ライフサイエンスコーパス: vanadium

1 pper, iron, and titanium), and ship traffic (vanadium).

2 agnetic impurities, manganese, chromium, and vanadium.

3 abundances of nickel, cobalt, chromium, and vanadium.

4 black carbon, nickel, silicon, titanium, and vanadium.

5 .013 for copper, 0.13 for zinc and 0.015 for vanadium.

6 hosphorus, manganese, iron, zinc, copper and vanadium.

7 anium or other elements, such as aluminum or vanadium.

8 Similar trends were observed for vanadium.

9 uent decrease of the electron density in the vanadium 3d levels.

10 which significantly enhance the recovery of vanadium - 4-(2-pyridylazo) resorcinol (PAR) chelate.

11 robes within the water pools, measured using vanadium-51 NMR spectroscopy, indicate a significant dro

12 Measured changes in concentrations of vanadium, a specific marker for heavy fuel oil combustio

13 dium, the role of molybdenum availability on vanadium acquisition and the contribution of alternative

14 Here we demonstrated an all-vanadium (all-V) continuous-flow photoelectrochemical st

15 ohols by an oxyvanadium catalyst to generate vanadium allenoates and the activation of allyl carbonat

16 sh, determining the uptake and metabolism of vanadium allows for a better understanding of the potent

17 pure titanium (cp-Ti) and titanium-aluminum-vanadium alloy (Ti-6Al-4V) disks were used.

18 crease in numbers of V(5+)-reducing cells in vanadium-amended columns compared to controls.

19 Vanadium, an important pollutant produced from anthropog

20 oyed was associated with a 20.0% increase in vanadium and an 18.3% increase in elemental carbon.

21 is achieved by the sputter-deposited nickel-vanadium and gold pad metal layers and copper interconne

22 etween prenatal exposure to higher levels of vanadium and increased risk of adverse birth outcomes, s

23 Vanadium and its surface oxides were studied as a potent

24 High enrichments of molybdenum and vanadium and low pyrite sulphur isotope values (Delta(34

25 We measured urinary concentrations of vanadium and other metals simultaneously using inductive

26 ic alcohols and allylic carbonates, engaging vanadium and palladium catalysts, is an exemplary case o

27 ng to the significant pi-bonding between the vanadium and the oxide ligand.

28 thesis of the first tin-bridged bis(benzene) vanadium and trovacene sandwich compounds and the invest

29 implementation of traditional RFBs, such as vanadium and Zn-Br2 RFBs, is limited due to a number of

30 5 mV s(-1), corresponding to 0.89 charge per vanadium) and excellent cyclability (62.5 mAh g(-1) in f

31 ll as for the implant constituents titanium, vanadium, and aluminum.

32 he PM2.5 constituents calcium, black carbon, vanadium, and zinc.

33 um, nickel, lead, sulfur, silicon, titanium, vanadium, and zinc.

34 In adults, exposed birds had higher vanadium, and, following the final exposure, higher bica

35 gated for their bioweathering effects on the vanadium- and lead-containing insoluble apatite group mi

36 ic (bcc) metals, such as liquid tantalum and vanadium, are successfully vitrified to form metallic gl

37 the phonon dispersion of single-crystalline vanadium as a function of pressure to 45 GPa.

38 as components (SO2, NO, NO2, H2O, and O2) on vanadium at 500-600 degrees C were investigated by therm

39 rst water oxidation catalyst containing only vanadium atoms as metal centers is reported.

40 tive purposes, we demonstrate the concept on vanadium based perovskites where we reveal an unpreceden

41 f materials have been considered, where both vanadium-based and titanium-based materials are recommen

42 We confirmed the use of the alternative vanadium-based nitrogenase in the Nostoc cyanobiont of t

43 Recent studies on (Ph4P-d20)2[V(C8S8)3], a vanadium-based qubit, demonstrate that millisecond T2 ti

44 particulate filters (DPF), Cu zeolite-, and vanadium-based selective catalytic reduction (SCR) catal

45 n PM from the engine fitted with a prototype vanadium-based selective catalytic reductors (V-SCR) ret

46 evalence as a contaminant, the potential for vanadium bioremediation has not been widely studied.

