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1 um is strongly regulated by the abundance of molybdenum.
6 how that previously unknown halo-substituted molybdenum alkylidene species are exceptionally reactive
7 A new family of structurally well-defined molybdenum alkylidyne catalysts for alkyne metathesis, w
8 demonstration is given for a nickel-chromium-molybdenum alloy film of 150 nm thickness that was produ
9 re we show that PdMo bimetallene-a palladium-molybdenum alloy in the form of a highly curved and sub-
11 d to prevent this softening effect in nickel-molybdenum alloys with grain sizes below 10 nanometres(3
14 nanosheet degradation and release of soluble molybdenum and sulfur species, and generates protons tha
15 ic ligands eta(2)-coordinated to tungsten or molybdenum and the use of these reactions in the synthes
20 sential minerals (cobalt, copper, manganese, molybdenum, and zinc), 4 metals with some evidence of no
21 the interplay between excitons and trions in molybdenum- and tungsten-based transition metal dichalco
22 is of the present work, we conclude that all molybdenum- and tungsten-containing formate dehydrogenas
25 ge protein (MoSto) deposits large amounts of molybdenum as polyoxomolybdate clusters in a heterohexam
27 veals a previously unsuspected transition in molybdenum at high pressure and high temperature, which
29 ases, which use vanadium or iron in place of molybdenum at their active site, might play a more promi
31 ) ball-shaped species containing 154 and 132 molybdenum atoms, and a {PMo(12)}C{Mo(124)Ce(4)} = [H(16
32 died the occurrence of vanadium, the role of molybdenum availability on vanadium acquisition and the
39 120 Ce6 } to afford two half-closed gigantic molybdenum blue clusters {Mo180 } (1) and {Mo130 Ce6 } (
40 bsequently template the assembly of gigantic molybdenum-blue wheel {Mo(154)} = [Mo(154)O(462)H(14)(H(
41 To address the issues, here, hydrophilic molybdenum boride (MoB) nanoparticles are presented as a
43 Here we report a high-slope melting curve in molybdenum by synchrotron X-ray diffraction analysis of
44 solution-phase synthesis route to phase-pure molybdenum carbide (alpha-MoC(1-x)) nanoparticles (NPs)
45 platinum (Pt) atomically dispersed on alpha-molybdenum carbide (alpha-MoC) enables low-temperature (
46 synthesized layered gold (Au) clusters on a molybdenum carbide (alpha-MoC) substrate to create an in
47 t is obtained from a cobalt-substituted bulk molybdenum carbide (beta-Mo(2)C:Co) through a two-step s
48 sed bifunctional catalyst consisting of iron-molybdenum carbide (Fe3 Mo3 C) and IrMn nanoalloys is de
50 dy on the Raman spectra of 2D alpha-Mo(2) C (molybdenum carbide), a promising member in MXene family,
53 the well-known leaching problem of supported molybdenum catalysts (i.e., loss of Mo species thus caus
55 aspidosperma alkaloid includes an efficient molybdenum-catalyzed enantioselective ring-closing metat
56 et al. have described, while performing the molybdenum-catalyzed epoxidation reaction of olefins usi
57 e observe a magnetic interaction between the molybdenum center and one of the iron/sulfur centers, pe
58 recapture of unspent white phosphorus by the molybdenum center can be achieved by post-photolysis hea
59 lectron paramagnetic resonance signal of the molybdenum center in its Mo(V) state and demonstrated th
62 the sulfo group of the oxidized and reduced molybdenum center, Mo(6+) horizontal lineS and Mo(4+)-SH
63 in our understanding of the structure of the molybdenum center, we propose a reaction mechanism invol
67 m the taper junction between Cobalt-Chromium-Molybdenum (CoCrMo) and Titanium (Ti) components (fretti
73 malonic encephalopathy protein 1 (ETHE1) and molybdenum cofactor (MoCo) deficiencies are hereditary d
74 8 are known to be present in humans: MOCS1, molybdenum cofactor biosynthesis; LIAS, lipoic acid bios
75 ral other radical SAM enzymes, including the molybdenum cofactor biosynthetic enzyme MoaA and the RNA
85 reflect the exciton-trion coherence time in molybdenum compounds, but are shown to provide a lower b
86 hing and cooking for most water samples, the molybdenum concentration in the cooked rice doubled (2.2
92 kinetics and spectroscopic properties of the molybdenum-containing, NAD(+)-dependent FdsABG formate d
96 ransformation of dopamine to m-tyramine by a molybdenum-dependent dehydroxylase from Eggerthella lent
