ライフサイエンスコーパス: molybdenum

1 o be a major source of vanadium, nickel, and molybdenum.

2 rce micronutrients in addition to nickel and molybdenum.

3 um is strongly regulated by the abundance of molybdenum.

4 s of nickel (0.5-270 nM), cobalt (0.5-6 nM), molybdenum (10-5600 nM) and tungsten (0.3-8 nM) in Hydra

5 Molybdenum (98)Mo/(95)Mo isotope ratios are a sediment p

6 We have investigated the nature of the molybdenum active site of the arsenite oxidase from the

7 ordination plays a critical role in defining molybdenum active site redox chemistry and reactivity in

8 enzymes that oxidize sulfite to sulfate at a molybdenum active site.

9 y of the various surface orientations toward molybdenum adsorption is controlled by the speciation of

10 how that previously unknown halo-substituted molybdenum alkylidene species are exceptionally reactive

11 An iron-molybdenum alloy powder was extensively deformed by high

12 Here we report the synthesis of a molybdenum ammonia complex supported by terpyridine and

13 layer, and a silicon substrate covered with molybdenum and a carbon layer.

14 idic to neutral conditions, precipitation of molybdenum and hydrolysis of tetrathiomolybdate were obs

15 local and electronic structures of both the molybdenum and sulfur elements for the as prepared mater

16 l mechanism in which hydrogen atoms bound to molybdenum and sulfur sites recombine to form H2 has a b

17 nanosheet degradation and release of soluble molybdenum and sulfur species, and generates protons tha

18 ic ligands eta(2)-coordinated to tungsten or molybdenum and the use of these reactions in the synthes

19 Here, using molybdenum and tungsten isotope measurements on iron met

20 Mono- and bis-terphenyl complexes of molybdenum and tungsten with general composition M2(Ar')

21 Molybdenum and vanadium nitrogenases are capable of conv

22 The molybdenum and vanadium nitrogenases are two homologous

23 Higher quartiles of barium, molybdenum, and antimony were associated with greater HO

24 is of the present work, we conclude that all molybdenum- and tungsten-containing formate dehydrogenas

25 ompton scattering peaks of the X-ray source (molybdenum anode).

26 Molybdenum, antimony, tungsten, and uranium were positiv

27 Molybdenum, antimony, tungsten, and uranium were positiv

28 on and chemical vapour deposition samples to molybdenum antisite in physical vapour deposition sample

29 Molybdenum, as a component of the iron-molybdenum cofact

30 veals a previously unsuspected transition in molybdenum at high pressure and high temperature, which

31 me, which, in its most common form, requires molybdenum at its active site.

32 ases, which use vanadium or iron in place of molybdenum at their active site, might play a more promi

33 The molybdenum atom of Escherichia coli nitrate reductase A

34 nd bidentate coordination to the active site molybdenum atom.

35 Pores with only molybdenum atoms on their edges lead to higher fluxes, w

36 ate ligand that bridges the quadruply bonded molybdenum atoms, were prepared from the reaction of the

37 Molybdenum availability is critical to life in lakes, ju

38 died the occurrence of vanadium, the role of molybdenum availability on vanadium acquisition and the

39 It is, therefore, important to assess molybdenum availability to the lacustrine environment in

40 With 1.0 to 5.0 mole % of a molybdenum-based catalyst, which may be delivered in the

41 th complete diastereoselectivity by a chiral molybdenum-based complex, tandem conjugate reduction/int

42 Molybdenum-based materials have been considered as alter

43 Molybdenum-based molecular alkylidyne complexes of the t

44 gical nitrogen fixation, most probably using molybdenum-based nitrogenase as opposed to other variant

45 The pseudo-octahedral molybdenum benzylidyne complex [TolC identical withMo(ON

46 Detection of SRP is based on molybdenum blue chemistry with Sn(II) chloride dihydrate

47 120 Ce6 } to afford two half-closed gigantic molybdenum blue clusters {Mo180 } (1) and {Mo130 Ce6 } (

