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1 um is strongly regulated by the abundance of molybdenum.
2           Newly discovered tris(diisocyanide)molybdenum(0) complexes are Earth-abundant isoelectronic
3                                              Molybdenum (98)Mo/(95)Mo isotope ratios are a sediment p
4       We have investigated the nature of the molybdenum active site of the arsenite oxidase from the
5 enzymes that oxidize sulfite to sulfate at a molybdenum active site.
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-
10                                      An iron-molybdenum alloy powder was extensively deformed by high
11 d to prevent this softening effect in nickel-molybdenum alloys with grain sizes below 10 nanometres(3
12            Here we report the synthesis of a molybdenum ammonia complex supported by terpyridine and
13 in the fruit from C.IZC were associated with molybdenum and nickel found in the soil.
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
16                                  Here, using molybdenum and tungsten isotope measurements on iron met
17                                              Molybdenum and vanadium nitrogenases are capable of conv
18                  Higher quartiles of barium, molybdenum, and antimony were associated with greater HO
19 ace metal(loid)s, such as arsenic, antimony, molybdenum, and tungsten.
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
23 ompton scattering peaks of the X-ray source (molybdenum anode).
24                                              Molybdenum, antimony, tungsten, and uranium were positiv
25 ge protein (MoSto) deposits large amounts of molybdenum as polyoxomolybdate clusters in a heterohexam
26                                              Molybdenum, as a component of the iron-molybdenum cofact
27 veals a previously unsuspected transition in molybdenum at high pressure and high temperature, which
28 me, which, in its most common form, requires molybdenum at its active site.
29 ases, which use vanadium or iron in place of molybdenum at their active site, might play a more promi
30 nd bidentate coordination to the active site molybdenum atom.
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
33                  With 1.0 to 5.0 mole % of a molybdenum-based catalyst, which may be delivered in the
34                                              Molybdenum-based materials have been considered as alter
35                                              Molybdenum-based molecular alkylidyne complexes of the t
36            Depending on the reaction type, a molybdenum-based monoaryloxide pyrrolide or chloride (MA
37                              Polyoxometalate molybdenum blue (MB) complexes typically exist as discre
38                 Detection of SRP is based on molybdenum blue chemistry with Sn(II) chloride dihydrate
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
42         We have synthesized four binary bulk molybdenum borides Mo2 B, alpha-MoB, beta-MoB, and MoB2
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
49                                              Molybdenum carbide (Mo(2) C), a class of unterminated MX
50 dy on the Raman spectra of 2D alpha-Mo(2) C (molybdenum carbide), a promising member in MXene family,
51                   Alkyne cross-metathesis of molybdenum carbyne complex [TolC identical withMo(OCCH3(
52                                              Molybdenum carbyne complexes [RC identical withMo(OC(CH3
53 the well-known leaching problem of supported molybdenum catalysts (i.e., loss of Mo species thus caus
54 in metathesis using tungsten, ruthenium, and molybdenum catalysts are presented.
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
60 sfer of the substrate Calpha hydrogen to the molybdenum center in the course of the reaction.
61 necting the FMN of FdsB with the active-site molybdenum center of FdsA.
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
64  formate to a molybdenum-sulfur group of the molybdenum center.
65 minance of the Mo=O group over (high-valent) molybdenum chemistry can be challenged.
66                             In this study, a molybdenum coated T-shaped slotted quartz tube atom trap
67 m the taper junction between Cobalt-Chromium-Molybdenum (CoCrMo) and Titanium (Ti) components (fretti
68 EN for further modification to form the iron-molybdenum cofactor (FeMo-co) of nitrogenase.
69                       The [Mo:7Fe:9S:C] iron-molybdenum cofactor (FeMoco) of nitrogenase is the large
70 ntaining iron-sulfur cluster called the iron-molybdenum cofactor (FeMoco).
71                                              Molybdenum cofactor (Moco) biosynthesis is a highly cons
72 o-7,8-dihydro-GTP (3',8-cH(2)GTP) during the molybdenum cofactor (Moco) biosynthesis.