98 a distinct group of largely uncharacterized molybdenum-dependent enzymes that likely mediate primary
99 ctronic structure of the E. coli periplasmic molybdenum-dependent methionine sulfoxide reductase (Msr
100 n functional maturation of other cytoplasmic molybdenum-dependent nitrate reductases may be phylogene
105 ca generated a hydrophobic environment for a molybdenum diamine (Mo-diamine) precursor solution, enab
106 exchange appears to occur by formation of a molybdenum dihydride or dihydrogen complex, resulting fr
107 e lithium-storage capacity of the mesoporous molybdenum dioxide electrode is not based on a conversio
109 olymerized by a carbon-supported single-site molybdenum-dioxo catalyst to terephthalic acid (PTA) and
110 terostructures assembled from incommensurate molybdenum diselenide (MoSe(2)) and tungsten disulfide (
111 ley excitons trapped in a moire potential in molybdenum diselenide (MoSe(2))/tungsten diselenide (WSe
113 negative circularly polarized emission in a molybdenum diselenide/tungsten diselenide (MoSe(2)/WSe(2
115 s have been well established for crystalline molybdenum disulfide (c-MoS2) but not for amorphous moly
121 l layers of hexagonal boron nitride (BN) and molybdenum disulfide (MoS(2)) crystals on single-walled
123 t reports of various photodetectors based on molybdenum disulfide (MoS(2)) field effect transistors s
124 2D) transition-metal dichalcogenides such as molybdenum disulfide (MoS(2)) have been demonstrated to
129 res, nanopores constructed in a monolayer of molybdenum disulfide (MoS(2)) stand out as powerful devi
130 transition metal dichalcogenides, including molybdenum disulfide (MoS(2)), have previously been cons
131 tly synthesize a 2D semiconductor, monolayer molybdenum disulfide (MoS(2)), in arbitrary patterns on
132 em, the hydrogen evolution reaction (HER) at molybdenum disulfide (MoS(2)), where higher electrocatal
133 ly crosslinked hydrogels from defect-rich 2D molybdenum disulfide (MoS2 ) nanoassemblies and polymeri
135 the edge and basal-plane sites of monolayer molybdenum disulfide (MoS2 ) synthesized by chemical vap
136 lable fabrication of a large array of hybrid molybdenum disulfide (MoS2) - silicon dioxide (SiO2) one
137 ntrol over large area growth of high quality molybdenum disulfide (MoS2) and other types of 2D dichal
138 nsition metal dichalcogenides (TMDs) such as molybdenum disulfide (MoS2) and tungsten disulfide (WS2)
141 tems in numerous environmental applications, molybdenum disulfide (MoS2) nanosheets stand out as a pr
142 iated nanosheets of two-dimensional metallic molybdenum disulfide (MoS2) on thin plastic substrates c
143 report on flexible and wavelength-selective molybdenum disulfide (MoS2) phototransistors using monol
144 tial of the applicability of two-dimensional molybdenum disulfide (MoS2) structures, in various elect
145 perties of metallic (1T phase) nanosheets of molybdenum disulfide (MoS2) through covalent chemical fu
147 mbine these two advantages and demonstrate a molybdenum disulfide (MoS2) two-dimensional steep-slope
148 )-vacancies created on the basal plane of 2H-molybdenum disulfide (MoS2) using argon plasma exposure
149 rphous nickel-cobalt complexes with 1T phase molybdenum disulfide (MoS2) via hydrazine-induced phase
150 led fabrication of quantum dots in monolayer molybdenum disulfide (MoS2), and quantum dot arrays with
151 conductor interface, as epitaxial graphene - molybdenum disulfide (MoS2), is of great interest from t
152 these properties of monolayer TMDs, such as molybdenum disulfide (MoS2), on standard Si-based substr
157 o-dimensional (2D) layered materials, namely molybdenum disulfide and black phosphorus field effect t
158 e apply this method to the specific cases of molybdenum disulfide and graphene oxide particles, dispe
159 en the intensities of the two Raman bands of molybdenum disulfide and graphene oxide, we demonstrate
160 using a combination of solution-processed 2D-molybdenum disulfide and graphene-oxide (GO) that can be
161 , incorporated as an interface layer between molybdenum disulfide and hafnium dioxide in a bottom-gat
162 he full dielectric tensors of nanometer-thin molybdenum disulfide and hexagonal boron nitride microcr
163 isting of chemical vapor deposited monolayer molybdenum disulfide and solution-processed semiconducti
165 ructures made of single-layer semiconducting molybdenum disulfide contacting conductive graphene.
