ライフサイエンスコーパス: Mo

1 Mo concentrations ranged from <1 to 149 mug/L.

2 9m)Tc-NaTcO4 was produced from enriched (100)Mo (99.815%) with a cyclotron (24 MeV; 2 h of irradiatio

3 ; OHMT = 2,6-dimesitylphenoxide) to give 14e Mo(NAr)(CHCMe2Ph)(OHMT)Cl in solution as a mixture of sy

4 nd to be especially reactive because the 14e Mo(NR)(CHR')(OR'')Cl core is accessible through dissocia

5 Herein, reductive pathways of MoO(S2)2bpy (Mo-bpy) (bpy = 2,2'-bipyridine) are presented from both

6 ctra that reveal (NEt4)[MoO(S2)2picolinate] (Mo-pic) is stable in a d6-DMSO solution after heating at

7 -28.3%; Fe, -26.7%; Zn, -21.9%; Mg, -22.7%; Mo, -40.4%; K, -22.4%; and Ca, -19.5%.

8 nt uncertainties and requires the (92)Nb/(92)Mo ratio in the early solar system to be at least 50% lo

9 Here by performing (7)Li-/(95)Mo-nuclear magnetic resonance (NMR) spectroscopy, we dir

10 Molybdenum (98)Mo/(95)Mo isotope ratios are a sediment paleo proxy for the red

11 y measuring both the perturbation of the (95)Mo/(96)Mo and (97)Mo/(96)Mo isotopic ratios and the tota

12 ring both the perturbation of the (95)Mo/(96)Mo and (97)Mo/(96)Mo isotopic ratios and the total amoun

13 urbation of the (95)Mo/(96)Mo and (97)Mo/(96)Mo isotopic ratios and the total amount of molybdenum in

14 he perturbation of the (95)Mo/(96)Mo and (97)Mo/(96)Mo isotopic ratios and the total amount of molybd

15 Molybdenum (98)Mo/(95)Mo isotope ratios are a sediment paleo proxy for

16 (99)Mo, the parent of the widely used medical isotope (99m)T

17 Results from a 51.8-GBq (99)Mo production run are presented.

18 We report results for the production of (99)Mo from the accelerator-driven subcritical fission of an

19 We report results for the production of (99)Mo from the accelerator-driven subcritical fission of an

20 eparation, recovery, and purification of (99)Mo were demonstrated using a recycled uranyl sulfate sol

21 Conclusion: The (99)Mo yield and purity were found to be unaffected by reuse

22 The (99)Mo yield and purity were found to be unaffected by reuse

23 of N2 occurs at the FeMo-cofactor, a 7Fe-9S-Mo-C-homocitrate cluster.

24 d the presence of two Al layers in between a Mo-B sublattice.

25 lectrocatalyst is described, which employs a Mo-coating on a metal surface to achieve selective H2 ev

26 S), we have determined the active state of a Mo-promoted Pt/C catalyst (NanoSelect) for the liquid-ph

27 meter range can be grown on graphene using a Mo-Cu alloy catalyst.

28 ,6-tri-tert-butylphenoxyl radical to yield a Mo-alkylimido ([Mo horizontal lineNR](+)) complex (R = 2

29 tride complex upon N-C bond cleavage, and a [Mo horizontal lineNH](+) complex is formed by protonatio

30 olytic cleavage of all three H atoms from a [Mo-NH3](+) complex using the 2,4,6-tri-tert-butylphenoxy

31 selectivity is observed with boron-activated Mo(NC6F5)(CHR')(OHIPT)(Cl)(PPhMe2).

32 lphenoxyl radical to yield a Mo-alkylimido ([Mo horizontal lineNR](+)) complex (R = 2,4,6-tri-tert-bu

33 Microcystin-LR binds also Mo(6+), Cu(2+), and Mn(2+).

34 ox center is of broad interest for amorphous Mo-S (a-MoSx) electrocatalytic materials and anion-redox

35 le to that of a zirconia-supported analogue (Mo-ZrO2) prepared in a similar fashion.

