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 ding on the use of diatomites high or low in vanadium.

8 Similar trends were observed for vanadium.

9 hed, that identify the metallic 1T-phase and vanadium 3d(1) electronic configuration in monolayer VSe

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

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

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

13 y apple juices exhibited significantly lower vanadium amounts than clear apple juices, filter aids us

14 Vanadium, an important pollutant produced from anthropog

15 ter concentrations of other elements such as vanadium and copper.

16 VS(4) is one such promising material, with vanadium and disulfide anions [S(2)](2-) forming one-dim

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

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

19 Alternative vanadium and iron-only nitrogenases that are homologous

20 Vanadium and its surface oxides were studied as a potent

21 Changes in vanadium and manganese were largest and appeared to have

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

23 The strong colocalization of vanadium and P signal intensities demonstrated that vana

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

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

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

27 5 mV s(-1), corresponding to 0.89 charge per vanadium) and excellent cyclability (62.5 mAh g(-1) in f

28 al function (chromium, nickel, tungsten, and vanadium), and 12 with known toxicity (antimony, arsenic

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

30 r, iron, potassium, nickel, sulfur, silicon, vanadium, and zinc) in particulate matter with diameter

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

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

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

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

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

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

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

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

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

40 aper and less environmentally hazardous than vanadium-based batteries, but they have shorter lifetime

41 h other traditionally studied catalysts like vanadium-based catalysts and provides an important piece

42 This system was validated with the study of vanadium-based catalysts during propane oxydehydrogenati

43 te this catalytic system from less selective vanadium-based catalysts.

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

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

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

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

48 with increasing boron chain condensation in vanadium borides: Using a -23 mV overpotential decrement

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 Additionally, insights into heterogeneous vanadium catalysis are provided when parallels can be dr

52 ly hydrolyzed into imides and amides through vanadium catalysis.

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

54 given to mechanistic and kinetics studies of vanadium-catalyzed reactions including oxidations of alk

55 chloride ion to a coordinatively unsaturated vanadium center within a cluster that bears a single oxy

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

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

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

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

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

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

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

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

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

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

66 tions catalyzed by homogeneous and supported vanadium complexes from 2008 to 2018 are summarized and

67 Oxalate-vanadium complexes markedly reduced the vanadinite stabi

68 Vanadium compounds have been reported to have antidiabet

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

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

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

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

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

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

75 As vanadium concentration increases, the saturation magneti

76 The TISF can be manipulated by changing the vanadium concentration.

77 lter aid selection was shown to modulate the vanadium concentrations in clarified beverages.

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

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

80 Ln-vanadium concentrations were linearly associated with th

81 Plasma vanadium concentrations were measured and compared betwe

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

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

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

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

86 Vanadium contamination is a growing environmental hazard

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

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

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

90 The vanadium-dependent chloroperoxidase Mcl24 was discovered

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

92 c analysis of S. japonica revealed that most vanadium-dependent haloperoxidase genes involved in iodi

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

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

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

96 2-diarylhydrazines to the bis(imino)pyridine vanadium dinitrogen complex, [{((iPr)BPDI)V(THF)}2(mu2-N

97 To date, vanadium dioxide (VO(2) ) is the only known simple trans

98 combining hexagonal boron nitride (hBN) and vanadium dioxide (VO(2) ).

99 Vanadium dioxide (VO(2)) features a pronounced, thermall

100 Vanadium dioxide (VO(2)) is one of the most extensively

101 using a multilayered device, comprised of a vanadium dioxide (VO(2)) thin film on a silicon substrat

102 te the infrared emission from a thin film of vanadium dioxide (VO(2)).

103 ential strongly correlated electron compound vanadium dioxide (VO(2)).

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

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

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

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

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

109 Vanadium dioxide (VO2) is an archetypical correlated ele

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

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

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

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

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

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

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

117 , the insulator-to-metal phase transition of vanadium dioxide effectively renders the structure achir

118 Vanadium dioxide exhibits a first-order phase transition

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

120 ng 3D-chiral metallic inclusions and achiral vanadium dioxide inclusions.

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

122 metric transmission at room temperature when vanadium dioxide is in its insulator phase.

123 generator network using capacitively coupled Vanadium Dioxide nano-oscillators.

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

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

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

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

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

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

130 We perform experiments on vanadium dioxide VO(2) films, which exhibit a first-orde

131 ure is based on thin films of tungsten-doped vanadium dioxide where the tungsten fraction is judiciou

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

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

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

135 photoinduced insulator-metal transitions in vanadium dioxide.

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

137 Vanadium displays the highest cradle-to-gate environment

138 The titanium disulfide coated vanadium disulfide cathode exhibits an operating voltage

139 However, vanadium disulfide exhibits poor stability due to large

140 Here we report that vanadium disulfide flakes can be rendered stable in the

141 al dichalcogenides which are semiconductors, vanadium disulfide is metallic and conductive.

