戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 2NiO4+delta as a model system for a combined paramagnetic (17)O NMR and DFT methodology, the approach
2 he photohole leads to conversion of Ag(+) to paramagnetic Ag(2+).
3  In this system, a gadolinium-based nonionic paramagnetic agent is used in conjunction with magnetic
4 tudied computationally, and the contributing paramagnetic and diamagnetic factors were extracted.
5 taining samples are ferromagnetic at 5 K and paramagnetic at 300 K.
6 studying the local environment of Li ions in paramagnetic battery materials, the use of (17)O NMR in
7 istance between the magnet and the measuring paramagnetic bead with unfolding/folding steps.
8 netic sticks that capture protein A/G-coated paramagnetic beads bound to antibody-luciferase-labeled
9 s, were chemically coupled to the surface of paramagnetic beads for the sensitive detection of ricin
10 ceeding 0.2 eV, indicating that the observed paramagnetic behavior around 10K is due to superparamagn
11  Magnetization studies revealed nearly ideal paramagnetic behavior at high temperatures for both radi
12 conductors (MIECs) have been hampered by the paramagnetic behavior of these systems.
13  displays Pauli-like temperature independent paramagnetic behavior, with chiTIP = 6 x 10(-4) emu mol(
14 he pyrene knots, enabling the formation of a paramagnetic carbon structure with high spin density.
15 s by selectively doping one component with a paramagnetic center in order to measure the domain size
16 erage distance between the F nucleus and the paramagnetic center.
17                         The incorporation of paramagnetic centers into NPs offers new opportunities t
18 the existence of exchange coupling among the paramagnetic centers mediated by the conduction electron
19 the nanostructure, the photoluminescence and paramagnetic characteristic of Gd2O3:Eu(3+) nanorods wer
20 c exchange coupling to enable observation of paramagnetic chemical exchange saturation transfer (PARA
21 us solid-solid transition in a 2D crystal of paramagnetic colloidal particles is induced by a magneti
22 /EDTA extracts of a grassland soil, of which paramagnetic contaminations were removed with sodium sul
23 Es) and heteronuclear (1)H-(15)N NOEs if the paramagnetic contribution to the longitudinal relaxation
24 ysis reveals the dominating influence of the paramagnetic contribution yielding a highly deshielded a
25                                  The largest paramagnetic contribution, which originates from the cou
26                                          The paramagnetic contributions to the (13)C NMR chemical shi
27 hancement (sPRE) in the presence of an inert paramagnetic cosolute allows the assessment of protein d
28                                          For paramagnetic Cr(III), EPR (HYSCORE) spectroscopy shows h
29                            The complement of paramagnetic Cu(II) ions in the Mnx protein complex was
30 al (delta(orb), temperature-independent) and paramagnetic (delta(para), temperature-dependent) contri
31                                     However, paramagnetic DNP polarizing agents can have deleterious
32  In magnetically doped semiconductors, where paramagnetic dopants (such as Mn(2+), Co(2+) and so on)
33 onance tuning (MRET), which occurs between a paramagnetic 'enhancer' and a superparamagnetic 'quenche
34                     Mechanistic and electron paramagnetic (EPR) spectroscopic data supports the concl
35 ne-electron reduction yields a spin-coupled, paramagnetic Fe(III)/Fe(IV) intermediate, denoted X, who
36                                         This paramagnetic Fe3O4@GO composite (1microm size range) was
37 oglobin (oxyHb) with reversibly bound O2, or paramagnetic ferric methemoglobin (metHb).