36 ) and Mo-doped BiVO4 (BiVO4:Mo) powders embedded into a gold (

37 We propose that Co(2+) and Mo(4+) centres promote the initial discharge of water (a

38 tion underestimates reactive Cu, Cr, As, and Mo, that is, elements with a particularly high affinity

39 of sites at the interface between the Co and Mo atoms on the MoS2 basal surface and we ascribe the hi

40 e defects formed after dissolution of Co and Mo cations.

41 yte antigen-DR was determined on all DCs and Mo, along with CCR2 on CD14/CD16 Mo.

42 ic example of an M-cluster mimic with Fe and Mo positioned at opposite ends of the cluster.

43 wer crust to produce high levels of HREE and Mo.

44 concentrations, but are depleted in HREE and Mo.

45 ncluding Ni(II), Zn(II), Al(III), Ti(IV) and Mo(VI), are anchored as metal-oxide,hydroxide clusters t

46 lybdenum center, Mo(6+) horizontal lineS and Mo(4+)-SH, are suggested to be the direct hydride accept

47 tween the formal Mo(VI) horizontal lineS and Mo(IV)-SH states, and by modeling chronoamperometry data

48 ed daily allowance for Zn, to 70% for Mn and Mo).

49 Ti and Nd, moderately siderophile Cr, Ni and Mo, and highly siderophile Ru record different stages of

50 metals (Ag, Cd, Sb, Tl, but also V, Ni, and Mo which are enriched in bitumen) has been declining in

51 ee-living N fixation in response to N, P and Mo fertilizers.

52 ively determine the extent to which N, P and Mo stimulate or suppress N fixation, and if environmenta

53 landscape P gradient, and manipulated P and Mo to seedlings in a shadehouse.

54 OF of 27-34 s-1 and 42-48 s-1 for Mo-pic and Mo-pym and onset potentials of 240 mV and 175 mV for Mo-

55 tentials of 240 mV and 175 mV for Mo-pic and Mo-pym respectively reveal these complexes as promising

56 by the anisotropic growth rates of the S and Mo edges under low sulfur chemical potential.

57 ue, it triggers the co-assembly of Mo(V) and Mo(VI) species into the giant clusters.

58 red distribution of (Mo/Nb)O6 octahedra and (Mo/Nb)O4 tetrahedra.

59 [Ar2N3]Mo(N)(O-t-Bu) serves as a catalyst or precursor for the

60 [Ar2N3]Mo(N)(O-t-Bu), which contains the conformationally rigid

61 aminants, including SO4, Ca, Mn, Fe, Se, As, Mo, and V above background levels, were also identified

62 Although the average Mo oxidation state in La2MoO5 is 4+, the very different

63 Concentrations of dissolved Al, As, B, Mo, Na, S, and V all significantly decreased after biore

64 the morphological reconstruction of the bare Mo-terminated edge.

65 r main classes of materials, i.e., Rh-based, Mo-based, modified Fischer-Tropsch and modified methanol

66 he miR-34a expression varied greatly between Mo from different tissues, correlating inversely with th

67 Bifunctional Mo complexes, [CpMo(CO)(kappa(3)-P2N2)](+) (P2N2 = 1,5-d

68 ) and Mo-doped BiVO4 (BiVO4:Mo) powders embedded into a gold (Au) layer.

69 Both Mo-pic and (NEt4)[MoO(S2)2pyrimidine-2-carboxylate] (Mo-

70 ndence of inhibitor-binding affinity on both Mo oxidation state and inhibitor electron-donor strength

71 A series of pi-bound Mo-quinonoid complexes supported by pendant phosphines h

72 dination at higher Mo loadings, indicated by Mo K-edge X-ray absorption spectra.

73 ver, regulation of siderophore production by Mo- and V-limitation has been difficult to confirm and k

74 pressed by N fertilization and stimulated by Mo fertilization.