48 We have synthesized four binary bulk molybdenum borides Mo2 B, alpha-MoB, beta-MoB, and MoB2

49 Here we report a high-slope melting curve in molybdenum by synchrotron X-ray diffraction analysis of

50 platinum (Pt) atomically dispersed on alpha-molybdenum carbide (alpha-MoC) enables low-temperature (

51 synthesized layered gold (Au) clusters on a molybdenum carbide (alpha-MoC) substrate to create an in

52 sed bifunctional catalyst consisting of iron-molybdenum carbide (Fe3 Mo3 C) and IrMn nanoalloys is de

53 bbed Mo2 C@NC that is composed of ultrasmall molybdenum carbide (Mo2 C) nanoparticles embedded within

54 Molybdenum carbide has been proposed as a possible alter

55 study the benzene hydrogenation reactions on molybdenum carbide nanoparticles (MCNPs) in the process

56 Alkyne cross-metathesis of molybdenum carbyne complex [TolC identical withMo(OCCH3(

57 Molybdenum carbyne complexes [RC identical withMo(OC(CH3

58 the well-known leaching problem of supported molybdenum catalysts (i.e., loss of Mo species thus caus

59 in metathesis using tungsten, ruthenium, and molybdenum catalysts are presented.

60 aspidosperma alkaloid includes an efficient molybdenum-catalyzed enantioselective ring-closing metat

61 e observe a magnetic interaction between the molybdenum center and one of the iron/sulfur centers, pe

62 lectron paramagnetic resonance signal of the molybdenum center in its Mo(V) state and demonstrated th

63 sfer of the substrate Calpha hydrogen to the molybdenum center in the course of the reaction.

64 the sulfo group of the oxidized and reduced molybdenum center, Mo(6+) horizontal lineS and Mo(4+)-SH

65 The intramolecular combination of a molybdenum center, redox-active ligand, and Lewis acid r

66 in our understanding of the structure of the molybdenum center, we propose a reaction mechanism invol

67 formate to a molybdenum-sulfur group of the molybdenum center.

68 N2 at the FeMo cofactor, a sulfur-rich iron-molybdenum cluster (FeMoco).

69 m the taper junction between Cobalt-Chromium-Molybdenum (CoCrMo) and Titanium (Ti) components (fretti

70 EN for further modification to form the iron-molybdenum cofactor (FeMo-co) of nitrogenase.

71 The [Mo:7Fe:9S:C] iron-molybdenum cofactor (FeMoco) of nitrogenase is the large

72 n centers purportedly accumulate on the iron-molybdenum cofactor (FeMoco) of nitrogenase, and their r

73 ntaining iron-sulfur cluster called the iron-molybdenum cofactor (FeMoco).

74 The molybdenum cofactor (Moco) is an essential redox cofacto

75 The molybdenum cofactor (Moco) is essential for all kingdoms

76 brane is involved in iron-sulfur cluster and molybdenum cofactor assembly in the cytosol, but the tra

77 ization of proteins at inhibitory receptors, molybdenum cofactor biosynthesis and other diverse funct

78 gh the action of two enzymes, MoaA and MoaC (molybdenum cofactor biosynthesis protein A and C, respec

79 8 are known to be present in humans: MOCS1, molybdenum cofactor biosynthesis; LIAS, lipoic acid bios

80 xy-scyllo-inosamine dehydrogenase (BtrN) and molybdenum cofactor biosynthetic enzyme (MoaA).

81 ral other radical SAM enzymes, including the molybdenum cofactor biosynthetic enzyme MoaA and the RNA

82 Molybdenum cofactor deficiency (MoCD) is an autosomal re

83 Molybdenum cofactor deficiency (MoCD) is characterised b

84 Molybdenum, as a component of the iron-molybdenum cofactor of nitrogenase, is essential for sym

85 Here we report on MOlybdenum COfactor Sulfurase (MOCOS), an enzyme involve

86 We establish that a predicted heme-molybdenum cofactor-containing protein, and a complex po

87 Restoration of molybdenum cofactor-dependent enzyme activities results

88 n of nitrite to NO through reaction with its molybdenum cofactor.