38 prosthetic groups of the globin chains: from paramagnetic ferrous Hb to diamagnetic ferrous oxyhemogl
39 s that coat the entire enzyme surface with a paramagnetic field of sufficient strength to determine i
40                    Importantly, an identical paramagnetic fingerprint was observed in the presence of
41                      Excessive production of paramagnetic free radicals in nonhippocampus brain tissu
42 it qualitatively resembles V(CO)6 , the only paramagnetic homoleptic metal carbonyl isolable under am
43 e technique transfers spin polarization from paramagnetic impurities at nanodiamond surfaces to (1)H
44 atial and temporal properties of the surface paramagnetic impurities provide insight to prolonging th
45 -field theory (LDA+DMFT) we characterize its paramagnetic insulating and metallic phases, showing the
46 ctron spectroscopy-the band structure of the paramagnetic insulating phase of Ca2RuO4 and show how it
47 resence of magnetic interactions between the paramagnetic interlayer V ions and a Kondo screening of
48 hich phases have different concentrations of paramagnetic ions, the phases can provide different reso
49  ZnS crystalline lattice related to specific paramagnetic ions.
50 a have recently been discovered in oxides of paramagnetic Ir(4+) ions, widely known as 'iridates'.
51 clusters caused by spin interactions between paramagnetic iron atoms.
52 he same sample preparation (i.e., mutations, paramagnetic labeling, and reconstitution in lipid bilay
53                        We present a covalent paramagnetic lanthanide-binding tag (LBT) for increasing
54  are invoked by the covalent attachment of a paramagnetic lanthanoid chelating tag to the ligand of i
55 e induced throughout a 40-nm-thick amorphous paramagnetic layer through proximity to ferromagnets, me
56 that probe the local environment around O in paramagnetic Li-ion cathode materials are essential in o
57                               We introduce a paramagnetic ligand tagging approach that enables locali
58  in bulk material and still in excess of the paramagnetic limit.
59 l nitronyl nitroxides via the interaction of paramagnetic lithium derivatives as C-nucleophiles with
60 ic materials, such as diamagnetic copper and paramagnetic manganese, to overcome the Stoner criterion
61 levitation (MagLev) of diamagnetic or weakly paramagnetic materials suspended in a paramagnetic solut
62  of solid diamagnetic objects suspended in a paramagnetic medium.
63 nd magnetic properties of giant 3d and 3d/4f paramagnetic metal clusters in moderate oxidation states
64     In nuclear magnetic resonance (NMR), the paramagnetic metal ion interacting with the sugars cause
65              This is especially true for the paramagnetic metal LaNiO3, which can become insulating a
66 ntiferromagnetic insulator SrMnO3 and the 5d paramagnetic metal SrIrO3 is enormously strong, yielding
67 resonance (EPR) spectroscopy to characterize paramagnetic metal-organic and free radical species from
68 ntiferromagnetic Mott insulating state and a paramagnetic metallic state.
69                      The results show that a paramagnetic Mo(V) species is generated when reduced enz
70 ound state and around room temperatures, are paramagnetic Mott insulators.
71                    In this study we focus on paramagnetic NAMI analogs of a general structure [4-R-py
72 ted aggregation of fluorescent reporters and paramagnetic nanoparticle in a sandwich immunoassay was
73                                              Paramagnetic nature of Mn(2+) and its close resemblance
74                                          The paramagnetic nature of protein complexes is found to ser
75                            The effect of the paramagnetic nature of these complexes on the (1)H and (
76                        The reactivity of two paramagnetic nickel(I) compounds, CpNi(NHC) (where Cp=cy
77                                          The paramagnetic nitroxide spin label was attached to Cys re
78                                          The paramagnetic nitroxides (spin-adducts) formed as a resul
79 ith some success for many decades to explain paramagnetic NMR pseudocontact shifts, and has been the
80                       A detailed analysis of paramagnetic NMR shifts in a series of isostructural lan
81                                        Using paramagnetic NMR spectroscopy with a lanthanoid tag, we
82 developed a novel docking strategy guided by paramagnetic NMR that positions a triple-helical collage
83 elds (30 mT and above), the (29)Si and (13)C paramagnetic nuclear spin baths are decoupled.
84        For the large class of materials with paramagnetic or diamagnetic response, simple functional
85 le to MIECs and other functionally important paramagnetic oxides.