75 pecies agglomerate and convert into carbided Mo nanoparticles.

76 nd (NEt4)[MoO(S2)2pyrimidine-2-carboxylate] (Mo-pym) are shown to be homogenous electrocatalysts for

77 s had a more profound expansion of CD14/CD16 Mo when compared with nonseptic burned patients.

78 all DCs and Mo, along with CCR2 on CD14/CD16 Mo.

79 monocytic myeloid-derived suppressor cells (Mo-MDSC) in psoriasis patients and examine the implicati

80 monocytic myeloid-derived suppressor cells (Mo-MDSCs) have been shown to suppress T-cell activation

81 the oxidized and reduced molybdenum center, Mo(6+) horizontal lineS and Mo(4+)-SH, are suggested to

82 ed an increased CCR2 expression on classical Mo (CD14/CD16), which was paralleled by greater chemokin

83 eptor type 2 (CCR2) expressions on classical Mo.

84 alizing Weyl physics in the layered compound Mo(x)W(1-x)Te2, where non-saturating magneto-resistance

85 oriasis being a hyperinflammatory condition, Mo-MDSCs were elevated in psoriatic patient peripheral b

86 hile the prismatic Mo2O8 dimers only contain Mo(3+) (d(3)), a result directly confirmed by density fu

87 In contrast, Mo-ZrO2 led to significant leaching and close to 80 wt %

88 also demonstrated that psoriatic and control Mo-MDSCs both induce regulatory T-cell conversion from n

89 ration less efficiently than healthy control Mo-MDSCs.

90 RNAs for NOX5 indicated that NOX5 controlled Mo-DC differentiation by regulating the JAK/STAT/MAPK an

91 e results show the importance of controlling Mo speciation to achieve the desired product formation,

92 The pathways controlling Mo-DC differentiation are not fully understood.

93 l amidinate (CPAM) bis(carbonyl) complex [Cp*Mo{N(iPr)C(Ph)N(iPr)}(CO)2] (Cp*=eta(5)-C5Me5) serves as

94 , with the exception of multifloral (Ca, Cr, Mo, Se), common heather (Mg, Na), bearberry (Ba, Fe, Pb)

95 l carbonyl complexes ([M(bpy)(CO)4], M = Cr, Mo, W) are potentially promising CO2 reduction electroca

96 ucted for six different elements (C, Al, Cu, Mo, Gd, and W) using 40 fs, 800 nm Ti: Sapphire laser.

97 pendent monocytes into monocyte-derived DCs (Mo-DCs) in the lungs after F. tularensis LVS pulmonary i

98 ed maturation of human monocyte-derived DCs (Mo-DCs).

99 oss of Mo species thus causes deactivation), Mo-SIM demonstrated no loss in the metal loading before

100 phobic environment for a molybdenum diamine (Mo-diamine) precursor solution, enabling direct growth o

101 n state in La2MoO5 is 4+, the very different Mo-Mo distances reflect the fact that the Mo2O10 dimers

102 Exposure to AC downregulated Mo miR-34a expression, resulting in a positive feedback

103 nstrate that the NOX5-p22phox complex drives Mo-DC differentiation, and thus could be critical for im

104 OX5 expression was strongly increased during Mo-DC differentiation, but not during Mo-macrophage diff

105 during Mo-DC differentiation, but not during Mo-macrophage differentiation.

106 and examine the implication of dysregulated Mo-MDSC function.

107 (VSFG) measurements of the electrocatalyst [Mo(bpy)(CO)4] at platinum and gold electrodes.

108 intermediate, (eta(5)-C5Me5)[N(Et)C(Ph)N(Et)]Mo(Cl)(NHSiMe3) (V), and XOSiMe3 as a co-product.

109 mido complex, (eta(5)-C5Me5)[N(Et)C(Ph)N(Et)]Mo(NSiMe3) (3), with a 1:2 mixture of iPrOH and Me3SiCl

110 l allow hydrogen to bind directly to exposed Mo atoms.