89 Analogous molybdenum complexes promote dihydrogen evolution from c

90 Molybdenum complexes with the general formula Mo(NR)(CHR

91 Here we describe a molybdenum compound, supported by a terphenyl-diphosphin

92 hing and cooking for most water samples, the molybdenum concentration in the cooked rice doubled (2.2

93 Molybdenum-containing formate dehydrogenase H from Esche

94 kinetics and spectroscopic properties of the molybdenum-containing, NAD(+)-dependent FdsABG formate d

95 ler than the pathway for biosynthesis of the molybdenum-dependent cofactor (FeMo-co) equivalent.

96 drogenase component termed Hyd-3), FdhF (the molybdenum-dependent formate dehydrogenase-H), and three

97 The active site of the molybdenum-dependent nitrogenase is the unique carbide-c

98 e it is not vulnerable to autoinhibition via molybdenum desulfuration.

99 ca generated a hydrophobic environment for a molybdenum diamine (Mo-diamine) precursor solution, enab

100 exchange appears to occur by formation of a molybdenum dihydride or dihydrogen complex, resulting fr

101 e lithium-storage capacity of the mesoporous molybdenum dioxide electrode is not based on a conversio

102 Here, we demonstrate a mesoporous molybdenum dioxide material with abnormal lithium-storag

103 ichalcogenides: molybdenum disulfide (MoS2), molybdenum diselenide (MoSe2) and tungsten diselenide (W

104 f interlayer shear modes emerge in few-layer molybdenum diselenide grown by chemical vapor deposition

105 brations in a model bilayered semiconductor, molybdenum diselenide.

106 Here, we incorporate molybdenum diselenide/hexagonal boron nitride (MoSe2/hBN

107 Two-dimensional molybdenum disulfide (2D MoS2) presents extraordinary op

108 s have been well established for crystalline molybdenum disulfide (c-MoS2) but not for amorphous moly

109 gen-doped graphene sheets (N-RGO) supporting molybdenum disulfide (MoS(2)) nanoparticles with high-pe

110 Increasing the active edge sites of molybdenum disulfide (MoS2 ) is an efficient strategy to

111 raphene quantum dots (GQDs) interacting with molybdenum disulfide (MoS2 ) monolayers induce an effect

112 ly crosslinked hydrogels from defect-rich 2D molybdenum disulfide (MoS2 ) nanoassemblies and polymeri

113 The emerging molybdenum disulfide (MoS2 ) offers intriguing possibili

114 the edge and basal-plane sites of monolayer molybdenum disulfide (MoS2 ) synthesized by chemical vap

115 lable fabrication of a large array of hybrid molybdenum disulfide (MoS2) - silicon dioxide (SiO2) one

116 ntrol over large area growth of high quality molybdenum disulfide (MoS2) and other types of 2D dichal

117 nsition metal dichalcogenides (TMDs) such as molybdenum disulfide (MoS2) and tungsten disulfide (WS2)

118 Monolayer molybdenum disulfide (MoS2) has emerged as a model syste

119 Monolayer Molybdenum Disulfide (MoS2) is a promising anode materia

120 Mono- and multi-layered molybdenum disulfide (MoS2) is considered to be one of t

121 The prototypical 2D material molybdenum disulfide (MoS2) is reported to have a maximu

122 (sharp tip and flat punch, respectively) on molybdenum disulfide (MoS2) multi-walled nanotubes (MWNT

123 tems in numerous environmental applications, molybdenum disulfide (MoS2) nanosheets stand out as a pr

124 iated nanosheets of two-dimensional metallic molybdenum disulfide (MoS2) on thin plastic substrates c

125 report on flexible and wavelength-selective molybdenum disulfide (MoS2) phototransistors using monol

126 mechanical resonators based on exfoliated 2D molybdenum disulfide (MoS2) structures, and focus on inv

127 tial of the applicability of two-dimensional molybdenum disulfide (MoS2) structures, in various elect

128 observation of the elastic deformation of 2D molybdenum disulfide (MoS2) thin films using an ordinary

129 perties of metallic (1T phase) nanosheets of molybdenum disulfide (MoS2) through covalent chemical fu

