetic circular dichroism (MCD) spectroscopy to valida
84 ed photodissociation (IRPD), absorption, and magnetic circular dichroism (MCD) spectroscopy, coupled
90 uency electron paramagnetic resonance (EPR), magnetic circular dichroism (MCD), and nuclear magnetic
91 In the current study, resonance Raman (rR), magnetic circular dichroism (MCD), and nuclear magnetic
92 on, we employed electronic absorption (Abs), magnetic circular dichroism (MCD), and resonance Raman s
93 K-edge X-ray absorption, UV-vis absorption, magnetic circular dichroism (MCD), and resonance Raman s
94 X were studied with circular dichroism (CD), magnetic circular dichroism (MCD), and variable temperat
96 ng a combination of circular dichroism (CD), magnetic circular dichroism (MCD), and variable-temperat
100 A combination of circular dichroism (CD), magnetic circular dichroism (MCD), and variable-temperat
101 als were studied by magnetic susceptibility, magnetic circular dichroism (MCD), and X-ray magnetic ci
102 riety of spectroscopic methods ((119)Sn-NMR, magnetic circular dichroism (MCD), electron paramagnetic
103 UV/visible absorption, variable-temperature magnetic circular dichroism (MCD), EPR, and resonance Ra
104 bination of near-IR circular dichroism (CD), magnetic circular dichroism (MCD), variable temperature
106 DHBD, EC 1.13.11.39), has been studied using magnetic circular dichroism (MCD), variable-temperature
107 roscopy, we have used electronic absorption, magnetic circular dichroism (MCD), variable-temperature,
108 , to our knowledge, the first tabletop X-ray magnetic circular dichroism measurements at the N4,5 abs
109 ic spectrum, and use them to implement X-ray magnetic circular dichroism measurements in a tabletop-s
112 n (mu-XRD) using a focused X-ray beam, X-ray Magnetic Circular Dichroism - Photo Emission Electron Mi
113 characteristic feature of NI is the intense magnetic circular dichroism pseudo-A feature (a pair of
114 utagenesis, ligand-binding measurements, and magnetic circular dichroism, resonance Raman, and electr
115 Detailed low-temperature absorption and magnetic circular dichroism, resonance Raman, and electr
117 -temperature absorption, circular dichroism, magnetic circular dichroism, resonance Raman, EPR and X-
118 UV-visible absorption, variable temperature magnetic circular dichroism, resonance Raman, Mossbauer,
124 rption, electron paramagnetic resonance, and magnetic circular dichroism spectra of these variants pr
125 rbance, electron paramagnetic resonance, and magnetic circular dichroism spectra showed a high spin f
126 53 nm, shoulder at approximately 585 nm) and magnetic circular dichroism spectra that are nearly iden
127 ibe detailed time-resolved mass spectral and magnetic circular dichroism spectral data recorded as he
128 sm, and variable-temperature, variable-field magnetic circular dichroism spectroscopic experiments ha
130 In the present study, in situ Mossbauer and magnetic circular dichroism spectroscopic studies combin
132 resonance (EPR), electronic absorption, and magnetic circular dichroism spectroscopies have been per
136 e cofactor were monitored with time-resolved magnetic circular dichroism spectroscopy after photodiss
138 e for a methyl-Ni(III) species; furthermore, magnetic circular dichroism spectroscopy identified the
141 ar structure differences, Mossbauer spectra, magnetic circular dichroism spectroscopy, and integer-sp
142 raction, electronic absorption spectroscopy, magnetic circular dichroism spectroscopy, magnetic susce
143 ion, and variable temperature/variable field magnetic circular dichroism spectroscopy, provide strong
147 Resonance Raman and variable-temperature magnetic circular dichroism studies of heme-free prepara
151 n of these systems on surfaces, ranging from magnetic circular dichroism to magnetic force microscopy
152 ant, but its lifetime agrees with a reported magnetic circular dichroism transient, which has been at
153 esized and studied by electronic absorption, magnetic circular dichroism, transmission electron micro
154 d using a combination of circular dichroism, magnetic circular dichroism, variable-temperature variab
156 n of UV/visible/near-IR variable-temperature magnetic circular dichroism (VTMCD) and EPR spectroscopi
157 zed protein and EPR and variable-temperature magnetic circular dichroism (VTMCD) studies of the as-pr
158 the combination of EPR, variable-temperature magnetic circular dichroism (VTMCD), and resonance Raman
159 -visible absorption and variable-temperature magnetic circular dichroism (VTMCD), EPR, and resonance
160 /NIR absorption, CD and variable-temperature magnetic circular dichroism (VTMCD), EPR, and X-ray abso
161 ation of variable-temperature variable-field magnetic circular dichroism (VTVH MCD) and powder/single
162 AS), and variable-temperature-variable-field magnetic circular dichroism (VTVH MCD) spectroscopy, we
163 e, using variable-temperature variable field magnetic circular dichroism (VTVH MCD) spectroscopy.
164 tein, a variable-temperature, variable-field magnetic circular dichroism (VTVH-MCD) spectroscopic stu
166 ts, X-ray absorption spectroscopy, and X-ray magnetic circular dichroism, we have determined the natu
167 r characterization by electronic absorption, magnetic circular dichroism, X-ray absorption, magnetic
168 N@C(80) endofullerene was studied with X-ray magnetic circular dichroism (XMCD) and a magnetometer wi
169 xial Fe/graphene interface by means of X-ray magnetic circular dichroism (XMCD) and density functiona
174 , x-ray absorption spectroscopy (XAS), x-ray magnetic circular dichroism (XMCD), and specular/off-spe
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