111 he acquisition of the nitrogenase co-factors Mo and V.

112 cide with a dramatic increase of metals (Fe, Mo, Pb, Mn and As) in the fossils and their host rocks.

113 he Mo2Fe6S8(SPh)3 is capable of N2 fixation, Mo itself is not necessary to carry out this process.

114 The incorporation of a fluorinated Mo(II)2 paddlewheel, B, into analogous Zn(II)8(L(B))6 an

115 ed by completing the solar cells as follows: Mo/CZTSSe/CdS/i-ZnO/Al:ZnO/Ni/Al.

116 The TOF of 27-34 s-1 and 42-48 s-1 for Mo-pic and Mo-pym and onset potentials of 240 mV and 175

117 m known CCR disposal sites, and analyzed for Mo and inorganic geochemistry indicators, including boro

118 ed arbitrarily by alloying, for example, for Mo(x)W(1-x)Te2 monolayers.

119 nd onset potentials of 240 mV and 175 mV for Mo-pic and Mo-pym respectively reveal these complexes as

120 highest value of delta(iso) is observed for Mo and the lowest for Ta, the values for W and Re being

121 of molybdate precursors are reduced to form {Mo(V)2(acetate)} structures under the coordination effec

122 sis, the Mo center cycles between the formal Mo(VI) horizontal lineS and Mo(IV)-SH states, and by mod

123 olybdenum complexes with the general formula Mo(NR)(CHR')(OR'')(Cl)(MeCN) (R = t-Bu or 1-adamantyl; O

124 molybdenum oxide cluster, {Mo132} (formula: [Mo(VI)72Mo(V)60O372(CH3COO)30(H2O)72](42-)), with system

125 Pivalonitrile can be removed (>95%) from Mo(NAr)(CHCMe2Ph)(OHMT)(Cl)(t-BuCN) (Ar = 2,6-diisopropy

126 d, phase-engineering of few-layer MoTe2 from Mo nanoislands is reported.

127 es, PdCl2, and CO gas, released ex situ from Mo(CO)6, were assembled to generate sulfonyl isocyanates

128 the stepwise removal of three H atoms from [Mo-NH3](+) and formation of [Mo horizontal lineNR](+).

129 the interaction between initially generated [Mo(bpy)(CO)4](*-) and the electrode is critical in enabl

130 The products of heterolytic cleavage of H2, Mo hydride complexes bearing protonated amines, [CpMo(H)

131 ce elements (As, Ba, Cu, Fe, Mn, Cd, Cr, Hg, Mo, Ni, Pb, Se, Sb, Sn, and Zn) in three different pulse

132 ence that these carbonatitic magmas had high Mo concentrations.

133 ore than 300 years for groundwater with high Mo concentrations support a geogenic source of Mo to the

134 d back to tetrahedral coordination at higher Mo loadings, indicated by Mo K-edge X-ray absorption spe

135 ppressive capabilities compared to DC-HIL(+) Mo-MDSC found in melanoma patients, suggesting contextua

136 The expanded population of DC-HIL(+) Mo-MDSC in psoriasis patients, however, display inferior

137 ort the identification of Late Triassic HREE-Mo-rich carbonatites in the northernmost Qinling orogen.

138 echanisms by LDH phases, by using changes in Mo geometry as powerful molecular-scale probe.

139 l combustion residues (CCRs) are enriched in Mo, and thus present a potential anthropogenic contamina

140 bly mechanisms of the two metalloclusters in Mo-nitrogenase and giving a brief account of the possibl

141 de phosphate reduced form oxidases (NOXs) in Mo-DC differentiation.

142 mitochondria and interacted with p22phox in Mo-DC.

