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1 ntain metal ions including silver, iron, and chromium.
2 omium intake exceeding our estimated ADI for chromium.
3 nmental availability of toxic metals such as chromium.
4 xicology Program: a case study on hexavalent chromium.
5 he role of welding-related exposures such as chromium.
6 elium due to the antiferromagnetic nature of chromium.
7 , undergoing oxidation/reduction rather than chromium.
8 tri- or tetramerization in combination with chromium.
9 ricarbonyl(1-chloro-2-deuteriomethylbenzene) chromium(0) was computed, showing that reasonable predic
10 ine concentrations, and results for GFR from chromium-51 ((51)Cr) EDTA excretion measurements ((51)Cr
12 gnetism by hydrostatic pressure in elemental chromium, a simple cubic metal that demonstrates a subtl
13 Here we describe electrical measurements on chromium--a simple metal and quintessential spin density
14 r structures composed of iron, titanium, and chromium accounting for the magnetic properties of these
17 is a novel thin-strut (81 microm), platinum chromium alloy PES designed to improve radial strength,
23 ains elevated pseudo-total concentrations of chromium and nickel, this soil is not a significant sour
24 ications; and steel alloying elements (e.g., chromium and niobium) as well as elements used in high-t
27 r aerobic conditions, the levels of arsenic, chromium, and boron in leachate decreased up to 96%, 49%
28 ching of metals/metalloids (arsenic, copper, chromium, and boron) from treated wood in aged mature co
29 n to lead, metals such as aluminum, cadmium, chromium, and manganese require further investigation.
31 of redox-active substances, such as arsenic, chromium, and pharmaceutical products, through oxidation
34 tu formed tricarbonyl(eta(6)-2-methylindenyl)chromium anion with a series of Pd and Pt metallacycles
35 character of the tricarbonyl(eta(6)-indenyl)chromium anion, of which the main property is to behave
37 our-electron oxidative addition of O2 to one chromium atom, which involves a spin-forbidden transform
40 c oxidations, this oxidation is catalytic in chromium because oxygen, not the chromium reagent, is th
42 on center (CGC(Et)Ti) covalently linked to a chromium bis(thioether)amine ethylene trimerization cent
43 se, iron, copper and zinc) and heavy metals (chromium, cadmium, lead and nickel) were determined in v
44 on between non-heteroatom-stabilized alkynyl chromium carbene complexes prepared in situ and furfural
45 a the macrocyclization of a chlorovinylidene chromium carbenoid onto a pendant aldehyde to generate t
46 n the metal matrix with in-situ formation of chromium carbide (Cr7C3) at the CNT/copper (Cu) interfac
47 l for a persistent, if not perpetual, deadly chromium carcinogenic cycle exists in the cellular milie
48 discovery of an easily accessible bimetallic chromium catalyst is reported for this transformation.
55 e established several systems based on zinc, chromium, cobalt, and aluminum catalysts for the ring-op
56 terpene-based cyclic anhydrides catalyzed by chromium, cobalt, and aluminum salen complexes is report
57 y occurring trace metals, including arsenic, chromium, cobalt, nickel, and lead, likely due to the mi
60 present a rare class of mononuclear, neutral chromium complexes with a three-coordinate high-spin chr
61 As one of the world's leading producers of chromium compounds, the U.S. is facing growing challenge
62 t weight with a mean of 15.9 +/- 3.5 ppm and chromium concentrations ranged from 2.0 to 73.6 ppm wet
65 ntents of aluminium, barium, boron, calcium, chromium, copper, iron, magnesium, manganese, nickel, ph
66 on-metal-arene complexes such as bis(benzene)chromium Cr(eta(6)-C(6)H(6))(2) are historically importa
68 al chromate (Cr2O7(2-)) anions consisting of chromium Cr(VI) was used as a model environmental stress
70 ort for the first time the use of hexavalent chromium (Cr(VI)) as an electrocatalyst in electrochemic
74 the reduction of the highly toxic hexavalent chromium (Cr(VI)) were investigated using Shewanella one
75 damage response (DDR) induced by hexavalent chromium (Cr(VI)), but the molecular mechanism remains u
77 uding Lead (Pb), Mercury (Hg), Arsenic (As), Chromium (Cr) and Cadmium (Cd) are considered to be high
79 permanent modifiers, has been developed for chromium (Cr) determination in food of plant origin by t
80 The behavior of metal contaminants such as chromium (Cr) during struvite precipitation, however, re
85 ting the aquatic and human health impacts of chromium (Cr) necessitates one to determine its speciati
86 icrobial activities on the transformation of chromium (Cr) remediation products has generally been ov
87 ese (Mn), iron (Fe), copper (Cu), zinc (Zn), chromium (Cr)) and heavy metals (cadmium (Cd), lead (Pb)
88 tion of naturally occurring As, cobalt (Co), chromium (Cr), and nickel (Ni) from wetland sediments ca
90 , arsenic (As), lead (Pb), cadmium (Cd), and chromium (Cr), from primary anthropogenic sources in Chi
92 d in the depletion of some elements [such as chromium (Cr)] in the bulk silicate Earth relative to ch
107 was applied to chromium speciation and total chromium determination in real samples and gave recoveri
110 with all DES compared with BMS, with cobalt-chromium EES, platinum chromium-EES, SES, and BES also h
111 with BMS, with cobalt-chromium EES, platinum chromium-EES, SES, and BES also having lower target-vess
112 fidic seafloor and that the record of Mo and chromium enrichments through time is consistent with the
114 (PtCr-EES) compared with a predicate cobalt chromium everolimus-eluting stent (CoCr-EES) in patients
115 monstrated that the second-generation cobalt-chromium everolimus-eluting stent (CoCr-EES) is superior
116 the thin-strut, fluoropolymer-coated cobalt-chromium everolimus-eluting stent (CoCr-EES) may be asso
117 ing Absorb BVS (n=2164) or the Xience cobalt-chromium everolimus-eluting stent (CoCr-EES; n=1225).