142 ess, enabling it to stabilize the underlying vanadium disulfide material.

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

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

145 ed due to the high manufacturing cost of the vanadium electrolyte, which is currently prepared using

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

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

148 Vanadium had the largest odds ratio (for fourth vs. firs

149 Vanadium had the largest odds ratio (for fourth vs. firs

150 Vanadium has previously been linked to elevated toxicity

151 The chemistry of vanadium has seen remarkable activity in the past 50 yea

152 Herein we demonstrate that vanadium(III) acetylacetonate (V(acac)(3) ) is an effici

153 Here, we report the vanadium(III) complex mer-[V(ddpd)(2)][PF(6)](3) yieldin

154 Our comprehensive study demonstrates that vanadium(III) complexes with d(2) electron configuration

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

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

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

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

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

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

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

162 copper, mercury, molybdenum, lead, tin, and vanadium--in relation to young-onset breast cancer (diag

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

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

165 re and high-temperature annealing on lithium-vanadium-iron-phosphate (LiFe(0.75)V(0.10)PO(4)) glass m

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

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

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

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

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

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

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

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

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

175 nductor, VI(3) , which is based on honeycomb vanadium layers separated by an iodine-iodine van der Wa

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

177 of specific filter aids with highly variable vanadium levels in beer, wine, and fruit juices.

178 irst, the previously reported broad range of vanadium levels was confirmed in 68 commercial beverages

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

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

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

182 ecting the composition and morphology of the vanadium membrane.

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

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

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

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

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

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

189 Vanadium, nickel, and arsenic increased with time on dia

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

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

192 Vanadium, nickel, cadmium, and tin were increased in pre

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

194 Although salts of such metals as vanadium, niobium, cerium, and manganese were found to f

195 ater CO Faradaic efficiency than Pd-modified vanadium nitride (Pd/VN) and commercial Pd/C catalysts.

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

197 Here, we elucidate the contribution of vanadium nitrogenase (V-Nase) to BNF by cyanolichens acr

198 Recent work indicates that vanadium nitrogenase may play a role in the global biolo

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

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

201 Molybdenum and vanadium nitrogenases are capable of converting carbon m

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

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

204 ey have a different transition metal, either vanadium or iron, at their active sites.

205 Nanolayers of iron, vanadium, or nickel, 10 to 30 nm thin, produce open-circ

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

207 ains disordered on cycling while its average vanadium oxidation state varies from 3 to 4.5.

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

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

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

211 serve as a molecular model for halogen-doped vanadium oxide (VO(2)) materials that have recently attr

212 m temperature of 68-70 degrees C as shown by vanadium oxide (VO(2)), compared with other transition m

213 odoping that has recently been described for vanadium oxide (VO(2)).

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

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

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

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

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

219 The vanadium oxide nanosheets engaged by structural water ac

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

221 the highly disordered potassium-intercalated vanadium oxide nanosheets.

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

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

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

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

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

227 Generation of the oxygen-deficient vanadium oxide, [V(6)O(6)(OC(2)H(5))(12)](1-), was confi

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

229 loride-substituted variants of the Lindqvist vanadium-oxide cluster were obtained via two distinct ch

230 Here we report that orthorhombic vanadium oxides (V(2) O(5) ) supports highly reversible

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

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

233 strictive magnetic metal has been shown with vanadium oxides and our findings here prove that this me

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

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

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

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

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

239 n substantial and highly variable amounts of vanadium, particularly in all analyzed diatomite (38-368

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

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

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

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

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

245 cularly in all analyzed diatomite (38-368 mg vanadium per kg filter aid), but not in perlite products

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

247 The sodium vanadium phosphate/sodium full cells with composite elec

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

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

250 dium contamination, and novel approaches for vanadium recovery.

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

252 (ESS): lithium iron phosphate (LFP) battery, vanadium redox flow battery (VRFB), and liquid air energ

253 The vanadium redox flow battery is considered one of the mos

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

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

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

257 thesis of two closely related metastable tin vanadium selenides via near-diffusionless reactions at l

258 utcomes for the crystallization of templated vanadium selenites.

259 he role of different oxygen species bound to vanadium sites.

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

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

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

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

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

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

266 zation increases, which is optimal at ~4 at% vanadium; the highest doping level ever achieved for V-d

267 filtration experiments (170 L/batch) proved vanadium to be released from diatomite (Kieselguhr), inc

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

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

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

271 ixation is catalyzed by the molybdenum (Mo), vanadium (V) and iron (Fe)-only nitrogenase metalloenzym

272 Vanadium (V) and iron-only Nases have been suggested as

273 e capacity even in the presence of competing vanadium (V) ions in aqueous medium.

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

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

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

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

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

281 oom temperature with a molecular catalyst of vanadium (V)-oxo dimer.

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

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

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

296 sols, while others (e.g., cadmium, titanium, vanadium) were rarely found.

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

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

299 vely associated with achieved hemoglobin and vanadium while positively associated with arsenic.

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