143 Here, we propose a tunable Weyl state in Mo(x)W(1-x)Te2 where Weyl nodes are formed by touching p

144 icates that the enhanced PL due to increased Mo-O bonding leads to p-type compensation doping, and is

145 ility of efferocytosis to polarize ingesting Mo uniquely and to reduce their host-defense functions,

146 icrobial ClO4(-) reductase, which integrates Mo(MGD)2 complex (MGD = molybdopterin guanine dinucleoti

147 ed a defect in monocyte differentiation into Mo-DCs that was phenotypically similar to MR1(-/-) mice.

148 fferentiation of inflammatory monocytes into Mo-DCs.

149 During the reaction, the initial isolated Mo oxide species agglomerate and convert into carbided M

150 The results show that isolated Mo-oxo species present after calcination are converted b

151 rons to the well-characterized "as-isolated" Mo(V) oxidation state is needed to initiate the catalyti

152 nance signal of the molybdenum center in its Mo(V) state and demonstrated the direct transfer of the

153 microg/g) when using water containing >1mg/L Mo.

154 is procedure leads to the formation of large Mo-blue ring-shaped anion {Mo154}, which contains the su

155 Groundwater typically has low Mo (<2 mug/L), and elevated levels are associated with a

156 comb complex proto-oncogene BMI1 [B lymphoma Mo-MLV insertion region 1 homolog (mouse)] is essential

157 In this regard, monolayer (ML) MX2 (M = Mo, W; X = S, Se) has drawn increasing attention due to

158 Monolayer MX2 (M = Mo, W; X = S, Se) has recently been drawn much attention

159 ormula M(NR)(CHR')(OR'')(Cl)(L) in which M = Mo or W, NR = N-2,6-diisopropylphenyl or NC6F5, and L is

160 6-7 transition-metal dichalcogenides, MX2 (M=Mo, W, Tc, Re; X=S, Se, Te).

161 esident murine and human tissue macrophages (Mo).

162 Meanwhile, Mo geometry evolves from tetrahedral to octahedral on th

163 n multifloral honey (Al, As, Be, Ca, Cr, Mn, Mo, Ni, Se, Th and U), common heather (Co, K, Mg, Na, V)

164 Ce, Co, Cs, Cu, Eu, Fe, Ga, Gd, La, Lu, Mn, Mo, Nb, Nd, Ni, Pr, Rb, Sm, Te, Ti, Tl, Tm, U, V, Y, Zn

165 ations of Ag, As, Ba, Cu, Co, Fe, K, Mg, Mn, Mo, Na, Ni, Se, Sb, U and Th (p<0.05, all) among honeys.

166 found for Ba, Ca, Cd, Co, Cu, K, Li, Mg, Mn, Mo, P, Pb, Se, Sr, Tl and Zn; and high dialyzability rat

167 Molybdenum (Mo) is an essential trace nutrient but has negative heal

168 ortance of N, phosphorus (P) and molybdenum (Mo) availability in controlling free-living N fixation r

169 millisecond laser on a pristine molybdenum (Mo) surface to measure surface melting and mass loss.

170 The molybdenum (Mo)- and vanadium (V)-nitrogenases are two homologous me

171 Two distinct monocyte (Mo)/macrophage (Mp) subsets (Ly6C(low) and Ly6C(high)) o

172 y DCs is derived from circulating monocytes (Mo) and has a key role in inflammation and infection.

173 to investigate the alterations in monocytes (Mo) and dendritic cells (DCs) in septic burned patients

174 sperse, porous heterogeneous catalyst, named Mo-SIM, and its structure on the node was elucidated bot

175 Metathetical exchange of the new Mo-N amido bond of V by a second equivalent of Me3SiCl t

176 5 P4 , Co2 P), and their base metals (W, Ni, Mo, Co); their activity, stability, and degradation beha

177 So far no Mo horizontal lineCHCl complexes, which are required int

178 The catalytic activity of Mo-SIM was tested for the epoxidation of cyclohexene.

179 bon steel with high silicon and additions of Mo and V for secondary hardening.

180 One potential advantage of Mo is its higher specific heat of vaporization, which co

181 ersible formation of a significant amount of Mo(4+) following lithiation.