86   The simple, rapid magnetic manipulation of paramagnetic particles (PMPs) paired with the wide range
87                                              Paramagnetic particles heavily decorated with anti-ERalp
88      In the case of palladium, a mononuclear paramagnetic Pd(I) derivative was readily isolated from
89 ase and heavily damped electromagnons in the paramagnetic phase of LiCrO2.
90 s C) are insulators with lower ferrimagnetic-paramagnetic phase transition temperature.
91 voltage reversibly drives a ferromagnetic-to-paramagnetic phase transition.
92                    Our results show that the paramagnetic (PM) to HO and LMAFM phase transitions are
93  a recently developed multifunctional trityl paramagnetic probe and electron paramagnetic resonance (
94  reversible exchange processes as functional paramagnetic probes.
95 ight-controlled effects observed for GNRs on paramagnetic properties and activities of surrounding mo
96 dependent effects of gold nanorods (GNRs) on paramagnetic properties of nitroxide spin probes.
97 ethylpiperidine core do not appear, implying paramagnetic properties.
98 rising the cation channel TRPV4 fused to the paramagnetic protein ferritin.
99 d-state quenching via (1) energy transfer or paramagnetic quenching by the Co(II) species and (2) exc
100 henylazoimidazole-based PDLs that switch the paramagnetic ratio of the investigated nickel species by
101  Electron spin decoupling can mitigate these paramagnetic relaxation effects.
102   The structure was modeled using long-range paramagnetic relaxation enhancement (PRE) distance restr
103                                  Here we use paramagnetic relaxation enhancement (PRE) measured by NM
104                                  Here we use paramagnetic relaxation enhancement (PRE) NMR spectrosco
105 1)H nuclear Overhauser enhancement (NOE) and paramagnetic relaxation enhancement (PRE) techniques.
106 nuclear magnetic resonance experiments using paramagnetic relaxation enhancement (PRE), which is sens
107 how that the accurate measurement of solvent paramagnetic relaxation enhancement (sPRE) in the presen
108                                      Solvent paramagnetic relaxation enhancement analysis showed that
109                               We propose NMR paramagnetic relaxation enhancement as a new tool to det
110                               Intermolecular paramagnetic relaxation enhancement broadening of IL-8 (
111 coupling data, amide protection factors, and paramagnetic relaxation enhancement distances, in combin
112                                              Paramagnetic relaxation enhancement experiments confirm
113                             Fluorescence and paramagnetic relaxation enhancement experiments showed t
114                                              Paramagnetic relaxation enhancement has been proven a po
115                                              Paramagnetic relaxation enhancement is an NMR technique
116                                    Moreover, paramagnetic relaxation enhancement studies show that Tr
117 n with liposomes is mapped by intermolecular paramagnetic relaxation enhancement using Gd(3+)-tagged
118                                 Fluorine NMR paramagnetic relaxation enhancement was evaluated as a v
119 are encounter complexes using intermolecular paramagnetic relaxation enhancement, a highly sensitive
120                   Subsequent measurements by paramagnetic relaxation enhancement, analytical ultracen
121 r tags that can aid in the interpretation of paramagnetic relaxation enhancement, double electron-ele
122                                              Paramagnetic relaxation enhancement- and CSP-NMR-guided
123 scopy, residual dipolar couplings (RDCs) and paramagnetic relaxation enhancements (PREs).
124                                      Solvent paramagnetic relaxation enhancements (sPREs) proved to b
125                                              Paramagnetic relaxation enhancements also reveal an exte
126 of spin-label conformers against intradomain paramagnetic relaxation enhancements with a genetic algo
127                        Both DFT and electron paramagnetic resonance (EPR) analyses further indicate t
128                                     Electron paramagnetic resonance (EPR) analysis detected signals o
129                                     Electron paramagnetic resonance (EPR) and electron-nuclear double
130                        In contrast, electron paramagnetic resonance (EPR) and nuclear magnetic resona
131 ted in more detail by time-resolved electron paramagnetic resonance (EPR) and quantum chemical calcul
132 d by continuous wave (CW) and pulse electron paramagnetic resonance (EPR) characterization.