118 the clinical outcomes with a novel platinum chromium everolimus-eluting stent (PtCr-EES) compared wi
121 discontinuation before 30 days after cobalt chromium everolimus-eluting stent implantation was stron
123 umerically excess stroke and PCI with cobalt-chromium everolimus-eluting stent with numerically incre
125 al studies have in fact reported that cobalt-chromium everolimus-eluting stents (CoCr-EES) coated wit
127 At a median follow-up of 3.8 years, cobalt-chromium everolimus-eluting stents (EES) were associated
129 ention (PCI) with fluoropolymer-based cobalt-chromium everolimus-eluting stents (PCI group, 948 patie
130 ruption is safe in patients receiving cobalt chromium everolimus-eluting stents remains controversial
134 olution-growth of ZnO nanowires using a thin chromium film as a nucleation inhibitor and Au size-sele
136 antitatively extract all forms of hexavalent chromium from the standard reference materials (SRM) can
137 the 3sigma line-edge roughness of 70-nm-wide chromium grating lines from 8.4 nm to less than 1.5 nm,
139 II) solids of environmental relevance, i.e., chromium hydroxide Cr(OH)3(s), chromium oxide Cr2O3(s),
140 MFCs were examined at three types of shocks (chromium, hypochlorite and acetate) in a batch-mode cham
141 ) method for the determination of hexavalent chromium i.e. Cr(VI) in food samples is established with
144 molecular analog of SnO) and binary dimeric chromium(II) bis(mu2,kappa(2),kappa(2)) derivative [Cr2(
147 ern half based on nerol and acetoacetate and chromium(II)-mediated Reformatsky reactions as a powerfu
149 rhenium(I)-based charge-transfer state to a chromium(III) acceptor can be fully accounted for by For
150 electronically conductive solid solution of chromium(iii) and aluminium oxides in the corundum struc
151 The optimized constant for the monomeric chromium(III) complex was in between those of the iron(I
153 roughput methodology was employed to produce chromium(III) complexes suitable for the surface modific
154 the coordination chemistry and stability of chromium(III) complexes with natural organic matter (NOM
160 didate, [Cr(OH)6](3-), which was formed from chromium(III) perchlorate and pH adjusted with ethylened
166 S results showed a predominance of monomeric chromium(III)-NOM complexes at low pH (<5), in which onl
176 ly use of 10 products tested would result in chromium intake exceeding our estimated ADI for chromium
187 action between aquaethylenediaminebis(peroxo)chromium(IV) and glutathione at neutral pH exhibits a cy
189 pproach involves deposition of an additional chromium layer (superlayer) onto a bonded system, where
190 iciencies for five metals (arsenic, cadmium, chromium, lead and nickel) were compared under varying c
191 ion batteries, the leached concentrations of chromium, lead, and thallium exceeded the California reg
194 oncentrations of Arsenic, Antimony, Cadmium, Chromium, Lead, Selenium and Vanadium were evaluated in
196 e highest to the lowest quartiles of toenail chromium levels was 0.80 (0.66-0.98; Plinear trend = 0.0
199 ments (selenium, molybdenum, cobalt, copper, chromium, manganese) and eight non-essential, potentiall
205 tals, termed M-Pt3Ni/C, where M is vanadium, chromium, manganese, iron, cobalt, molybdenum (Mo), tung
208 alyzed with regard to heavy metals (cadmium, chromium, mercury, and lead) and flame retardants (Penta
209 lements (aluminium, cadmium, cobalt, copper, chromium, mercury, manganese, molybdenum, nickel, lead a
210 in (20 muM) and the heme oxygenase inhibitor chromium mesoporphyrin IX (CrMP, 5 muM) abolished the tr
212 oach where chlorinated analytes reacted with chromium metal to form H(2) and minor amounts of HCl.