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
76                                              Molybdenum cofactor deficiency (MoCD) is an autosomal re
77       Molybdenum, as a component of the iron-molybdenum cofactor of nitrogenase, is essential for sym
78                            Here we report on MOlybdenum COfactor Sulfurase (MOCOS), an enzyme involve
79 sphate (cPMP), requires the bicistronic gene molybdenum cofactor synthesis 1 (MOCS1).
80           We establish that a predicted heme-molybdenum cofactor-containing protein, and a complex po
81  P(4) molecule from a mononuclear cyclo-P(4) molybdenum complex.
82                                    Analogous molybdenum complexes promote dihydrogen evolution from c
83                                              Molybdenum complexes with the general formula Mo(NR)(CHR
84                           Here we describe a molybdenum compound, supported by a terphenyl-diphosphin
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
87                          Bacterial genes for molybdenum-containing and tungsten-containing enzymes ar
88                                          The molybdenum-containing dehydrogenase FdsABG is a soluble
89 ime-reducing component (MARC) is a mammalian molybdenum-containing enzyme.
90 ce of "nitrite reductases" such as heme- and molybdenum-containing enzymes.
91                                              Molybdenum-containing formate dehydrogenase H from Esche
92 kinetics and spectroscopic properties of the molybdenum-containing, NAD(+)-dependent FdsABG formate d
93                                              Molybdenum contamination is a concern in mining regions
94 rins are reported in the literature, related molybdenum corroles are very less reported.
95                    Treatment of the neutral, molybdenum cyclo-P(4) complexes Mo(eta(4) -P(4) )I(2) (C
96 ransformation of dopamine to m-tyramine by a molybdenum-dependent dehydroxylase from Eggerthella lent
97                      Here, we characterize a molybdenum-dependent enzyme from the human gut bacterium
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
101                                              Molybdenum-dependent nitrogenase consists of two protein
102                       The active site of the molybdenum-dependent nitrogenase is the unique carbide-c
103      Re-doped (n-type) and Nb-doped (p-type) molybdenum di-sulfide (MoS(2)) field-effect transistors
104 d through the selective electrodeposition of Molybdenum (di)oxide (MoO(2)).
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
108            Here, we demonstrate a mesoporous molybdenum dioxide material with abnormal lithium-storag
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
112 brations in a model bilayered semiconductor, molybdenum diselenide.
113  negative circularly polarized emission in a molybdenum diselenide/tungsten diselenide (MoSe(2)/WSe(2
114                              Two-dimensional molybdenum disulfide (2D MoS2) presents extraordinary op
115 s have been well established for crystalline molybdenum disulfide (c-MoS2) but not for amorphous moly
116          2D semiconductors such as monolayer molybdenum disulfide (MoS(2) ) are promising material ca
117                                              Molybdenum disulfide (MoS(2) ) is a multifunctional mate
118                                 For example, molybdenum disulfide (MoS(2) ) is a natural uniaxial vdW
119                              Forming pits on molybdenum disulfide (MoS(2) ) monolayers is desirable f
120                                              Molybdenum disulfide (MoS(2) ) nanosheet is a two-dimens
121 l layers of hexagonal boron nitride (BN) and molybdenum disulfide (MoS(2)) crystals on single-walled
122        Among the family of 2D nanomaterials, molybdenum disulfide (MoS(2)) features distinct characte
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
125                                              Molybdenum disulfide (MoS(2)) laminar membranes have rec
126                         Two-dimensional (2D) molybdenum disulfide (MoS(2)) nanomaterials are an emerg
127                                  Few-layered molybdenum disulfide (MoS(2)) nanosheets are poised to b
128                                          The molybdenum disulfide (MoS(2)) nanosheets functionalized
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
134                                 The emerging molybdenum disulfide (MoS2 ) offers intriguing possibili
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)
139                                    Monolayer molybdenum disulfide (MoS2) has emerged as a model syste
140                      Mono- and multi-layered molybdenum disulfide (MoS2) is considered to be one of t
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
146                         Here, we demonstrate molybdenum disulfide (MoS2) transistors with a 1-nm phys
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
153                                              Molybdenum disulfide (MoS2), with its active edge sites,
154 tomic force microscope tip on a thin film of molybdenum disulfide (MoS2).