47 N-N bond cleavage to yield the corresponding vanadium bis(amido) derivatives, ((iPr)BPDI)V(NHAr)2 (Ar

48 n-C4H10, and C2H4, while substitution of one vanadium by a phosphorus atom yields the reactive [VPO4]

49 esults indicate the uptake and metabolism of vanadium by H. azteca.

50 n phosphatase and coordinating ligand to the vanadium can be established resulting in a dramatic enha

51 results may be the first documentation that vanadium can substitute for phosphorus in biological pro

52 New two-dimensional niobium and vanadium carbides have been synthesized by selective etc

53 ly hydrolyzed into imides and amides through vanadium catalysis.

54 n of a phenolic lignin model compound with a vanadium catalyst results in the oxidative cleavage of t

55 O bond cleavage depends on the choice of the vanadium catalyst.

56 ransient allenyl enolate intermediate of the vanadium-catalyzed Meyer-Schuster rearrangement with ald

57 A novel vanadium-catalyzed one-pot domino reaction of 1,2-diketo

58 ly linear V(III)N2V(III) core and where each vanadium center antiferromagnetically couples to give a

59 ands with concomitant 2e(-) reduction at the vanadium center.

60 tions, revealing V(3+)/d(2) character of the vanadium center.

61 spin-free ligand, which served to shield the vanadium centers against solvent nuclear spins.

62 ve the detailed coordination environments of vanadium centers in large biological molecules.

63 e obtained after reduction into nitrite by a vanadium chloride reagent.

64 However, the concentration of vanadium chloride used in this protocol brings coloratio

65 This finding biochemically links a vanadium chloroperoxidase to microbial natural product b

66 several of its main alloying elements (i.e., vanadium, chromium, manganese, and niobium).

67 nsition metals, termed M-Pt3Ni/C, where M is vanadium, chromium, manganese, iron, cobalt, molybdenum

68 t opens the way to the use of less expensive vanadium clusters as water oxidation catalysts in artifi

69 We report a vanadium complex in a nuclear-spin free ligand field tha

70 ce involving an N-heterocyclic carbene and a vanadium complex that results in cleavage of both the N-

71 complexes with early metals, the homoleptic vanadium complex, [V(L)3 ] (1), and its monocation, [V(L

72 strate, affording the first eta(2)-[N2H3](-) vanadium complex.

73 erization of the first stable two-coordinate vanadium complexes are described.

74 s point to a frameshift in ligand design for vanadium complexes as phosphatase inhibitors and are con

75 Oxalate-vanadium complexes markedly reduced the vanadinite stabi

76 Vanadium compounds have been proposed to have beneficial

77 Vanadium compounds have been reported to have antidiabet

78 escription of the antidiabetic properties of vanadium compounds is described here in the context of r

79 ted and dramatic enhancement of antidiabetic vanadium compounds may result.

80 Studies of antidiabetic vanadium compounds, specifically the organic vanadate es

81 have been reported of a number of promising vanadium compounds.

82 ell as high price, toxicity, and scarcity of vanadium compounds.

83 rticipants in the highest quartile of plasma vanadium concentration had a notably lower risk of newly

84 We found a substantial reduction in vanadium concentrations after the fuel change and a 28-7

85 Urinary Ln-vanadium concentrations showed non-linear dose-response

86 Our results suggested that plasma vanadium concentrations were inversely associated with n

87 Ln-vanadium concentrations were linearly associated with th

88 Plasma vanadium concentrations were measured and compared betwe

89 Analyses showed that plasma vanadium concentrations were significantly lower in case

90 for gestational age per unit increase in Ln-vanadium concentrations.