166 tiscale structural and electronic control of molybdenum disulfide foam to synergistically promote the
169 th a notable advantage in terms of capacity, molybdenum disulfide has been considered a promising ano
170 roach for large-scale and highly crystalline molybdenum disulfide monolayers using a solution-process
171 roscopy studies reveal that the single-layer molybdenum disulfide nucleates at the graphene edges.
172 ch, where MoOx/MoS2 core-shell nanowires and molybdenum disulfide sheets are exposed to dilute aqueou
173 abricate arrays of hybrid superlattices with molybdenum disulfide that could be used in electrical ca
174 trates the validity of multiscale control in molybdenum disulfide via overall consideration of the ma
175 functional theory calculations indicate that molybdenum disulfide with moderate cobalt doping content
178 that hydrazine acts as an electron dopant in molybdenum disulfide, increasing its conductivity, while
179 n single flakes of atomically thin CVD-grown molybdenum disulfide, using non-degenerate femtosecond p
180 stigating the hydrogen evolution reaction on molybdenum disulfide, where it is shown that the basal p
182 dified with gold nanoparticle decorated on a molybdenum disulfide/chitosan (Au@MoS(2)/Ch) nanocomposi
183 a field-effect transistor biosensor based on molybdenum disulfide/graphene (MoS(2)/graphene) hybrid n
185 ydrogen evolution reaction (HER; refs ,,,,), molybdenum disulphide (MoS2) is known to contain active
186 ort properties of nanostructured flower-like molybdenum disulphide grown by hydrothermal route has be
188 systematic modulation of the carrier type in molybdenum ditelluride (MoTe2 ) field-effect transistors
189 are performed on atomic layers of hexagonal molybdenum ditelluride (MoTe2), a prototypical transitio
191 n in the infrared region from a monolayer of molybdenum ditelluride on a silicon photonic-crystal cav
193 near-field ThermoPhotoVoltaics, specifically molybdenum-doped indium oxide, dysprosium-doped cadmium
195 prepared via low pressure chalcogenation of molybdenum film, decreases by up to two orders of magnit
198 The third one remains free and generates molybdenum hydride moieties as the active site under H2
201 Reaction of a solvent-stabilized cationic molybdenum imido alkylidene N-heterocyclic carbene (NHC)
202 e monoalkoxide complexes as well as cationic molybdenum imido alkylidene triflate complexes have been
204 levels of manganese, iron, copper, zinc and molybdenum in rice were reduced during washing and cooki
205 6)Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is
206 Specifically, proteins that a) utilize a molybdenum ion as a cofactor and b) are involved in the
207 y revised oxidation state assignment for the molybdenum ion, providing the first spatially resolved p
208 aphy and EPR spectroscopy of the nitrogenase molybdenum iron (MoFe) proteins from two phylogeneticall
210 ngstrom crystal structure of the nitrogenase molybdenum-iron (MoFe) protein captured under physiologi
211 ogenase is most commonly associated with the molybdenum-iron cofactor called FeMoco or the M-cluster,
213 O(12) solid-electrolyte-based molten lithium-molybdenum-iron(II) chloride battery (denoted as Li-Mo-F
217 er with new, experimental data, we show that molybdenum isotopic fractionation is driven by preferenc
218 ed carbon nanotubes, graphene nanoplatelets, molybdenum(IV) sulfide flakes, neodymium(III) oxide nano
220 s including barium, cadmium, cobalt, cesium, molybdenum, lead, antimony, thallium, tungsten, and uran
221 -arsenic, cobalt, chromium, copper, mercury, molybdenum, lead, tin, and vanadium--in relation to youn