130 Here, we demonstrate molybdenum disulfide (MoS2) transistors with a 1-nm phys

131 mbine these two advantages and demonstrate a molybdenum disulfide (MoS2) two-dimensional steep-slope

132 )-vacancies created on the basal plane of 2H-molybdenum disulfide (MoS2) using argon plasma exposure

133 rphous nickel-cobalt complexes with 1T phase molybdenum disulfide (MoS2) via hydrazine-induced phase

134 l edge states of a single atomic membrane of molybdenum disulfide (MoS2), a transition metal dichalco

135 led fabrication of quantum dots in monolayer molybdenum disulfide (MoS2), and quantum dot arrays with

136 conductor interface, as epitaxial graphene - molybdenum disulfide (MoS2), is of great interest from t

137 monolayer transition-metal dichalcogenides: molybdenum disulfide (MoS2), molybdenum diselenide (MoSe

138 these properties of monolayer TMDs, such as molybdenum disulfide (MoS2), on standard Si-based substr

139 Molybdenum disulfide (MoS2), with its active edge sites,

140 tomic force microscope tip on a thin film of molybdenum disulfide (MoS2).

141 ndeed, we show basal plane activation of 1T' molybdenum disulfide and a lowering of DeltaG(H) from +1

142 he full dielectric tensors of nanometer-thin molybdenum disulfide and hexagonal boron nitride microcr

143 germanium as the source and atomically thin molybdenum disulfide as the channel, a vertical heterost

144 , we report that the thermal conductivity of molybdenum disulfide can be modified by electrochemical

145 mulations, that a nanopore in a single-layer molybdenum disulfide can effectively reject ions and all

146 sts a potential way to design newly advanced molybdenum disulfide catalysts through modulating the in

147 cm(-2), performing among the best of current molybdenum disulfide catalysts.

148 ructures made of single-layer semiconducting molybdenum disulfide contacting conductive graphene.

149 for 2H to +0.18 eV for 1T', comparable to 2H molybdenum disulfide edges on Au(111), one of the most a

150 tiscale structural and electronic control of molybdenum disulfide foam to synergistically promote the

151 The optimized three-dimensional molybdenum disulfide foam with uniform mesopores, vertic

152 Recently, molybdenum disulfide has been attracted considerable att

153 th a notable advantage in terms of capacity, molybdenum disulfide has been considered a promising ano

154 Layered molybdenum disulfide has demonstrated great promise as a

155 These changes alter the energetics of molybdenum disulfide interactions with hydrogen (DeltaG(

156 roach for large-scale and highly crystalline molybdenum disulfide monolayers using a solution-process

157 Here we unambiguously solve the structure of molybdenum disulfide monolayers using high-resolution tr

158 ly used gold nanoparticles when supported on molybdenum disulfide nanoribbons matrix (MoS2 NRs-Au NPs

159 ssisted strategy for the synthesis of narrow molybdenum disulfide nanosheets with edge-terminated str

160 roscopy studies reveal that the single-layer molybdenum disulfide nucleates at the graphene edges.

161 orrelation technique, we show that monolayer molybdenum disulfide photodetector can have intrinsic re

162 ch, where MoOx/MoS2 core-shell nanowires and molybdenum disulfide sheets are exposed to dilute aqueou

163 mainly on synthesizing highly nanostructured molybdenum disulfide that allows the exposure of a large

164 trates the validity of multiscale control in molybdenum disulfide via overall consideration of the ma

165 functional theory calculations indicate that molybdenum disulfide with moderate cobalt doping content

166 ce and Raman spectra of a bare bilayer MoS2 (Molybdenum disulfide).

167 Presently, for molybdenum disulfide, a promising catalyst for artificia

168 Two-dimensional layered materials, such as molybdenum disulfide, are emerging as an exciting materi

169 that hydrazine acts as an electron dopant in molybdenum disulfide, increasing its conductivity, while

170 n single flakes of atomically thin CVD-grown molybdenum disulfide, using non-degenerate femtosecond p

171 stigating the hydrogen evolution reaction on molybdenum disulfide, where it is shown that the basal p

172 ble band gap that can be as large as that of molybdenum disulfide.