91 ed creatinine-corrected urinary vanadium (Ln-vanadium) concentrations as continuous variables and cat

92 composed of nitrides of either molybdenum or vanadium, containing either copper or nickel catalysts,

93 Synchrotron based V 1s XANES spectroscopy of vanadium-containing fine-particle PM from the V-SCR iden

94 lso relevant to remedial treatments for lead/vanadium contamination, and novel approaches for vanadiu

95 The redox chemistry of vanadium controls its occurrence in the aquatic environm

96 plexes are reviewed, and the potency of such vanadium coordination complexes as antidiabetic agents i

97 has a nonlinear [N-V-N = 123.47(9) degrees ] vanadium coordination.

98 The vanadium-dependent chloroperoxidase Mcl24 was discovered

99 biochemical characterization of a bacterial vanadium-dependent chloroperoxidase, NapH1 from Streptom

100 ment of the cofactor in the resting state of vanadium-dependent chloroperoxidases (VCPO).

101 t contains two genes encoding rare bacterial vanadium-dependent haloperoxidase (VHPO) genes.

102 rin A and isomeric merochlorin B by a single vanadium-dependent haloperoxidase, thus completing the r

103 Vanadium-dependent haloperoxidases (VHPOs) perform two-e

104 Vanadium-dependent haloperoxidases are generally conside

105 pha-hydroxyketone rearrangement catalysed by vanadium-dependent haloperoxidases to account for these

106 In a small-scale reaction, vanadium-dependent nitrogenase has previously been shown

107 excitation, accompanied by faster motions of vanadium dimers that are more complex than simple dilati

108 2-diarylhydrazines to the bis(imino)pyridine vanadium dinitrogen complex, [{((iPr)BPDI)V(THF)}2(mu2-N

109 An archetypal correlated material is vanadium dioxide (VO(2)), which is insulating only at te

110 Vanadium dioxide (VO2) exhibits a first-order metal-insu

111 The preparation of thermochromic vanadium dioxide (VO2) films in an economical way is of

112 The insulator-metal transition (IMT) of vanadium dioxide (VO2) has remained a long-standing chal

113 The complex phase transitions of vanadium dioxide (VO2) have drawn continual attention fo

114 The insulator-to-metal phase transition in vanadium dioxide (VO2) is a canonical example of such co

115 Vanadium dioxide (VO2) is an archetypical correlated ele

116 ntrol of aluminum-doped zinc oxide (Al:ZnO) /vanadium dioxide (VO2) multilayered thin films, where th

117 Single-crystalline vanadium dioxide (VO2) nanostructures have attracted an

118 amically tunable broadband absorber based on vanadium dioxide (VO2) phase transition.

119 ces activated by microstructural change of a vanadium dioxide (VO2) thin film.

120 that exploits insulator-metal transition in Vanadium Dioxide (VO2) to efficiently solve vertex color

121 Vanadium dioxide (VO2) with its unique sharp resistivity

122 across the insulator-to-metal transition in vanadium dioxide (VO2), to design a hybrid-phase-transit

123 nce, silicon) that provide limited activity, vanadium dioxide (VO2), which exhibits an insulator-to-m

124 rived from the metal-insulator transition of vanadium dioxide at 68 degrees C.

125 Vanadium dioxide exhibits a first-order phase transition

126 s ranging from 240 to 340 kelvin in metallic vanadium dioxide in the vicinity of its metal-insulator

127 ervation of an insulator-metal transition in vanadium dioxide induced by a terahertz electric field.

128 triggered functionalities, we demonstrate a vanadium dioxide integrated photonic metamaterial as a t

129 Vanadium dioxide is particularly intriguing because both

130 Here, by leveraging the phase-change of a vanadium dioxide nanolayer, we demonstrate broadband all

131 , visualize the phase transition dynamics in vanadium dioxide nanoparticles.