133                        We show that electron paramagnetic resonance (EPR) combined with atomic absorp
134  of MCR-ALS, for the first time, on electron paramagnetic resonance (EPR) imaging data sets that will
135                               Pulse electron paramagnetic resonance (EPR) is being applied to ever mo
136                              Pulsed electron paramagnetic resonance (EPR) measurements enabled the in
137                               Using electron paramagnetic resonance (EPR) of a bifunctional spin labe
138                                     Electron paramagnetic resonance (EPR) of biomolecules spin-labele
139      High-frequency (263 GHz) pulse electron paramagnetic resonance (EPR) of the NH2Y*s reported the
140             Moreover, our extensive electron paramagnetic resonance (EPR) results demonstrate that th
141                     Biochemical and electron paramagnetic resonance (EPR) spectroscopic analyses demo
142             Here, we used hyperfine electron paramagnetic resonance (EPR) spectroscopic methods, comb
143       In-situ temperature dependent electron paramagnetic resonance (EPR) spectroscopic studies show
144 family by magnetometry, optical and electron paramagnetic resonance (EPR) spectroscopies and modellin
145 ption (XAS), and emission (XES) and electron paramagnetic resonance (EPR) spectroscopies in the solid
146 and continuous wave (CW) and pulsed electron paramagnetic resonance (EPR) spectroscopies revealed tha
147 oupled to UV/visible absorption and electron paramagnetic resonance (EPR) spectroscopies support a me
148 uclear Magnetic Resonance (NMR) and Electron Paramagnetic Resonance (EPR) spectroscopies to distingui
149 ctron-electron resonance (DEER) and electron paramagnetic resonance (EPR) spectroscopies.
150  (Ph4P)2[VO(C3S4O)2] (4), by pulsed electron paramagnetic resonance (EPR) spectroscopy and compared t
151                    A combination of electron paramagnetic resonance (EPR) spectroscopy and computatio
152 e been employed in combination with electron paramagnetic resonance (EPR) spectroscopy at defined ele
153 n of magnetic anisotropy using both electron paramagnetic resonance (EPR) spectroscopy for its experi
154                                     Electron paramagnetic resonance (EPR) spectroscopy is a powerful
155 el was fitted to 180 data points of electron paramagnetic resonance (EPR) spectroscopy measurements o
156 , we report that absorption-display electron paramagnetic resonance (EPR) spectroscopy of nonirradiat
157      In the first use of high-field electron paramagnetic resonance (EPR) spectroscopy to characteriz
158 his series of molecules with pulsed electron paramagnetic resonance (EPR) spectroscopy to determine t
159 mplex, as demonstrated by (1)H NMR, electron paramagnetic resonance (EPR) spectroscopy, equilibrium d
160 Mnx protein complex was examined by electron paramagnetic resonance (EPR) spectroscopy.
161 ometry, continuous wave, and pulsed electron paramagnetic resonance (EPR) spectroscopy.
162 ) analysis and multifrequency pulse electron paramagnetic resonance (EPR) spectroscopy.
163 nx protein complex were examined by electron paramagnetic resonance (EPR) spectroscopy.
164 escence (PL) microscopy imaging and electron paramagnetic resonance (EPR) spectroscopy.
165 able temperature using steady-state electron paramagnetic resonance (EPR) spectroscopy.
166            The compound exhibits an electron paramagnetic resonance (EPR) spectrum with an unusually
167 n aqueous solution using an in situ electron paramagnetic resonance (EPR) spin trapping technique and
168 ional trityl paramagnetic probe and electron paramagnetic resonance (EPR) technique for in vivo concu
169 transferring spin polarization from electron paramagnetic resonance (EPR) to NMR.
170 stigated by time-resolved and pulse electron paramagnetic resonance (EPR) with laser excitation.