173 d electronic response of synthetic monolayer molybdenum disulfide.

174 ectricity in a free-standing single layer of molybdenum disulphide (MoS(2)) and a measured piezoelect

175 a range of 2D materials including graphene, molybdenum disulphide (MoS2) and black phosphorus.

176 A nanocomposite formed from molybdenum disulphide (MoS2) and graphene quantum dots (

177 ansition metal dichalcogenide family such as molybdenum disulphide (MoS2) and tungsten diselenide (WS

178 bility 4-inch wafer-scale films of monolayer molybdenum disulphide (MoS2) and tungsten disulphide, gr

179 Two-dimensional (2D) molybdenum disulphide (MoS2) atomic layers have a strong

180 Ultrathin molybdenum disulphide (MoS2) has emerged as an interesti

181 ydrogen evolution reaction (HER; refs ,,,,), molybdenum disulphide (MoS2) is known to contain active

182 hes have been demonstrated for the growth of molybdenum disulphide (MoS2) on insulating substrates, b

183 , the growth of ultra-high-quality monolayer molybdenum disulphide appears a primary task for the com

184 ressure-induced nanoindentation of monolayer molybdenum disulphide from a tailored nanopattern, and d

185 ort properties of nanostructured flower-like molybdenum disulphide grown by hydrothermal route has be

186 olation of the two-dimensional semiconductor molybdenum disulphide introduced a new optically active

187 Defects in two-dimensional monolayer molybdenum disulphide may be responsible for large varia

188 investigation of point defects in monolayer molybdenum disulphide prepared by mechanical exfoliation

189 embrane with exceptional strength, monolayer molybdenum disulphide subjected to biaxial strain can em

190 ected for thicker crystals such as monolayer molybdenum disulphide, bilayer graphene or multilayer hB

191 reduction performance of vertically aligned molybdenum disulphide.

192 systematic modulation of the carrier type in molybdenum ditelluride (MoTe2 ) field-effect transistors

193 are performed on atomic layers of hexagonal molybdenum ditelluride (MoTe2), a prototypical transitio

194 hexagonal and monoclinic phases of monolayer molybdenum ditelluride (MoTe2).

195 n in the infrared region from a monolayer of molybdenum ditelluride on a silicon photonic-crystal cav

196 Molybdenum ditelluride, MoTe2 , is emerging as an import

197 near-field ThermoPhotoVoltaics, specifically molybdenum-doped indium oxide, dysprosium-doped cadmium

198 There is a linear correlation between the molybdenum Em value and both enzyme activity and the abi

199 ive catalysis in mARC and other pyranopterin molybdenum enzymes that catalyze this one-electron trans

200 Treatment of the bis(imino)pyridine molybdenum eta(6)-benzene complex ((iPr)PDI)Mo(eta(6)-C6

201 Finally, molybdenum-free chalcogels containing only Fe4S4 cluster

202 Molybdenum has been reported as a limiting nutrient for

203 For both protocols, molybdenum hexacarbonyl was used as a solid source of CO

204 The third one remains free and generates molybdenum hydride moieties as the active site under H2

205 sm involves protonation of the electron rich molybdenum hydride site (Volmer-Heyrovsky mechanism), le

206 The group 6 molybdenum(II) cyclopentadienyl amidinate (CPAM) bis(car

207 hemMatrix) were used to separate (99m)Tc and molybdenum in 4N NaOH.

208 The isotopic composition of molybdenum in five samples of glassy debris from the 194

209 levels of manganese, iron, copper, zinc and molybdenum in rice were reduced during washing and cooki

210 availability of bioessential metals such as molybdenum in the ocean was limited.

211 6)Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is

212 ptured at crack tips during the straining of molybdenum inside a transmission electron microscope at

213 y revised oxidation state assignment for the molybdenum ion, providing the first spatially resolved p

214 aphy and EPR spectroscopy of the nitrogenase molybdenum iron (MoFe) proteins from two phylogeneticall

215 an be used to photosensitize the nitrogenase molybdenum-iron (MoFe) protein, where light harvesting r

216 f carbon monoxide (CO)-inhibited nitrogenase molybdenum-iron (MoFe)-protein at 1.50 angstrom resoluti

217 a reduction product bound to the active-site molybdenum-iron cofactor (FeMo-co).