132 Owing to its small size the vanadium dioxide nanowire-based microthermometer has a l

133 ow a new type of microthermometer based on a vanadium dioxide nanowire.

134 insulator phase transition in single-crystal vanadium dioxide nanowires (NWs) is engineered to be a g

135 ealized with phase-change materials, such as vanadium dioxide or chalcogenide glasses, which exhibit

136 gin of the phase transition remains elusive, vanadium dioxide serves as a testbed for correlated-elec

137 and full mapping in spectroscopic studies of vanadium dioxide systems, which is commonly substituted

138 the epitaxial quality and microstructures of vanadium dioxide thin films and understanding the metal-

139 ulator transition behaviors of the epitaxial vanadium dioxide thin films deposited on Al2O3 (0001) su

140 The well-known metal-insulator transition in vanadium dioxide, a popular candidate for ultrafast opti

141 xploiting the hysteretic phase transition of vanadium dioxide, an all-solid, rewritable metacanvas on

142 The M1 form of vanadium dioxide, which exhibits a reversible insulator-

143 oluene (TNT) was investigated using films of vanadium dioxide.

144 action measurements on intact lithium/silver vanadium diphosphate (Li/Ag2VP2O8) electrochemical cells

145 Vanadium displays the highest cradle-to-gate environment

146 Nano-sized vanadium-doped LFP (V-LFP) was synthesized using a conti

147 that the unit cell is unaffected in-plane by vanadium doping changes, and remains unchanged over a th

148 insufficient availability of molybdenum and vanadium, elements essential to the production of high-y

149 nadate occurs via sigma-bond metathesis, and vanadium enolate is directly involved in the key C-C bon

150 e report a large spin Hall angle observed in vanadium films sputter-grown at room temperature, which

151 es, resulted in prolonged removal of aqueous vanadium for a period of at least two years.

152 The trace metal vanadium had a significant effect on the biogeography of

153 o umbrella structure, however, is present in vanadium haloperoxidase (VHPOs) enzymes and metal-organi

154 Vanadium has previously been linked to elevated toxicity

155 Vanadium has the potential to leach into the environment

156 eport the first mononuclear three-coordinate vanadium(II) complex [(nacnac)V(ODiiP)] and its activati

157 The vanadium(II) primary amido derivative V{N(H)Ar(iPr6)}2 [

158 mputational studies support an assignment as vanadium(III) complexes with chelate radical anions, [BP

159 n prepared via the thermolysis of metastable vanadium(III)-azido precursors.

160 organic-organic hybrid material, imidazolium vanadium(III,IV) oxyfluoride [C3 H5 N2 ][V9 O6 F24 (H2 O

161 drazine, formation of the bis(imino)pyridine vanadium imide amide compounds, ((iPr)BPDI)V(NHAr)NAr, w

162 first measurements of the oxidation state of vanadium in diesel vehicle PM emissions.

163 amples include selenium in colored glass and vanadium in pigments.

164 was developed to quantify the trace level of vanadium in real water and food samples by graphite furn

165 le, and, importantly, the oxidation state of vanadium in sub-milligram masses of environmental aeroso

166 ten percent simply by changing the amount of vanadium in the dendritic phase.

167 a tissue increased with the concentration of vanadium in the exposure water.

168 The concentrations of vanadium in the H. azteca tissue increased with the conc

169 tion of five-coordinate trigonal bipyramidal vanadium inhibitors by comparison with the reported vana

170 lts have revealed the coordination change of vanadium ions (from 5+1 to 6) at around 4 GPa.

171 caled-up reaction featuring 20 milligrams of vanadium-iron protein, the catalytic component of vanadi

172 Vanadium is a commercially important metal that is relea

173 mmiscibility of redox electrolytes and where vanadium is replaced by organic molecules.