223 and irreversibly deactivate the diamagnetic molybdenum metallacyclobutadiene complex through a multi
226 essful incorporation of atomically dispersed molybdenum (Mo) atoms into the framework of nanosized MF
228 over the importance of N, phosphorus (P) and molybdenum (Mo) availability in controlling free-living
232 ulsed Nd:YAG millisecond laser on a pristine molybdenum (Mo) surface to measure surface melting and m
233 Cd), cobalt (Co), mercury (Hg), nickel (Ni), molybdenum (Mo), lead (Pb), antimony (Sb), tin (Sn), and
234 ogical nitrogen fixation is catalyzed by the molybdenum (Mo), vanadium (V) and iron (Fe)-only nitroge
235 y microbial action is dependent on the metal molybdenum (Mo), which is required by nitrate reductase
242 emical vapor deposition growth of nonlayered molybdenum nitride to passivate its surface, which enabl
247 ron-only nitrogenases that are homologous to molybdenum nitrogenases are also found in archaea and ba
248 ytic coatings composed of nitrides of either molybdenum or vanadium, containing either copper or nick
251 al synthetic reactions of a 2.9 nm spherical molybdenum oxide cluster, {Mo132} (formula: [Mo(VI)72Mo(
252 e recent past in a few cases, Keplerate-type molybdenum oxide-based porous, spherical clusters, short
253 ree strategy is carried out to prepare mixed molybdenum oxides as an advanced anode material for lith
255 e bulk of disordered lithium nickel titanium molybdenum oxides using a standard solid-state method to
258 tinuous efforts have been made to synthesize molybdenum-oxo complexes of different ligand environment
259 olefins using alkyl hydroperoxides, that the molybdenum-oxo moiety is an active catalytic species.
261 in PL and carrier lifetime due to increased molybdenum-oxygen bonding compared to that of traditiona
262 ntified reduced Pt covered with an amorphous molybdenum oxyhydroxide hydrate with a local structural
264 ns (50 ng of pure approximately 0.75 nm size molybdenum polyoxometalate (POM) anions on 25 mug ( appr
266 cesium (Ptrend = 0.29), 1.76 (1.24-2.50) for molybdenum (Ptrend = 0.01), 0.79 (0.56-1.13) for lead (P
267 d alpha-MoB and beta-Mo2 C phases, while the molybdenum richest phase Mo2 B show significantly lower
268 n of grain boundaries through relaxation and molybdenum segregation was used to prevent this softenin
270 din-2-one selectively cleave the propagating molybdenum species in the ring-opening alkyne metathesis
272 olution structure of the radiation sensitive molybdenum storage protein, demonstrate soaking of the d
273 num disulfide (c-MoS2) but not for amorphous molybdenum sulfide (a-MoSx), which exhibits significantl
277 ynthesized a new phase of sub-stoichiometric molybdenum sulfide (s-MoSx) on sulfur-enriched copper su
281 ing of nanocomposite layer of zinc oxide and molybdenum sulphide (ZnO/MoS2) over unclad core of optic
285 leted and low-enriched U alloyed with 10 wt% molybdenum that has different nominal enrichments of 0.2
286 above 4 x 10(7) for barium and 4 x 10(5) for molybdenum; the chemical yields of cesium are more than
289 xial van der Waals semiconductor alpha-phase molybdenum trioxide (alpha-MoO(3) ) has recently receive
290 spersion contours in bilayers of alpha-phase molybdenum trioxide (alpha-MoO(3)), arising when the rot
291 ppropriate ligands within complexes based on molybdenum, tungsten and ruthenium has led to reactivity
292 he bioresorbable materials (e.g., magnesium, molybdenum, tungsten, silicon, germanium, silicon dioxid
293 ynthesis and characterization of two new oxo-molybdenum(V)-corrolato complexes are described herein.
296 g activity significantly higher than that of molybdenum(VI) oxide powder and comparable to that of a