171                                     Electron paramagnetic resonance (EPR), absorption, and magnetic c
172 visible-near-infrared (UV-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear magnetic re
173    We have used chemical synthesis, electron paramagnetic resonance (EPR), and circular dichroism to
174  magnetic circular dichroism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption,
175      Here, we used a combination of electron paramagnetic resonance (EPR), stopped flow freeze quench
176 at these probes in combination with electron paramagnetic resonance (EPR)-based spectroscopy and imag
177  using site-directed spin labelling electron paramagnetic resonance (SDSL EPR) spectroscopy.
178 as investigated with spectroscopic (electron paramagnetic resonance [EPR] and UV-vis) and theoretical
179                                     Electron paramagnetic resonance analysis showed that MCPyV sT coo
180                                 The electron paramagnetic resonance analysis suggests that with the e
181 acterization of the intermediate by electron paramagnetic resonance and (13)C, (57)Fe electron nuclea
182 e/spin exchange rates determined by electron paramagnetic resonance and by molecular structural level
183                     Continuous-wave electron paramagnetic resonance and electron-nuclear double-reson
184 man cytochrome P450 3A4 (CYP3A4) by electron paramagnetic resonance and fluorescence spectroscopy.
185 been characterized by 9 and 130 GHz electron paramagnetic resonance and high-field electron nuclear d
186  at pH 1, which is characterized by electron paramagnetic resonance and in situ X-ray absorption spec
187 derived from a combined analysis of electron paramagnetic resonance and inductively coupled plasma sp
188  analyzed by X-ray crystallography, electron paramagnetic resonance and optical spectroscopy, and den
189 and nitric oxide bioavailability by electron paramagnetic resonance and phosphorylation of vasodilato
190                                     Electron paramagnetic resonance and solution magnetic moment dete
191  obtained from variable-temperature electron paramagnetic resonance and ultraviolet-visible spectrosc
192  application of Raman spectroscopy, electron paramagnetic resonance and UV-vis absorption spectroscop
193 m nitrite in erythrocytes including electron paramagnetic resonance detection of nitrosyl hemoglobin,
194               Using spin probes and electron paramagnetic resonance detection, we confirmed that carn
195 erformance of nanometer-range pulse electron paramagnetic resonance distance measurements (pulsed ele
196 e probed the protomer arrangement by solvent paramagnetic resonance enhancement, analysis of chemical
197 of these mutants led us to a set of electron paramagnetic resonance experiments that provide evidence
198 is study, continuous-wave and pulse electron paramagnetic resonance in a native outer-membrane prepar
199                                     Electron paramagnetic resonance measurements confirmed the D1-D5
200 ion of the triplet ground state via electron paramagnetic resonance measurements.
201                                     Electron paramagnetic resonance shows that their binding globally
202      We have also characterized the electron paramagnetic resonance signal of the molybdenum center i
203                     Furthermore, an electron paramagnetic resonance signal was observed when the N-be
204 we are able to clearly identify the electron paramagnetic resonance signals for four of the iron/sulf
205 quency-domain Fourier-transform THz electron paramagnetic resonance spectra obtained on Mn2Os.7MeOH a
206  by pressure-induced changes in the electron paramagnetic resonance spectra of a nitroxide side chain
207     Here we report the first pulsed electron paramagnetic resonance spectra of actinide compounds.
208 nfrared, electronic absorption, and electron paramagnetic resonance spectra of MeC3Me ((3)3) are comp
209        Electrochemical analysis and electron paramagnetic resonance spectra suggest that in aerobic c
210 d by in situ vis-NIR absorption and electron paramagnetic resonance spectroelectrochemistry.
211                                     Electron paramagnetic resonance spectroscopic spin-trapping exper
212  in-depth time-resolved optical and electron-paramagnetic resonance spectroscopic study of two crypto
213           Time-resolved optical and electron paramagnetic resonance spectroscopies show that photogen
214 erized by UV-visible, Mossbauer and electron paramagnetic resonance spectroscopies.