218 Here we present new molybdenum isotope data, which demonstrate that the area

219 Nonnatural molybdenum isotopic compositions were observed, reflecti

220 rmediates which collectively support a novel molybdenum(IV)-based catalytic cycle as being operative.

221 er composed of polyanionic trimeric units of molybdenum(IV).

222 s including barium, cadmium, cobalt, cesium, molybdenum, lead, antimony, thallium, tungsten, and uran

223 females had higher bile acid, globulin, and molybdenum levels, and males, higher corticosterone.

224 ected in natural ecosystems, particularly in molybdenum-limited habitats.

225 rly in compartments (e.g., organelles) where molybdenum may be limiting.

226 and irreversibly deactivate the diamagnetic molybdenum metallacyclobutadiene complex through a multi

227 th high regioselectivity (>98%) along with a molybdenum metallacyclobutadiene complex.

228 Here, the authors report a palladium-molybdenum mixed catalyst for the selective hydrodeoxyge

229 over the importance of N, phosphorus (P) and molybdenum (Mo) availability in controlling free-living

230 Molybdenum (Mo) is an essential trace nutrient but has n

231 to aromatic hydrocarbons over catalysts with molybdenum (Mo) nanostructures supported on shape-select

232 ulsed Nd:YAG millisecond laser on a pristine molybdenum (Mo) surface to measure surface melting and m

233 vanadium, chromium, manganese, iron, cobalt, molybdenum (Mo), tungsten, or rhenium.

234 The molybdenum (Mo)- and vanadium (V)-nitrogenases are two h

235 nts of organic matter from diazotrophs using molybdenum (Mo)-nitrogenases.

236 The use of such molybdenum monoaryloxide chloride complexes enables the

237 Here we show that molybdenum monoaryloxide chloride complexes furnish high

238 The reaction is promoted by a molybdenum monoaryloxide pyrrolide complex and affords p

239 obalt, copper, chromium, mercury, manganese, molybdenum, nickel, lead and zinc) were assayed in a coh

240 bide into the M cluster, the cofactor of the molybdenum nitrogenase from Azotobacter vinelandii.

241 ytic coatings composed of nitrides of either molybdenum or vanadium, containing either copper or nick

242 Using a 10 nm thick molybdenum oxide (MoO3-x) layer as a transparent and low

243 (1,2-CS) reactions of aldoses, i.e., various molybdenum oxide and molybdate species, nickel(II) diami

244 al synthetic reactions of a 2.9 nm spherical molybdenum oxide cluster, {Mo132} (formula: [Mo(VI)72Mo(

245 ree strategy is carried out to prepare mixed molybdenum oxides as an advanced anode material for lith

246 The well mixed molybdenum oxides at the microscale and the involvement

247 e bulk of disordered lithium nickel titanium molybdenum oxides using a standard solid-state method to

248 The well-defined silica-supported molybdenum oxo alkyl species ( identical withSiO-)MoO(CH

249 in PL and carrier lifetime due to increased molybdenum-oxygen bonding compared to that of traditiona

250 ntified reduced Pt covered with an amorphous molybdenum oxyhydroxide hydrate with a local structural

251 nes highly dispersed palladium and ultrafine molybdenum phosphate nanoparticles on silica.