182 for samples containing different amounts of Mo indicate that interfacial sites are an order of magni

183 itical value, it triggers the co-assembly of Mo(V) and Mo(VI) species into the giant clusters.

184 a biosynthetic scaffold for the cofactor of Mo-nitrogenase (designated the M-cluster).

185 phase, contain significant concentrations of Mo (~17 ppm), reinforcing the inference that these carbo

186 Further, this delayed differentiation of Mo-DCs in MR1(-/-) mice was responsible for the delayed

187 e report that the equation of state (EOS) of Mo is obtained by an integrated technique of laser-heate

188 he cold compression and thermal expansion of Mo have been measured up to 80 GPa at 300 K, and 92 GPa

189 i arc length can be changed as a function of Mo concentration, thus tuning the topological strength.

190 is observation motivated an investigation of Mo(NMe2 )4 as a volatile precursor for the atomic layer

191 The syn isomer of Mo(NAr)(CHCMe2Ph)(OHMT)Cl binds pivalonitrile most stron

192 upported molybdenum catalysts (i.e., loss of Mo species thus causes deactivation), Mo-SIM demonstrate

193 gen abstraction and oxygenation mechanism of Mo-MnLOX by controlling oxygen access to the pentadiene

194 The phenotypes of Mo and DCs, particularly CCR2 expression on Mo, are not

195 creening reveals the very high reactivity of Mo(NMe2 )4 with H2 S for the low-temperature synthesis o

196 Reduction of Mo(IV) CO adducts of carbide and silylcarbyne species al

197 We tracked chemical reduction of Mo-bpy with UV-vis spectroscopy using sodium napthalenid

198 However, little is known about the role of Mo-MDSCs and their functional relationship to T-cell sup

199 Our group has recently described a series of Mo-S molecular HER catalysts based on a MoO(S2)2L2 struc

200 concentrations support a geogenic source of Mo to the groundwater, rather than CCR-induced contamina

201 ime indicators to investigate the sources of Mo in drinking-water wells from shallow aquifers in a re

202 The stability of Mo-SIM was further confirmed computationally, with densi

203 The electronic structures of Mo carbide and carbyne species were investigated quantum

204 Adoptive transfer of Mo-DCs to MAIT cell-deficient mice (MR1(-/-) mice) rescu

205 that contains a disordered distribution of (Mo/Nb)O6 octahedra and (Mo/Nb)O4 tetrahedra.

206 e H atoms from [Mo-NH3](+) and formation of [Mo horizontal lineNR](+).

207 ely avoiding the need for the generation of [Mo(bpy)(CO)4](2-).

208 Chemical reduction of [Mo horizontal lineNR](+) generates a terminal Mo identic

209 Once the concentration of {Mo(V)2(acetate)} reaches a critical value, it triggers t

210 ring type architecture (yield 4.3 % based on Mo).

211 nd decrease in human leukocyte antigen-DR on Mo and DCs in burned patients with sepsis compared with

212 Mo and DCs, particularly CCR2 expression on Mo, are not fully explored in severely burned patients w

213 With CCR2 level on Mo before sepsis onset being higher than postsepsis, CCR

214 the fact that the Mo2O10 dimers contain only Mo(5+) (d(1)), while the prismatic Mo2O8 dimers only con

215 fixation depends on soil nutrients (N, P or Mo), but recent evidence shows that fixation may also di

216 achieved by tuning the growth temperature or Mo:Se precursor ratio.

217 c activity increases in the following order: Mo(VI) < Ti(IV) < Al(III) < Zn(II) < Ni(II).