215 n, magnetic circular dichroism, and electron paramagnetic resonance spectroscopies.
216 azyl (DPPH) assay and by the use of electron paramagnetic resonance spectroscopy (EPR).
217                    Furthermore, our electron paramagnetic resonance spectroscopy and circular dichroi
218                 Rapid freeze-quench electron paramagnetic resonance spectroscopy and rapid chemical-q
219  pre-steady state kinetic analyses, electron paramagnetic resonance spectroscopy and single crystal X
220  of Singlet Oxygen Sensor Green, by electron paramagnetic resonance spectroscopy and the induction of
221 nd characterized by IR, UV-vis, and electron paramagnetic resonance spectroscopy as well as by quantu
222              Using high-power pulse electron paramagnetic resonance spectroscopy at Q-band frequencie
223                                     Electron paramagnetic resonance spectroscopy has been long known
224 molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a pivotal r
225                         Here, using electron paramagnetic resonance spectroscopy in combination with
226         Site-directed spin-labeling electron paramagnetic resonance spectroscopy is a useful tool to
227                                     Electron paramagnetic resonance spectroscopy of BciD indicated th
228 Electronic and variable-temperature electron paramagnetic resonance spectroscopy of the mixed-valence
229 on, near-UV circular dichroism, and electron paramagnetic resonance spectroscopy provide evidence tha
230                          Tests with electron paramagnetic resonance spectroscopy showed that Ag NPs w
231  cavities, and variable-temperature electron paramagnetic resonance spectroscopy shows that a dilute
232 tion spectroscopy and freeze-quench electron paramagnetic resonance spectroscopy support the presence
233 rein, voltammetry was combined with electron paramagnetic resonance spectroscopy to identify and defi
234  we use site-directed spin-labeling electron paramagnetic resonance spectroscopy to investigate confo
235 he use of time-resolved optical and electron paramagnetic resonance spectroscopy to probe singlet fis
236 ) in its resting conformation using electron paramagnetic resonance spectroscopy together with bioche
237 is-copper six-porphyrin nanoring by electron paramagnetic resonance spectroscopy via measurement of t
238 e mechanism of maltose stimulation, electron paramagnetic resonance spectroscopy was used to study th
239                               Using electron paramagnetic resonance spectroscopy we have characterize
240 troscopies, cyclic voltammetry, and electron paramagnetic resonance spectroscopy.
241 mal chemical vapor deposition, from electron paramagnetic resonance spectroscopy.
242 ated, and EPFRs on PM quantified by electron paramagnetic resonance spectroscopy.
243 nfirmed by site-directed spin-label electron paramagnetic resonance spectroscopy.
244 y delocalized spin, as evidenced by electron paramagnetic resonance spectroscopy.
245 )-derived radical was identified by electron paramagnetic resonance spin trapping, immunospin trappin
246          Radical clock experiments, electron paramagnetic resonance studies and density functional th
247                                     Electron paramagnetic resonance studies verify a clocklike transi
248                 Characterization by electron paramagnetic resonance techniques of several variants of
249                               Using electron paramagnetic resonance techniques, we characterized the
250 a,meso,beta fused structures, using electron paramagnetic resonance techniques.
251  porphyrin oligomers is explored by electron paramagnetic resonance techniques.