252 ns (50 ng of pure approximately 0.75 nm size molybdenum polyoxometalate (POM) anions on 25 mug ( appr

253 Molybdenum precipitates preferentially under reducing co

254 re necessary intermediates in the process of molybdenum precipitation under anoxic conditions, there

255 cesium (Ptrend = 0.29), 1.76 (1.24-2.50) for molybdenum (Ptrend = 0.01), 0.79 (0.56-1.13) for lead (P

256 d alpha-MoB and beta-Mo2 C phases, while the molybdenum richest phase Mo2 B show significantly lower

257 complexes of the metals chromium to nickel, molybdenum, ruthenium to palladium, and tungsten to plat

258 Here we use patterned seeds of molybdenum source material to grow flakes of MoS2 at pre

259 din-2-one selectively cleave the propagating molybdenum species in the ring-opening alkyne metathesis

260 olution structure of the radiation sensitive molybdenum storage protein, demonstrate soaking of the d

261 num disulfide (c-MoS2) but not for amorphous molybdenum sulfide (a-MoSx), which exhibits significantl

262 Crystalline and amorphous molybdenum sulfide (Mo-S) catalysts are leaders as earth

263 Molybdenum sulfide (MoS2) is widely recognized for its c

264 ne, boron nitride (BN), zinc oxide (ZnO) and molybdenum sulfide (MoS2) nanoribbons, toward more reali

265 Amorphous molybdenum sulfide (MoSx) is covalently anchored to redu

266 s paper, we report the study of an amorphous molybdenum sulfide (MoSx) proton reducing electrocatalys

267 ynthesized a new phase of sub-stoichiometric molybdenum sulfide (s-MoSx) on sulfur-enriched copper su

268 The molybdenum sulfide aerogel exhibits high adsorption sele

269 The ammonium sites present in the molybdenum sulfide chalcogel network are ion-exchangeabl

270 We report the synthesis of ion-exchangeable molybdenum sulfide chalcogel through an oxidative coupli

271 se of most transition metal dichalcogenides (molybdenum sulfide, cobalt diselenide and so on).

272 Redox processes of molybdenum-sulfide (Mo-S) compounds are important in the

273 Molybdenum sulfides are very attractive noble-metal-free

274 ur material is fabricated by growing ternary molybdenum sulfoselenide particles on self-standing poro

275 ng direct hydride transfer from formate to a molybdenum-sulfur group of the molybdenum center.

276 ing of nanocomposite layer of zinc oxide and molybdenum sulphide (ZnO/MoS2) over unclad core of optic

277 The addition of molybdenum sulphide in the transducer layer increases th

278 eve the highest intrinsic HER activity among molybdenum-sulphide-based catalysts.

279 Also, using molybdenum telluride as a test case, we performed X-ray

280 Here we show that the flux of molybdenum to a Mesoproterozoic lake was 1 to 2 orders o

281 high-temperature alloys (e.g., tungsten and molybdenum), to vulnerability to supply restriction.

282 trioxide nanopaper, assembled via ultralong molybdenum trioxide nanobelts, displays an excellent ave

283 A flexible transparent molybdenum trioxide nanopaper, assembled via ultralong m

284 Molybdenum trioxide thin films of different thicknesses

285 oying a surface carrier transfer method with molybdenum trioxides.

286 ppropriate ligands within complexes based on molybdenum, tungsten and ruthenium has led to reactivity

287 Molybdenum-, tungsten-, and ruthenium-based complexes th

288 r-edge spectra of irreversibly laser excited Molybdenum using an average of only few x-ray pulses wit

289 A series of novel molybdenum(V) and tungsten(VI) oxoazides was prepared st

290 Most molybdenum(V) and tungsten(VI) oxoazides were fully char

291 Most molybdenum(VI) and tungsten(VI) dioxoazides were fully c

292 Molybdenum(VI) and tungsten(VI) dioxodiazide, MO2(N3)2 (

293 g activity significantly higher than that of molybdenum(VI) oxide powder and comparable to that of a

294 Molybdenum(VI) oxide was deposited on the Zr6 node of th

295 ions indicating that the dissociation of the molybdenum(VI) species from the node of NU-1000 is ender

296 iological nitrogen fixation and suggest that molybdenum was bioavailable in the mid-Archaean ocean lo

297 l loading before and after catalysis, and no molybdenum was detected in the reaction mixture.

298 An important case is molybdenum, which has long been speculated to undergo an

299 transitions has never been reported for pure molybdenum, while transformation coupled with plasticity

300 nded contact, formed through the reaction of molybdenum with the SWNT to form carbide, also exhibited