218 gen, the rice blast fungusMagnaporthe oryzae(Mo), was expressed inPichia pastoris.Mo-MnLOX was deglyc

219 Other Mo(NR)(CHR')(OR'')(Cl)(L) complexes can be activated thr

220 Our analysis indicates an oxidized Mo(VI) active site with a structure that is far from equ

221 The results show that a paramagnetic Mo(V) species is generated when reduced enzyme is expose

222 starts with a lag phase period when partial Mo(VI) centers of molybdate precursors are reduced to fo

223 oryzae(Mo), was expressed inPichia pastoris.Mo-MnLOX was deglycosylated, purified to homogeneity, an

224 molybdenum eta(6)-benzene complex ((iPr)PDI)Mo(eta(6)-C6H6) ((iPr)PDI, 2,6-(2,6-iPr2C6H3N horizontal

225 icantly, the weakened N-H bonds in ((iPr)PDI)Mo(NH3)2(eta(2)-C2H4) enabled hydrogen atom abstraction

226 rearrangement of the arene to form ((iPr)PDI)Mo(NH3)2(eta(2)-C6H6).

227 mately 10 equiv of ammonia can be formed per Mo with a maximum efficiency in electrons of approximate

228 The acetonitrile or pivalonitrile Mo(NR)(CHR')(OR'')(Cl)(L) complexes are found to be espe

229 eterminant of fixation, with P (and possibly Mo) only influencing fixation following tree-fall distur

230 rently under debate, and whether the primary Mo coordination sphere remains saturated or one of the l

231 In addition, psoriatic Mo-MDSCs expressed reduced surface expression of program

232 the regulatory T cells induced by psoriatic Mo-MDSCs displayed decreased suppressive functionality.

233 nt previous research demonstrating psoriatic Mo-MDSC are unable to suppress autologous and heterologo

234 Cao et al. describe psoriatic Mo-MDSC that produce increased IL-23, IL-1b, and CCL4 cy

235 esults suggest that aberrations in psoriatic Mo-MDSCs prevent proper suppression of effector T-cell e

236 Freshly isolated psoriatic Mo-MDSCs directly suppressed CD8 T-cell proliferation le

237 n of the surface protein DC-HIL on psoriatic Mo-MDSC.

238 plane of s-MoSx contains chemically reactive Mo-rich sites that can undergo dynamic dissociative adso

239 ot on gp91phox/NOX2, as shown by the reduced Mo-DC differentiation observed in chronic granulomatous

240 hat monosilylation, and a more electron-rich Mo center, favors deoxygenative pathways.

241 Z selectivity as compared to when other Ru-, Mo-, or W-based complexes are utilized.

242 icro- and macro-nutrients, such as Na, P, S, Mo, Zn, and Fe.

243 that are created local to the observed Co-S-Mo interfacial sites.

244 fractal arrays at the atomic scale for the S-Mo-S(Co) 2D- layers that conform the spherically shaped

245 fluence on the catalytic properties of the S-Mo-S(Co) system.

246 ments (Na, K, V, Ni, Co, Cu, Zn, Ga, As, Se, Mo, Cd, Sn, Sb, Ba, W, and Pb), including air toxics wer

247 bbon growth is narrowly defined by proper Se:Mo ratios, as corroborated experimentally using differen

248 a diffusion barrier to the phase-segregated Mo and allows nanometer-thin Mo2 C to be grown.

249 Herein is presented two water soluble Mo-S complexes based around the [MoO(S2)2L2]1- motif.

250 rmation of the catalytically active species [Mo(bpy)(CO)3](2-) via a second pathway at more positive

251 , K, Ca, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Sr, Mo, Cd, Sn, Sb, Ba, Hg, Pb, Bi, Th, and U) in green coff

252 rystalline and amorphous molybdenum sulfide (Mo-S) catalysts are leaders as earth abundant materials

253 Redox processes of molybdenum-sulfide (Mo-S) compounds are important in the function of materia

254 o horizontal lineNR](+) generates a terminal Mo identical withN nitride complex upon N-C bond cleavag

255 A terminal Mo phosphide was prepared through the group transfer of

256 onstrating that the multiple bonded terminal Mo identical withC moiety is an intermediate on the path

257 persulfide reduction to form the tetragonal Mo(VI) complex [MoOS3](2-).