252 ransmission electron microscopy and electron paramagnetic resonance to show that the presence of anio
253 directed spin labeling coupled with electron paramagnetic resonance to test the first 88 amino acids
254 e spectroscopically (UV/visible and electron paramagnetic resonance) distinct heme environments were
255 g structure determination with EPR (electron paramagnetic resonance) spectroscopy and simulation, sho
256  assessed by electronic absorption, electron paramagnetic resonance, and Mn K-edge X-ray absorption m
257  high-resolution mass spectrometry, electron paramagnetic resonance, and nuclear magnetic resonance s
258 n characterized by resonance Raman, electron paramagnetic resonance, and X-ray absorption spectroscop
259 its metallocofactors by UV-visible, electron paramagnetic resonance, hyperfine sublevel correlation (
260 oscopy, nuclear magnetic resonance, electron paramagnetic resonance, infrared and Raman spectroscopy,
261 terizations (electronic absorption, electron paramagnetic resonance, X-ray absorption spectroscopies)
262       SAMCA is cleaved by PhDph2, yielding a paramagnetic (S = 1/2) species, which is assigned to a c
263 n application example, droplets containing a paramagnetic salt and doxorubicin (leukemia drug) are ma
264                                              Paramagnetic salts are compared in terms of solubility,
265                                    Different paramagnetic salts with chim from approximately 4500 to
266 manipulation, where droplets instead contain paramagnetic salts with molar magnetic susceptibilities
267 the two radicals is imagined to react with a paramagnetic scavenger via spin-selective electron trans
268 etwork solid composed of Fe(III) centers and paramagnetic semiquinoid linkers, (NBu4)2Fe(III)2(dhbq)3
269 This work demonstrates that lanthanide-based paramagnetic shift reagents can be designed to detect im
270 7)Fe hyperfine coupling interaction with the paramagnetic signal, which indicates that the iron-sulfu
271  novel spin-orbit state within the nominally paramagnetic SIO.
272 The methodology for studying (17)O shifts in paramagnetic solids described in this work will be usefu
273 weakly paramagnetic materials suspended in a paramagnetic solution in a magnetic field gradient provi
274 rticles heated or cooled in certain polar or paramagnetic solvents may behave as if they carry an ele
275                                         Such paramagnetic species are broadly found in nature and can
276        The detection and characterization of paramagnetic species by electron spin resonance (ESR) sp
277 e to identify for the first time the various paramagnetic species present in the native state of thes
278 n-group and transition-metal diamagnetic and paramagnetic species, and to bind strongly to metal cent
279 wn as a preferred technique for the study of paramagnetic species.
280                                 The electron paramagnetic spectroscopy of illuminated CdSe:CaI showed
281 ins usually lack reactive cysteines and that paramagnetic spin labels entering the periplasm are sele
282 e material of interest (doping/attachment of paramagnetic spin labels to biomolecules of interest).
283                               Using electron paramagnetic spin resonance (EPR), we show that this rot
284 tance due to weak localization and the Pauli paramagnetic spin susceptibility.
285   Using ESR to trace the reactionary path of paramagnetic spins or spin-active proxy molecules provid
286 sing ferromagnetic La2/3Sr1/3MnO3 (LSMO) and paramagnetic SrIrO3 (SIO) are synthesized with the preci
287                          Interestingly, this paramagnetic state admixes a zig-zag spin mode analogous
288 ition temperature (between ferromagnetic and paramagnetic states) using very small fields (smaller th
289 the addition of exogenous superoxide via the paramagnetic superoxide donor potassium dioxide or super
290            The antiaromatic state has a huge paramagnetic susceptibility, despite having no unpaired
291 rtant materials for electrical conductivity, paramagnetic susceptibility, optical nonlinearity, photo
292                  Other attempts use a strong paramagnetic suspension for the separation of purely dia
293                                           As paramagnetic systems are generally considered difficult
294 widely applicable to membrane proteins where paramagnetic tags can be introduced.
295           The orbital analysis shows how the paramagnetic terms, understood with a localized bond mod
296 tational manipulation of free-standing super-paramagnetic thin-film microplates using external magnet
297 lic chelates (e.g., DOTP(8-)) complexed with paramagnetic thulium (Tm(3+)), to generate pHe maps in r
298 oscopy and confirmed by the TN values of the paramagnetic to antiferromagnetic transition.
299 ell (SOFC) cathode material La2NiO4+delta, a paramagnetic transition-metal oxide.
300                            A novel system of paramagnetic vesicles was designed using ion pairs of ir

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top