213 lost from the taper junction between Cobalt-Chromium-Molybdenum (CoCrMo) and Titanium (Ti) component
214 s and early failures of some types of Cobalt-Chromium-Molybdenum alloy containing artificial hip impl
217 sm is attributed to atomic-scale disorder in chromium nanoparticles, leading to abundant unbalanced s
218 of some heavy metals such as cadmium, lead, chromium, nickel and cobalt in domestic cultivated and i
221 he fate of (in)organic contaminants, such as chromium or arsenic, and nitroaromatic compounds functio
222 eagents (based around toxic elements such as chromium or selenium) or expensive catalysts (such as pa
224 rive fundamental insights into mechanisms of chromium oxidation during combustion of solid fuels.
225 conductive CrOx bridges across a thin native chromium oxide barrier between the nanodots and an under
226 evance, i.e., chromium hydroxide Cr(OH)3(s), chromium oxide Cr2O3(s), and copper chromite Cu2Cr2O5(s)
227 e previously reported that the micronutrient chromium picolinate (CrP), with long-standing cardiovasc
229 pends on the long-term potential for reduced chromium precipitates to remain immobilized under oxidiz
233 Under oxidizing conditions, immobilized chromium reduced under predominantly denitrifying condit
234 In vitro lymphocyte proliferation assays, chromium-release assays, and development of antibodies w
235 nd chemical sequestration of N, Cl, and S by chromium result in quantitative conversion of compound-s
238 agent and polymer but with a novel platinum chromium scaffold designed for enhanced deliverability,
239 nding metal complexes, as exemplified by the chromium series, and the effect of the metal appears to
240 r drug-eluting stents: the thin-strut cobalt-chromium sirolimus-eluting Orsiro stent and the stainles
242 h is explained in terms of the occurrence of chromium/sodium vacancy antisite during desodiation and
246 novel method was developed by SAE-DLLME for chromium speciation in water and rice samples using 2-th
247 results challenge the old vision of "naked" chromium species (i.e., low coordinated) as the active s
250 s compared with an everolimus-eluting cobalt-chromium stent, was within the prespecified margin for n
252 It was discovered that the sulfur in sodium chromium sulfide is electrochemically active, undergoing
254 y, which was not observed for the nickel and chromium surfaces, indicating a titanium-specific biolog
255 ncipally M(2)delta to benzoate pi* with some chromium t(2g) participation, according to calculations
256 he safety and efficacy of the novel platinum chromium TAXUS Element paclitaxel-eluting stent (PES) co
257 ess in NaCrS2 where it is sulfur rather than chromium that works as the electrochemical active specie
261 ase features are analyzed for catalysts from chromium to gold for ionic hydrogenations, bifunctional
262 ed the ability to reduce the amount of toxic chromium to levels within the range of the EPA contamina
263 n of 3 pKa units for complexes of the metals chromium to nickel, molybdenum, ruthenium to palladium,
265 e differing redox behavior of molybdenum and chromium to provide constraints on seafloor redox evolut
266 radionuclides and metals such as uranium and chromium to sparingly soluble and less toxic forms.
267 is review paper has outlined the overview of chromium toxicity, conventional analytical techniques al
268 metabolic behavior was investigated for two chromium tricarbonyl derivatives of the antischistosomal
269 sensing using a novel Raman reporter, arene chromium tricarbonyl linked aminothiophenol (Cr(CO)3-ATP
271 ect microscopy to demonstrate that monolayer chromium triiodide (CrI3) is an Ising ferromagnet with o
272 hich NO is oxidized quantitatively to NO2 by chromium trioxide (CrO3), before conversion to NO2(-) an
274 2) (1) reacts rapidly with dioxygen to yield chromium(V) dioxo species (i-Pr2Ph)2nacnacCr(O)2 (2).
280 uction for practical applications where both chromium (VI) cations and organic dyes are the main poll
281 id, which is able to effectively remove both chromium (VI) cations and organic pollutants simultaneou
294 ts estimated for arsenic, lead, mercury, and chromium were 8, 14, 20, and 150 mug/g, respectively.
295 ,beta-unsaturated Fischer carbene complex of chromium with a propargyl ether bearing an alkenyl group
297 ude use of lasers, most recently the erbium, chromium:yttrium-scandium-gallium-garnet (Er,Cr:YSGG) la
299 ed outflow concentrations of iron, aluminum, chromium, zinc, and lead, likely due to leaching and mob
300 bon (EC) and nine trace elements: potassium, chromium, zinc, iron, titanium, arsenic, calcium, mangan
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