258 We conclude that Mo-MnLOX illustrates a partly unique variation of the st

259 cid with an applied potential confirmed that Mo-bpy maintains its structure during catalytic cycling.

260 NaNpth) as the reducing agent and found that Mo-bpy undergoes anionic persulfide reduction to form th

261 Herein we report that Mo(NMe2 )4 enables MoS2 film growth at record low temper

262 In this study, we revealed that Mo-DC differentiation was inhibited by NOX inhibitors an

263 ction pathways were explored, revealing that Mo=O may function as a proton relay.

264 The Mo coating was stable in acidic media for multiple hours

265 The Mo layer likely hinders O2 gas permeation, impeding cont

266 The Mo nitrogenase catalyzes the ambient reduction of N2 to

267 The Mo precursor plays a key role in determining the quality

268 The Mo-Mo bond length in the Mo2O10 dimers is 2.684(8) A, wh

269 The Mo-Pt3Ni/C showed the best ORR performance, with a speci

270 n involves formal addition of HCl across the Mo horizontal lineN imido bond through initial hydrogen-

271 This analogue, referred to as the Mo-cluster, is the first synthetic example of an M-clust

272 ite oxidases, the electrons generated at the Mo center are transferred to an external electron accept

273 lopment of a molecular motif inspired by the Mo-S catalytic materials and their active sites is of in

274 During catalysis, the Mo center cycles between the formal Mo(VI) horizontal li

275 corroborating the experimental data for the Mo-SIM material.

276 Prostaglandin (PG) E2 is involved in the Mo/Mp-mediated inflammatory response, however, the role

277 detailed new insight into the nature of the Mo species on zeolite ZSM-5 during methane dehydroaromat

278 3SiCl resulted in the rapid formation of the Mo(IV) dichloride, (eta(5)-C5Me5)[N(Et)C(Ph)N(Et)]MoCl2

279 Treatment of the Mo(IV) terminal imido complex, (eta(5)-C5Me5)[N(Et)C(Ph)

280 Moreover, the ability of the Mo-cluster to reduce C1 substrates to hydrocarbons sugge

281 We show that the Mo-DC differentiation was dependent on p22phox, and not

282 bitors (and substrates) bind directly to the Mo center.

283 We propose that inhibitors bind to the Mo following dissociation of a selenocysteine ligand to

284 ibited by selective inhibitor binding to the Mo(VI) horizontal lineS state.

285 ntial differences between cultures using the Mo- as opposed to the less efficient V-nitrogenase.

286 The [Mo:7Fe:9S:C] iron-molybdenum cofactor (FeMoco) of nitrog

287 ously been linked to efferocytosis by tissue Mo.

288 IL-23, IL-1b, and CCL4 cytokines compared to Mo-MDSC from healthy controls.

289 naling as a potential contributing factor to Mo-MDSC function.

290 by miR-34a provides one means of fine-tuning Mo behavior toward AC in specific tissue environments wi

291 e cyanobacterium Anabaena variabilis has two Mo-nitrogenases that function under different environmen

292 oferrin is almost completely repressed under Mo- and V-limitation.

293 n of all siderophores increases, while under Mo-limitation only catechol siderophore production is in

294 es as the nitrogen source was achieved using Mo(CO)6 as the reductant and origin of the CO.

295 6-norbornene skeleton, can be prepared using Mo(N-2,6-Me2C6H3)(CHCMe2Ph)(OHMT)(pyrrolide) (1) as the

296 y be the incorporation of finely dispersed V-Mo-Nb carbides in a ferrite matrix.

297 3 are generally within a factor three, while Mo is underestimated and Co, Ni and Zn in soils with pH

298 ile there are two types of Mo2O8 dimers with Mo-Mo bonds lengths of 2.22(2) and 2.28(2) A.

299 s the hydrogen evolution reaction (HER) with Mo-S electrocatalysts.

300 aries are predominantly terminated by zigzag Mo edge structure.