155                 Multiwalled carbon nanotubes molybdenum disulfide 3D nanocomposite (MWCNT-MoS(2) NC)
156 apse via threshold engineering in dual gated molybdenum disulfide and black phosphorus FETs.
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
164                      Tungsten diselenide and molybdenum disulfide channels were used selectively to p
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
167              The optimized three-dimensional molybdenum disulfide foam with uniform mesopores, vertic
168                                    Recently, molybdenum disulfide has been attracted considerable att
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
176 ce and Raman spectra of a bare bilayer MoS2 (Molybdenum disulfide).
177 aterials studied so far(12,13) (for example, molybdenum disulfide).
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
181 d electronic response of synthetic monolayer molybdenum disulfide.
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
184  a range of 2D materials including graphene, molybdenum disulphide (MoS2) and black phosphorus.
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
187 edge supercurrent in the Weyl superconductor molybdenum ditelluride (MoTe(2)).
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
190 hexagonal and monoclinic phases of monolayer molybdenum ditelluride (MoTe2).
191 n in the infrared region from a monolayer of molybdenum ditelluride on a silicon photonic-crystal cav
192                                              Molybdenum ditelluride, MoTe2 , is emerging as an import
193 near-field ThermoPhotoVoltaics, specifically molybdenum-doped indium oxide, dysprosium-doped cadmium
194          Treatment of the bis(imino)pyridine molybdenum eta(6)-benzene complex ((iPr)PDI)Mo(eta(6)-C6
195  prepared via low pressure chalcogenation of molybdenum film, decreases by up to two orders of magnit
196                                     Finally, molybdenum-free chalcogels containing only Fe4S4 cluster
197                                              Molybdenum has been reported as a limiting nutrient for
198     The third one remains free and generates molybdenum hydride moieties as the active site under H2
199 monocyanide complex and the three-coordinate molybdenum(III) complex Mo(N(t)BuAr)(3).
200                          A series of neutral molybdenum imido alkylidene N-heterocyclic carbene (NHC)
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
203                  The isotopic composition of molybdenum in five samples of glassy debris from the 194
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
209 itating electron transfer to the nitrogenase molybdenum iron-protein.
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,
212 -7S] cluster (P-cluster), both housed in the molybdenum-iron protein (MoFeP).
213 O(12) solid-electrolyte-based molten lithium-molybdenum-iron(II) chloride battery (denoted as Li-Mo-F
214 fe enzymes that are used in situations where molybdenum is limiting.
215                    We show that the distinct molybdenum isotopic compositions of CAIs cover almost th
216                                   Nonnatural molybdenum isotopic compositions were observed, reflecti
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
219 er composed of polyanionic trimeric units of molybdenum(IV).
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
222 ected in natural ecosystems, particularly in molybdenum-limited habitats.
223  and irreversibly deactivate the diamagnetic molybdenum metallacyclobutadiene complex through a multi
224 th high regioselectivity (>98%) along with a molybdenum metallacyclobutadiene complex.
225         Here, the authors report a palladium-molybdenum mixed catalyst for the selective hydrodeoxyge
226 essful incorporation of atomically dispersed molybdenum (Mo) atoms into the framework of nanosized MF
227                                 On land, low molybdenum (Mo) availability has been shown to limit BNF
228 over the importance of N, phosphorus (P) and molybdenum (Mo) availability in controlling free-living
229  MoS(2) flake using Pd and low-work-function molybdenum (Mo) contacts, respectively.
230                                              Molybdenum (Mo) is an essential micronutrient for most l
231                                              Molybdenum (Mo) is an essential trace nutrient but has n
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
236                                          The molybdenum (Mo)- and vanadium (V)-nitrogenases are two h
237 g), selenium (Se), iodine (I), zinc (Zn) and molybdenum (Mo).