174 We also showed that the acquisition of vanadium is strongly regulated by the abundance of molyb

175 When nuclear spin-free ligands are employed, vanadium(IV) complexes can show at low temperature suffi

176 ong-lived quantum coherence in spin systems, vanadium(IV) complexes have shown record phase memory ti

177 ovanadium(IV) in a square pyramidal versus a vanadium(IV) in an octahedral environment featuring the

178 e complex formation between luteolin (L) and vanadium(IV) oxide sulphate monohydrate (VOSO4.H2O) was

179 on dynamics and the quantum coherence of two vanadium(IV)-based potential molecular spin qubits in th

180 (II)-peroxysuccinate ferryl precursor, and a vanadium(IV)-oxo mimic of the ferryl intermediate in the

181 Vanadium K-edge X-ray absorption near edge structure (XA

182 replicate determinations at 0.5 mug L(-1) of vanadium level was found to be <5.0%.

183 s to evaluate the association between plasma vanadium levels and type 2 diabetes.

184 Mean plasma vanadium levels in participants with and without diabete

185 thm transformed creatinine-corrected urinary vanadium (Ln-vanadium) concentrations as continuous vari

186 sient absorption spectroscopy (FXTAS) at the vanadium M2,3 edge is used to track the insulator-to-met

187 t that the carbon capture performance of the vanadium membrane can potentially be strengthened by mat

188 ecting the composition and morphology of the vanadium membrane.

189 e observed timescales and d(2) nature of the vanadium metal centers are inconsistent with a Peierls d

190 to M(n) = 89200 g.mol(-1)) composed of d(5)-vanadium metal centers in the main chain, making it a ra

191 inyl substituents were deposited, along with vanadium metal, on the Au(100) surface.

192 in-film organic-based magnet V[MeTCEC]x (V = vanadium; MeTCEC = methyl tricaynoethylenecarboxylate) v

193 k of adverse birth outcomes, suggesting that vanadium might be a potential toxic metal for human bein

194 ical simulations, no other lead vanadate, or vanadium minerals were detected.

195 e was also estimated to be a major source of vanadium, nickel, and molybdenum.

196 itted in high quantities from the upgraders (vanadium, nickel, and zinc), and crustal elements (alumi

197 crystal structure, the elements of group V, vanadium, niobium and tantalum, show strong interactions

198 iron-dependent diazotophy are encoded by the vanadium nitrogen fixation (vnf) and alternative nitroge

199 Vanadium nitrogenase not only reduces dinitrogen to ammo

200 thus an atomically homologous active site in vanadium nitrogenase, highlights the importance and infl

201 the Fe-V cofactor of Azotobacter vinelandii vanadium nitrogenase.

202 ium-iron protein, the catalytic component of vanadium nitrogenase.

203 Molybdenum and vanadium nitrogenases are capable of converting carbon m

204 The molybdenum and vanadium nitrogenases are two homologous enzymes with di

205 f CO as a substrate for both molybdenum- and vanadium-nitrogenases strengthens the hypothesis that CO

206 ted that alternative nitrogenases, which use vanadium or iron in place of molybdenum at their active

207 f) gene clusters, whereas genes specific for vanadium- or iron-dependent diazotophy are encoded by th

208 clusters, which hold vanadyl groups, even if vanadium oxidation state is formally +3.

209 concomitant with a reversible change in the vanadium oxidation state, when alternating between oxidi

210 ycin A, including enolate SET oxidation, oxo-vanadium oxidation, and atom-transfer cyclization.

211 ncreased after the formation of complex with vanadium oxide (VO(+2)) cation.

212 y absorbing chemical species such as gaseous vanadium oxide and titanium oxide.

213 thickness, suggesting that the properties of vanadium oxide are sensitive to the supporting oxide.

214 the oxidative dehydrogenation of propane by vanadium oxide catalysts supported on silica are examine

215 pic data indicated that luteolin reacts with vanadium oxide cation (VO(+2)) through 4-carbonyl-5-hydr

216 titanium dioxide surface termination and the vanadium oxide layer thickness, suggesting that the prop

217 The vanadium oxide nanosheets engaged by structural water ac

218 ffects of structural water on the disordered vanadium oxide nanosheets will contribute to the explora

219 the highly disordered potassium-intercalated vanadium oxide nanosheets.

220 etal oxides such as titanium oxide (TiO) and vanadium oxide occur in the observable regions of the ve

221 Monomeric and dimeric vanadium oxide species are both considered and modeled b

222 on transmission electron microscopy to study vanadium oxide supported on titanium dioxide, which is o

223 ns reveal a reversible transformation of the vanadium oxide surface between an ordered and disordered

224 ent alterations in the surfaces of supported vanadium oxide upon reduction and oxidation.

225 The vanadium oxide-fluoride octahedra are ordered by the use

226 A series of strontium vanadium oxide-hydride phases prepared by utilizing a lo

227 rostructure of an FeSC and a Mott-insulating vanadium oxide.

228 us permitting a comparison to the well-known vanadium-oxide cation [V2O4](*+).

229 TiO2 and carbon nanotubes (CNTs) supported vanadium oxides (VOX/TiO2-CNTs) modified with MnOX and C

230 We hypothesize that decomposition of surface vanadium oxides and diffusion of surface oxygen into the

231 are unlikely to have adsorbed on the surface vanadium oxides at 600 degrees C after exposure for up t

232 r solute-solvent interactions with the polar vanadium-oxo moiety.

233 The structure consists of inorganic vanadium oxyfluoride slabs with kagome layers of V(4+) S

234 ter induces structural rearrangements of the vanadium-oxygen octahedra and enhances stability of the

235 gh-pressure study of anion-ordered strontium vanadium oxyhydride SrVO2H that H(-) is extraordinarily

236 with allyl carbonates using an unprecedented vanadium/palladium contemporaneous dual catalysis.

237 TMO) such as molybdenum tri-oxide (MoO(3) ), vanadium pent-oxide (V(2) O(5) ) or tungsten tri-oxide (

238 developed an inbred mouse model of ILD using vanadium pentoxide (V2O5), the most common form of a tra

239 y/energy (443 mAh g(-1) and 1,550 Wh kg(-1)) vanadium pentoxide from being used as the cathode materi

240 e resulting graphene-modified nanostructured vanadium pentoxide hybrids contain only 2 wt.

241 en developed, wherein stacked lamellas of 1D vanadium pentoxide nanofibres, intercalated with water m

242 a method to incorporate graphene sheets into vanadium pentoxide nanoribbons via the sol-gel process.

243 on the structural information obtained from vanadium-phosphatase complexes.

244 d vertically porous nanocomposite of layered vanadium phosphates (VOPO4) and graphene nanosheets with

245 -butane oxidation to maleic anhydride on the vanadium phosphorus oxide (VPO) surface.

246 ed from dynamometer samples containing total vanadium pools of only 0.2-2 ng and provide some of the

247 Collectively, the pH-dependent vanadium probes show CO(2) dissolves in the nanowater dr

248 water molecules in each droplet, changes in vanadium probes within the water pools, measured using v

249 m inhibitors by comparison with the reported vanadium-protein phosphatase complexes.

250 on of two active redox processes (silver and vanadium), providing a significant enhancement in the ca

251 dium contamination, and novel approaches for vanadium recovery.

252 a case study with an off-grid application of vanadium redox flow batteries (VRFBs).

253 structural stability, electronic conduction, vanadium redox reaction and lithium-ion diffusion suppor

254 : lithium-ion, lead-acid, sodium-sulfur, and vanadium-redox-flow.

255 Generally, the active form of vanadium remains elusive, although studies have been rep

256 Ce f states forming two Ce(3+) ions whereas vanadium remains fully oxidized (V(5+)).

257 utcomes for the crystallization of templated vanadium selenites.