238                          The reaction of the molybdenum-molybdenum triple-bonded dimer (CO)(2)CpMo=Mo
239                              The use of such molybdenum monoaryloxide chloride complexes enables the
240                            Here we show that molybdenum monoaryloxide chloride complexes furnish high
241                The reaction is promoted by a molybdenum monoaryloxide pyrrolide complex and affords p
242 emical vapor deposition growth of nonlayered molybdenum nitride to passivate its surface, which enabl
243                                              Molybdenum nitrogenase catalyzes the reduction of dinitr
244                                   The enzyme molybdenum nitrogenase converts atmospheric nitrogen gas
245                They are less widespread than molybdenum nitrogenase in bacteria and archaea, and they
246 e only been found in microbes that also have molybdenum nitrogenase.
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
249  esters and amides, or acids (in contrast to molybdenum- or tungsten-based alkylidenes).
250            Here, 2D ultrathin single-crystal molybdenum oxide (MoO(2) ) flakes that exhibit unexpecte
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
254                               The well mixed molybdenum oxides at the microscale and the involvement
255 e bulk of disordered lithium nickel titanium molybdenum oxides using a standard solid-state method to
256            The well-defined silica-supported molybdenum oxo alkyl species ( identical withSiO-)MoO(CH
257                                   Grafting a molybdenum oxo alkylidene on silica (partially dehydroxy
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.
260            The two-dimensional morphology of molybdenum oxycarbide (2D-Mo(2)CO(x)) nanosheets dispers
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
263 nes highly dispersed palladium and ultrafine molybdenum phosphate nanoparticles on silica.
264 ns (50 ng of pure approximately 0.75 nm size molybdenum polyoxometalate (POM) anions on 25 mug ( appr
265                While plenty of such works on molybdenum porphyrins are reported in the literature, re
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
269                    The iron atoms substitute molybdenum sites in MoS(2) crystals, as confirmed by tra
270 din-2-one selectively cleave the propagating molybdenum species in the ring-opening alkyne metathesis
271                                          The molybdenum storage protein (MoSto) deposits large amount
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
274                    Crystalline and amorphous molybdenum sulfide (Mo-S) catalysts are leaders as earth
275                                              Molybdenum sulfide (MoS2) is widely recognized for its c
276                                    Amorphous molybdenum sulfide (MoSx) is covalently anchored to redu
277 ynthesized a new phase of sub-stoichiometric molybdenum sulfide (s-MoSx) on sulfur-enriched copper su
278                           Redox processes of molybdenum-sulfide (Mo-S) compounds are important in the
279                                              Molybdenum sulfides are very attractive noble-metal-free
280 ng direct hydride transfer from formate to a molybdenum-sulfur group of the molybdenum center.
281 ing of nanocomposite layer of zinc oxide and molybdenum sulphide (ZnO/MoS2) over unclad core of optic
282                              The addition of molybdenum sulphide in the transducer layer increases th
283 eve the highest intrinsic HER activity among molybdenum-sulphide-based catalysts.
284                                  Also, using molybdenum telluride as a test case, we performed X-ray
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
287                                    Also, for molybdenum, thioanions dominated over oxyanions in many
288       Inner surface of T-SQT was coated with molybdenum to enhance the trapping efficiency.
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.
294                      The efficacy of the oxo-molybdenum(V)-corrolato complexes for the catalytic epox
295             The catalytic application of oxo-molybdenum(V)-corrolato complexes in the epoxidation rea
296 g activity significantly higher than that of molybdenum(VI) oxide powder and comparable to that of a
297                                              Molybdenum(VI) oxide was deposited on the Zr6 node of th
298 l loading before and after catalysis, and no molybdenum was detected in the reaction mixture.
299 ls of organochlorine pollutants, cobalt, and molybdenum were associated with lower BMI.
300                         An important case is molybdenum, which has long been speculated to undergo an

 
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