258 mapping was achieved obtaining titanium and vanadium signals from the metal implant as well as phosp

259 Such metal defects are favored at vanadium sites.

260 Particle size-resolved vanadium speciation data were obtained from dynamometer

261 emical modelling confirmed the complexity of vanadium speciation, and the significant effect of oxala

262 e V(IV) species was measured as the dominant vanadium species in diesel PM emissions.

263 To determine uptake of vanadium species in the biota, we exposed the benthic in

264 h increasing concentrations of two different vanadium species, V(IV) and V(V), for seven days.

265 presence of V(V), V(IV), and an unidentified vanadium species.

266 he V-SCR identified V(2)O(5) as the dominant vanadium species.

267 ocessing, but, with the notable exception of vanadium-tetracyanoethylene, magnetic transition tempera

268 Here, we studied the occurrence of vanadium, the role of molybdenum availability on vanadiu

269 Vanadium, the single most abundant trace metal in bitume

270 1.95) as the cathode, with or without adding vanadium to LSC.

271 The binding of the vanadium to the phosphatases is either as a five-coordin

272 se species with our recently reported set of vanadium tris(dithiolene) complexes.

273 ns that involve multiple oxidation states of vanadium (V(3+), V(4+) and V(5+)).

274 Vanadium (V) is increasingly recognized both as a medica

275 However, marine tests show that vanadium (V) is preferentially extracted over U and many

276 (K), nickel (Ni), sulfur (S), silicon (Si), vanadium (V), and zinc (Zn)) were developed.

277 indirect factor in controlling Se as well as vanadium (V), cobalt (Co), nickel (Ni), zinc (Zn), and a

278 ummary of the global biogeochemical cycle of vanadium (V), including both human-derived and natural f

279 We show that the vanadium (V)- and iron (Fe)-only "alternative" nitrogena

280 The vanadium (V)-nitrogenase of Azotobacter vinelandii catal

281 The molybdenum (Mo)- and vanadium (V)-nitrogenases are two homologous members of

282 Here we report an oxo-vanadium(V) aminotriphenolate complex that was found to

283 ation could enhance the reductive removal of vanadium(V) and inhibit the reoxidation of its reduction

284 mpounds the first structurally characterized vanadium(V) azides.

285 The reactive transport of uranium (U) and vanadium(V) from abandoned mine wastes collected from th

286 Vanadium(V) is an emerging contaminant in the most recen

287 ng growth in the presence of lead carbonate, vanadium(V) oxide and ammonium metavanadate, while abiot

288 Vanadium(V) oxoazide [VO(N3)3] was prepared through a fl

289 n the aquatic environment, but the impact of vanadium(V) speciation on the redox properties remains l

290 tics of four pH- and concentration-dependent vanadium(V) species in the presence and the absence of p

291 With molar ratios of phosphate to vanadium(V) varying from 0 to 1, phosphate accelerated t

292 solated by the reaction of tungstate(VI) and vanadium(V) with triethanolammonium ions (TEAH), acting

293 Two neutral and four-coordinate vanadium(V)-nitrido complexes have been prepared via the

294 ve nitrogenases that are dependent on either vanadium (VFe) or iron only (FeFe) for activity.

295 rve the metabolism of cobalt, manganese, and vanadium, we predict that DMT1 should contribute little

296 os (ORs) for increasing quartiles of urinary vanadium were 1.76 (95% CI 1.05-2.95) for Q2, 3.17 (1.96

297 imony, Cadmium, Chromium, Lead, Selenium and Vanadium were evaluated in cocoa powder and chocolate by

298 equires trigonal bipyramidal geometry of the vanadium when bound to the protein, such geometry can be

299 ging content of the beta stabilizing element vanadium while holding the volume fraction of dendritic

300 sess the association of prenatal exposure to vanadium with the risk of adverse birth outcomes in babi